Aspartyl protease inhibitors

Description of equivalent WO 03106405 A1

ASPARTYL PROTEASE INHIBITORS

PRIORITY CLAIM [0001] The present application claims priority to co-pending applications

U.S.S.N. 60/430,693, filed December 3, 2002, and U.S.S.N. 60/389,194, filed June 17, 2002; the entire contents of each of these applications are incorporated herein by reference.

BACKGROUND OF THE INVENTION [0002] Alzheimer's Disease is a progressive dementia in which massive deposits of aggregated protein breakdown products (β-amyloid plaques and neurofibrillary tangles) accumulate in the brain, resulting in the loss of memory, cognition, reasoning, judgement, orientation, and eventually death. Current therapies for the treatment of Alzheimer's Disease include, but are not limited to, donepezil and tacrine. These therapies are useful for improving the memory of patients during the early stages of Alzheimer's Disease, however they do not modify the progression of aggregated protein breakdown products underlying the pathology of Alzheimer's Disease. It would be desirable to develop therapies that would either stop or slow down this process of aggregation.

[0003] As described above, a defining feature of Alzheimer's Disease which is often used during clinical diagnosis is the presence of β-amyloid plaques and neurofibrillary tangles, β-amyloid plaques are predominantly composed of amyloid β peptide (Aβ (or βA4), which is derived by proteolysis of the amyloid precursor protein (APP). Proteolysis of the amyloid precursor protein is effected by several enzymes called secretases. More specifically, cleavage of APP at the N-terminus of the Aβ peptide by β-secretase and at the C-terminus by one or more γ-secretases constitutes the β-amyloido genie pathway, i.e., the pathway by which Aβ is formed. It is believed that Aβ peptide accumulates as a result of this APP processing by β- secretase and thus inhibition of this enzyme's activity is desirable for the treatment of Alzheimer's Disease. For example, in vivo processing of APP at the β-secretase cleavage site is thought to be a rate limiting step in Aβ production, and is thus believed to be a therapeutic target for Alzheimer's Disease (Sabbagh et al. Alz. Dis. Rev. 1997, 3, 1-19). Recently, an aspartyl protease (known as BACE, Asp2, Me apsin) has been identified as the enzyme responsible for processing of APP at the β-secretase cleavage site (see, for example, Nassar, et al. Science, 1999, 286, 735- 741; Nan et al. Nature, 1999, 402, 533-537; Sinha et al. Nature, 1999, 402, 537-540; and Hussain et al. Mol. Cell. Neurosci.1999, 14, 419-427).

[0004] Because it is believed that BACE plays an important role in the development and patho genesis of Alzheimer's Disease, there has been increasing interest in the development of inhibitors of BACE as treatments (and possibly as preventative agents) for Alzheimer's Disease and other disorders caused by the accumulation of β-amyloid plaques. There remains a need, however, for the development of novel therapeutics capable of inhibiting the activity of this aspartyl protease. In particular, it would be desirable to develop therapeutics capable of selectively inhibiting BACE.

SUMMARY OF THE INVENTION [0005] As discussed above, there remains a need for the development of novel therapeutic agents and agents useful for treating disorders mediated by aspartyl proteases. The present invention provides novel compounds of general formula (I).

<img file="WO03106405A1_D0001.tif" />

(I) and pharmaceutical compositions thereof, as described generally and in subclasses herein, which compounds are useful as inhibitors of aspartyl proteases, and thus are useful, for example, for the treatment of Alzheimer's Disease. In certain embodiments, the invention provides pharmaceutical compositions comprising an inventive compound, wherein the compound is present in an amount effective to inhibit β-secretase activity. In certain other embodiments, the invention provides pharmaceutical compositions comprising an inventive compound and optionally further comprising an additional therapeutic agent. In yet other embodiments, the additional therapeutic agent is an agent for the treatment of Alzheimer's Disease. [0006] In yet another aspect, the present invention provides methods for inhibiting β-secretase activity in a patient or a biological sample, comprising administering to said patient, or contacting said biological sample with an effective inhibitory amount of a compound of the invention, h still another aspect, the present invention provides methods for treating any disorder involving β-secretase activity, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of the invention. In certain other embodiments, the invention provides a method for treating or preventing a disease characterized by β-amyloid deposits in the brain comprising administering to a patient a therapeutically effective amount of a compound of the invention.

[0007] In yet another aspect, the present invention provides methods for preparing compounds of the invention. In certain embodiments, the invention provides a method for synthesizing a compound having the structure:

<img file="WO03106405A1_D0002.tif" /> cn and pharmaceutically acceptable derivatives thereof; wherein R', R -R , R³', and X^!-X³ are defined in classes and subclasses herein; which method comprises steps of: i) providing a compound having the structure:

<img file="WO03106405A1_D0003.tif" /> wherein R', R², R³, R³ and X² are as defined above,

R^Pl is a nitrogen protecting group;

A is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=O)-, -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR⁵-, -C(=S)NR⁵-, -COO-, -(CHR⁵)_r, -O-, -CH₂NR⁵- or -NR⁵-, wherein each occurrence of R⁵ is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or - (heteroalkyl)heteroaryl moiety, and k is an integer from 1 to 3; and

B is a protecting group, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety, or is -VR^C, wherein V is -O-, -NR^D-, - C(=O)-, -S(=O)- or -SO₂-, wherein each occurrence of R and R is independently hydrogen, a protecting group or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety; ii) reacting the compound of step (i) under suitable conditions to generate a compound having the structure: <img file="WO03106405A1_D0004.tif" /> wherein U is -NHR^P2 or -N₃, wherein R^P2 is a nitrogen protecting group; iii) reacting the compound of step (ii) with suitable reagents to generate a compound having the structure:

<img file="WO03106405A1_D0005.tif" /> iv) reacting the compound of step (iii) with suitable reagents to generate the free amine having the structure :

<img file="WO03106405A1_D0006.tif" /> (I )

[0008] In certain embodiments, the method comprises synthesizing a compound having the following stereochemistry:

<img file="WO03106405A1_D0007.tif" /> (F^A).

[0009] In certain embodiments, the invention provides a method for synthesizing a compound having the structure:

<img file="WO03106405A1_D0008.tif" />

(I^") and pharmaceutically acceptable derivatives thereof; wherein R', R^R⁴, R³',

1 ^ and X -X are defined in classes and subclasses herein; which method comprises steps of: i) providing a compound having the structure:

H OH

R^p1"^Nγ ^{x B}

R² R³ wherein R², R³, and X² are as defined above,

R^P1 is a nitrogen protecting group;

A is absent, -MHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=0 , -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR⁵-, -C(=S)NR⁵-, -COO-, -(CHR⁵)_r, -O-, -CH₂NR⁵- or -NR⁵-, wherein each occurrence of R⁵ is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or - (heteroalkyl)heteroaryl moiety, and k is an integer from 1 to 3; and

B is a protecting group, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety, or is -VR^C, wherein V is -O-, -NR^D-, - C(=O)-, -S(=O)- or -SO₂-, wherein each occurrence of R and R is independently hydrogen, a protecting group or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety; ii) reacting the compound of step (i) under suitable conditions to generate a compound having the structure:

<img file="WO03106405A1_D0009.tif" /> wherein U is -NHR^P2 or -N₃, wherein R^p2 is a nitrogen protecting group; iii) reacting the compound of step (ii) with suitable reagents to generate a compound having the structure:

<img file="WO03106405A1_D0010.tif" /> iv) reacting the compound of step (iii) with suitable reagents to generate the free amine having the structure :

<img file="WO03106405A1_D0011.tif" /> (I^")

[0010] In certain embodiments, the method comprises synthesizing a compound having the following stereochemistry: <img file="WO03106405A1_D0012.tif" /> (F'^A).

BRIEF DESCRIPTION OF THE DRAWING [0011] Figure IA depicts a plasma concentration curve for an exemplary inventive compound.

[0012] Figure IB depicts a brain concentration curve for an exemplary inventive compound.

DEFINITIONS [0013] Certain compounds of the present invention, and definitions of specific functional groups are described in more detail below. For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75ⁿ Ed., inside cover, and specific functional groups are generally defined as described therein. Additionally, general principles of organic chemistry, as well as specific functional moieties and reactivity, are described in "Organic Chemistry", Thomas Sorrell, University Science Books, Sausalito: 1999, the entire contents of which are incorporated herein by reference. Furthermore, it will be appreciated by one of ordinary skill in the art that the synthetic methods, as described herein, utilize a variety of protecting groups. By the term "protecting group", has used herein, it is meant that a particular functional moiety, e.g., O, S, or N, is temporarily blocked so that a reaction can be carried out selectively at another reactive site in a multifunctional compound, hi preferred embodiments, a protecting group reacts selectively in good yield to give a protected substrate that is stable to the projected reactions; the protecting group must be selectively removed in good yield by readily available, preferably nontoxic reagents that do not attack the other functional groups; the protecting group may form an easily separable derivative (more preferably without the generation of new stereogenic centers); and the protecting group has a minimum of additional functionality to avoid further sites of reaction. As detailed herein, oxygen, sulfur, nitrogen and carbon protecting groups may be utilized. For example, in certain embodiments, as detailed herein, certain exemplary oxygen protecting groups are utilized. These oxygen protecting groups include, but are not limited to methyl ethers, substituted methyl ethers (e.g., MOM (methoxymethyl ether), MTM (methylthiomethyl ether), BOM (benzyloxymethyl ether), PMBM (p- methoxybenzyloxymethyl ether), to name a few), substituted ethyl ethers, substituted benzyl ethers, silyl ethers (e.g., TMS (trimethylsilyl ether), TES (triethylsilylether), TIPS (triisopropylsilyl ether), TBDMS (t-butyldimethylsilyl ether), tribenzyl silyl ether, TBDPS (t-butyldiphenyl silyl ether), to name a few), esters (e.g., formate, acetate, benzoate (Bz), trifluoroacetate, dichloroacetate, to name a few), carbonates, cyclic acetals and ketals. In certain other exemplary embodiments, nitrogen protecting groups are utilized. These nitrogen protecting groups include, but are not limited to, carbamates (including methyl, ethyl and substituted ethyl carbamates (e.g., Troc), to name a few) amides, cyclic imide derivatives, N-Alkyl and N-Aryl amines, imine derivatives, and enamine derivatives, to name a few. Certain other exemplary protecting groups are detailed herein, however, it will be appreciated that the present invention is not intended to be limited to these protecting groups; rather, a variety of additional equivalent protecting groups can be readily identified using the above criteria and utilized in the present invention. Additionally, a variety of protecting groups are described in "Protective Groups in Organic Synthesis" Third Ed. Greene, T.W. and Wuts, P.G., Eds., John Wiley &amp; Sons, New York: 1999, the entire contents of which are hereby incorporated by reference

[0014] It will be appreciated that the compounds, as described herein, may be substituted with any number of substituents or functional moieties. In general, the term "substituted" whether preceded by the term "optionally" or not, and substituents contained in formulas of this invention, refer to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent. When more than one position in any given structure may be substituted with more than one substituent selected from a specified group, the substituent may be either the same or different at every position. As used herein, the term "substituted" is contemplated to include all permissible substituents of organic compounds, hi a broad aspect, the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and non-aromatic substituents of organic compounds. For purposes of this invention, heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valencies of the heteroatoms. Furthermore, this invention is not intended to be limited in any manner by the permissible substituents of organic compounds. Combinations of substituents and variables envisioned by this invention are preferably those that result in the formation of stable compounds useful in the treatment and prevention, for example of disorders, as described generally above. The term "stable", as used herein, preferably refers to compounds which possess stability sufficient to allow manufacture and which maintain the integrity of the compound for a sufficient period of time to be detected and preferably for a sufficient period of time to be useful for the purposes detailed herein.

[0015] The term "aliphatic", as used herein, includes both saturated and unsaturated, straight chain (i.e., unbranched), branched, cyclic, or polycyclic aliphatic hydrocarbons, which are optionally substituted with one or more functional groups. As will be appreciated by one of ordinary skill in the art, "aliphatic" is intended herein to include, but is not limited to, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and cycloalkynyl moieties. Thus, as used herein, the term "alkyl" includes straight, branched and cyclic alkyl groups. An analogous convention applies to other generic terms such as "alkenyl", "alkynyl" and the like. Furthermore, as used herein, the terms "alkyl", "alkenyl", "alkynyl" and the like encompass both substituted and unsubstituted groups. In certain embodiments, as used herein, "lower alkyl" is used to indicate those alkyl groups (cyclic, acyclic, substituted, unsubstituted, branched or unbranched) having 1-6 carbon atoms.

[0016] In certain embodiments, the alkyl, alkenyl and alkynyl groups employed in the invention contain 1-20 aliphatic carbon atoms, certain other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-4 carbon atoms. Illustrative aliphatic groups thus include, but are not limited to, for example, methyl, ethyl, n- propyl, isopropyl, cyclopropyl, -CH₂-cyclopropyl, allyl, n-butyl, sec-butyl, isobutyl, tert-butyl, cyclobutyl, -CH₂-cyclobutyl, n-pentyl, sec-pentyl, isopentyl, tert-pentyl, cyclopentyl, -CH -cyclopentyl-n, hexyl, sec-hexyl, cyclohexyl, -CH -cyclohexyl moieties and the like, which again, may bear one or more substituents. Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, 1- methyl-2-buten-l-yl, and the like. Representative alkynyl groups include, but are not limited to, ethynyl, 2-propynyl (propargyl), 1-propynyl and the like. [0017] The term "alkoxy" (or "alkyloxy"), or "thioalkyl" as used herein refers to an alkyl group, as previously defined, attached to the parent molecular moiety through an oxygen atom or through a sulfur atom. In certain embodiments, the alkyl group contains 1-20 aliphatic carbon atoms. In certain other embodiments, the alkyl group contains 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the alkyl group contains 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl group contains 1-4 aliphatic carbon atoms. Examples of alkoxy, include but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, n- butoxy, tert-butoxy, neopentoxy and n-hexoxy. Examples of thioalkyl include, but are not limited to, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, and the like.

[0018] The term "alkylamino" refers to a group having the structure - NHR'wherein R' is allcyl, as defined herein. The term "dialkylamino" refers to a group having the structure -N(R')₂, wherein R' is alkyl, as defined herein. The term "aminoalkyl" refers to a group having the structure NH R'-, wherein R' is alkyl, as defined herein. In certain embodiments, the alkyl group contains 1-20 aliphatic carbon atoms, hi certain other embodiments, the alkyl group contains 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the alkyl group contains 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl group contains 1-4 aliphatic carbon atoms. Examples of alkylamino include, but are not limited to, methylamino, ethylamino, iso-propylamino and the like.

[0019] Some examples of substituents of the above-described aliphatic (and other) moieties of compounds of the invention include, but are not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; alkylaryl; alkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI; Br; I; -OH; -NO₂; -CN; -CF₃; -CH₂CF₃; -CHC1₂; -CH₂OH; -CH₂CH₂OH; - CH₂NH₂; -CH₂SO₂CH₃; -C(O)R_x; -C0₂(R_x); -CON(R_x)₂; -OC(O)R_x; -OCO₂R_x; - OCON(R_x)₂; -N(R_X)₂; -S(O)R_x; -S(O)₂R_x; -NR_x(CO)R_x wherein each occurrence of R_x independently includes, but is not limited to, aliphatic, heteroaliphatic, aryl, heteroaryl, alkylaryl, or alkylheteroaryl, wherein any of the aliphatic, heteroaliphatic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl substituents described above and herein may be substituted or unsubstituted. Additional examples of generally applicable substituents are illustrated by the specific embodiments shown in the Examples that are described herein.

[0020] hi general, the terms "aromatic moiety" and "heteroaromatic moiety", as used herein, refer to stable mono- or polycyclic, heterocyclic, polycyclic, and polyheterocyclic unsaturated moieties having preferably 3-14 carbon atoms, each of which may be substituted or unsubstituted. It will also be appreciated that aromatic and heteroaromatic moieties, as defined herein may be attached via an alkyl or heteroalkyl moiety and thus also include -(alkyl)aromatic, -(heteroalkyl)aromatic, - (heteroalkyl)heteroaromatic, and -(heteroalkyl)heteroaromatic moieties. Thus, as used herein, the phrases "aromatic or heteroaromatic moieties" and "aromatic, heteroaromatic, -(alkyl)aromatic, -(heteroalkyl)aromatic,

(heteroalkyl)heteroaromatic, and -(heteroalkyl)heteroaromatic" are interchangeable. Substituents include, but are not limited to, any of the previously mentioned substituents, i.e., the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound. [0021] The term "aryl", as used herein, does not differ significantly from the common meaning of the term in the art, and refers to a mono- or bicyclic carbocyclic ring system having one or two aromatic rings including, but not limited to, phenyl, naphthyl, tetrahydronaphthyl, indanyl, indenyl and the like.

[0022] The term "heteroaryl", as used herein, does not differ significantly from the common meaning of the term in the art, and refers to a cyclic aromatic radical having from five to ten ring atoms of which one ring atom is selected from S, O and N; zero, one or two ring atoms are additional heteroatoms independently selected from S, O and N; and the remaining ring atoms are carbon, the radical being joined to the rest of the molecule via any of the ring atoms, such as, for example, pyridyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, and the like. [0023] It will be appreciated that aryl and heteroaryl groups (including bicyclic aryl groups) can be unsubstituted or substituted, wherein substitution includes replacement of one or more of the hydrogen atoms thereon independently with any one or more of the following moieties including, but not limited to: aliphatic; heteroaliphatic; aryl; heteroaryl; alkylaryl; alkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI; Br; I; -OH; -NO₂; -CN; -CF₃; -CH₂CF₃; -CHC1₂; -CH₂OH; -CH₂CH₂OH; - CH₂NH₂; -CH₂SO₂CH₃; -C(O)R_x; -CO₂(R_x); -CON(R_x)₂; -OC(0)R_x; -OCO₂R_x; - OCON(R_x)₂; -N(R_X)₂; -S(O)R_x; -S(O)₂R_x; -NR_x(CO)R_x wherein each occurrence of R_x independently includes, but is not limited to, aliphatic, heteroaliphatic, aryl, heteroaryl, alkylaryl, or alkylheteroaryl, wherein any of the aliphatic, heteroaliphatic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl substituents described above and herein may be substituted or unsubstituted. Additionally, it will be appreciated, that any two adjacent groups taken together may represent a 4, 5, 6, or 7- membered cyclic, substituted or unsubstituted aliphatic or heteroaliphatic moiety. Additional examples of generally applicable substituents are illustrated by the specific embodiments shown in the Examples that are described herein. [0024] The term "cycloalkyl", as used herein, refers specifically to cyclic moieties having three to seven, preferably three to ten carbon atoms. Suitable cycloalkyls include, but are not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like, which, as in the case of other aliphatic, heteroaliphatic or heterocyclic moieties, may optionally be substituted with substituents including, but not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; alkylaryl; alkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI; Br; I; -OH; -NO₂; -CN; -CF₃; -CH₂CF₃; -CHC1₂; -CH₂OH; - CH₂CH₂OH; -CH₂NH₂; -CH₂SO₂CH₃; -C(O)R_x; -CO₂(R_x); -CON(R_x)₂; -OC(O)R_x; - OCO₂R_x; -OCON(R_x)₂; -N(R_X)₂; -S(O)R_x; -S(0)₂R_x; -NR_x(CO)R_x wherein each occurrence of R_x independently includes, but is not limited to, aliphatic, heteroaliphatic, aryl, heteroaryl, alkylaryl, or alkyllieteroaryl, wherein any of the aliphatic, heteroaliphatic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl substituents described above and herein may be substituted or unsubstituted. Additionally, it will be appreciated that any of the cycloahphatic or cycloheteroaliphatic moieties described above and herein may comprise an aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl moiety fused thereto. Additional examples of generally applicable substituents are illustrated by the specific embodiments shown in the Examples that are described herein. [0025] The term "heteroaliphatic", as used herein, refers to aliphatic moieties in which one or more carbon atoms in the main chain have been substituted with a heteroatom. Thus, a heteroaliphatic group refers to an aliphatic chain which contains one or more oxygen sulfur, nitrogen, phosphorus or silicon atoms, e.g., in place of carbon atoms. Heteroaliphatic moieties may be branched, unbranched, cyclic or acyclic and include saturated and unsaturated heterocycles such as morpholino, pyrrolidinyl, etc. In certain embodiments, heteroaliphatic moieties are substituted by independent replacement of one or more of the hydrogen atoms thereon with one or more moieties including, but not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; alkylaryl; alkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI; Br; I; -OH; -NO ; -CN; -CF₃; - CH₂CF₃; -CHC1₂; -CH₂OH; -CH₂CH₂OH; -CH₂NH₂; -CH₂SO₂CH₃; -C(O)R_x; - C0₂(R_x); -CON(R_x)₂; -OC(O)R_x; -OCO₂R_x; -OCON(R_x)₂; -N(R_X)₂; -S(O)R_x; - S(O)₂R_x; -NR_x(CO)R_x wherein each occurrence of R_x independently includes, but is not limited to, aliphatic, heteroaliphatic, aryl, heteroaryl, alkylaryl, or alkylheteroaryl, wherein any of the aliphatic, heteroaliphatic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and wherein any of the aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl substituents described above and herein may be substituted or unsubstituted.

[0026] In general, the term "cycloahphatic", as used herein, refer to a cyclic aliphatic moiety, wherein the term aliphatic is as defined above. A cycloahphatic moiety may be substituted or unsubstituted and saturated or unsaturated. Substituents include, but are not limited to, any of the previously mentioned substituents, i.e., the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound. In certain embodiments, cycloahphatic compounds include but are not limited to monocyclic, or polycyclic aliphatic hydrocarbons and bridged cycloalkyl compounds, which are optionally substituted with one or more functional groups. As will be appreciated by one of ordinary skill in the art, "cycloahphatic" is intended herein to include, but is not limited to, cycloalkyl, cycloalkenyl, and cycloalkynyl moieties, which are optionally substituted with one or more functional groups. Illustrative cycloahphatic groups thus include, but are not limited to, for example, cyclopropyl, -CH₂-cyclopropyl, cyclobutyl, -CH₂-cyclobutyl, cyclopentyl, -CH₂-cyclopentyl, cyclohexyl, -CH₂- cyclohexyl, cyclohexenylethyl, cyclohexanylethyl, norborbyl moieties and the like, which again, may bear one or more substituents.

[0027] hi general, the term "cycloheteroaliphatic", as used herein, refers to a cyclic heteroaliphatic moiety, wherein the term heteroaliphatic is as defined above. A cycloheteroaliphatic moiety may be substituted or unsubstituted and saturated or unsaturated. Substituents include, but are not limited to, any of the previously mentioned substituents, i.e., the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound. The term "cycloheteroaliphatic" encompasses "heterocycloalkyl", "heterocycle" or

"heterocyclic" moieties, as defined herein.

[0028] Additionally, it will be appreciated that any of the cycloahphatic or cycloheteroaliphatic moieties described above and herein may comprise an aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety fused thereto. Additional examples of generally applicable substituents are illustrated by the specific embodiments shown in the Examples that are described herein.

[0029] The terms "halo" and "halogen" as used herein refer to an atom selected from fluorine, chlorine, bromine and iodine.

[0030] The term "haloalkyl" denotes an alkyl group, as defined above, having one, two, or three halogen atoms attached thereto and is exemplified by such groups as chloromethyl, bromoethyl, trifluoromethyl, and the like.

[0031] The term "acyl", as used herein, refers to a group having the general formula -C(=0)R, where R is an aliphatic, heteroaliphatic, heterocycle, aromatic or heteroaromatic moiety, as defined herein.

[0032] The term "heterocycloalkyl", "heterocycle" or "heterocyclic", as used herein, refers to compounds which combine the properties of heteroaliphatic and cyclic compounds and include, but are not limited to, saturated and unsaturated mono- or polycyclic cyclic ring systems having 5-16 atoms wherein at least one ring atom is a heteroatom selected from O, S and N (wherein the nitrogen and sulfur heteroatoms may be optionally be oxidized), wherein the ring systems are optionally substituted with one or more functional groups, as defined herein. In certain embodiments, the term "heterocycloalkyl", "heterocycle" or "heterocyclic" refers to a non-aromatic 5-, 6- or 7- membered ring or a polycyclic group wherein at least one ring atom is a heteroatom selected from O, S and N (wherein the nitrogen and sulfur heteroatoms may be optionally be oxidized), including, but not limited to, a bi- or tri-cyclic group, comprising fused six-membered rings having between one and three heteroatoms independently selected from oxygen, sulfur and nitrogen, wherein (i) each 5- membered ring has 0 to 2 double bonds, each 6-membered ring has 0 to 2 double bonds and each 7-membered ring has 0 to 3 double bonds, (ii) the nitrogen and sulfur heteroatoms may be optionally be oxidized, (iii) the nitrogen heteroatom may optionally be quaternized, and (iv) any of the above heterocyclic rings may be fused to an aryl or heteroaryl ring. Representative heterocycles include, but are not limited to, heterocycles such as furanyl, thiofuranyl, pyranyl, pyrrolyl, thienyl, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolyl, oxazolidinyl, isooxazolyl, isoxazolidinyl, dioxazolyl, thiadiazolyl, oxadiazolyl, tetrazolyl, triazolyl, thiatriazolyl, oxatriazolyl, thiadiazolyl, oxadiazolyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, isothiazolidinyl, dithiazolyl, dithiazolidinyl, tetrahydrofuryl, and benzofused derivatives thereof. In certain embodiments, a "substituted heterocycle, or heterocycloalkyl or heterocyclic" group is utilized and as used herein, refers to a heterocycle, or heterocycloalkyl or heterocyclic group, as defined above, substituted by the independent replacement of one, two or three of the hydrogen atoms thereon with but are not limited to aliphatic; cycloahphatic; heteroaliphatic; heterocyclic; aromatic; heteroaromatic; aryl; heteroaryl; alkylaryl; heteroalkylaryl; alkylheteroaryl; heteroalkylheteroaryl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; CI; Br; I; - OH; -NO₂; -CN; -CF₃; -CH₂CF₃; -CHC1₂; -CH₂OH; - CH₂CH₂OH; -CH₂NH₂; -CH₂SO₂CH₃; -C(O)R_x; -CO₂(R_x); -CON(R_x)₂; -OC(O)R_x; - OCO₂R_X; -OCON(R_x)₂; -N(R_X)₂; -S(0)₂R_x; -NR_x(CO)R_x wherein each occurrence of R_x independently includes, but is not limited to, aliphatic, cycloahphatic, heteroaliphatic, heterocyclic, aromatic, heteroaromatic, aryl, heteroaryl, alkylaryl, alkylheteroaryl, heteroalkylaryl or heteroalkylheteroaryl, wherein any of the aliphatic, cycloahphatic, heteroaliphatic, heterocyclic, alkylaryl, or alkylheteroaryl substituents described above and herein may be substituted or unsubstituted, branched or unbranched, saturated or unsaturated, and wherein any of the aromatic, heteroaromatic, aryl or heteroaryl substitutents described above and herein may be substituted or unsubstituted. Additional examples or generally applicable substituents are illustrated by the specific embodiments shown in the Examples, which are described herein.

[0033] The phrase, "pharmaceutically acceptable derivative", as used herein, denotes any pharmaceutically acceptable salt, ester, or salt of such ester, of such compound, or any other adduct or derivative which, upon administration to a patient, is capable of providing (directly or indirectly) a compound as otherwise described herein, or a metabolite or residue thereof. Pharmaceutically acceptable derivatives thus include among others pro-drugs. A pro-drug is a derivative of a compound, usually with significantly reduced pharmacological activity, which contains an additional moiety that is susceptible to removal in vivo yielding the parent molecule as the pharmacologically active species. An example of a pro-drug is an ester which is cleaved in vivo to yield a compound of interest. Pro-drugs of a variety of compounds, and materials and methods for derivatizing the parent compounds to create the pro-drugs, are known and may be adapted to the present invention. Certain exemplary pharmaceutical compositions and pharmaceutically acceptable derivatives will be discussed in more detail herein below.

[0034] The term "treating", as used herein generally means that the compounds of the invention can be used in humans or animals with at least a tentative diagnosis of disease. The compounds of the invention will delay or slow the progression of the disease thereby giving the individual a more useful life span.

[0035] The term "preventing" as used herein means that the compounds of the present invention are useful when administered to a patient who has not been diagnosed as possibly having the disease at the time of administration, but who would normally be expected to develop the disease or be at increased risk for the disease. The compounds of the invention will slow the development of disease symptoms, delay the onset of disease, or prevent the individual from developing the disease at all. Preventing also includes administration of the compounds of the invention to those individuals thought to be predisposed to the disease due to age, familial history, genetic or chromosomal abnormalities, and/or due to the presence of one or more biological markers for the disease, such as a known genetic mutation of APP or APP cleavage products in brain tissues or fluids.

[0036] As used herein the term "biological sample" includes, without limitation, cell cultures or extracts thereof; biopsied material obtained from an animal (e.g., mammal) or extracts thereof; and blood, saliva, urine, feces, semen, tears, or other body fluids or extracts thereof. For example, the term "biological sample" refers to any solid or fluid sample obtained from, excreted by or secreted by any living organism, including single-celled micro-organisms (such as bacteria and yeasts) and multicellular organisms (such as plants and animals, for instance a vertebrate or a mammal, and in particular a healthy or apparently healthy human subject or a human patient affected by a condition or disease to be diagnosed or investigated). The biological sample can be in any form, including a solid material such as a tissue, cells, a cell pellet, a cell extract, cell homogenates, or cell fractions; or a biopsy, or a biological fluid. The biological fluid may be obtained from any site (e.g. blood, saliva (or a mouth wash containing buccal cells), tears, plasma, serum, urine, bile, cerebrospinal fluid, amniotic fluid, peritoneal fluid, and pleural fluid, or cells therefrom, aqueous or vitreous humor, or any bodily secretion), a transudate, an exudate (e.g. fluid obtained from an abscess or any other site of infection or inflammation), or fluid obtained from a joint (e.g. a normal joint or a joint affected by disease such as rheumatoid arthritis, osteoarthritis, gout or septic arthritis). The biological sample can be obtained from any organ or tissue (including a biopsy or autopsy specimen) or may comprise cells (whether primary cells or cultured cells) or medium conditioned by any cell, tissue or organ. Biological samples may also include sections of tissues such as frozen sections taken for histological purposes. Biological samples also include mixtures of biological molecules including proteins, lipids, carbohydrates and nucleic acids generated by partial or complete fractionation of cell or tissue homogenates. Although the sample is preferably taken from a human subject, biological samples may be from any animal, plant, bacteria, virus, yeast, etc. The term animal, as used herein, refers to humans as well as non-human animals, at any stage of development, including, for example, mammals, birds, reptiles, amphibians, fish, worms and single cells. Cell cultures and live tissue samples are considered to be pluralities of animals. In certain exemplary embodiments, the non- human animal is a mammal (e.g., a rodent, a mouse, a rat, a rabbit, a monkey, a dog, a cat, a sheep, cattle, a primate, or a pig). An animal may be a transgenic animal or a human clone. If desired, the biological sample may be subjected to preliminary processing, including preliminary separation techniques.

DESCRIPTION OF CERTAIN PREFERRED EMBODIMENTS OF THE INVENTION

[0037] As noted above, there has been increasing interest in recent years in the development of aspartyl protease inhibitors, particularly BACE inhibitors, as therapeutic agents for the treatment of Alzheimer's Disease and other disorders caused by the accumulation of β-amyloid plaques. It has been generally accepted by the scientific community that potential new leads for aspartyl inhibitor small molecules must comprise an aspartate binding hydroxyl group to retain aspartyl protease inhibitory activity (See for example, Ajay et al, "Designing Libraries woth CNS Activity", J. Med. Chem., 42:4942-4951, 1999, see especially the paragraph bridging columns 1 and 2 on page 4942 of this article). The present invention demonstrates that amino analogs (i.e., where the hydroxyl group has been replaced with an amino group) are unexpectedly equally promising (if not superior) aspartyl protease inhibitors as their hydroxy-containing counterparts. In fact, the present invention shows that certain amino-containing inventive compounds possess several superior biological properties over their hydroxy-containing counterparts (e.g., increased potency in cells, increased selectivity for the BACE enzyme, and/or superior ADME properties).

[0038] Thus, the present invention provides novel amino-containing compounds capable of inhibiting the activity of BACE. More generally, the compounds of the invention are inhibitors of proteases, and more specifically inhibitors of aspartyl proteases. In certain embodiments of special interest, the inventive compounds are useful for the treatment or prevention of disorders characterized by β amyloid deposits or plaques. In certain exemplary embodiments, the compounds are useful for the treatment of Alzheimer's Disease.

[0039] Compounds of this invention include those generally set forth above and described specifically herein, and are illustrated in part by the various classes, subgenera and species disclosed herein.

[0040] Additionally, the present invention provides pharmaceutically acceptable derivatives of the inventive compounds, and methods of treating a subject using these compounds, pharmaceutical compositions thereof, or either of these in combination with one or more additional therapeutic agents.

[0041] 1) General Description of Compounds of the Invention [0042] hi certain embodiments, the compounds of the invention include compounds of the general formula (I) as further defined below:

<img file="WO03106405A1_D0013.tif" />

(I) and pharmaceutically acceptable derivatives thereof; wherein R° is hydrogen, an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or a nitrogen protecting group, or a prodrug moiety; or R°, taken together with R' or a substituent present on X , may form a cycloheteroaliphatic moiety;

R' is hydrogen or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R', taken together with R°, R² or a substituent present on R¹, may form a cycloheteroaliphatic moiety;

R¹ is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R¹, taken together with R', may form a cycloheteroaliphatic moiety;

X¹ is -C(=O)-, -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=O)-₅ -NC(=S)-, -N-C(=N- C N , -NS(O₂)-, -CHR^X1A-, -SO₂-, -COO-, -C(=0)C(R^X1A)₂-, or -SC(=O)- wherein each occurrence of R is independently hydrogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R² is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R², taken together with R', may form a cycloheteroaliphatic moiety;

R is hydrogen, halogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R³ is hydrogen, halogen, or lower alkyl;

R is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R⁴, taken together with a substituent present on X² or X³, may form a cycloahphatic, cycloheteroaliphatic, aromatic, or heteroaromatic moiety;

X² is absent, <img file="WO03106405A1_D0014.tif" /> or - N(R^X2A)CH(R^X2A')Y- wherein each occurrence of R^X2A is independently hydrogen or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R taken together with R° may form a cycloheteroaliphatic moiety, each occurrence of Y is

independently <img file="WO03106405A1_D0015.tif" />^x . wherein, for each independent occurrence of t, ²⁸ is hydrogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R^X2A or one occurrence of R ²³ taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aromatic or heteroaromatic moiety, and wherein each occurrence of j and t is independently an integer from 1 to 4; and

X³ is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=0)- , -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR^X3A-, -C(=S)NR^X3A-, -COO-, -(CHR^x3A)_k-, -0-, -CH₂NR^X3A-_; or -NR^X3A-, wherein each occurrence of R^X3A is independently hydrogen, an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R^X3A taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aromatic or heteroaromatic moiety, and k is an integer from 1 to 3; wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aromatic, heteroaromatic, aryl and heteroaryl moieties may be substituted or unsubstituted.

[0043] In certain embodiments of compounds described directly above and compounds as described in certain classes and subclasses herein, one or more of the following groups do not occur simultaneously as defined:

(i) R', R°, R³ and R³ are each hydrogen; R² is alkyl, cycloalkylalkyl or aralkyl; -X²-X³-R⁴ together represents -CHR^eC(=O)NHCH(R^w)C(=O)NR^xR^y, wherein R^e is hydrogen or alkyl, R is alkyl, and one of R^x or R^y represents hydrogen and the other represents hydrogen, alkyl, aryl, aralkyl, l-alkoxycarbonyl-2- phenylethyl, 1 -alkoxycarbonyl-2-(imidazol-4-yl)ethyl, 2-(imidazol- 1 -yl)ethyl, indanyl, heterocyclyl-alkyl, carboxyalkyl, alkoxycarbonylalkyl, aryloxycarbonylalkyl, aralkoxycarbonylalkyl or a group of the formula -A-N(R^a)(R^b) in which A represents alkylene and R^a and R each represents alkyl or R^a and R^b together represent a pentamethylene group in which one methylene group can be replaced by NH, N-alkyl, N-alkanoyl, N-aralkoxycarbonyl, O, S, SO, or SO₂; or R^x and R^y together with the nitrogen atom to which they are attached represent a 1,2,3,4-tetrahydroisoquinoline ring; and -X^R¹ together represents an alkoxycarbonyl, aralkoxycarbonyl, alkanoyl, aralkanoyl, aroyl, cycloalkylcarbonyl, heterocyclylcarbonyl, heterocyclyl-alkanoyl, 6- (dibenylcarbamoyl)-4-oxohexanoyl moiety or an acyl group of an α-amino acid in which the amino group is substituted by an alkoxycarbonyl, aralkoxycarbonyl, diaralkylcarbamoyl, diaralkylalkanoyl, or aralkanoyl moiety; wherein the term "aroyl" refers to an acyl group derived from from an arylcarboxylic acid such as benzoyl, 1-naphthoyl, 2-naphthoyl, etc., and the term "aralkanoyl" refers to an acyl group derived from an aryl-substituted alkanecarboxylic acid; whereby the term "aryl" alone or in each of the aralkyl, aryloxycarbonylalkyl, aralkoxycarbonylalkyl or N-aralkoxycarbonyl moieties refers to a phenyl or naphthyl group optionally substituted with one or emore substituents selected from alkyl, hydroxy, alkoxy and halogen;

(ii) R', R°, R³ and R^3' are each hydrogen; X¹ is -C(=O)-, -SO₂-, N(R^x)SO₂, N(R^x)C(=O) or SC(=0), wherein R^x is hydrogen, Ci-salkyl or joined together with R¹ either directly to form a 5-7 membered heterocycle such as pyrrolidinyl or piperidinyl, or through a heteroatom selected from N, O and S, to form a 6-membered heterocycle with the nitrogen to which they are attached such as morpholinyl, piperazyl, or N-Ci. ₃alkyl-piperazyl; R¹ is a substituted or unsubstituted Cι_₆alkyl, a 5-6 membered heterocycle or a 6-10 carbon atoms aryl moiety substituted with Cι_-4alkyl, Cμ₃alkoxy, hydroxy, halogen, N(R^a)₂, C(=O)OR^a, -C(=O)N(R^a)₂, -SO₂N(R^a)₂, CH₂N(R^a)₂, N(R^a)C(=O)R^a or N(R^a)SO₂R^a; R² is OR^a, N(R^a)₂, Cι.₄alkenyl-R^c or -[CR R^c]_nR^c; and -X²-X³-R⁴ together represent -CH(R^d)C(=O)NHCH(R^e)C(=O)-Y-[CR^fR^g]_mR⁸, wherein m is an integer from 0 to 5, Y is O or NH, R^d and R^e are independently hydrogen, OR^a, N(R^a)₂, C_Malkenyl-R^c or -[CR R^c]„R^c wherein n is an integer from 0 to 5, R^a is hydrogen or Cι. alkyl, R is hydrogen, hydroxy or Cι_-4alkyl and R^c is hydrogen, substituted or unsubstituted aryl, 5- or 6-membered heterocycle, Cι_-6alkyl or Ci-βalkenyl, C_3-7cycloalkyl, 5- to 7-membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring, benzofuryl, indolyl, azabicyclo C_7-ncycloalkyl or benzopiperidinyl; R is hydrogen, substituted or unsubstituted Cι_₆alkyl or (CH₂CH₂O)_pCH₃ or (CH₂CH₂O)_pH wherein p is an integer from 0 to 5, and R^g is hydrogen, or substituted or unsubstituted aryl, heterocycle, 5- to 7-membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring;

(iii) R', R°, R³ and R^3' are each hydrogen; X¹ is -C(=O)-, -SO₂-, N(R^x)SO₂, N(R^x)C(=0) or SC(=O) , wherein R is hydrogen, Cι_-5alkyl or joined together with R¹ either directly to form a 5-7 membered heterocycle such as pyrrolidinyl or piperidinyl, or through a heteroatom selected from N, O and S, to form a 6-membered heterocycle with the nitrogen to which they are attached such as morpholinyl, piperazyl, or N- . ₃alkyl-piperazyl; R¹ is a substituted or unsubstituted Cι_-6alkyl, a 5-6 membered heterocycle or a 6-10 carbon atoms aryl moiety substituted with C_1- alkyl, C_1-3alkoxy, hydroxy, halogen, N(R^a)₂, C(=O)OR^a, -C(=O)N(R^a)₂, -SO₂N(R^a)₂, CH₂N(R^a)₂, N(R^a)C(=O)R^a or N(R^a)SO₂R^a; R² is OR^a, N(R^a)₂, Cι_₄alkenyl-R° or -[CR R^c]_nR^c; and -X²-X³-R⁴ together represent -CH(R^d)C(=O)-Y-[CR^fR^g]_mR⁸, wherein m is an integer from 0 to 5, Y is O or NH, R^d is hydrogen, OR^a, N(R^a)₂, Cι.₄alkenyl-R^c or - [CR^bR^c]_nR^c; wherein n is an integer from 0 to 5, R^a is hydrogen or Cμ₄alkyl, R is hydrogen, hydroxy or Cι- alkyl and R^c is hydrogen, substituted or unsubstituted aryl, 5- or 6-membered heterocycle, Cι_₆alkyl or Cι_-6alkenyl, C_3-7cycloalkyl, 5- to 7- membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring, benzofuryl, indolyl, azabicyclo C₇-ncycloalkyl or benzopiperidinyl; R is hydrogen, substituted or unsubstituted Cι.₆alkyl or (CH₂CH₂θ)_pCH₃ or (CH₂CH₂θ)_pH wherein p is an integer from 0 to 5, and R^g is hydrogen, or substituted or unsubstituted aryl, heterocycle, 5- to 7-membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring;

(iv) R' and R are each hydrogen; R is hydrogen, -C(=0)H, -Cι_-4alkyl or - COOR^a; X¹ is -C(=O)-, -S0₂-, N(R^x)SO₂, N(R^x)C(=O) or SC(=O), wherein R^x is hydrogen, Ci-salkyl or joined together with R¹ either directly to form a 5-7 membered heterocycle such as pyrrolidinyl or piperidinyl, or through a heteroatom selected from N, O and S, to form a 6-membered heterocycle with the nitrogen to which they are attached such as morpholinyl, piperazyl, or N-Cι_-3alkyl-piperazyl; R¹ is a substituted or unsubstituted Cι_₆alkyl, a 5-6 membered heterocycle or a 6-10 carbon atoms aryl moiety substituted with Cι_ alkyl, Cι_-3alkoxy, hydroxy, halogen, N(R )₂, C(=O)OR^a, - C(=O)N(R^a)₂, -SO₂N(R^a)₂, CH₂N(R^a)₂, N(R^a)C(=O)R^a or N(R^a)SO₂R^a; R² is OR^a, N(R^a)₂, C alkenyl-R^c or -[CR^bR^c]_nR^c; R³ is hydrogen, OR^a, N(R^a)₂, C alkenyl-R^c or -[CR R^c]_nR^c; and -X²-X³-R⁴ together represent -CH(R^d)C(=0)NHCH(R^e)C(=O Y-[CR^fR^g]_mR^g, wherein m is an integer from 0 to 5, Y is O or NH, R^d and R^e are independently hydrogen, OR^a, N(R^a)₂, Cι_-4alkenyl-R^c or -[CR^bR^c]_nR^c wherein n is an integer from 0 to 5, R^a is hydrogen or Cι_-4alkyl, R is hydrogen, hydroxy or Cι_-4alkyl and R^c is hydrogen, substituted or unsubstituted aryl, 5- or 6-membered heterocycle, Cι_-6alkyl or Cι_₆alkenyl, C_3-7cycloalkyl, 5- to 7-membered carbocyclic or 7- to 10- membered bicyclic carbocyclic ring, benzofuryl, indolyl, azabicyclo C₇_πcycloalkyl or benzopiperidinyl; R^f is hydrogen, substituted or unsubstituted Cι_-6alkyl or (CH₂CH₂0)_pCH₃ or (CH₂CH₂O)_pH wherein p is an integer from 0 to 5, and R^s is hydrogen, or substituted or unsubstituted aryl, heterocycle, 5- to 7-membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring;

(v) R' and R³ are each hydrogen; R° is hydrogen, -C(=O)H, -Cι_-4alkyl or - COOR^a; X¹ is -C(=0)-, -SO₂-, N(R^x)SO₂, N(R^x)C(=O) or SC(=0), wherein R^x is hydrogen, Cι_-5alkyl or joined together with R¹ either directly to form a 5-7 membered heterocycle such as pyrrolidinyl or piperidinyl, or through a heteroatom selected from N, O and S, to form a 6-membered heterocycle with the nitrogen to which they are attached such as morpholinyl, piperazyl, or N-Cι_-3alkyl-piperazyl; R¹ is a substituted or unsubstituted Cι_₆alkyl, a 5-6 membered heterocycle or a 6-10 carbon atoms aryl moiety substituted with Cχ.₄alkyl, Cι_-3alkoxy, hydroxy, halogen, N(R^a)₂, C(=O)OR^a, - C(=O)N(R^a)₂, -S0₂N(R^a)₂, CH₂N(R^a)₂, N(R^a)C(=0)R^a or N(R^a)SO₂R^a; R² is OR^a, N(R^a)₂, Cι_-4alkenyl-R^c or -[CR^bR^c]_nR^c; R³ is hydrogen, OR^a, N(R^a)₂, Cι_-4alkenyl-R^c or -[CR^bR^c]_nR^c; and -X²-X³-R⁴ together represent -CH(R^d)C(=O)-Y-[CR^fR^g]_mR⁸, wherein is an integer from 0 to 5, Y is O or NH, R^d is hydrogen, OR^a, N(R^a)₂, C_\. ₄alkenyl-R^c or -[CR^bR^c]_nR^c; wherein n is an integer from 0 to 5, R^a is hydrogen or . ₄alkyl, R^b is hydrogen, hydroxy or Cι_-4alkyl and R^c is hydrogen, substituted or unsubstituted aryl, 5- or 6-membered heterocycle, Cι.₆alkyl or Cμ₆alkenyl, C₃. ₇cycloalkyl, 5- to 7-membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring, benzofuryl, indolyl, azabicyclo C_7-πcycloalkyl or benzopiperidinyl; R^f is hydrogen, substituted or unsubstituted Cι_₆alkyl or (CH₂CH₂O)_pCH₃ or (CH₂CH₂0)_pH wherein p is an integer from 0 to 5, and R⁸ is hydrogen, or substituted or unsubstituted aryl, heterocycle, 5- to 7-membered carbocyclic or 7- to 10-membered bicyclic carbocyclic ring; and

(vi) R°, R', R³ and R^3' are each hydrogen; R² is Cι_-6alkyl, C_2-6alkenyl, C_3-₇cycloalkyl, aryl, heteroaryl, T-Cι_-6alkyl, T-C_2-6alkenyl, wherein T is aryl, heteroaryl or C_3-7cycloalkyl; R^X¹ together represent W wherein W is R^x, R^xCO, R^xOCO, R^xOCH(R^y)CO, R^xNHCH(R^y)CO, R^xSCH(R^y)CO, R^xSO₂, R^xSO or an amino acid with a blocked or unblocked amino terminus, wherein R^x and R^y are each independently hydrogen, Cι_-6alkyl, C_3-7cycloalkyl, aryl, heteroaryl, T-Cι_₆alkyl or T- (CH₂)„CH(T)(CH₂)_n wherein n is an integer from 1 to 4; and -X -X³-R⁴ together represent -CH(R^a)C(=X)CHR R^c, wherein X is (OH,H) or O; R^a is hydrogen, C_. ₆alkyl, C_2-6alkenyl, C_3-7cycloalkyl, aryl, heteroaryl, T-Cι_-6alkyl or T-C₂.₆alkenyl; R is hydrogen or OH; and R^c is Y, (CHR^w)_n-Y or =CR^z(CHR^w)_n-Y, wherein Y is hydrogen, OH, -NR^wR^q, aryl, heteroaryl or CO-Z, n is an integer from 1 to 4, Z is OH, -NR R^q, OR^w or an amino acid with a blocked or unblocked carboxy terminus, R^q is H, Cι_₆alkyl or arylCι_-6alykl, and R^z and R^w are each independently hydrogen, Ci. ₆alkyl, C_3- cycloalkyl, aryl, heteroaryl, T-Cι_₆alkyl or T-C₂-₆alkenyl.

[0044] In certain embodiments, the present invention defines particular classes of compounds which are of special interest. For example, one class of compounds of special interest includes those compounds of Formula I wherein:

R° is hydrogen, an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, a nitrogen protecting group, or a prodrug moiety;

R' is hydrogen or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R¹ is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

X¹ is -C(=O)-, -S(=O)-, -C(-NH)-, -C(=S)-, -NC(=0)-, -NC(=S)-, -N-C(=N- C N)-, -NS(O₂)-, -CHR^X1A-, -SO₂-, -COO-, -C(=O)C(R^xlA)₂-, or -SC(=O)- wherein each occurrence of R^X1A is independently hydrogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R² is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R is hydrogen, halogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R is hydrogen, halogen, or lower alkyl;

R⁴ is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

X² is absent, -NR^X2A-, -(CHR^-, -NR ^2AY-, or -(CHR^jY- wherein each occurrence of R^X2A is independently hydrogen or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, each occurrence of Y is independently

<img file="WO03106405A1_D0016.tif" /> * wherein, for each independent occurrence of t, R is hydrogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, and wherein each occurrence of j and t is independently an integer from 1 to 4; and

X³ is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=0)- , -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - CONR^X3A-, -COO-, -(CHR^X3A)_k-, -O-, or -NR^X3A-, wherein each occurrence of R^X3A is independently hydrogen, an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, and k is an integer from 1 to 3; wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aromatic, heteroaromatic, aryl and heteroaryl moieties may be substituted or unsubstituted.

[0045] Another class of compounds of special interest includes those compounds wherein the compound has the stereochemistry as shown in Formula (I^A):

R' NHR°

R _ .xl „.R⁴

X¹ Υ X "x^3'

R² R³ R^3' (I^A) [0046] Another class of compounds of special interest includes those compounds wherein in the compound of formula (I^A) above, R³' is hydrogen, X² is CHR^X2A, R° and R , taken together, form a 5-membered heterocyclic moiety and the compound has the Formula (I^B):

<img file="WO03106405A1_D0017.tif" /> d^B)

[0047] Another class of compounds of special interest includes those compounds

A *__ "VI _ wherein, in the compound of formula (I ) above, R is hydrogen, X is CHR , R and R , taken together, form a 6-membered heterocyclic moiety and the compound has the Formula (I^c):

<img file="WO03106405A1_D0018.tif" />

(i^c) [0048] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (I) above, R is hydrogen, X is CHMe and the compound has the Formula (I^D):

<img file="WO03106405A1_D0019.tif" /> d^D)

[0049] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (I) above, R³ is hydrogen, X³ is absent, X² is -

CH(Me)Y- where Y is <img file="WO03106405A1_D0020.tif" />² and the compound has the Formula (I ):

<img file="WO03106405A1_D0021.tif" />

[0050] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (I) above, R³ is hydrogen, X³ is absent, X² is -

CH(Me)Y- where Y is <img file="WO03106405A1_D0022.tif" />² and the compound has the Formula (I^F)

<img file="WO03106405A1_D0023.tif" /> d^F)

[0051] Another class of compounds of special interest includes compounds of Formula (II) wherein R' and R³ are each hydrogen, and X² is CHR^X2A:

<img file="WO03106405A1_D0024.tif" />

(II) [0052] Another class of compounds of special interest includes those compounds wherein the compound of formula (II) above has the stereochemistry as shown in Formula (II^A):

<img file="WO03106405A1_D0025.tif" /> (II^A) [0053] Another class of compounds of special interest includes those compounds wherein in the compound of formula (II^A) above, R° and R^X2A, taken together, form a

5-membered heterocyclic moiety and the compound has the Formula (II^B):

<img file="WO03106405A1_D0026.tif" /> (H^B) [0054] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (II^A) above, R° and R ²^ taken together, form a 6-membered heterocyclic moiety and the compound has the Formula (II^C):

<img file="WO03106405A1_D0027.tif" /> (H^C)

[0055] Another class of compounds of special interest includes those compounds wwhheerreeiinn,, iinn tthhee ccoommppoound of formula (II) above, R^X2 is methyl and the compound has the Formula (II^D):

<img file="WO03106405A1_D0028.tif" /> (II^D)

[0056] Another class of compounds of special interest includes compounds of

Formula (III) wherein R' and R^3' are each hydrogen, X² is CHR^X2A and X³ is -

C(=0)NH-:

<img file="WO03106405A1_D0029.tif" /> (III) [0057] Another class of compounds of special interest includes those compounds wherein the compound of fomiula (III) above has the stereochemistry as shown in Formula (III^A):

<img file="WO03106405A1_D0030.tif" />

(in^A)

[0058] Another class of compounds of special interest includes those compounds wherein in the compound of formula (III^A) above, R° and R^X2A, taken together, form a 5-membered heterocyclic moiety and the compound has the Formula (III^B):

<img file="WO03106405A1_D0031.tif" />

(III^B)

[0059] Another class of compounds of special interest includes those compounds wherein in the compound of formula (III^A) above, R° and R^X2A, taken together, form a 6-membered heterocyclic moiety and the compound has the Formula (III^C):

<img file="WO03106405A1_D0032.tif" />

(III^C)

[0060] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (III), above R^X2A is methyl, and the compound has the Formula (III^D):

<img file="WO03106405A1_D0033.tif" /> (III^D)

[0061] Another class of compounds of special interest includes compounds of Formula (IV) wherein R' and R^3' are each hydrogen, X² is CHR ^2A and X¹ is -C(=O

<img file="WO03106405A1_D0034.tif" /> (IV)

[0062] Another class of compounds of special interest includes those compounds wherein the compound of formula (IV) above has the stereochemistry as shown in

Formula (IV^A):

H NHR° R^X2A R Υ^ X _^^{^}X³ „. O R² R³

(IV^A)

[0063] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (IV^A) above, R° and R ^{' X2A}, taken together, form a 5-membered heterocyclic moiety and the compound has the Formula (IV ):

<img file="WO03106405A1_D0035.tif" />

[0064] Another class of compounds of special interest includes those compounds wherein in the compound of formula (IV ) above R and R X2A , taken together, form a 6-membered heterocyclic moiety and the compound has the Formula (IV ):

<img file="WO03106405A1_D0036.tif" />

(IV^C)

[0065] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (IV), above R^X2A is methyl, and the compound has the Formula (IV^D):

<img file="WO03106405A1_D0037.tif" />

(IV^D)

[0066] Another class of compounds of special interest includes compounds of Formula (V) wherein R' and R^3' are each hydrogen, X¹ is -C(=O)-, X² is CHR^X2A and X³ is -C(=O)NH-: <img file="WO03106405A1_D0038.tif" />

(V) [0067] Another class of compounds of special interest includes those compounds wherein the compound of formula (V) above has the stereochemistry as shown in Formula (V^A):

<img file="WO03106405A1_D0039.tif" /> (V^A) [0068] Another class of compounds of special interest includes those compounds wherein, in the compound of formula V^A) above, R° and R ^2A, taken together, form a 5-membered heterocyclic moiety and the compound has the Formula (V^B):

<img file="WO03106405A1_D0040.tif" />

[0069] Another class of compounds of special interest includes those compounds wherein in the compound of formula V^A) above, R° and R^X2A, taken together, form a 6-membered heterocyclic moiety and the compound has the Formula (V^c):

<img file="WO03106405A1_D0041.tif" />

[0070] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (V) above, R^X2A is methyl, and the compound has the Formula (V^D):

<img file="WO03106405A1_D0042.tif" />

(V^D) [0071] Another class of compounds of special interest includes compounds of Formula (VI) wherein R' and R³ are each hydrogen, and X² is -NR³^-:

<img file="WO03106405A1_D0043.tif" /> (VI) [0072] Another class of compounds of special interest includes those compounds wherein the compound of formula (VI) above has the stereochemistry as shown in Formula (VI^A):

<img file="WO03106405A1_D0044.tif" /> (VI^A)

[0073] Another class of compounds of special interest includes those compounds wherein R° and R^X2A, taken together, form a heterocyclic moiety and the compound has the structure as shown in Formula (VI^B):

<img file="WO03106405A1_D0045.tif" /> wherein n is 0 or 1.

[0074] Another class of compounds of special interest includes compounds of Formula (VII) wherein R' and R³ are each hydrogen, X¹ is -C(=O)- and X² is -

NR^X2A-:

<img file="WO03106405A1_D0046.tif" /> (VII)

[0075] Another class of compounds of special interest includes those compounds wherein the compound of formula (VII) above has the stereochemistry as shown in Formula (VII^A):

<img file="WO03106405A1_D0047.tif" /> (VII^A)

[0076] Another class of compounds of special interest includes compounds of Formula (VIII) wherein R' and R³ are each hydrogen, X¹ is -C(=O)- and X² is NH:

<img file="WO03106405A1_D0048.tif" /> (VIII) [0077] Another class of compounds of special interest includes those compounds wherein the compound of foπnula (VIII) above has the stereochemistry as shown in Formula (VIII^A):

<img file="WO03106405A1_D0049.tif" /> (VIII^A)

[0078] Another class of compounds of special interest includes compounds of

Formula (I) wherein R' and R³' are each hydrogen, X¹ is -C(=O)-, X² and X³ are both

absent and R is a cyclic moiety <img file="WO03106405A1_D0050.tif" /> the compounds have the general structure as shown in Formula (IX):

<img file="WO03106405A1_D0051.tif" /> (IX) wherein X⁴, X⁵, X⁶, X⁷ and X⁸ are connected by either a single or double bond, as valency permits, and are each independently -C(=0)-, CHR , NR ^', N, O, CH, CR , wherein each occurrence of R is independently hydrogen, halogen, alkyl, heteroalkyl, aryl, or heteroaryl, or is WR^X , wherein W is -O-, -S-, -NH-, -CO-, -SO₂- , -COO- or -CONH-, and R^X" is hydrogen, alkyl, heteroalkyl, aryl, or heteroaryl, or two occurrences of R^x taken together represent a cycloalkyl, heterocycloalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety. [0079] hi certain embodiments of the compounds as described directly above:

<img file="WO03106405A1_D0052.tif" /> a moiety having the structure:

<img file="WO03106405A1_D0053.tif" />

[0080] Another class of compounds of special interest includes compounds of Foπnula (I) wherein R' and R³' are each hydrogen, X¹ is -C(=O)-, X² is absent, X³ is NHSO₂ and the compounds have the structure as shown in Formula (X):

<img file="WO03106405A1_D0054.tif" /> (X)

[0081] Another class of compounds of special interest includes those compounds of Foπnula (I) wherein X¹ is -C(=O)- and the compound has the structure as shown in Formula (XI):

<img file="WO03106405A1_D0055.tif" />

[0082] Another class of compounds of special interest includes those compounds wherein in the compound of formula (XI) above, R is hydrogen and R and R , taken together, form a 6-membered heterocyclic moiety and the compound has the Formula (XI^A):

<img file="WO03106405A1_D0056.tif" /> (XI^A) wherein W is C or N, n is an integer from 0 to 3, and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl.

[0083] Another class of compounds of special interest includes those compounds of formula (I) wherein X¹ is CHR^xlA and the compound has the structure as shown in Formula (XII):

<img file="WO03106405A1_D0057.tif" />

(XII)

[0084] Another class of compounds of special interest includes those compounds wherein in the compound of formula (XII) above, R' and R³ are each hydrogen and R^X1A and R², taken together, form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety and tthhee ccoommppooiund has the Formula (XII^A)

<img file="WO03106405A1_D0058.tif" />

(Xir A)_\ wherein n is 1 or 2, m is an integer from 0 to 4, and each occuπence of R^2A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, or wherein any two adjacent occurrences of R^2A may form an cycloahphatic, heterocyclic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety. [0085] Another class of compounds of special interest includes those compounds wherein in the compound of formula (XII) above, R' and R³ are each hydrogen and R^X1A and R², taken together, form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety and the compound has the Formula (XII^B):

<img file="WO03106405A1_D0059.tif" />

(XII^B) [0086] Another class of compounds of special interest includes compounds of Formula (I) wherein R^3' is hydrogen, X¹ is -C(=V , X² is CHR^, X³ is - C(=W)NR^X3A-, and the compound has the Formula (XIII):

<img file="WO03106405A1_D0060.tif" /> (XIII) wherein V is O, S, or (H,H) and W is O, S, (H,H) or NH.

[0087] Another class of compounds of special interest includes those compounds wherein the compound of formula (XIII) above has the stereochemistry as shown in

Formula (XIII^A):

<img file="WO03106405A1_D0061.tif" /> (XIII^A)

[0088] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (XIII^A) above, V is (H, H), W is -O- and the compound has the Formula (XIII^B):

<img file="WO03106405A1_D0062.tif" /> (XIII^B) [0089] Another class of compounds of special interest includes those compounds wherein in the compound of formula (XIII^A) above V is O, W is (H, H) and the compound has the Formula (XIII ):

R' NHR° R^X2A R^X3A

RγN Λ _/N,_R4

O R² R³ (XIII^C)

[0090] Another class of compounds of special interest includes those compounds wherein, in the compound of formula (XIII^B) above, R^X2A is methyl and the compound has the Formula (XIII^D):

<img file="WO03106405A1_D0063.tif" /> (XIII^D)

[0091] Another class of compounds of special interest includes those compounds wherein in the compound of formula (XIII^C) above R^X2A is methyl and the compound has the Formula (XIII^E):

<img file="WO03106405A1_D0064.tif" />

(Xiir E)\

[0092] In certain exemplary embodiments, for each of classes of compounds described above, R° is hydrogen. In certain other exemplary embodiments, for each of classes of compounds described above, R° is a prodrug moiety. In certain other exemplary embodiments, for each of the classes of compounds as described above, R³ is hydrogen; R² is substituted or unsubstituted lower alkyl, lower alkylamino, lower heteroaryl, -(CH₂)cycloalkyl,-(CH₂)heterocycloalkyl, -(CH₂)aryl, -(CH₂)heteroaryl, optionally substituted with one or more occurrences of R^2A, wherein R^2A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -OR^2B, -SR^2B, - N(R^2B)₂, -SO₂N(R^2B)₂, -C(=O)N(R^2B)₂, halogen, -CN, -NO₂, -C(=O)OR^2B, - N(R^2B)C(=0)R^2c, wherein each occcurrence of R^2B and R^2C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl; R¹ is alkyl, alkenyl, heteroalkyl, heteroalkenyl, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkyl)heteroaryl, wherein R¹ is optionally substituted with one or more occurrences of R^1A, wherein R^1A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -OR^1B, - SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, ~C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, - N(R^1B)C(=0)R^lc; or or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; and R⁴ is alkyl, alkenyl, heteroalkyl, heteroalkenyl, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl - (heteroalkyl)aryl, or -(heteroalkyl)heteroaryl, optionally substituted with one or more occurrences of R^4A wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -CN, -NO₂, -C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl.

[0093] A number of important subclasses of each of the foregoing classes deserve separate mention; these subclasses include subclasses of the foregoing classes in which:

[0094] i) R¹ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl or alkenyl;

[0095] ii) R¹ is substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -

(alkyl)heteroaryl or heterocyclic;

[0096] iii) R¹ is one of:

<img file="WO03106405A1_D0065.tif" />

wherein R , IA is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, (alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or -N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^lc, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; R^1D is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, acyl or a nitrogen protecting group; wherein n and p are each independently integers from 0 to 3 and r is an integer from 1 to 6; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkylheteroaryl moieties may be substituted or unsusbtituted; [0097] iv) R¹ is one of:

<img file="WO03106405A1_D0066.tif" /> wherein each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, - SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, -N(R^1B)C(=O)R^lc or ι D ι f 1 R i f

— N(R )SO₂R ; wherein each occcurrence of R and R is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein n and p are each independenly an integer from 0 to 4; or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0098] v) R¹ is one of:

<img file="WO03106405A1_D0067.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; ; or R^1D and R^1E taken together form a 5-8 membered heterocyclic ring; or R^1E and one occuπence of R^1A, taken together, form a substituted or unsubstituted, saturated or unsaturated heterocyclic ring; each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, -N(R^1B)C(=O)R^lc or - N(R^1B)SO₂R^lc; and each occcurrence of R^1B and R ^c is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein n and p are each independenly an integer from 0 to 4; or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0099] vi) R¹ is:

<img file="WO03106405A1_D0068.tif" /> wherein R ^D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; ; or R^1D and R^1E taken together form a 5-8 membered heterocyclic ring; or R^1E and one occurrence of R^1A, taken together, form a substituted or unsubstituted, saturated or unsaturated heterocyclic ring; each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, -N(R^1B)C(=O)R^lc or - N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein n and p are each independenly an integer from 0 to 4; or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0100] vii) R¹ is:

wherein <img file="WO03106405A1_D0069.tif" /> heteroaryl, -(alkyl)aryl or - (alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, - CN, -NO₂, -C(=O)OR^1B, -N(R^1B)C(=O)R^lc or -N(R^1B)S0₂R^1C, wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1B and R^1C, taken together with the atoms to which they are attached, foπn a substituted or unsubstituted heterocyclic moiety; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0101] viii) R¹ is:

<img file="WO03106405A1_D0070.tif" /> wherein R^1A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -

(alkyl)heteroaryl, -OR^lc, -SR^1C, -N(R^1C)₂, -SO₂N(R^lc)₂, -C(=O)N(R^lc)₂, halogen, - CN, -NO₂, -C(=O)OR^lc, -N(R^lc)C(=O)R^1D, wherein each occcurrence of R^lc and R^1D is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl; and R^1B is hydrogen or laower alkyl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, - (alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0102] ix) R¹ is: <img file="WO03106405A1_D0071.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; ; or R^1D and R^1E taken together form a 5-8 membered heterocyclic ring; or R^1E and one occmxence of R ^A, taken together, form a substituted or unsubstituted, saturated or unsaturated heterocyclic ring; each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, -N(R^1B)C(=O)R^lc, wherein each occcurrence of R^1B and R^lc is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein n and p are each independenly an integer from 0 to 4; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0103] x) R¹ is:

<img file="WO03106405A1_D0072.tif" /> wherein R^1A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, - CN, -NO₂, -C(=0)OR^1B, -N(R^1B)C(=O)R^lc, wherein each occcurrence of R^1B and R^lc is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0104] xi) R¹ is:

<img file="WO03106405A1_D0073.tif" /> wherein R^1A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^lc, -SR^1C, -N(R^1C)₂, -SO₂N(R^lc)₂, -C(=O)N(R^lc)₂, halogen, - CN, -NO₂, -C(=O)OR^lc, -N(R^lc)C(=O)R^1D, wherein each occcurrence of R^1C andR^1D is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl; and R^1B is hydrogen or laower alkyl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, - (alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0105] xii) compounds of subsets vi)-xi) wherein R^1A is methyl, methoxy or halide;

[0106] xiii) compounds of subsets vi)-xi) wherein R^1A is methyl, methoxy or

F;

[0107] xiv) compounds of subsets vi)-xi) wherein R^{1 A} is methyl;

[0108] xv) compounds of subsets viii) and xi) wherein R^1B is hydrogen, methyl or ethyl; [0109] xvi) R¹ is:

<img file="WO03106405A1_D0074.tif" /> wherein R^1A and R^1B are each independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted;

[0110] xvii) compounds of subset xvi) wherein R^1A and R^1B are each independently cyclic or acyclic lower alkyl;

[0111] xviii) compounds of subset xvi) wherein R^1A and R^1B are each independently methyl, ethyl, propyl, butyl, pentyl, isopropyl, isobutyl, sec-butyl, isopentyl or cyclopropyl; [0112] xix) R¹ is:

<img file="WO03106405A1_D0075.tif" /> wherein R^1A and R^1C are each independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -C(=O)R^1D, -S0₂R^1D or a nitrogen protecting group, or R^1A and R^1C, taken together with the nitrogen atom to which they are attached, form a substituted or unsubstituted heterocyclic moiety; and R^1B and R^1D are each independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted;

[0113] xx) compounds of subset xix) wherein R^1B is substituted or unsubstituted, linear or branched, cyclic or acyclic lower alkyl; R^1A is lower alkyl; and R^lc is -SO₂R^1D wherein R^1D is lower alkyl;

[0114] xxi) compounds of subset xix) wherein R^1B is substituted or unsubstituted, linear or branched, cyclic or acyclic lower alkyl; R^1A and R^1C, taken together with the nitrogen atom to which they are attached, form a 5- or 6-membered cyclic sulfonamide moiety; [0115] xxii) R¹ is one of:

<img file="WO03106405A1_D0076.tif" /> wherein each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, - SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(-O)OR^1B, -N(R^1B)C(=0)R^1C or -N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; R^1D is linear or branched lower alkyl and n and p are independently integers from 0 to 3; [0116] xxiii) compounds of subset xxii) wherein p is 1 ;

[0117] xxiv) R¹ is one of: <img file="WO03106405A1_D0077.tif" /> xxv) R¹ is one of:

<img file="WO03106405A1_D0078.tif" />

[0119] xxvi) R² is lower alkyl, -CH₂NR^2AR^2B or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R , wherein R^2C is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^2D, -SR^2D, -N(R^2D)₂, -SO₂N(R^2D)₂, -C(=O)N(R^2D)₂, halogen, -CN, -NO₂, - C(=O)OR^2D, -N(R^2D)C(=0)R^2B, wherein each occcurrence of R^2D and R^2E is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; and wherein R^2A and R^2B are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted;

[0120] xxvii) R² is lower alkyl, -CH₂NR^2AR^2B or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R , wherein

R is hydrogen, alkyl, alkoxy or halogen; and wherein R and R are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0121] xxviii) R² is one of: <img file="WO03106405A1_D0079.tif" /> wherein R^2A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkylheteroaryl, -OR^2B, -SR^2B, -N(R^2B)₂, -SO₂N(R^2B)₂, -C(=O)N(R^2B)₂, halogen, - CN, -NO₂, -C(=O)OR^2B, -N(R^2B)C(=O)R^2C, wherein each occcuπence of R^2B and R^2C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl, wherein q and s are each independently integers from 0 to 3 and u is an integer from 1 to 6; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0122] xxix) R² is one of: <img file="WO03106405A1_D0080.tif" /> wherein each occcurrence of R »2A , is independently hydrogen or lower alkyl; each occurrence of X is independently a halogen; s is an integer from 0 to 3 and u is an integer from 1 to 6; whereby each of the foregoing alkyl moieties may be linear or branched, substituted or unsubstituted and cyclic or acylic; [0123] xxx) compounds of subset xxix) wherein X is chlorine or fluorine;

[0124] xxxi) compounds of subset xxix) wherein each occurrence of X is fluorine;

[0125] xxxii) compounds of subset xxix) wherein R^2A is methyl;

[0126] xxxiii) R² is one of:

<img file="WO03106405A1_D0081.tif" />

[0127] xxxiv) R² is one of: <img file="WO03106405A1_D0082.tif" />

[0128] xxxv) R² is one of:

<img file="WO03106405A1_D0083.tif" />

[0129] xxxvi) R² is one of:

<img file="WO03106405A1_D0084.tif" />

[0130] xxxvii) R³ is hydrogen or halogen; [0131] xxxviii) R³ is hydrogen or F; [0132] xxxix) R³ is hydrogen; [0133] xl) R³ is hydrogen, methyl or halogen; [0134] xli) R³ is hydrogen, methyl or F; [0135] xlii) R³ is hydrogen; [0136] xliii) one of R³ and R³ is halogen; [0137] xliv) R³ and R³ are each independently hydrogen or F; [0138] xlv) R³ and R³ are each F; [0139] xlvi) R³ and R³ are each hydrogen;

[0140] xlvii) X¹ is -C(=O)-;

[0141] xlviii) X¹ is CHR^X1A and R^X1A is hydrogen or linear or branched substituted or unsubstituted alkyl;

[0142] xlix) X¹ is CH₂;

[0143] 1) X² is CHR^X2A and R^X2A is hydrogen or linear or branched substituted or unsubstituted alkyl;

[0144] li) X² is CHR^X2A and R^X2A is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl or benzyl;

[0145] hi) X² is CHR^X2A and R^X2A is methyl, ethyl or isopropyl;

[0146] liii) X² is CHMe

[0147] liv) X² is -NR^X2A- and R^X2A is hydrogen or linear or branched substituted or unsubstituted alkyl;

[0148] lv) X² is -NR^{X A}- and R^MA is C1-C3 alkyl;

[0149] lvi) X² is NH;

[0150] lvii) X^z is NHY where Y is <img file="WO03106405A1_D0085.tif" /> where each occurrence

R ²³ is independently hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety; whereby each of the foregoing aliphatic and heteroaliphatic moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, saturated or unsaturated, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted;

[0151] lviii) <img file="WO03106405A1_D0086.tif" /> where each occurrence R^X2B is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, -

(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(hetero alkyl)hetero aryl moiety; whereby each of the foregoing aliphatic and heteroaliphatic moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, saturated or unsaturated, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0152] lix) X² is absent;

[0153] lx) X³ is (CHR^X3A)_k, -CH₂NH-, -C(=O)NH-, or -S0₂-, wherein each occurrence of R^X3A is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or —

(heteroalkylheteroaryl moiety, and k is an integer from 1 to 3 and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted;

[0154] lxi) X³ is absent;

[0155] lxii) X³ is CHR^X3A, X² is -NR ² - and R^X2A and R^X3A are each independently hydrogen or linear or branched substituted or unsubstituted alkyl;

[0156] lxiii) X³ is CHR^X3A and X² is NH; wherein R^X3A is hydrogen or linear or branched substituted or unsubstituted alkyl;

[0157] lxiv) X³ is CH₂ and X² is NH;

[0158] lxv) X² is CHR^X2A and X³ is CH₂NH; wherein R^X2A is hydrogen or linear or branched substituted or unsubstituted alkyl;

[0159] lxvi) X² is CHR^X2A and X³ is -C(=O)NH-; wherein R^X2A is hydrogen or linear or branched substituted or unsubstituted alkyl;

[0160] lxvii) R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^4B, -SR^4B, -

N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -CN, -NO₂, -C(=O)OR^4B, -

N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteoraryl, -(alkyl)aryl or -

(alkyl)hetero aryl;

[0161] lxviii) R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH2)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen;

[0162] lxix) R⁴ is one of: <img file="WO03106405A1_D0087.tif" />

(R*^A)_V<img file="WO03106405A1_D0088.tif" />

<img file="WO03106405A1_D0089.tif" /> wherein each occurrence of R^4A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, - SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -CN, -NO₂, -C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein v and w are each independently integers from 0 to 3 and x is an integer from 1 to 6; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted; [0163] lxx) R⁴ is one of:

<img file="WO03106405A1_D0090.tif" /> wherein each occcurrence of R^4A is independently hydrogen, lower alkyl or C(=O)OR^4B, wherein R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; each occurrence of X is independently a halogen; w is an integer from 0 to 3 and x is an integer from 1 to 6; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted;

[0164] lxxi) compounds of subset lxx) wherein w is 1 ;

[0165] lxxii) compounds of subset lxx) wherein w is 0;

[0166] lxxiii) compounds of subset lxx) wherein x is 1, 3 or 4;

[0167] lxxiv) compounds of subset lxx) wherein X is chlorine or fluorine;

[0168] lxxv) compounds of subset lxx) wherein each occurrence of X is fluorine;

[0169] lxxvi) compounds of subset lxx) wherein R ^A is methyl;

[0170] lxxvii) R is one of:

<img file="WO03106405A1_D0091.tif" /> wherein R^4A is hydrogen, hydroxyl, lower alkyl, lower alkoxy, halogen, C(=O)OR^4B, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteoraryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl or -(heteroalkylheteroaryl;

[0171] lxxviii) R is one of:

<img file="WO03106405A1_D0092.tif" />

[0172] lxxix) R⁴ is one of: <img file="WO03106405A1_D0093.tif" />

[0173] lxxx) R is one of:

<img file="WO03106405A1_D0094.tif" />

[0174] lxxxi) R is one of:

<img file="WO03106405A1_D0095.tif" />

[0175] lxxxii) R', R°, R³ and R³ ' are each hydrogen, X¹ is -C(=O , X³ is -

C(=O)NH-, R¹ is as described in subset xxiv, R² is as described in subset xxxiv, X² is as described in subset li, and R⁴ is as described in subset lxxx; and or [0176] lxxxiii) R', R°, R³ and R³ ' are each hydrogen, X¹ is -C(=O)-, X³ is -

C(=O)NH-, R¹ is as described in subset xxv, R² is as described in subset xxxv, X² is as described in subset Iii, and R⁴ is as described in subset lxxxi [0177] It will be appreciated that for each of the classes and subclasses described above and herein, any one or more occurrences of aliphatic or heteroaliphatic may independently be substituted or unsubstituted, cyclic or acyclic, linear or branched, saturated or unsaturated and any one or more occurrences of aryl, heteroaryl, cycloahphatic, cycloheteroaliphatic may be substituted or unsubstituted. [0178] The reader will also appreciate that all possible combinations of the variables described in i)- through lxxxiii) above (e.g., R', R°, R¹, X¹, R², R³, R³ , X², X³ and R⁴, among others) are considered part of the invention. Thus, the invention encompasses any and all compounds of formula I generated by taking any possible permutation of variables R', R^υ, R .1¹, v Xl¹, R^z, R^J, R 3⁵' , X X^J and \ and other variables/substituents (e.g., R , X1A , r R.X2A , Y, R X3A , _π R4A , etc.) as further defined for R',

R _&gt;o^υ, R¹, X¹, R , R^J, R &gt;3^J' , X\ X^ό and R⁴, described in i)- through lxxxiii) above. [0179] As the reader will appreciate, compounds of particular interest include, among others, those which share the attributes of one or more of the foregoing subclasses. Some of those subclasses are illustrated by the following sorts of compounds:

[0180] I. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0096.tif" /> wherein R° is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -alkylaryl, - heteroalkylaryl, -alkyllieteroalkyl, -heteroalkylheteroaryl, a nitrogen protecting group or a prodrug moiety;

R¹ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R² is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R³ is hydrogen, halogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R⁴ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R⁴, taken together with a substituent present on X³, may form a cycloahphatic, cycloheteroaliphatic, aryl, or heteroaryl moiety;

R^X2A is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkyl)heteroaryl moiety;

Y is independently absent or <img file="WO03106405A1_D0097.tif" /> wherein, for each independent occurrence of t, R^X2B is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkylheteroaryl, -(heteroalkylaryl, or - (heteroalkyl)heteroaryl moiety; t is an integer from 1 to 4; and

X³ is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=0)- , -S(=O)-, -C(=NH)-, -C(=S , -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -S0₂-, - C(-O)NR^X3A-, -C(=S)NR^X3A-, -COO-, (CHR^X3A)_k, -O-, -CH₂NR ^3A-, or -NR^X3A-, wherein each occuπence of R^X3A is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R^X3A taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aryl or heteroaryl moiety, and k is an integer <img file="WO03106405A1_D0098.tif" /> wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, - (hetero alkyl) aryl, and -(heteroalkylheteroaryl moieties may be substituted or unsubstituted.

[0181] In certain embodiments, R³ is halogen, h certain exemplary embodiments, R³ is F.

[0182] h certain embodiments for compounds as described directly above, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0099.tif" />

[0183] In certain exemplary embodiments, R^X2A is a substituted or unsubstituted, linear or branched lower alkyl moiety. In certain other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety.

[0184] II. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0100.tif" /> wherein AR¹ is a su stituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; and R°, R², R³, R⁴ and ^'R^X2 are defined generally above and in classes and subclasses herein.

[0185] hi certain exemplary embodiments, R° is hydrogen and the compound has the structure: <img file="WO03106405A1_D0101.tif" /> [0186] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH2)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, - CN, -NO₂, -C(=O)OR^4B, -N(R^4B)C(=0)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, -(heteroalkylheteroaryl. [0187] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0188] III. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0102.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety and AR² is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; and R , R , R and R are defined generally above and in classes and subclasses herein. [0189] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0103.tif" />

[0190] In certain exemplary embodiments, AR² is ^-fluorophenyl and the compound has the structure: <img file="WO03106405A1_D0104.tif" />

[0191] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0105.tif" />

[0192] IV. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0106.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic moiety; and R°, R², R³ and R^X2A are defined generally above and in classes and subclasses herein.

[0193] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0107.tif" />

[0194] V. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0108.tif" /> wherein R° is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, (alkyl)heteroaryl, or a nitrogen protecting group or a prodrug moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl moiety, or R', taken together with a substituent present on R¹, may form a cycloheteroaliphatic moiety;

R¹ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety; or R¹, taken together with R', may form a cycloheteroaliphatic moiety;

R² is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R³ is hydrogen, halogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkyl)heteroaryl moiety;

R⁴ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R⁴, taken together with a substituent present on X , may form a cycloahphatic, cycloheteroaliphatic, aryl, or heteroaryl moiety;

R^MA is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

Y is independently absent or <img file="WO03106405A1_D0109.tif" /> wherein for each independent occurrence of t, R^X2B is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -

(heteroalkylheteroaryl moiety; t is an integer from 1 to 4; and

X³ is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=O)~ , -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -S0₂-, - C(=O)NR^X3A-, -C(=S)NR^X3A-, -COO-, (CHR^X3A)_k, -O-, -CH₂NR^X3A-, or -NR^X3A-, wherein each occuπence of R^X3A is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkylheteroaryl, -(heteroalkylaryl, or -(heteroalkyl)heteroaryl moiety, or R^X3A taken together with R⁴ may form a cycloaliphatic, cycloheteroaliphatic, aryl or heteroaryl moiety, and k is an integer from 1 to 3; wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, - (heteroalkyl)aryl, and -(heteroalkylheteroaryl moieties may be substituted or unsubstituted.

[0195] hi certain embodiments, R³ is halogen. hi certain exemplary embodiments, R³ is F.

[0196] In certain embodiments for compounds as described directly above, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0110.tif" />

[0197] h certain exemplary embodiments, R^X2A is a substituted or unsubstituted, linear or branched lower alkyl moiety. In certain other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -

(alkyl)heteroaryl or heterocyclic moiety. In certain embodiments, R', taken together with a substituent present on R¹, may form a 5- or 6-membered heterocyclic moiety.

[0198] h other exemplary embodiments, R¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on R¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0111.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or- N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; and wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain other embodiments, R^1E taken together with one occurrence of R^1A, may form a 5- or 6-membered heterocyclic moiety. In certain embodiments, R° is hydrogen.

[0199] VI. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0112.tif" /> wherein AR¹ is a su stituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R², R³, R⁴ and R^X2A are defined generally above and in classes and subclasses herein.

[0200] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0113.tif" /> [0201] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkylheteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, - CN, -NO2, -C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl.

[0202] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occuπences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0203] VII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof): <img file="WO03106405A1_D0114.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety, and AR² is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R , R , R and R are defined generally above and in classes and subclasses herein.

[0204] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0115.tif" /> [0205] In certain exemplary embodiments, AR² is ^-fluorophenyl and the compound has the structure:

<img file="WO03106405A1_D0116.tif" />

[0206] In certain exemplary embo ments, R° i hyd and the compound has the structure:

<img file="WO03106405A1_D0117.tif" />

[0207] VIII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0118.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic moiety; and R°, R², R³ and R^X2A are defined generally above and in classes and subclasses herein.

[0208] h certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0119.tif" />

[0209] In certain embodiments, Ak is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl.

[0210] hi certain embodiments, for compounds of classes VI- VIII, AR¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on AR¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0120.tif" /> wherein R⁴ is as defined generally above and in classes and subclasses herein, or is AR² or Ak as defined above and in classes and subclasses herein;

R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1E&gt; and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -S0₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(-O)R^lc or- N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^lc, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R° is hydrogen. [0211] IX. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0121.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -

(alkyl)heteroaryl or heterocyclic moiety; R' is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or, taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R², R³ and R⁴ are defined generally above and in classes and subclasses herein, hi certain exemplary embodiments, R° is a prodrug moiety.

[0212] In certain exemplary embodiments, R° is a prodrug moiety. In certain other embodiments, R' is hydrogen.

[0213] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occuπences of

R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -

(alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -

CN, -NO₂, -C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -

(alkyl)aryl or -(alkyl)heteroaryl.

[0214] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of

R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0215] X. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0122.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety, and AR² is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; R' is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or, taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R² and R³ are defined generally above and in classes and subclasses herein.

[0216] In certain exemplary embodiments, R° is a prodrug moiety. In certain other embodiments, R' is hydrogen.

[0217] In certain exemplary embodiments, AR² is ^-fluorophenyl and the compound has the structure:

<img file="WO03106405A1_D0123.tif" />

[0218] In certain exemplary embodiments, R° is a prodrug moiety. In certain other embodiments, R' is hydrogen.

[0219] XI. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0124.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; R' is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or, taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic moiety; and R°, R² and R³ are defined generally above and in classes and subclasses herein.

[0220] In certain exemplary embodiments, R° is a prodrug moiety, hi certain other embodiments, R' is hydrogen. h certain embodiments, Ak is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl. [0221] In certain embodiments, for compounds of classes IX-XI above, AR¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on

AR¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0125.tif" /> wherein R is as defined generally above and in classes and subclasses herein, or is AR² or Ak as defined above and in classes and subclasses herein;

R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)_2. - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=0)OR^1B, N(R^1B)C(=O)R^lc or - N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R° is a prodrug moiety. [0222] In certain exemplary embodiments, for compounds of classes II-IV above, R^X2A is methyl, ethyl or isopropyl.

[0223] In certain exemplary embodiments, for compounds of classes II-IV and IV-XI above, R° and R³ are each hydrogen.

[0224] In certain exemplary embodiments, for compounds of classes II-IV above, R and R are each hydrogen; AR is a moiety having one of the structures:

<img file="WO03106405A1_D0126.tif" />

<img file="WO03106405A1_D0127.tif" />

<img file="WO03106405A1_D0128.tif" />

R² is a moiety having one of the structures:

<img file="WO03106405A1_D0129.tif" />

<img file="WO03106405A1_D0130.tif" /><img file="WO03106405A1_D0131.tif" />

<img file="WO03106405A1_D0132.tif" />

R is methyl, ethyl, propyl or benzyl; and R is a moiety having one of the structures:

<img file="WO03106405A1_D0133.tif" />

[0225] In certain exemplary embodiments, for compounds of classes II-IV above, R° and R³ are each hydrogen; AR¹ is a moiety having one of the structures:

<img file="WO03106405A1_D0134.tif" />

R is a moiety having one of the structures: <img file="WO03106405A1_D0135.tif" />

R is methyl, ethyl or isopropyl; and R is a moiety having one of the structures:

<img file="WO03106405A1_D0136.tif" />

[0226] XII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0137.tif" /> wherein R°-R⁴ are as defined generally above and in classes and subclasses herein, and R and each occurrence of R are each independently hydrogen, aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, and t is an integer from 1 to 4.

[0227] h certain other exemplary embodiments for compounds as described directly above, t is 2, R^X2A is methyl and one occurrence of R^X2B is isopropyl, and the compound has the structure:

<img file="WO03106405A1_D0138.tif" /> wherein R »^uo, R _πι¹, R^z, R^J and R⁴ are as defined generally above and in classes and subclasses herein.

[0228] In certain exemplary embodiments, R^X2A is a substituted or unsubstituted, linear or branched lower alkyl moiety. In certain other exemplary embodiments, R° is hydrogen, hi yet other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl or heterocyclic moiety. [0229] XIII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0139.tif" /> wherein AR¹ is substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -

(alkyl)heteroaryl or heterocyclic moieties; and R°, R², R³ and R⁴ are as defined generally above and in classes and subclasses herein.

[0230] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0140.tif" />

[0231] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkylheteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, - CN, -N0₂, -C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl.

[0232] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0233] XIV. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0141.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety, and AR² is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; and R , R and R are defined generally above and in classes and subclasses herein. [0234] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0142.tif" />

[0235] In certain exemplary embodiments, AR² is phenyl and the compound has the structure:

<img file="WO03106405A1_D0143.tif" />

[0236] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0144.tif" />

[0237] XV. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0145.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic moiety; and R , R and R are defined generally above and in classes and subclasses herein.

[0238] h certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0146.tif" /> [0239] In certain embodiments, Ak is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl.

[0240] XVI. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0147.tif" /> wherein R°-R⁴ are as defined generally above and in classes and subclasses herein, R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl moiety, or R', taken together with a substituent present on R¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and

Y Δ "V R

R and each occurrence of R are each independently hydrogen, aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, and t is an integer

[0241] In certain other exemplary embodiments for compounds as described directly above, t is 2, R^X2A is methyl and one occurrence of R^X2B is isopropyl, and the compound has the structure:

<img file="WO03106405A1_D0148.tif" /> wherein R°, R¹, R², R³ and R⁴ are as defined generally above and in classes and subclasses herein.

[0242] In certain exemplary embodiments, R is a substituted or unsubstituted, linear or branched lower alkyl moiety, h certain other exemplary embodiments, R° is hydrogen, hi yet other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl or heterocyclic moiety.

[0243] In other exemplary embodiments, R¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on R¹ forms a cycloheteroaliphatic moiety and the compound has the structure: <img file="WO03106405A1_D0149.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -N0₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or - N(R^1B)S0₂R^1C; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain other embodiments, R^1E, taken together with one occurrence of R^1A, may foπn a 5- or 6-membered heterocyclic moiety. In certain embodiments, R° is hydrogen.

[0244] XVII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0150.tif" /> wherein AR¹ is substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moieties; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R², R³ and R⁴ are as defined generally above and in classes and subclasses herein.

[0245] hi certain exemplary embodiments, R° is hydrogen and the compound has the structure: <img file="WO03106405A1_D0151.tif" />

[0246] hi certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, - CN, -NO₂, -C(=0)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl.

[0247] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0248] XVIII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0152.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety, and AR is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; R^r is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R² and R³ are defined generally above and in classes and subclasses herein.

[0249] h certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0153.tif" /> [0250] In certain exemplary embodiments, AR² is phenyl and the compound has the structure:

<img file="WO03106405A1_D0154.tif" />

[0251] In certain exemplary embodiments, R is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0155.tif" />

[0252] XIX. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0156.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic moiety; and R°, R² and R³ are defined generally above and in classes and subclasses herein.

[0253] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0157.tif" />

In certain embodiments, Ak is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl.

[0254] In certain embodiments, for compounds of classes XVII-XIX above,

AR¹ is a carboxamide-substituted phenyl moiety and the compound has the structure: <img file="WO03106405A1_D0158.tif" /> wherein R &gt;4 . is as defined generally above and in classes and subclasses herein, or is AR² or Ak as defined above and in classes and subclasses herein;

R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occuπence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(-O)OR^1B, N(R^1B)C(=O)R^lc or - N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^lc, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain other embodiments, R^1E, taken together with one occurrence of R^1A, may form a 5- or 6-membered heterocyclic moiety.

[0255] In certain exemplary embodiments, for each of the compounds of classes I-XIX above, R³ is hydrogen, lower alkyl or halogen. In certain other exemplary embodiments, for each of the compounds of classes I-XIX above, R is hydrogen, methyl or F. h certain other exemplary embodiments, for each of the compounds of classes I-XIX above, R is hydrogen. In certain other exemplary embodiments, for each of the compounds of classes I-XIX above, R³ is halogen. In certain other exemplary embodiments, for each of the compounds of classes I-XIX above, R³ is F.

[0256] XX. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0159.tif" /> wherein R° is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -alkylaryl, - heteroalkylaryl, -alkyllieteroalkyl, -heteroalkylheteroaryl, a nitrogen protecting group or a prodrug moiety;

R¹ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R² is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R³ is hydrogen, halogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R⁴ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkylheteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R⁴, taken together with R or a substituent present on Y, may form a cycloahphatic, cycloheteroaliphatic, aryl, or heteroaryl moiety;

R^X2A is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R^X2A is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R^X2A taken together with R⁴ may foπn a cycloahphatic, cycloheteroaliphatic, aryl or heteroaryl moiety; and

Y is <img file="WO03106405A1_D0160.tif" /> wherein for each independent occurrence of t, R^X2B is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -

(alkyl)heteroaryl, -(heteroalkylaryl, or -(heteroalkylheteroaryl moiety, or one occurrence of R ²³ taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aryl or heteroaryl moiety; t is an integer from 1 to 4; wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -

(heteroalkyl)aryl, and -(heteroalkylheteroaryl moieties may be substituted or unsubstituted. [0257] In certain exemplary embodiments for compounds as described directly above, R° and R^X2A are each hydrogen, and the compound has the structure:

<img file="WO03106405A1_D0161.tif" />

[0258] In certain other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl or heterocyclic moiety.

[0259] XXI. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0162.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; and R°, R² and R⁴ are defined generally above and in classes and subclasses herein. [0260] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0163.tif" />

[0261] h certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl or phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -CN, -NO₂, - C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl.

[0262] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl or phenyl, wherein the phenyl group is optionally substituted with one or more occuπences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen. [0263] XXII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0164.tif" /> wherein R°-R² and R⁴ are as defined generally above and in classes and subclasses herein, t is an integer from 1 to 3, and R and each occurrence of R are each independently hydrogen, aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl. [0264] In certain other exemplary embodiments for compounds as described directly above, R &gt;X2A is methyl, t is 2, one occurrence of R X2B is isopropyl, and the compound has the structure:

<img file="WO03106405A1_D0165.tif" /> wherein R°, R¹, R² and R⁴ are as defined generally above and in classes and subclasses herein.

[0265] h certain exemplary embodiments, R^X2A is a substituted or unsubstituted, linear or branched lower alkyl moiety. In certain other exemplary embodiments, R° is hydrogen. In yet other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl or heterocyclic moiety.

[0266] XXIII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0166.tif" /> wherein AR¹ is substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moieties; and R°, R² and R⁴ are as defined generally above and in classes and subclasses herein. [0267] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0167.tif" />

[0268] hi certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, - CN, -NO₂, -C(=0)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkylheteroaryl.

[0269] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0270] XXIV. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0168.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic , and AR² are is a substituted or unsubstituted aryl,

O 9 heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; and R and R are defined generally above and in classes and subclasses herein.

[0271] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0169.tif" />

[0272] In certain exemplary embodiments, AR is phenyl and the compound has the structure: <img file="WO03106405A1_D0170.tif" />

[0273] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0171.tif" />

[0274] XXV. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0172.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic moiety; and R° and R² are as defined generally above and in classes and subclasses herein.

[0275] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0173.tif" />

[0276] In certain embodiments, Ak is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl.

[0277] XXVI. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0174.tif" /> wherein R° is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, or a nitrogen protecting group or a prodrug moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl moiety, or R', taken together with a substituent present on R¹, may form a cycloheteroaliphatic moiety;

R¹ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R¹ taken together with R may form a cycloheteroaliphatic moiety;

R² is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R³ is hydrogen, halogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R⁴ is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or R⁴, taken together with R^X2A or a substituent present on Y, may form a cycloahphatic, cycloheteroaliphatic, aryl, or heteroaryl moiety; jl^K2A is hydrogen or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety;

R^X2A is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkyl)heteroaryl moiety, or s ^' ^^2A taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aryl or heteroaryl moiety; and

<img file="WO03106405A1_D0175.tif" /> wherein for each independent occurrence of t, R^X2B is hydrogen, or an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -

(alkyl)heteroaryl, -(heteroalkyl)aryl, or -(heteroalkylheteroaryl moiety, or one occurrence of R^X2B taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aryl or heteroaryl moiety; t is an integer from 1 to 4; wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -

(heteroalkyl)aryl, and -(heteroalkylheteroaryl moieties may be substituted or unsubstituted. [0278] In certain exemplary embodiments for compounds as described directly above, R° and R^X2A are each hydrogen, and the compound has the structure:

<img file="WO03106405A1_D0176.tif" />

[0279] In certain other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl or heterocyclic moiety.

[0280] hi other exemplary embodiments, R¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on R¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0177.tif" /> wherein R and R are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or - ι TI i f* 1 R 1 c¹

N(R )Sθ₂R ; wherein each occcuπence of R andR is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain other embodiments, R^1E, taken together with one occurrence of R^1A, may form a 5- or 6-membered heterocyclic moiety. In certain embodiments, R° is hydrogen.

[0281] XXVII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0178.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R² and R⁴ are defined generally above and in classes and subclasses herein.

[0282] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0179.tif" />

[0283] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl or phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -CN, -NO₂, - C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl.

[0284] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl or phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0285] In certain embodiments, AR¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on AR¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0180.tif" /> wherein R is as defined generally above and in classes and subclasses herein, or is AR² or Ak as defined above and in classes and subclasses herein; R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or- N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain other embodiments, R^1E, taken together with one occurrence of R^1A may form a 5- or 6-membered heterocyclic moiety. In certain embodiments, R° is hydrogen.

[0286] XXVIII. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0181.tif" /> wherein R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl moiety, or R', taken together with a substituent present on R¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; R°- R² and R⁴ are as defined generally above and in classes and subclasses herein, t is an

* "-) * ' V"9R integer from 1 to 4, and R and each occurrence of R are each independently hydrogen, aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl. [0287] In certain other exemplary embodiments for compounds as described directly above, R ^ is methyl, t is 2, one occurrence of R ^2B is isopropyl, and the compound has the structure:

<img file="WO03106405A1_D0182.tif" /> wherein R', R°, R¹, R² and R⁴ are as defined generally above and in classes and subclasses herein.

[0288] h certain exemplary embodiments, R^X3A is a substituted or unsubstituted, linear or branched lower alkyl moiety. In certain other exemplary embodiments, R° is hydrogen. In yet other exemplary embodiments, R¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl or heterocyclic moiety.

[0289] In other exemplary embodiments, R¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on R¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0183.tif" /> wherein R ^D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, foπn a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or-

N(R<img file="WO03106405A1_D0184.tif" /> is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^ID and R^1E are each independently hydrogen, methyl, ethyl or propyl. . In certain other embodiments, R^1E, taken together with one occurrence of R^1A, may form a 5- or 6-membered heterocyclic moiety, h certain embodiments, R is hydrogen.

[0290] XXIX. Compounds having the structure (and pharmaceutically acceptable derivatives thereof): <img file="WO03106405A1_D0185.tif" /> wherein AR¹ is substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moieties; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R°, R² and R⁴ are as defined generally above and in classes and subclasses herein.

[0291] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0186.tif" />

[0292] In certain other exemplary embodiments, R ι4 is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH2)phenyl, wherein the phenyl group is optionally substituted with one or more occuπences of R^4A wherein R^4A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, -SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, - CN, -NO₂, -C(=O)OR^4B, -N(R^4B)C(=O)R^4c, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl.

[0293] In certain other exemplary embodiments, R⁴ is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl, phenyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^4A, wherein R^4A is hydrogen, hydroxyl, alkyl, alkoxy or halogen.

[0294] XXX. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0187.tif" /> wherein AR¹ is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, (alkyl)heteroaryl or heterocyclic , and AR² is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; and R° and R² are defined generally above and in classes and subclasses herein.

[0295] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0188.tif" />

[0296] In certain exemplary embodiments, AR .2 : is phenyl and the compound has the structure:

<img file="WO03106405A1_D0189.tif" />

[0297] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0190.tif" />

[0298] XXXI. Compounds having the structure (and pharmaceutically acceptable derivatives thereof):

<img file="WO03106405A1_D0191.tif" /> wherein AR is a substituted or unsubstituted aryl, heteroaryl, -(alkyl)aryl, - (alkyl)heteroaryl or heterocyclic moiety; R' is an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl moiety, or R', taken together with a substituent present on AR¹, may form a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; Ak is a substituted or unsubstituted, linear or branched, cyclic or acyclic, saturated or unsaturated aliphatic or heteroaliphatic

0 9 moiety; and R and R are as defined generally above and in classes and subclasses herein. [0299] In certain exemplary embodiments, R° is hydrogen and the compound has the structure:

<img file="WO03106405A1_D0192.tif" />

[0300] In certain embodiments, Ak is substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl.

[0301] In certain embodiments, for compounds of classes XXIX-XXXI above, AR¹ is a carboxamide-substituted phenyl moiety, R taken together with a substituent on AR¹ forms a cycloheteroaliphatic moiety and the compound has the structure:

<img file="WO03106405A1_D0193.tif" /> wherein R⁴ is as defined generally above and in classes and subclasses herein, or is AR² or Ak as defined above and in classes and subclasses herein;

R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C( ))OR^1B, N(R^1B)C(=O)R^lc or- N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)lιeteroaryl, or R^1B and R^lc, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein a is 0 or 1 and n is an integer from 0 to 3. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. . In certain other embodiments, R , taken together with one occurrence of R ^A, may form a 5- or 6-membered heterocyclic moiety. In certain embodiments, R° is hydrogen.

[0302] In certain embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently one of: <img file="WO03106405A1_D0194.tif" />

wherein R^1A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, - CN, -N0₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or -N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; R^1D is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, acyl or a nitrogen protecting group; wherein n and p are each independently integers from 0 to 3 and r is an integer from 1 to 6. In certain embodiments, in compounds where R' is not hydrogen, R', taken together with one occuπence of R^1A, may form a 5- or 6-membered heterocyclic moiety. [0303] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R¹ and/or AR¹ are each independently one of: <img file="WO03106405A1_D0195.tif" /> wherein each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, - SO₂N(R^1B)₂, -C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or -N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^lc, taken together with the atoms to which they are attached, fonn a substituted or unsubstituted heterocyclic moiety; wherein n and p are each independenly an integer from 0 to 4. In certain embodiments, in compounds where R' is not hydrogen, R', taken together with one occurrence of R^1A, may form a 5- or 6- membered heterocyclic moiety.

[0304] In other exemplary embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently one of:

<img file="WO03106405A1_D0196.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; wherein R^1D and R^1E taken together form a 5-8 membered heterocyclic ring; each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^IB)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, N(R^1B)C(=0)R^1C or - N(R^1B)S0₂R^1C; and each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein n and p are each independenly an integer from 0 to 4. In certain exemplary embodiments, p is 0. In certain embodiments, in compounds where R' is not hydrogen, R', taken together with one occurrence of R^1A, may form a 5- or 6-membered heterocyclic moiety.

[0305] In other embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently one of:

<img file="WO03106405A1_D0197.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; ; or R^1D and R^1E taken together form a 5-8 membered heterocyclic ring; or R^1E and one occuπence of R^1A, taken together, form a substituted or unsubstituted, saturated or unsaturated heterocyclic ring; each occurrence of R^1A and R^1B is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^lc, -SR^1C, -N(R^1C)₂, - S0₂N(R^IC)₂, -C(=O)N(R^lc)₂, halogen, -CN, -NO₂, -C(=O)OR^lc, -N(R^lc)C(=O)R^1D, wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein n is an integer from 0 to 4.

[0306] In other embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently a carboxamide-substituted phenyl moiety having the structure:

<img file="WO03106405A1_D0198.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -S0₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -N0₂, -C(=O)OR^1B, N(R^1B)C(=O)R^lc or- N(R^1B)SO₂R^lc; wherein each occcurrence of R^1B and R^1C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; wherein n is an integer from 0 to 4. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain embodiments, R° is hydrogen.

[0307] In other exemplary embodiments, R^1E and one occurrence of R^1A, taken together, form a 5- or 6-membered heterocyclic moiety and the carboxamide- substituted phenyl moiety has the structure:

<img file="WO03106405A1_D0199.tif" /> wherein a is 0 or 1 and n is from 0 to 4. [0308] In other exemplary embodiments, R^1D and R^1E are each propyl and the carboxamide-substituted phenyl moiety has the structure:

<img file="WO03106405A1_D0200.tif" /> wherein R^1A is halogen, or substituted or unsusbtituted, linear or branched lower alkyl or lower alkoxy.

[0309] In yet other exemplary embodiments, R^1D and R^1E, taken together, form a substituted or unsusbtituted piperazine moiety and the carboxamide-substituted phenyl moiety has the structure:

<img file="WO03106405A1_D0201.tif" /> wherein R^1A is halogen, or substituted or unsusbtituted, linear or branched lower alkyl or lower alkoxy, and R^1B is hydrogen or substituted or unsubstituted lower alkyl.

[0310] In certain embodiments, for each of the four carboxamide-substituted phenyl moieties described directly above, R° is hydrogen. In certain other embodiments, R^1A is methyl, methoxy or halide. In certain exemplary embodiments, R^1A is methyl, methoxy or F. In yet other exemplary embodiments, R^1A is methyl. In certain other embodiments, R^1B is hydrogen, methyl or ethyl.

[0311] hi other exemplary embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently a sulfonamide-substituted phenyl moiety having the structure:

<img file="WO03106405A1_D0202.tif" /> wherein R^1D and R^1E are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; or R^1D and R^1E, taken together, form a 5-8 membered heterocyclic ring; and each occuπence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, -SO₂N(R^1B)₂, - C(=O)N(R^1B)₂, halogen, -CN, -NO₂, -C(=O)OR^1B, -N(R^1B)C(=0)R^1C, wherein each occcurrence of R^1B and R^lc is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein n is an integer from 0 to 4. In certain embodiments, R^1D and R^1E are each independently hydrogen, methyl, ethyl or propyl. In certain embodiments, R° is hydrogen. [0312] In other exemplary embodiments, R^1D and R^1E are each propyl and the sulfonamide-substituted phenyl moiety has the structure:

<img file="WO03106405A1_D0203.tif" /> wherein R^1A is halogen, or substituted or unsusbtituted, linear or branched lower alkyl or lower alkoxy.

[0313] In yet other exemplary embodiments, R^1D and R^1E, taken together, form a substituted or unsusbtituted piperazine moiety and the sulfonamide-substituted phenyl moiety has the structure:

<img file="WO03106405A1_D0204.tif" /> wherein R^1A is halogen, or substituted or unsusbtituted, linear or branched lower alkyl or lower alkoxy, and R^1B is hydrogen or substituted or unsubstituted lower alkyl.

[0314] In certain embodiments, for each of the three sulfonamide-substituted phenyl moieties described directly above, R° is hydrogen. In certain other embodiments, R^1A is methyl, methoxy or halide. hi certain exemplary embodiments, R^1A is methyl, methoxy or F. hi yet other exemplary embodiments, R^1A is methyl. In certain other embodiments, R^1B is hydrogen, methyl or ethyl.

[0315] In other exemplary embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently a moiety having the structure:

OR^1A

wherein R^1A and R^1B are each in Adependently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^lc, -SR^1C, -N(R^1C)₂, -SO₂N(R^lc)₂, - C(=O)N(R^lc)₂, halogen, -CN, -NO₂, -C(=O)OR^lc, -N(R^lc)C(=O)R^1D, wherein each occcurrence of R^1C and R^1D is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl. In certain embodiments, R^1A and R^1B are each independently cyclic or acyclic lower alkyl. In certain embodiments, R^1A and R^1B are each independently methyl, ethyl, propyl, butyl, pentyl, isopropyl, isobutyl, sec-butyl, isopentyl or cyclopropyl. [0316] In other exemplary embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently a moiety having the structure:

<img file="WO03106405A1_D0205.tif" /> wherein R^1A and R^1C are each independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl, -(alkylheteroaryl, -C(=O)R^1D, -SO₂R^1D or a nitrogen protecting group, or R^1A and R^lc, taken together with the nitrogen atom to which they are attached, form a substituted or unsubstituted heterocyclic moiety; and R^1B and R^1D are each independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted. In certain embodiments, R^1B is substituted or unsubstituted, linear or branched, cyclic or acyclic lower alkyl; R^1A is lower alkyl; and R^1C is -SO R^1D wherein R^1D is lower alkyl. In certain embodiments, R^1B is substituted or unsubstituted, linear or branched, cyclic or acyclic lower alkyl; R^1A and R^1C, taken together with the nitrogen atom to which they are attached, form a 5- or 6- membered cyclic sulfonamide moiety.

[0317] In other exemplary embodiments, for compounds of classes I-XXXI above, R¹ and/or AR¹ are each independently a moiety having one of the following structures:

<img file="WO03106405A1_D0206.tif" /> wherein each occurrence of R^1A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^1B, -SR^1B, -N(R^1B)₂, - SO₂N(R^1B)₂, -C(=0)N(R^1B)₂, halogen, -CN, -NO₂, -C(=0)OR^1B, -N(R^1B)C(=0)R^1C or <img file="WO03106405A1_D0207.tif" /> is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl) aryl or -(alkyl)heteroaryl, or R^1B and R^1C, taken together with the atoms to which they are attached, form a substituted or unsubstituted heterocyclic moiety; R^1D is linear or branched lower alkyl and n and p are independently integers from 0 to 3. In certain embodiments, p is 1. [0318] hi yet other exemplary embodiments, for compounds of classes I-

XXXI above, R¹ and/or AR¹ are each independently a moiety having one of the following structures:

<img file="WO03106405A1_D0208.tif" />

[0319] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R¹ and/or AR¹ are each independently a moiety having one of the following structures: <img file="WO03106405A1_D0209.tif" />

[0320] In certain exemplary embodiments, for compounds of classes I-XXXI above, R² is lower alkyl or -(CH )phenyl, wherein the phenyl group is optionally substituted with one or more occuπences of R^2A, wherein R^2A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, -OR^2B, -SR^2B, - N(R^2B)₂, -S0₂N(R^2B)₂, -C(=O)N(R^2B)₂, halogen, -CN, -NO₂, -C(=O)OR^2B, - N(R^2B)C(=O)R^2C, wherein each occcurrence of R^2B and R^2C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl.

[0321] In certain other exemplary embodiments, for compounds of classes I-

XXXI above, R² is lower alkyl, -CH₂NR^2AR^2B or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R , wherein R is hydrogen, alkyl, alkoxy or halogen; and wherein R^2A and R^2B are each independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted.

[0322] In certain other exemplary embodiments, for compounds of classes I-

XXXI above, R² is lower alkyl or -(CH₂)phenyl, wherein the phenyl group is optionally substituted with one or more occurrences of R^2A, wherein R^2A is hydrogen, alkyl, alkoxy or halogen.

[0323] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R² is one of: <img file="WO03106405A1_D0210.tif" />

,2A. .

^,R ^ r&gt; "ζ*^ °^D^ ^(R ^&gt;

<img file="WO03106405A1_D0211.tif" /> wherein R^2A is hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or - (alkyl)heteroaryl, -OR^2B, -SR^2B, -N(R^2B)₂, -SO₂N(R^2B)₂, -C(=O)N(R^2B)₂, halogen, - CN, -NO₂, -C(=O)OR^2B, -N(R^2B)C(=O)R^2C, wherein each occcurrence of R^2B and R^2C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl, wherein q and s are each independently integers from 0 to 3 and u is an integer from 1 to 6; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted.

[0324] In still other exemplary embodiments, for compounds of classes I-

XXXI above, R² is one of: <img file="WO03106405A1_D0212.tif" /> wherein each occcuπence of R^2A is independently hydrogen or lower alkyl; each occurrence of X is independently a halogen; s is an integer from 0 to 3 and u is an integer from 1 to 6; whereby each of the foregoing alkyl moieties may be linear or branched, substituted or unsubstituted and cyclic or acylic. In certain embodiments, X is chlorine or fluorine. In certain other embodiments, each occurrence of X is fluorine. In yet other embodiments, R^2A is methyl.

[0325] In still other embodiments, for compounds of classes I-XXXI above,

R² is one of:

<img file="WO03106405A1_D0213.tif" />

[0326] In certain exemplary embodiments, for compounds of classes I-XXXI above, R is one of:

<img file="WO03106405A1_D0214.tif" />

[0327] In certain exemplary embodiments, for compounds of classes I-XXXI above, R is one of:

<img file="WO03106405A1_D0215.tif" />

[0328] In certain exemplary embodiments, for compounds of classes I-XXXI above, R is one of:

<img file="WO03106405A1_D0216.tif" />

[0329] In certain other exemplary embodiments, for compounds of classes I-

A 9

XXXI above, R and/or AR are each independently one of: <img file="WO03106405A1_D0217.tif" /> wherein each occuπence of R^4A is independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, - SO₂N(R^4B)₂, -C(=O)N(R^4B)₂, halogen, -CN, -NO₂, -C(-O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcurrence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein v and w are each independently integers from 0 to 3 and x is an integer from 1 to 6. [0330] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or AR² are each independently one of:

<img file="WO03106405A1_D0218.tif" /> wherein each occcurrence of R^4A is independently hydrogen, lower alkyl or C(=O)OR^4B, wherein R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; each occurrence of X is independently a halogen; w is an integer from 0 to 3 and x is an integer from 1 to 6. In certain embodiments, w is 0. In other embodiments, w is 1. In certain other exemplary embodiments, x is 1, 3 or 4. In yet other exemplary embodiments, X is chlorine or fluorine. In yet other embodiments, R^4A is hydrogen or methyl; In certain other embodiments, AR² is phenyl or -(CH₂)phenyl, wherein the phenyl group is substituted at the para position with one occurrence of R^4A, wherein R^4A is hydrogen, hydroxyl, lower alkyl, lower alkoxy, halogen, C(=0)OR^4B, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl. [0331] In certain other embodiments, for compounds of classes I-XXXI above, R⁴ and/or AR² are each independently phenyl or -(CH₂)phenyl, wherein the phenyl group is substituted at the para position with one occurrence of R^4A, wherein R^4A is hydrogen, hydroxyl, lower alkyl, lower alkoxy, halogen, C(=O)OR^4B, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or ~(alkyl)heteroaryl. [0332] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or AR² are each independently one of:

<img file="WO03106405A1_D0219.tif" /> wherein R^4A is hydrogen, hydroxyl, lower alkyl, lower alkoxy, halogen, C(=O)OR^4B, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteoraryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl or -(heteroalkylheteroaryl; [0333] hi yet other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or AR² are each independently one of:

<img file="WO03106405A1_D0220.tif" />

[0334] In certain other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or Ak are each independently a substituted or unsubstituted, linear or branched, cyclic or acyclic alkyl. In certain exemplary embodiments, R⁴ and/or Ak are each independently one of: <img file="WO03106405A1_D0221.tif" /> wherein each occurrence of R &gt;4A i ^■s independently hydrogen, alkyl, heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkylheteroaryl, -OR^4B, -SR^4B, -N(R^4B)₂, - S0₂N(R^4B)₂, -C(=0)N(R^4B)₂, halogen, -CN, -N0₂, -C(=O)OR^4B, -N(R^4B)C(=O)R^4C, wherein each occcuπence of R^4B and R^4C is independently hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein v and w are each independently integers from 0 to 3 and x is an integer from 1 to 6. In certain embodiments, w is 1.

[0335] In certain other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or Ak are each independently one of:

<img file="WO03106405A1_D0222.tif" /> wherein each occcurrence of R^4A is independently hydrogen, lower alkyl or C(=O)OR^4B, wherem R^4B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl; each occurrence of X is independently a halogen; w is an integer from 0 to 3 and x is an integer from 1 to 6; whereby each of the foregoing alkyl and heteroalkyl moieties may be linear or branched, substituted or unsubstituted, cyclic or acylic, and each of the foregoing aryl, heteroaryl, -(alkyl)aryl and -(alkyl)heteroaryl moieties may be substituted or unsusbtituted. [0336] In certain other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or Ak are each independently one of: <img file="WO03106405A1_D0223.tif" />

<img file="WO03106405A1_D0224.tif" /><img file="WO03106405A1_D0225.tif" /> wherein R^4A is hydrogen, hydroxyl, lower alkyl, lower alkoxy, halogen, C(=O)OR^4B, aryl, heteroaryl, -(alkyl)aryl or -(alkyl)heteroaryl, wherein R ^B is hydrogen, lower alkyl, lower heteroalkyl, aryl, heteoraryl, -(alkyl)aryl, - (alkyl)heteroaryl, -(heteroalkyl)aryl or -(heteroalkylheteroaryl. [0337] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or Ak are each independently one of:

<img file="WO03106405A1_D0226.tif" />

[0338] In yet other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or Ak are each independently one of:

<img file="WO03106405A1_D0227.tif" />

[0339] hi yet other exemplary embodiments, for compounds of classes I-

XXXI above, R⁴ and/or Ak are each independently one of:

<img file="WO03106405A1_D0228.tif" />

[0340] It will also be appreciated that for each of the subgroups I-XXXI described above, a variety of other subclasses are of special interest, including, but not limited to those classes described above i)-lxx) and classes, subclasses and species of compounds described above and in the examples herein.

[0341] Some of the foregoing compounds can comprise one or more asymmetric centers, and thus can exist in various isomeric forms, e.g., stereoisomers and/or diastereomers. Thus, inventive compounds and pharmaceutical compositions thereof may be in the form of an individual enantiomer, diastereomer or geometric isomer, or may be in the form of a mixture of stereoisomers. hi certain embodiments, the compounds of the invention are enantiopure compounds, h certain other embodiments, mixtures of stereoisomers or diastereomers are provided. [0342] Furthermore, certain compounds, as described herein may have one or more double bonds that can exist as either the Z or E isomer, unless otherwise indicated. The invention additionally encompasses the compounds as individual isomers substantially free of other isomers and alternatively, as mixtures of various isomers, e.g., racemic mixtures of stereoisomers. In addition to the above-mentioned compounds per se, this invention also encompasses pharmaceutically acceptable derivatives of these compounds and compositions comprising one or more compounds of the invention and one or more pharmaceutically acceptable excipients or additives. Compounds of the invention may be prepared by crystallization of compound of formula (I) under different conditions and may exist as one or a combination of polymorphs of compound of general formula (I) forming part of this invention. For example, different polymorphs may be identified and/or prepared using different solvents, or different mixtures of solvents for recrystallization; by performing crystallizations at different temperatures; or by using various modes of cooling, ranging from very fast to very slow cooling during crystallizations. Polymorphs may also be obtained by heating or melting the compound followed by gradual or fast cooling. The presence of polymorphs may be determined by solid probe NMR spectroscopy, IR spectroscopy, differential scanning calorimetry, powder X-ray diffractogram and/or other techniques. Thus, the present invention encompasses inventive compounds, their derivatives, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them.

[0343] 2) Synthetic Overview: [0344] The practitioner has a a well-established literature of peptide chemistry to draw upon, in combination with the information contained herein, for guidance on synthetic strategies, protecting groups, and other materials and methods useful for the synthesis of the compounds of this invention, including compounds containing the various R', R°, R¹, R², R³ and R^3' substituents and X¹, X² and X³ moieties. [0345] The various patent documents and other references cited herein provide helpful background information on preparing compounds similar to the inventive compounds described herein or relevant intermediates, as well as information on fonnulation, uses, and administration of such compounds which may be of interest.

[0346] Moreover, the practitioner is directed to the specific guidance and examples provided in this document relating to various exemplary compounds and intermediates thereof.

[0347] As described above, the present invention provides novel compounds, specifically compounds having the following general structure:

<img file="WO03106405A1_D0229.tif" />

(I) and pharmaceutically acceptable derivatives thereof; wherein R° is hydrogen, an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or a nitrogen protecting group, or a prodrug moiety; or R°, taken together with R' or a substituent present on X , may form a cycloheteroaliphatic moiety;

R' is hydrogen or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R', taken together with R°, R² or a substituent present on R¹, may form a cycloheteroaliphatic moiety;

R¹ is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R¹ taken together with R may form a cycloheteroaliphatic moiety;

X¹ is -C(=0)-, -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=O)-, -NC(=S)-, -N-C(=N- C N)-, -NS(O₂)-, -CHR^X1A-, -SO₂-, -COO-, -C(=O)C(R^xlA)₂-, or -SC(=0)- wherein each occurrence of R is independently hydrogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety; . R² is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R², taken together with R', may form a cycloheteroaliphatic moiety;

R³ is hydrogen, halogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety;

R³ is hydrogen, halogen, or lower alkyl;

R⁴ is an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R⁴, taken together with a substituent present on X² or X³, may form a cycloahphatic, cycloheteroaliphatic, aromatic, or heteroaromatic moiety;

X² is absent, <img file="WO03106405A1_D0230.tif" /> or - N(R^X2A)CH(R^X2A)Y- wherein each occurrence of R^X2A is independently hydrogen or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R taken together with R° may form a cycloheteroaliphatic moiety, each occurrence of Y is

independently <img file="WO03106405A1_D0231.tif" />^x . wherein, for each independent occurrence of t,

R^X2B is hydrogen, or an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R or one occurrence of R taken together with R may form a cycloahphatic, cycloheteroaliphatic, aromatic or heteroaromatic moiety, and wherein each occurrence of j and t is independently an integer from 1 to 4; and

X³ is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=0)- , -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR^X3A-, -C(=S)NR^X3A-, -COO-, -(CHR^x3A)_k-, -O-, ,CH₂NR^X3A-_; or ,NR^X3A-, wherein each occurrence of R^X3A is independently hydrogen, an aliphatic, heteroaliphatic, aromatic or heteroaromatic moiety, or R^X3A taken together with R⁴ may form a cycloahphatic, cycloheteroaliphatic, aromatic or heteroaromatic moiety, and k is an integer from 1 to 3; wherein each of the foregoing aliphatic or heteroaliphatic moieties may be independently substituted or unsubstituted, linear or branched, cyclic or acyclic, and each of the foregoing aromatic, heteroaromatic, aryl and heteroaryl moieties may be substituted or unsubstituted.

[0348] It will be appreciated that for compounds as generally described above, certain classes of compounds are of special interest. For example, one class of compounds of special interest includes those compounds wherein the compound has the stereochemistry as shown in Formula (I^A):

<img file="WO03106405A1_D0232.tif" /> (I^A)

[0349] Another class of compounds of special interest includes those ccoommppoouunnddss wwhheerreeiinn RR'',, RR° aanndd RR³ are each hydrogen and the compound has the structure as shown in Formula (IF):

<img file="WO03106405A1_D0233.tif" />

(II')

[0350] Another class of compounds of special interest includes those compounds wherein the compound has the stereochemistry as shown in Formula

(II'^A):

<img file="WO03106405A1_D0234.tif" /> (II'^A)

[0351] In yet another aspect of the invention, methods for producing inteπnediates useful for the preparation of compounds of fonnulae (I) and (I^A), through the formation of the free amino derivatives (I') and (T^A), are provided, embodiments of said methods being depicted generally in Schemes A and Ai-.

<img file="WO03106405A1_D0235.tif" />

Scheme A <img file="WO03106405A1_D0236.tif" />

Scheme Ai

[0352] Alternatively, substituent R³' may be introduced at a later stage in the synthesis, as depicted for example in Schemes A₂ and A :

<img file="WO03106405A1_D0237.tif" />

<img file="WO03106405A1_D0238.tif" />

(0

Scheme A2

<img file="WO03106405A1_D0239.tif" /> [0353] In certain embodiments, the inventive method comprises i) providing a compound having the structure:

<img file="WO03106405A1_D0240.tif" /> wherein R', R², R³, R³ and X² are as defined generally above and in classes and subclasses herein,

R^pl is a nitrogen protecting group;

A is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=O)-, -S(=O)-, -C(=NH)-, -C(=S)~, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR⁵-, -C(=S)NR⁵-, -COO-, -(CHR⁵) , -O-, -CH₂NR⁵- or -NR⁵-, wherein each occuπence of R⁵ is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or - (heteroalkylheteroaryl moiety, and k is an integer from 1 to 3; and

B is a protecting group, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety, or is -NR^C, wherein N is -0-, -ΝR^D-, - C(=O)-, -S(=0)- or -SO₂-, wherein each occurrence of R and R is independently hydrogen, a protecting group or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety; ii) reacting the compound of step (i) under suitable conditions to generate a compound having the structure:

<img file="WO03106405A1_D0241.tif" /> wherein U is -NHR^P2 or -N₃, wherein R^p2 is a nitrogen protecting group; iii) reacting the compound of step (ii) with suitable reagents to generate a compound having the structure:

<img file="WO03106405A1_D0242.tif" /> iv) reacting the compound of step (iii) with suitable reagents to generate the free amine having the structure :

<img file="WO03106405A1_D0243.tif" /> (T) wherein R', R¹, R², R³, R^3', R⁴, X¹, X² and X³ are as defined generally above and in classes and subclasses herein. [0354] In certain embodiments, the present invention encompasses methods for the preparation of compounds having the general formula (I'A), and classes and subclasses herein.

<img file="WO03106405A1_D0244.tif" /> (I'^A)

[0355] In certain embodiments, the method comprises: i) providing a compound having the structure:

<img file="WO03106405A1_D0245.tif" />

wherein R', R², R , R and X are as defined above,

R^pl is a nitrogen protecting group;

A is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=O)-, -S(=O)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR⁵-, -C(=S)NR⁵-, -COO-, -(CHR⁵) , -O-, -CH₂NR⁵- or -NR⁵-, wherein each occuπence of R⁵ is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or - (heteroalkylheteroaryl moiety, and k is an integer from 1 to 3; and

B is a protecting group, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety, or is -VR^C, wherein V is -O-, -NR^D-, - C(=O)-, -S(=0)- or -SO₂-, wherein each occurrence of R^c and R^D is independently hydrogen, a protecting group or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety; ii) reacting the compound of step (i) under suitable conditions to generate a compound having the structure:

<img file="WO03106405A1_D0246.tif" /> wherein U is -NHR^P2 or -N₃, wherein R^p2 is a nitrogen protecting group; iii) reacting the compound of step (ii) with suitable reagents to generate a compound having the structure:

<img file="WO03106405A1_D0247.tif" /> iv) reacting the compound of step (iii) with suitable reagents to generate the free amine having the structure (I'^A):

<img file="WO03106405A1_D0248.tif" /> (I'^A) wherein R', R¹, R², R³, R^3', R⁴, X¹, X² and X³ are as defined generally above and in classes and subclasses herein.

[0356] In yet another aspect of the invention, methods for producing intermediates useful for the preparation of compounds of formulas (I") and (I"^A) are provided, embodiments of said methods being depicted generally in Schemes A4 and

A₅:

<img file="WO03106405A1_D0249.tif" />

Scheme A₄

<img file="WO03106405A1_D0250.tif" />

ill Scheme As

[0357] hi certain embodiments, the inventive method comprises i) providing a compound having the structure:

<img file="WO03106405A1_D0251.tif" /> wherein R², R³, and X² are as defined above,

R^pl is a nitrogen protecting group;

A is absent, -NHCO-, -NHSO₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=O)-, -S(=O)-, -C(=NH)-, -C(=S , -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=0)NR⁵-, -C(=S)NR⁵-, -COO-, -(CHR⁵) , -O-, -CH₂NR⁵- or -NR⁵-, wherein each occurrence of R⁵ is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, -(alkyl)heteroaryl, -(heteroalkyl)aryl, or - (heteroalkylheteroaryl moiety, and k is an integer from 1 to 3; and

B is a protecting group, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - f* r_

(alkyl)aryl or -(alkyl)heteroaryl moiety, or is -NR , wherem V is -O-, -ΝR -, -

C(=O)-, -S(=O)- or -SO₂-, wherein each occurrence of R and R is independently hydrogen, a protecting group or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety; ii) reacting the compound of step (i) under suitable conditions to generate a compound having the structure:

<img file="WO03106405A1_D0252.tif" /> wherein U is -ΝHR^P2 or -N₃, wherein R^P2 is a nitrogen protecting group; iii) reacting the compound of step (ii) with suitable reagents to generate a compound having the structure:

<img file="WO03106405A1_D0253.tif" /> iv) reacting the compound of step (iii) with suitable reagents to generate the free amine having the structure : <img file="WO03106405A1_D0254.tif" />

wherein R¹, R², R³, R⁴, X¹, X² and X³ are as defined generally above and in classes and subclasses herein.

[0358] In certain embodiments, the present invention encompasses methods for the preparation of compounds having the general formula (I"A), and classes and subclasses herein.

<img file="WO03106405A1_D0255.tif" />

(i^"A)

[0359] In certain embodiments, the method comprises: i) providing a compound having the structure:

<img file="WO03106405A1_D0256.tif" />

wherein R², R³, and X² are as defined above,

R^P1 is a nitrogen protecting group;

A is absent, -NHCO-, -NHS0₂-, -NHCONH-, -NHCOO-, -CH₂NH-, -C(=O)-, -S(=0)-, -C(=NH)-, -C(=S)-, -NC(=S)N-, -N-C(=N-C N)N-, -NS(O₂)N-, -SO₂-, - C(=O)NR⁵-, -C(=S)NR⁵-, -COO-, -(CHR⁵)_r-, -O-, -CH₂NR⁵- or -NR⁵-, wherein each occurrence of R⁵ is independently hydrogen, an aliphatic, heteroaliphatic, aryl, heteroaryl, -(alkyl)aryl, i -(alkyl)heteroaryl, -(heteroalkyl)aryl, or - (heteroalkylheteroaryl moiety, and k is an integer from 1 to 3; and

B is a protecting group, or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety, or is -VR^C, wherein V is -O-, -NR^D-, - C(=O)-, -S(=O)- or -SO₂-, wherein each occurrence of R and R is independently hydrogen, a protecting group or an aliphatic, heteroaliphatic, aryl, heteroaryl, - (alkyl)aryl or -(alkyl)heteroaryl moiety; ii) reacting the compound of step (i) under suitable conditions to generate a compound having the structure:

<img file="WO03106405A1_D0257.tif" /> wherein U is -NHR or -N , wherein R is a nitrogen protecting group; iii) reacting the compound of step (ii) with suitable reagents to generate a compound having the structure:

<img file="WO03106405A1_D0258.tif" /> iv) reacting the compound of step (iii) with suitable reagents to generate the free amine having the structure (I"^A):

<img file="WO03106405A1_D0259.tif" /> (I"^A) wherein R , R , R , R , X , X and X are as defined generally above and in classes and subclasses herein.

[0360] In certain exemplary embodiments, compounds (and methods of synthesis thereof) are provided wherein the compounds having the general formula (I"^A) as shown in Scheme B below:

<img file="WO03106405A1_D0260.tif" />

Scheme B wherein each of R¹, X¹, RP¹, R², X³, and R⁴ are as defined above and R^p3 is an oxygen protecting group.

[0361] It will be appreciated that in certain embodiments, as depicted in

Scheme B, step i) involves providing a oxo-tetrahydro-furan-2-yl (as described in the Examples herein). Subsequent ring opening, protection, oxidation and stereoselective reduction yields the desired compound of provided in step i). Subsequent reduction to an azide in step ii) and reaction with a suitable reagent (to yield -X^R¹) is also effected. Finally, reaction with a suitable reagent to generate -X³-R⁴ and deprotection yields the desired compound. It will be appreciated that a variety of methods can be utilized to effect these transformations, including those detailed in the specification herein, and additional general guidance as also described herein.

[0362] In certain exemplary embodiments, compounds (and methods of synthesis thereof) are provided wherein the compounds having the general formula (VI') as shown in Scheme C below: <img file="WO03106405A1_D0261.tif" />

(vr)

Scheme C [0363] It will be appreciated that in certain embodiments, as depicted in

Scheme C, the inventive method involves providing an epoxide (as described in the Examples herein). Subsequent ring opening, protection, oxidation and reductive animation yields the free amine shown above. Further protection and deprotecting steps and diversification reactions (to yield -X^R¹) and -X³-R⁴ the desired compound (VT). It will be appreciated that a variety of methods can be utilized to effect these transformations, including those detailed in the specification herein, and additional general guidance as described herein.

[0364] Additionally, it will appreciated that compounds having the general structures depicted above, wherein X is SO₂ can be effected using the methodology generally described herein and also methodology described in 5,585,397, the entire contents of which are hereby incorporated by reference.

[0365] Numerous suitable prodrug moieties, and information concerning their selection, synthesis and use are well known in the art. Examples of prodrug moieties of interest include, among others, prodrug moieties that can be attached to primary or secondary amine-containing functionalities. For instance, prodrug moieties of interest include those that can be attached to group NHR⁰. Examples of such prodrug moieties include the following: For the synthesis of the prodrug groups, see Borchardt, R. T. et. al., J. Org. Chem. 1997, 43, 3641-3652. <img file="WO03106405A1_D0262.tif" />

R¹ = all natural, unnatural amino acids

For the synthesis of the prodrug group: Zhou, X-X. et. al., PCT WO 99/51613. <img file="WO03106405A1_D0263.tif" />

R1 = C1-C4 alkyl, cycloalkyl, oxyalkyl, aminoalkyl, etc.

R² = all natural, unnatural amino acids

For the synthesis of the prodrug groups, see EΞzra, A. et. al., J. Med. Chem. 2000, 43, 3641-3652. <img file="WO03106405A1_D0264.tif" /> R¹ , R² = all natural, unnatural amino acids

[0366] The present invention encompasses any prodrug form of the compounds described herein. Although certain other exemplary prodrug moieties generated from the inventive compounds amino group are detailed herein, it will be appreciated that the present invention is not intended to be limited to these prodrug moieties; rather, a variety of additional prodrug moieties can be readily identified by a person skilled in the relevant art.

[0367] 3) Pharmaceutical Compositions

[0368] As discussed above, certain of the compounds as described herein exhibit activity generally as inhibitors of aspartyl proteases and more specifically as inhibitors of β-secretase enzyme activity, and have the ability to halt or reduce the production of A β from APP and reduce or eliminate the formation of β-amyloid deposits in the brain. Thus, the compounds are useful for treating humans or animals suffering from a condition characterized by a pathological form of β -amyloid peptide, such as β-amyloid plaques, and for helping to prevent or delay the onset of such a condition. Thus, in certain embodiments, compounds of the invention are useful for treating Alzheimer's disease, for helping prevent or delay the onset of Alzheimer's disease, for treating patients with MCI (mild cognitive impairment) and preventing or delaying the onset of Alzheimer's disease in those who would progress from MCI to AD, for treating Down's syndrome, for treating humans who have Hereditary Cerebral Hemmorhage with Amyloidosis of the Dutch-Type, for treating cerebral amyloid angiopathy and preventing its potential consequences, i.e. single and recurrent lobal hemorrhages, for treating other degenerative dementias, including dementias of mixed vascular and degenerative origin, dementia associated with Parkinson's disease, dementia associated with progressive supranuclear palsy, dementia associated with cortical basal degeneration, and diffuse Lewy body type Alzheimer's disease. The compounds and compositions of the invention are particularly useful for treating or preventing Alzheimer's disease. When treating or preventing these diseases, the compounds of the invention can either be used individually or in combination.

[0369] Accordingly, in another aspect of the present invention, pharmaceutical compositions are provided, which comprise any one of the compounds described herein (or a prodrug, pharmaceutically acceptable salt or other pharmaceutically acceptable derivative thereof), and optionally comprise a pharmaceutically acceptable carrier. In certain embodiments, these compositions optionally further comprise one or more additional therapeutic agents. Alternatively, a compound of this invention may be administered to a patient in need thereof in combination with the administration of one or more other therapeutic agents. For example, additional therapeutic agents for conjoint administration or inclusion in a pharmaceutical composition with a compound of this invention may be an approved agent for the treatment of Alzheimer's Disease, or it may be any one of a number of agents undergoing approval in the Food and Drug Administration that ultimately obtain approval for the treatment any disorder suffering from a condition characterized by a pathological form of β-amyloid peptide. It will also be appreciated that certain of the compounds of present invention can exist in free form for treatment, or where appropriate, as a pharmaceutically acceptable derivative thereof. According to the present invention, a phaπnaceutically acceptable derivative includes, but is not limited to, pharmaceutically acceptable salts, esters, salts of such esters, or a pro-drug or other adduct or derivative of a compound of this invention which upon administration to a patient in need is capable of providing, directly or indirectly, a compound as otherwise described herein, or a metabolite or residue thereof. [0370] As used herein, the term "pharmaceutically acceptable salt" refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts of amines, carboxylic acids, and other types of compounds, are well known in the art. For example, S.M. Berge, et al. describe pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 66: 1-19 (1977), incorporated herein by reference. The salts can be prepared in situ during the final isolation and purification of the compounds of the invention, or separately by reacting a free base or free acid function with a suitable reagent, as described generally below. For example, a free base function can be reacted with a suitable acid. Furthermore, where the compounds of the invention carry an acidic moiety, suitable pharmaceutically acceptable salts thereof may, include metal salts such as alkali metal salts, e.g. sodium or potassium salts; and alkaline earth metal salts, e.g. calcium or magnesium salts. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2- hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p- toluenesulfonate, undecanoate, valerate salts, and the like. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, loweralkyl sulfonate and aryl sulfonate.

[0371] Additionally, as used herein, the term "pharmaceutically acceptable ester" refers to esters that hydrolyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Suitable ester groups include, for example, those derived from pharmaceutically acceptable aliphatic carboxylic acids, particularly alkanoic, alkenoic, cycloalkanoic and alkanedioic acids, in which each alkyl or alkenyl moiety advantageously has not more than 6 carbon atoms. Examples of particular esters include formates, acetates, propionates, butyrates, acrylates and ethylsuccinates.

[0372] Furthermore, the term "pharmaceutically acceptable prodrugs" as used herein refers to those prodrugs of the compounds of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the issues of humans and lower animals with undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention. The term "prodrug" refers to compounds that are rapidly transformed in vivo to yield the parent compound of the above formula, for example by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and N. Stella, Pro-drugs as Novel Delivery Systems, Vol. 14 of the A.C.S. Symposium Series, and in Edward B. Roche, ed., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference.

[0373] As described above, the pharmaceutical compositions of the present invention additionally comprise a pharmaceutically acceptable carrier, which, as used herein, includes any and all solvents, diluents, or other liquid vehicle, dispersion or suspension aids, surface active agents, isotonic agents, thickening or emulsifying agents, preservatives, solid binders, lubricants and the like, as suited to the particular dosage form desired. Remington's Phaπnaceutical Sciences, Sixteenth Edition, E. W. Martin (Mack Publishing Co., Easton, Pa., 1980) discloses various carriers used in formulating pharmaceutical compositions and known techniques for the preparation thereof. Except insofar as any conventional carrier medium is incompatible with the compounds of the invention, such as by producing any undesirable biological effect or otherwise interacting in a deleterious manner with any other component(s) of the pharmaceutical composition, its use is contemplated to be within the scope of this invention. Some examples of materials which can serve as pharmaceutically acceptable carriers include, but are not limited to, sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatine; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil, sesame oil; olive oil; corn oil and soybean oil; glycols; such as propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogenfree water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.

[0374] Liquid dosage forms for oral administration include, but are not limited to, pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3- butylene glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, geπn, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents. [0375] Injectable preparations, for example, sterile mjectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3- butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables. [0376] The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use.

[0377] hi order to prolong the effect of a drug, it is often desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension or crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution that, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle. Injectable depot may form are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include (poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.

[0378] Compositions for rectal or vaginal administration are preferably suppositories which can be prepared by mixing the compounds of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.

[0379] Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules, hi such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically acceptable excipient or carrier such as sodium citrate or dicalcium phosphate and/or a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar— agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate,'h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage fonn may also comprise buffering agents. [0380] Solid compositions of a similar type may also be employed as fillers in soft and hard- filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like. The solid dosage fonns of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polethylene glycols and the like. [0381] The active compounds can also be in micro-encapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings, release controlling coatings and other coatings well known in the pharmaceutical formulating art. In such solid dosage forms the active compound may be admixed with at least one inert diluent such as sucrose, lactose and starch. Such dosage forms may also comprise, as in normal practice, additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such as magnesium stearate and microcrystalline cellulose, hi the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes.

[0382] Dosage fonns for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable caπier and any needed preservatives or buffers as may be required. Ophthalmic formulation, eardrops, and eye drops are also contemplated as being within the scope of this invention. Additionally, the present invention contemplates the use of transdermal patches, which have the added advantage of providing controlled delivery of a compound to the body. These dosage may form are made by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.

[0383] It will also be appreciated that the compounds and pharmaceutical compositions of the present invention can be formulated and employed in combination therapies, that is, the compounds and phannaceutical compositions can be formulated with or administered concurrently with, prior to, or subsequent to, one or more other desired therapeutics or medical procedures. For example, compounds of the invention can be used in combination, with each other, or with other therapeutic agents or approaches used to treat or prevent the conditions described above and herein. Exemplary agents include, but are not limited to: acetylcholine esterase inhibitors such as tacrine (tetrahydroaminoacridine, marketed as COGNEX®), donepezil hydrochloride (marketed as Aricept® and rivastigmine (marketed as Exelon®); gamma-secretase inhibitors; anti-inflammatory agents such as cyclooxygenase II inhibitors; anti-oxidants such as Vitamin E and ginkolides; immunological approaches, such as, for example, immunization with A β peptide or administration of anti-A β peptide antibodies; statins; and direct or indirect neurotropic agents such as Cerebrolysin®, AIT-082 (Emilieu, 2000, Arch. Neurol. 57:454), and other neurotropic agents of the future. The particular combination of therapies (therapeutics or procedures) to employ in a combination regimen will take into account compatibility of the desired therapeutics and/or procedures and the desired therapeutic effect to be achieved. It will also be appreciated that the therapies employed may achieve a desired effect for the same disorder (for example, an inventive compound may be administered concurrently with another Alzheimer's agent), or they may achieve different effects (e.g., control of any adverse effects). In certain embodiments, the pharmaceutical compositions of the present invention further comprises one or more additional therapeutically active ingredients (e.g., palliative). For purposes of the invention, the term "Palliative" refers to treatment that is focused on the relief of symptoms of a disease and/or side effects of a therapeutic regimen, but is not curative. For example, palliative treatment encompasses painkillers, antinausea medications and anti-sickness drugs.

[0384] 4) Research Uses, Pharmaceutical Uses and Methods of

Treatment

[0385] Research Uses

[0386] According to the present invention, the inventive compounds may be assayed in any of the available assays known in the art for identifying compounds having protease inhibitory activity. For example, the assay may be cellular or non- cellular, in vivo or in vitro, high- or low-throughput format, etc. [0387] In certain exemplary embodiments, compounds of this invention were assayed for their ability to inhibit aspartyl proteases, more specifically BACE. [0388] Thus, in one aspect, compounds of this invention which are of particular interest include those which:

• are inhibitors of aspartyl proteases;

• exhibit the ability to inhibit BACE (β-secretase enzyme activity);

• exhibit the ability to inhibit A β peptide production;

. exhibit the ability to halt or reduce the production of A β from APP and reduces or eliminates the formation of β-amyloid deposits in the brain; are useful for treating mammals (e.g., humans) or animals suffering from a condition characterized by a pathological form of β-amyloid peptide, such as β- amyloid plaques, and for helping to prevent or delay the onset of such a condition;

• exhibit a favorable therapeutic profile (e.g. , safety, efficacy, and stability). [0389] In certain embodiments, compounds of the invention are aspartyl protease inhibitors. In certain exemplary embodiments, inventive compounds are selective BACE inhibitors. In certain exemplary embodiments, inventive compounds have ^BACEκ,^app &lt; 10 μM. In certain other embodiments, inventive compounds have ^BACEj^^app &lt;- -^. ^ ^ j_{n ceπam 0}ther embodiments, inventive compounds have ^BACE_K,^a_P^p_{≤ 5 μM}_ _{In certam omer} embodiments, inventive compounds have ^BACEκ ^pp &lt; 2.5 μM. In certain other embodiments, inventive compounds have ^BACEκ,^app &lt; 1 μM. In certain other embodiments, inventive compounds have ^BACEκ, ^pp &lt; 750 nM. In certain other embodiments, inventive compounds have ^BACEjQ^app &lt; 500 nM. In certain other embodiments, inventive compounds have ^BACEK_;^app &lt; 250 nM. In certain other embodiments, inventive compounds have ^BACEκ,^app &lt; 100 nM. In certain other embodiments, inventive compounds have ^BACEκ,^app &lt; 80 nM. In certain other embodiments, inventive compounds have ^BACE ,^app &lt; 60 nM. In certain other embodiments, inventive compounds have ^BACEκ,^app &lt; 50 nM. In certain other embodiments, inventive compounds have ^BACEκ,^app &lt; 30 nM. In certain other embodiments, inventive compounds have ^BACE ,^ap &lt; 20 nM. In certain other embodiments, inventive compounds have ^BACE ,^app &lt; 10 nM.

[0390] In certain embodiments, ^CatDκ,^app for compounds of the invention is &gt; 2 fold greater than ^BACEκ_;^app. In certain other embodiments, ^CatDκ.^app for compounds of the invention is &gt; 3 fold greater than ^BACEκ,^app. In certain other embodiments, ^CatDK_;^app for compounds of the invention is &gt; 4 fold greater than ^BACE ,^app. In certain other embodiments, ^CatDκ,^app for compounds of the invention is &gt; 5 fold greater than ^BACE_K;^a_{PP In certain} embodiments, ^CatDκ.^app for compounds of the invention is &gt; 7.5 fold greater than ^BACEκ,^app. In certain embodiments, ^CatDK_!^app for compounds of the invention is &gt; 10 fold greater than ^BACEκ_/^ap . In certain embodiments, ^{CatD app} for compounds of the invention is &gt; 25 fold greater than ^BACEκ_/^app. In certain embodiments, ^CatDK_/^app for compounds of the invention is &gt; 50 fold greater than ^BACE_K.^ap_{P In certain} embodiments, ^CatDK, P^p for compounds of the invention is &gt; 75 fold greater than ^BACEκ,^app. In certain embodiments, ^CatDK,^app for compounds of the invention is &gt; 100 fold greater than ^BACEK_.^{a p}. In certain embodiments, ^CatDκ,^app for compounds of the invention is ≥ 150 fold greater than ^BACEκ_;^app. In certain embodiments, ^CatDκ_;^app for compounds of the invention is &gt; 200 fold greater than ^BACE_K.^ap_{P In} ^^ embodiments, ^CatDK,^app for compounds of the invention is ≥ 250 fold greater than ^BACEκ,^ap . In certain embodiments, ^CatDK_;^app for compounds of the invention is &gt; 300 fold greater than ^BACEK,-^{a p}. In certain embodiments, ^CatDκ,^app for compounds of the invention is &gt; 500 fold greater than ^BACE ,^app. In certain embodiments, ^CatDκ.^app for compounds of the invention is &gt; 1000 fold greater than

BACE-g- app

[0391] In certain exemplary embodiments, inventive compounds have ^e IC50 values &lt;10 μM. In certain other embodiments, inventive compounds have ^e IC₅₀ values &lt; 7.5 μM. In certain other embodiments, inventive compounds have ^e IC50 values &lt; 5 μM. In certain other embodiments, inventive compounds have ^e IC₅₀ p 11 values &lt; 2.5 μM. h certain other embodiments, inventive compounds have IC₅Q values &lt; 1 μM. In certain other embodiments, inventive compounds have ^CellIC₅₀ values &lt; 750 nM. In certain other embodiments, inventive compounds have ^CellIC₅o values ≤ 500 nM. In certain other embodiments, inventive compounds have ^CellIC_5o values &lt; 250 nM. In certain other embodiments, inventive compounds have ^CellIC5₀ values &lt; 100 nM. In certain other embodiments, inventive compounds have ^CellIC5₀ values &lt; 80 nM. In certain other embodiments, inventive compounds have ^CellIC₅₀ values &lt; 60 nM. In certain other embodiments, inventive compounds have ^{C ll}IC₅o values &lt; 50 nM. In certain other embodiments, inventive compounds have ^CellIC₅₀ values &lt; 30 nM. In certain other embodiments, inventive compounds have ^CellIC₅o values &lt; 20 nM. In certain other embodiments, inventive compounds have IC5₀ values &lt; 10 nM.

[0392] Pharmaceutical Uses and Methods of Treatment

[0393] As discussed above, without wishing to be bound by any particular theory, certain of the compounds as described herein exhibit activity generally as inhibitors of aspartyl proteases and more specifically as inhibitors of β-secretase enzyme activity. In certain embodiments compounds exhibit the ability to halt or reduce the production of A β from APP and reduce or eliminate the formation of β- amyloid deposits in the brain and thus the compounds are useful for treating humans or animals suffering from a condition characterized by a pathological form of β- amyloid peptide, such as β-amyloid plaques, and for helping to prevent or delay the onset of such a condition (e.g., Alzheimer's Disease). Thus, in certain embodiments, compounds of the invention are useful for treating Alzheimer's disease, for helping prevent or delay the onset of Alzheimer's disease, for treating patients with MCI (mild cognitive impairment) and preventing or delaying the onset of Alzheimer's disease in those who would progress from MCI to AD, for treating Down's syndrome, for treating humans who have Hereditary Cerebral Hemmorhage with Amyloidosis of the Dutch-Type, for treating cerebral amyloid angiopathy and preventing its potential consequences, i.e. single and recurrent lobal hemoπhages, for treating other degenerative dementias, including dementias of mixed vascular and degenerative origin, dementia associated with Parkinson's disease, dementia associated with progressive supranuclear palsy, dementia associated with cortical basal degeneration, and diffuse Lewy body type Alzheimer's disease. The compounds and compositions of the invention are particularly useful for treating or preventing Alzheimer's disease. When treating or preventing these diseases, the compounds of the invention can either be used individually or in combination.

[0394] In certain embodiments, the method involves the administration of a therapeutically effective amount of the compound or a pharmaceutically acceptable derivative thereof to a subject (including, but not limited to a human or animal) in need of it.

[0395] As described in more detail herein, in certain embodiments, compounds of the invention are useful as inhibitors of aspartyl proteases. Generally, compounds of the invention exhibit the ability to inhibit aspartyl protease enzyme activity and thus compounds of the invention generally are useful for the treatment of disorders mediated by aspartyl protease enzyme activity. More specifically, compounds of the invention exhibit activity as inhibitors of β-secretase enzyme activity and A β peptide production. Thus, in certain embodiments, the present invention provides compounds useful for the treatment of disorders mediated by a pathological form of β-amyloid peptide, such as β amyloid plaques, and for helping to prevent or delay the onset of such a condition.

[0396] Thus, in certain embodiments, compounds of the invention are useful for treating Alzheimer's disease, for helping prevent or delay the onset of Alzheimer's disease, for treating patients with MCI (mild cognitive impairment) and preventing or delaying the onset of Alzheimer's disease in those who would progress from MCI to AD, for treating Down's syndrome, for treating humans who have Hereditary Cerebral Hemmorhage with Amyloidosis of the Dutch-Type, for treating cerebral amyloid angiopathy and preventing its potential consequences, i.e. single and recurrent lobal hemoπhages, for treating other degenerative dementias, including dementias of mixed vascular and degenerative origin, dementia associated with Parkinson's disease, dementia associated with progressive supranuclear palsy, dementia associated with cortical basal degeneration, and diffuse Lewy body type Alzheimer's disease. The compounds and compositions of the invention are particularly useful for treating or preventing Alzheimer's disease. When treating or preventing these diseases, the compounds of the invention can either be used individually or in combination.

[0397] Thus, as described above, in another aspect of the invention, a method for the treatment of disorders useful for the treatment (or prevention) of disorders mediated by a pathological form of β-amyloid peptide, such as β amyloid plaques, is provided comprising administering a therapeutically effective amount of a compound of Formula (I) or (I^A), or any classes and subclasses of these compounds as described herein, to a subject in need thereof. It will be appreciated that the compounds and compositions, according to the method of the present invention, may be administered using any amount and any route of administration effective for the treatment of disorders by a pathological form of β-amyloid peptide, such as β amyloid plaques. Thus, the expression "effective amount" as used herein, refers to a sufficient amount of agent to inhibit the production of A β peptide, and to exhibit a therapeutic effect. The exact amount required will vary from subject to subject, depending on the species, age, and general condition of the subject, the severity of the infection, the particular therapeutic agent, its mode of administration, and the like. The compounds of the invention are preferably formulated in dosage unit form for ease of administration and uniformity of dosage. The expression "dosage unit form" as used herein refers to a physically discrete unit of therapeutic agent appropriate for the patient to be treated. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient or organism will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well known in the medical arts (see, for example, Goodman and Gilman's, "The Pharmacological Basis of Therapeutics", Tenth Edition, A. Gilman, J.Hardman and L. Limbird, eds., McGraw- Hill Press, 155-173, 2001, which is incorporated herein by reference in its entirety). [0398] Another aspect of the invention relates to a method for inhibiting β- secretase activity in a biological sample or a patient, which method comprises administering to the patient, or contacting said biological sample with a compound of formula I or a composition comprising said compound. [0399] Furthermore, after formulation with an appropriate pharmaceutically acceptable carrier in a desired dosage, the pharmaceutical compositions of this invention can be administered to humans and other animals orally, rectally, parenterally, intracistemally, intravaginally, intraperitoneally, topically (as by powders, ointments, or drops), bucally, as an oral or nasal spray, or the like, depending on the severity of the infection being treated, hi certain embodiments, the compounds of the invention may be administered at dosage levels of about 0.001 mg/kg to about 50 mg/kg, from about 0.01 mg/kg to about 25 mg/kg, or from about 0.1 mg/kg to about 10 mg/kg of subject body weight per day, one or more times a day, to obtain the desired therapeutic effect. It will also be appreciated that dosages smaller than 0.001 mg/kg or greater than 50 mg/kg (for example 50-100 mg/kg) can be administered to a subject, hi certain embodiments, compounds are administered orally or parenterally.

TREATMENT KIT [0400] In other embodiments, the present invention relates to a kit for conveniently and effectively carrying out the methods in accordance with the present invention, hi general, the pharmaceutical pack or kit comprises one or more containers filled with one or more of the ingredients of the pharmaceutical compositions of the invention. Such kits are especially suited for the delivery of solid oral forms such as tablets or capsules. Such a kit preferably includes a number of unit dosages, and may also include a card having the dosages oriented in the order of their intended use. If desired, a memory aid can be provided, for example in the form of numbers, letters, or other markings or with a calendar insert, designating the days in the treatment schedule in which the dosages can be administered. Alternatively, placebo dosages, or calcium dietary supplements, either in a form similar to or distinct from the dosages of the pharmaceutical compositions, can be included to provide a kit in which a dosage is taken every day. Optionally associated with such container(s) can be a notice in the foπn prescribed by a governmental agency regulating the manufacture, use or sale of phaπnaceutical products, which notice reflects approval by the agency of manufacture, use or sale for human administration.

EQUIVALENTS [0401] The representative examples that follow are intended to help illustrate the invention, and are not intended to, nor should they be construed to, limit the scope of the invention. Indeed, various modifications of the invention and many further embodiments thereof, in addition to those shown and described herein, will become apparent to those skilled in the art from the full contents of this document, including the examples which follow and the references to the scientific and patent literature cited herein. It should further be appreciated that the contents of those cited references are incorporated herein by reference to help illustrate the state of the art. [0402] The following examples contain important additional information, exemplification and guidance that can be adapted to the practice of this invention in its various embodiments and the equivalents thereof.

EXEMPLIFICATION [0403] The compounds of this invention and their preparation can be understood further by the examples that illustrate some of the processes by which these compounds are prepared or used. It will be appreciated, however, that these examples do not limit the invention. Variations of the invention, now known or further developed, are considered to fall within the scope of the present invention as described herein and as hereinafter claimed.

[0404] EXAMPLE 1

[0405] This example describes the enzyme assay for detennining the apparent

Kj of the compounds of the present invention.

[0406] The BACE enzyme used for inhibition analyses, BACE-HT, was produced from baculovirus-infected insect cells, and corresponded to the pro form of the soluble N-terminal protease domain (residues 22-454, starting from the N-terminal methionine), followed by a short linker and C-terminal 6X His tag.

[0407] Compounds were tested for their ability to inhibit BACE hydrolysis of the internally quenched fluorescent substrate, FS-1 (Ermolieff et al, Biochemistry

39:12450-12456 (2000)):

FS1 : NH₂-Arg-Glu(ED ANS)-Glu-Val-Asn-Leu- -Asp-Ala-Glu-Phe-Lys(D ABCYL)- Arg-COOH

FS-2: MOCAc-Ser-Glu-Val-Asn-Leu- -Asp-Ala-Glu-Phe-Lys(DNP)-Arg-Arg- COOH where EDANS is 5-((2-aminoethyl)amino)napthalene-l-sulfonic acid; DABCYL is 4- ((4-dimethylamino)phenyl)azo)benzoic acid; MOCAc is 7-methoxycoumarin-4-yl) acetic acid; and DNP is 2,4-dinotriphenylacetic acid.

[0408] FS-1 and FS-2 correspond to the Swedish APP β-site sequence, flanked by either an EDANS or MOCAc fluorophore on the N-terminus and a DABCYL or DNP quenching group near the C-terminus. In the intact state, the DABCYL or DNP group quenches the EDANS or MOCAc (respectively) fluorescence by virtue of their close proximity. In the intact state, the DABCYL group quenches the EDANS fluorescence by virtue of their close proximity. Upon cleavage at the site indicated by the aπow by BACE, the quenching is relieved and fluorescence is observed using λ_ex_.itation = 350 nm and λ_emi_SSi_on = 490nm or λ_exCit_ation ⁼ 328 nm and λ_emi_ssi_on⁼ 440nm (MOCAc). For determination of apparent inhibition constant (Kj^app) for various inhibitors, the initial rates of FS-1 hydrolysis in the presence of various concentrations of inhibitors were measured and fit to the Morrison equation (Williams and Morrison, Methods Enzymol. 63: 437-467 (1979)):

[E]„ - [l]o - ,^app + V ([E]₀-[l]o-Ki^app)² + 4[E]₀Ki^app

V = Vo .

2[E]₀ where v is the initial rate measured in the presence of [I]_o, the inhibitor concentration, using an enzyme concentration [E]₀. v_o is the initial rate measured in the absence of inhibitor.

[0409] Inhibitors were resuspended in DMSO and serially diluted in DMSO at

20x final assay concentration. Compound dilutions (5 μL) were transfeπed to Black non-treated 96-well microtiter plates, and resuspended in 85 μL 35.3 μM FS1 substrate in 100 mM sodium acetate buffer, pH 4.5, containing 5.9% DMSO (i.e. 10% final DMSO in assay). Following brief equilibration to room temperature, the reactions were initiated by the addition of lOμL BACE-HT (lOOnM final concentration) and brief mixing. The increase in EDANS fluorescence over time was monitored on a Gemini XS fluorometric plate reader using Softmax pro software. Initial rates were fit to the Morrison equation and Kj^app's determined using Graphpad Prism software. A representative range of K;^app's for the compounds is between 1- 1000 nM. The range of K.^app's for preferred compounds is 0.1-500 nM. [0410] EXAMPLE 2

[0411] This example describes an illustrative set of cell-based assays for testing the ability of the compounds of the present invention to inhibit the secretion of the Aβ peptide from cells expressing high levels of the human amyloid precursor protein ("APP").

[0412] A representative set of such cells include A-204 rhabdomyosarcoma cells, human embryonic kidney 293 cells transiently transfected with APP, Chinese hamster ovary cells stably transfected with APP (CHO2B7), and H4 neuroghoma cells stably transfected with APP (H4 β695wt). The A-204 cells and HEK 293 cells were obtained from ATCC. For HEK 293 transient transfections, a pcDNA3 plasmid containing the human APP gene was obtained from Invitrogen, and cells were transfected with FuGENE 6 transfection reagent (Roche) following manufacturer's protocols. The CHO2B7 and H4 β695wt lines were obtained from Mayo Clinic (J. Neuroscience Methods 108(2): 171-9 (2001)).

[0413] The following media were used for the cell lines: DMEM + glucose, glutamine, sodium pyruvate, pyridoxine-HCl, antibiotics, and 10% FBS (A-204 cells); DMEM + glucose, glutamine, sodium pyruvate, pyridoxine-HCl, non-essential amino acids, antibiotics, and 10% FBS (HEK 293 cells); Ham's F-12 + antibiotics, 10% FBS, and 400 μg/ml Zeocin (CHO2B7 cells); and Opti-MEM (Invitrogen)+ antibiotics, 10% FBS, and 500 μg/ml geneticin(H4 β695wt cells). [0414] In the assay, cells were pre-treated with compounds for 1-2 hours to

"wash out" any Aβ in the secretory pathway prior to incubation with compounds for the conditioning period required to generate detectable concentrations of Aβ. The production of secreted Aβ in cultured cells was monitored by sandwich ELISA, using the anti-Aβ monoclonal antibodies 6E10 and 4G8 (Signet Laboratories). The antibody 6E10 (specific to amino acids 1-17 of Aβ) was immobilized to the plate and used for capture, and a biotinylated version of the antibody 4G8 (specific to amino acids 17-24 of Aβ) was used for detection, via subsequent treatment with Neutravidin- horseradish peroxidase conjugate and development with luminescent substrate. [0415] Cells were plated at 2.5xl0⁵ cells/well (HEK293 cells in 24 well poly-

D-lysine coated plate), 1.3 x 10⁵ cells/well (A-204 cells) (48 well plates) or 5 x 10⁴ cells/well (CH02B7 and H4APP cells) (96 well plates) in appropriate media (500 μL per well for 24 well plates, 300 μL per well for 48 well plates, 150 μL per well for 96 well plates) and grown at 37° C and 5% CO₂ for 16-20 h. Media was aspirated and replaced with appropriate media plus 0.1% DMSO and various concentrations of inhibitors, prepared by resuspension of the appropriate volume of a 1000X solution of inhibitor in DMSO with media on a separate plate. Cells and inhibitors were incubated for 1-2 hours, followed by aspiration of the media and replacement with fresh media solutions having the same concentrations of inhibitors. After a 4-24 hour incubation period (depending on cell type), conditioned media were collected and 100 μL of each sample applied to wells of Nunc Maxisorp white 96-well plates that had been previously coated with 10 μg/mL 6E10 antibody in 50 mM Na₂CO , (pH 9.0) overnight at 4° C, blocked with Superblock in PBS (Pierce Chemicals; PBS=10 mM sodium phosphate + 150 mM NaCl, pH 7.4) for 1 hour at room temperature, and washed 3 times in wash buffer (PBS plus 0.05% Tween 20). Binding was allowed to take place overnight at 4 °C, and plates were then washed 8 times and treated with 100 μL/well of 10 nM biotinylated 4G8 antibody in binding buffer (superblock in PBS plus 0.05%) Tween 20) for 1 hour at room temperature. Plates were washed 8 times, treated with 100 μL/well of 1.5 μg/ Neutravidin-horseradish peroxidase conjugate (Pierce Chemicals) for 40 minutes at room temperature, washed an additional 8 times, and developed with 100 μL/well Supersignal luminescent substrate (Pierce Chemicals) for 2 minutes. Luminescence was measured on a Gemini XS fluorescence/luminescence plate reader, and translated into Aβ concentrations using an internal standard curve of known Aβ concentrations (Aβ 1-40 obtained from Oncogene). In general, IC₅o's of the compounds of the present invention range from about 5X to about 15X the observed Kj^app's against the BACE enzyme as determined using the method of Example 1.

[0416] EXAMPLE 3

[0417] This example describes permeability experiments using MDCK cells.

[0418] MDCK cells, derived from canine kidney, were obtained from

American Type Culture Collection (ATCC, Rockville, MD). Cells were cultured in DMEM medium supplemented with 10% fetal bovine serum, 1 mM sodium pyruvate and 0.01 mg/ml gentamicin. Cells were maintained in a humidified atmosphere with 5% CO² at 37°C. For transport studies, cells were plated at a density of 50 x 10³ cells/cm² on 0.4 μm pore size Transwell™ polyester membranes (Corning, Corning, NY). Culture medium was replaced every two days until a tight cell monolayer was formed as measured by preliminary R123 peπneability measurements. Compounds, 10 μM, were placed in either the apical or basolateral compartment and the amount of drug in the opposite chamber was measured using LC/MS/MS or fluorometry. The permeability coefficient was calculated using the following equation:

P_app= (1/ACo) dQ/dt where A= surface area of the cell monolayers, Co is the initial concentration and dQ/dt represents the amount of drug flux in a specified time.

[0419] EXAMPLE 4

[0420] This example describes pharmacokinetic experiments for determining peak plasma and peak brain concentrations using Adult Swiss Weber mice. The peak brain concentration determination also served as a measure for assessing whether the compounds were able to cross the blood brain barrier.

[0421] Adult Swiss Webster mice were administered compounds via tail vein injection.

Plasma and brain tissue were collected at 0, 0.5, 1, 2, 3, 4, and 8 hrs. Blood was collected via cardiac puncture. Subsequently, animals were perfused intra-cardially with ice-cold saline; the brain was homogenized in 10 volumes of ice-cold Tris- buffered saline (20 mM Tris, 137 mM NaCl, pH 7.6) and was then frozen at -20 °C. Following extraction, compound concentrations in plasma and brain homogenates were measured by LC/MS/MS. Peak plasma and brain concentrations (C_maχ) and time to achieve these concentrations (T_max) were measured directly from concentration versus time profiles. Descriptive pharmacokinetic parameters were calculated using the WinNonlin software package (Pharsight Inc., Mountain View CA). Figure 1 A and IB are the plasma and brain concentration curves respectively for one of the compounds of the present invention (where each data point is an average concentration from three mice). This compound has a molecular weight of 626, has a Kj^app of about 35 nM with a 125 fold selectivity over Cat D, and has an IC₅₀ in cells of about 220 nM. [0422] EXAMPLE 5

[0423] This example compares the biological properties of a hydroxy- containing compound with an amino-containing compound. The two compounds are of the structure

<img file="WO03106405A1_D0265.tif" /> where R is either OH or NH . In a surprising and unexpected finding, the amino- containing compound possesses several superior biological properties over its hydroxy-containing counterpart.

[0424] As it can be seen in the following Table, the amino compound is more potent in cells, is more selective for the BACE enzyme, and show superior ADME properties than its hydroxy counterpart.

<img file="WO03106405A1_D0266.tif" />

[0425] Although both compounds show similar activity against the BACE enzyme (180 nM versus 150 nM), the amino compound is significantly more potent in cells (740 nM versus 2000 nM). Moreover, the amino compound displays over a three fold preference for BACE over Cat D. In contrast, the hydroxy counterpart displays a 7.5 fold preference for Cat D over BACE. In addition, although both the amino and hydroxy compounds were stable in human plasma (100% recovery at 1 hour), the amino compound is much more stable in liver microsomes than its hydroxy counterpart.

[0426] These trends appear to be a general phenomenon and have been observed in several scaffolds in addition to one exemplified above.

[0427] The K; for BACE and the IC₅₀ determinations were performed as described in Examples 1 and 2 respectively.

[0428] The Ki determination for Cat D was performed using the assay conditions derived from Haque et al, J. Med. Chem. 42: 1428-1440 (1999) and the following substrate: DABCYL-GLu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS where Nle is norleucine and DABCYL and EDANS are as previously defined.

[0429] Plasma stability was determined by incubating the compounds in human plasma at a concentration of 1 μM at 37 °C for 0, 30 and 60 minutes. Reactions were stopped by addition of acetonitrile. Protein was precipitated by centrifugation (3000 rpm x 10 min) then supernatants were analyzed for remaining parent compound by LC/MS/MS.

[0430] Metabolic stability was determined by incubating the compounds with human liver microsomes (100 μg/ml) in 100 mM Tris buffer pH 7.4 for 5 minutes at 37 °C. Metabolic reactions were started by addition of NADPH to give a final concentration of 1 μM. Reactions were stopped after 30 and 60 minutes by addition of acetonitrile. Protein was precipitated by centrifugation (3000 rpm x 10 min) then supernatants were analyzed for remaining parent compound by LC/MS/MS.

[0431] General Description of Synthetic Strategy:

[0432] According to the present invention, any available techniques can be used to make or prepare the inventive compounds or compositions including them. For example, a variety of solution phase synthetic methods such as those discussed in detail below may be used. Alternatively or additionally, the inventive compounds may be prepared using any of a variety combinatorial techniques, parallel synthesis and/or solid phase synthetic methods known in the art.

[0433] It will be appreciated as described below, that a variety of inventive compounds can be synthesized according to the methods described herein. The starting materials and reagents used in preparing these compounds are either available from commercial suppliers such as Aldrich Chemical Company (Milwaukee, WI), Bachem (Torrance, CA), Sigma (St. Louis, MO), or are prepared by methods well known to a person of ordinary skill in the art following procedures described in such references as Fieser and Fieser 1991, "Reagents for Organic Synthesis", vols 1-17, John Wiley and Sons, New York, NY, 1991; Rodd 1989 "Chemistry of Carbon Compounds", vols. 1-5 and supps, Elsevier Science Publishers, 1989; "Organic Reactions", vols 1-40, John Wiley and Sons, New York, NY, 1991; March 2001, "Advanced Organic Chemistry", 5th ed. John Wiley and Sons, New York, NY; and Larock 1989, "Comprehensive Organic Transformations", VCH Publishers. These schemes are merely illustrative of some methods by which the compounds of this invention can be synthesized, and various modifications to these schemes can be made and will be suggested to a person of ordinary skill in the art having regard to this disclosure.

[0434] The starting materials, intermediates, and compounds of this invention may be isolated and purified using conventional techniques, including filtration, distillation, crystallization, chromatography, and the like. They may be characterized using conventional methods, including physical constants and spectral data. [0435] General Reaction Procedures;

[0436] Unless mentioned specifically, reaction mixtures were stiπed using a magnetically driven stirrer bar. An inert atmosphere refers to either dry argon or dry nitrogen. Reactions were monitored either by thin layer chromatography, by proton nuclear magnetic resonance (NMR) or by high-pressure liquid chromatography (HPLC), of a suitably worked up sample of the reaction mixture. [0437] General Work Up Procedures;

[0438] Unless mentioned specifically, reaction mixtures were cooled to room temperature or below then quenched, when necessary, with either water or a saturated aqueous solution of ammonium chloride. Desired products were extracted by partitioning between water and a suitable water-immiscible solvent (e.g. ethyl acetate, dichloromethane, diethyl ether). The desired product containing extracts were washed appropriately with water followed by a saturated solution of brine. On occasions where the product containing extract was deemed to contain residual oxidants, the extract was washed with a 10%o solution of sodium sulphite in saturated aqueous sodium bicarbonate solution, prior to the aforementioned washing procedure. On occasions where the product containing extract was deemed to contain residual acids, the extract was washed with saturated aqueous sodium bicarbonate solution, prior to the aforementioned washing procedure (except in those cases where the desired product itself had acidic character). On occasions where the product containing extract was deemed to contain residual bases, the extract was washed with 10% aqueous citric acid solution, prior to the aforementioned washing procedure (except in those cases where the desired product itself had basic character). Post washing, the desired product containing extracts were dried over anhydrous magnesium sulphate, and then filtered. The crude products were then isolated by removal of solvent(s) by rotary evaporation under reduced pressure, at an appropriate temperature (generally less than 45°C). [0439] General Purification Procedures:

[0440] Unless mentioned specifically, chromatographic purification refers to flash column chromatography on silica, using a single solvent or mixed solvent as eluent. Suitably purified desired product containing elutes were combined and concentrated under reduced pressure at an appropriate temperature (generally less than 45°C) to constant mass. Final compounds were dissolved in 50% aqueous acetonitrile, filtered and transferred to vials, then freeze-dried under high vacuum before submission for biological testing.

[0441] Synthesis of Exemplary Compounds:

[0442] The practitioner has a well-established literature of amino acid and peptide chemistry to draw upon, in combination with the information contained in the many examples which follow, for guidance on synthetic strategies, protecting groups, and other materials and methods useful for the synthesis of the compounds of this invention, including compounds containing the various R°, R¹, R² and R³ substituents and X¹, X² and X³ moieties. Described generally below, are procedures and general guidance for the synthesis of compounds as described generally and in subclasses and species herein. In addition, synthetic guidance for the synthesis of amino acid derivatives and peptide analogues (and protease inhibitors more generally) can be found in U.S. Patent Nos: 5,585,397; 5,916,438 and 5,413,999; and Published PCT application WO 02/02505, the entire contents of which are hereby incorporated by reference. A derivative of Formula I, or a pharmaceutically-acceptable derivative or salt thereof, may be prepared using any of the available relevant chemical transformations, combined with protection and deprotection as desired or required. Such processes, when used to prepare a derivative of the formula I, or a pharmaceutically-acceptable salt thereof, are illustrated by the following representative examples. The various starting materials are either commercially available or may be obtained by standard procedures of organic chemistry. The preparation of such starting materials is described within the accompanying non- limiting Examples.

[0443] Unless otherwise indicated, starting materials are either commercially available, as indicated or are obtained through laboratory synthesis by anyone reasonably familiar with the art. [0444] EXAMPLE 6

[0445] This example describes how compounds of the formula

<img file="WO03106405A1_D0267.tif" /> were obtained where P is Boc, Tr, or Fmoc and R_A is substituted or unsubstituted aliphatic, aryl, or alkylaryl. These amino acids and amino acid like compounds were either purchased from commercial sources or prepared by the procedure described in

J. Org. Chem. 1999, 64, 3322 as shown in Scheme 1.

[0446 5]] Scheme 1.

<img file="WO03106405A1_D0268.tif" />

1.3 P = Boc, Tr, or Fmoc

[0447] Treatment of (R,R)-(-)-pseudoephedrine (1 eq) and glycine methyl ester hydrochloride 1.1(1.3 eq) in THF ("tetraliydrofuran") with lithium tert-butoxide (1.4 eq) works up with water to afford 2. Enolization of 2 in LiCI (3.2 eq) in THF by LHMDS (3.2 eq) and alkylation of R_AX affords L3. Hydrolysis of 3 under basic condition (NaOH, H₂O, refluxed) followed by protection of amine yields the desired product 1.4.

[0448] EXAMPLE 7

[0449] This example describes the preparation of a common intermediate

<img file="WO03106405A1_D0269.tif" /> which was prepared according to Scheme 2 and the procedure below. [0450] Scheme 2.

H TBSCI <img file="WO03106405A1_D0270.tif" /><img file="WO03106405A1_D0271.tif" />

2.1 2.2 2.3

O

DMPI ..N OTBS NaBH_{4 p}-N-. „OTBS MsCI M^ .OTBS

RA RA

2.4 2.5 2.6

NaN₃

,-N OTBS

[0451] Compound 2J. is prepared by the procedure described J. Am. Chem.

Soc. 2000,722, 3522, starting with the conesponding N-protected amino acid or N- protected amino acid like compound. Reduction of lactone 2Λ by LAH ("lithium aluminum hydride") gives the corresponding diol 2j2, which is followed by protection of the primary alcohol by TBSCI ("tert-butyl-dimethyl silyl chloride") (1 eq), and imidazole in CH₂C1₂ to afford compound 23. Oxidation of the secondary alcohol by Dess-Martin periodinane to ketone 2;4, and reduction of ketone 2Λ by NaBH₄ affords alcohol 2J5. Mesylate 2 is obtained by the treatment of alcohol 2_j5 with mesyl chloride. Addition of sodium azide to the mesylate 2J6 affords compound 1.

[0452] EXAMPLE 8

[0453] This example describes an alternate method to make compound 1 which is made according to Scheme 3 and the procedure below.

[0454] Scheme 3.

0

Λ [j I CH₃P(0)(OR)₂ H j? OR n-BuLi, -10°C-rt

OH p" V ΌCH₃ - _». P" -"^{' "}"OR -

RA RA n-BuLi, -78°C RA Ethyl Pyruvate

<img file="WO03106405A1_D0272.tif" />

[0455] Methyl ester 3 . is prepared by esterfication of the conesponding N- protected amino acid or N-protected amino acid like compound. Ketophosphonate 3.2 is made from methyl ester 3Λ by Claisen condensation with litho-dimethyl methylphosphonate. Wadsworth-Emmons reaction of ketophosphonate 3j2 with ethyl pyruvate affords olefin 33, which is followed by reduction by NaBH₄ to afford lactone 3 Hydrogenation of lactone 3_ followed by reduction by LAH gives diol 3.6. Protection of primary alcohol gives TBS ether 3_ 7. Mesylation of 3_;7 follow by the addition of sodium azide to the mesylate affords compound 1.

[0456] EXAMPLE 9

[0457] This example describes another alternate method to make compound 1 which is made according to Scheme 4 and the procedure below.

[0458] Scheme 4.

<img file="WO03106405A1_D0273.tif" />

4.1 4 2 -3 ref: J. Org. Chem. 1991,56, 4823-4826

<img file="WO03106405A1_D0274.tif" /> [0459] Compound 4 and 43 are prepared by the procedure described J. Org.

Chem. 1991,56, 4823, starting with the corresponding N-protected amino acid or N- protected amino acid like compound. Reduction of ketone 43 by NaBH₄, followed by hydrogenation gives the corresponding diol 44. Protection of the primary alcohol by TBSCI (1 eq), and imidazole in CH₂C1₂ affords compound 45. Mesylation of 4.5 followed by the addition of sodium azide to the mesylate 2\6 affords compound 1.

[0460] EXAMPLE 10

[0461] This example describes the synthesis of the following compound.

<img file="WO03106405A1_D0275.tif" /> which was prepared according to Scheme 5 and the procedure below.

[0462] Scheme 5.

<img file="WO03106405A1_D0276.tif" />

O

^TBSC _^I- Boc ^^ ^-"^ ^-_/^OTBS ™ &gt;■ Boc^- _^-^°^{TBS ΝaBH} ►-

5.3 5.4

<img file="WO03106405A1_D0277.tif" /> HATU, DIEA

<img file="WO03106405A1_D0278.tif" />

5.12

[0463] a) Compound 5.1: [3-Methyl-l-(4-methyl-5-oxo-tetrahydro- furan-2-yl)-butyl]- carbamic acid tert-butyl ester was prepared according to the procedure described inJ Am. Chem. Soc. 2000, 122, 3522.

[0464] b) Preparation of 5.2: A solution of LiAlH (40 mL, 1 M in

THF) was added dropwise to 5.7 g of [3-Methyl-l-(4-methyl-5-oxo-tetrahydro-furan- 2-yl)-butyl] -carbamic acid tert-butyl ester 5Λ in 40 ml of THF at 0 °C. The reaction solution was warmed to room temperature, stirred for 1.5 h and cooled to 0°C. A solution of 15%) NaHSO₄ in water was added dropwise to the reaction mixture until no further precipitate was formed (6 ml of NaHSO₄). The resulting solution was filtered and concentrated, and product ^2 (5.4g, 93 % yield) was used for next reaction without further purification. LCMS: 290(M+1).

[0465] c) Preparation of 53: TBSCl(2.82g, 18.8mmol) was added to the solution of diol 5;2 (5.4g, 18.8mmol) and imidazole (2.6g, 38.2 mmol) in 30 ml of CH C1₂. After 30 min stiπing, solvent was removed under reduced pressure. The reaction mixture was purified by column chromatography (40%&gt; ether / hexanes) to afford 6.5g (88% yield) of 53. LCMS: 404(M+1). 1H NMR( CDCl₃)δ: 4.7(1H, broad s), 3.72(1H, m), 3.6-3.4(3H, m), 3.2( 1H, broad s), 1.93 (1H, m), 1.7-1.55 (2H, m), 1.45( 10H, m), 1.35-1.25 (2H, m), 0.95-0.85(18H, m), 0.04 (6H, s). [0466] d) Preparation of 5.4: A solution of Dess-Martin periodinane

(5.5g, 13 mmol in 5.5 mL CH₂C1₂) was added to a solution of 53 (3.5g, 8.68 mmol) in 30 mL of CH₂C1₂. After stirring for 15 min, the reaction mixture was purified by column (20% ether / hexanes) to afford 5Λ (3.2g, 91%). LCMS: 402(M+1). [0467] e) Preparation of 5.5: To a solution of ketone 5Λ (3.2g, 8.0 mmol) in 50 mL of MeOH, NaBH₄ (0.3g) was added at -78 °C. The reaction mixture was stirred for 10 min at -30°C, and was concentrated under reduced pressure. The reaction mixture was then extracted by ether (3 x 50 mL) water (50 mL), washed with brine (50mL), and concentrated to afford 5 (2.6g, 81%&gt; yield) as 20:1 ratio of syn and anti isomer (determined by 1H NMR). LCMS: 404(M+1). [0468] f) Preparation of 5.6: Mesyl Chloride (l.lg, 9.7mmol) was added to the solution of alcohol 55 (2.6 g, 6.5mmol) and triethylamine (2 mL) in chloroform (20 mL) at 0°C. The resulting mixture was stirred for 60 min, and purified by column chromatography (20% ether / hexanes) to afford mesylate 5_Λϊ (2.5g, 80%). LCMS: 482 (M+l).

[0469] g) Preparation of 5.7: Sodium azide (3.4g) was added to a solution of mesylate 5 6 (2.5g) in DMF ("dimethylformamide") (20 mL). The reaction mixture was stirred for overnight at 75°C and then extracted (ether 5x50mL/water 50 mL). The combined organic solution was dried, concentrated and purified by column chromatography (10%, ether/hexanes) to afford desired product 5,7 (1.05g, 55%). LCMS: 429( M+l) 1H NMR( CDCl₃)δ: 4.43(1H, broad), 3.77(1H, m), 3.63 ( 1H, m), 3.49( 2H, m), 1.85 (1H, m), 1.7-1.6 (2H, m), 1.45( 10H, m), 1.35- 1.25 (2H, m), 1.0-0.88(18H, m), 0.05(6H, s) and syn isomer (0.19g). [0470] h) Preparation of 5.8: A solution of 4N HC1 in dioxane was added to a solution of compound 5 7 in MeOH. After stirring at room temperature for 60 min, the volatiles were removed by reduced pressure to afford 5.8, which was used as is without further purification.

[0471] i) Preparation of 5 ⁾: Method 1: To a mixture of compound 5 $ and N,N-dipropyl-isophthalamic acid in DMF, EDC ("l-(3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride")/HOBt ("1-hydroxybenzotriazole hydrate")/DIEA ("diisopropylethylamine") was added. The resulting solution was stiπed at room temperature overnight. IN HC1 (2 mL) was added to the solution, followed by addition of EtOAc (80 mL). After stiπing for 10 min, the organic layer was separated, washed with brine, and dried over MgSO₄. After removal of solvents, the residue was purified by column chromatography to afford 5j9. Method 2: To a mixture of 5-8 and N,N-dipropyl-isophthalamic acid in CH₂C1₂, HATU ("2-(lH- azabenzotriazole-l-yl)-l,3,3-tetramethyluronium")/DIEA was added. The resulting mixture was stirred at room temperature for 2 h. The volatiles were removed by reduced pressure and purified by column chromatography to afford 5.9. [0472] j) Preparation of 5.10: Compound 5.9 was oxidized by Jone's reagent, after being worked up and purified by column to give acid 5.10 LCMS: 460( M+l) 1H NMR( CD₃OD)δ: 7.92(1H, d), 7.80(1H, s), 7.5-7.6(2H, m), 4.33(1H, m), 3.59(1H, m), 3.51( 2H, t), 3.22 (3H, t), 2.70 (1H, m), 1.98( 1H, m), 1.80-1.35 (8H, m), 1.20(3H, t), 1.06-0.9(9H, m), 0.75(3H, t).

[0473] k) Preparation of 5.11: Method 1: To a mixture of compound

5.10 and 2-amino-N-benzyl-3-methyl-butyramide in DMF, EDC/HOBt/ DIEA was added. The resulting solution was stirred at room temperature overnight. IN HC1 (2 mL) was added to the solution, followed by addition of EtOAc (80 mL). After stirring for 10 min, the organic layer was separated, washed with brine and dried over MgSO . After removal of solvents, the residue was purified by column chromatography to afford 5.11. Method 2: To a mixture of 5.10 and 2-amino-N- benzyl-3-methyl-butyramide in CH₂C1₂, HATU/DIEA was added. The resulting mixture was stirred at room temperature for 2 h. The volatiles were removed by reduced pressure and purified by column chromatography to afford 5.11. [0474] 1) Preparation of 5.12: Method 1: Compound 5.11 was treated with 1M PhMe₃ in THF. The resulting mixture is stirred for several hours until the compound is consumed. The reaction mixture is concentrated and IN HC1 is added. The resulting mixture is stiπed overnight. 20 %&gt; NaOH(aq) is added dropwise until the solution reaches a pH of 12-13. Method 2: Hydrogenation of compound 5.11 by 10 % Pd-C in MeOH under hydrogen atmosphere afforded 5.12 which was purified by preparative HPLC. [0475] EXAMPLE 11

[0476] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0279.tif" /> which is prepared according to Scheme 6 and the procedure below.

[0477] Scheme 6. n-BuLi, -10°C-rt ► ^{Ethyl p}y^ruvate<img file="WO03106405A1_D0280.tif" />

<img file="WO03106405A1_D0281.tif" /> u OH • OH i H ^0Ms I jXλ^« -----_ L^_X^__ I _BOC . OTBS

2. NaN₃₆.₆ u _._ 6.7 ll J 6.8

<img file="WO03106405A1_D0282.tif" />

<img file="WO03106405A1_D0283.tif" />

[0478] a) Preparation of 62 A solution of dimethyl methylphosphonate 6Λ (3 A g, 215.4 mmol) in THF (250 mL) in a nitrogen atmosphere was cooled to -78 °C to which was added 2.0 M solution of butyl lithium (107 mL, 215.4 mmol) via canula in 20 min. The solution was stirred at -78 °C for 20 min, and a THF (150 mL) solution of N-Boc-L-phenylalanine methyl ester (10.0 g, 35.8 mmol) was slowly added via dropping funnel. The mixture was stiπed at -78 °C for lh. The reaction was then quenched with 10% AcOH (250 mL) and warmed to room temperature. The solution was extracted with EtOAc, and the combined organic extracts were washed with saturated aqueous ΝaHCO₃ and brine, and dried over MgSO₄. Solvents were evaporated and excess dimethyl methylphosphonate was removed by rotary evaporator under high vacuum at 90 °C water bath. The resulted oily product containing 5-10% dimethyl methylphosphonate (as shown by 1H NMR) was used without purification. 1H NMR (400 MHz, CDC1₃) δ ppm 1.29 (m, 6 H) 1.35 (s, 9 H) 2.92 (dd, J=14.24, 8.39 Hz, 1 H) 3.03 (dd, J=22.38, 13.73 Hz, 1 H) 3.22 (m, 2 H) 4.10 (m, 4 H) 4.55 (d, J=5.59 Hz, 1 H) 5.38 (d, J=7.88 Hz, 1 H) 7.20 (m, 5 H); MS: 422 (MNa⁺).

[0479] b) Preparation of Ethyl (5S,2Z)-2-methyl-[5-(tert- butoxycarbonyl)amino]-4-oxo-6-phenylhex-2-enonate 6__!3: A solution of the crude phosphonate 6_;2 (16.8 g, ca. 35.8 mmol) in THF (100 mL) in a nitrogen atmosphere was cooled to 0 °C to which was added 1.6 M solution of butyllithium (22.4 mL, 35.8 mmol) via syringe in 10 min. The solution was stiπed at 0 °C for 30 min, and ethyl pyruvate (7.1 mL, 63.2 mmol) was added slowly. The solution was continued to be stirred at 0 °C for 1 h and then at room temperature overnight. The reaction was quenched with saturated aqueous NH₄C1 (100 mL) and diluted with EtOAc (400 mL). The organic layer was separated, washed brine, and dried over MgSO . Solvents were evaporated and the residue was purified by column chromatography (silica gel, Hexane-EtOAc 5:1) to give oily pure product 63 (9.0 g, approximately 70% yield starting from 1). 1H NMR (400 MHz, ACETONE-D6) δ ppm 1.24 (t, J=7.12 Hz, 3 H) 1.33 (s, 9 H) 2.00 (d, J=1.27 Hz, 3 H) 2.86 (m, 1 H) 3.19 (dd, J=13.99, 5.09 Hz, 1 H) 4.18 (q, J=7.12 Hz, 2 H) 4.53 (m, 1 H) 6.13 (d, J=7.88 Hz, 1 H) 6.51 (d, J=1.27 Hz, 1 H) 7.22 (m, 5 H); MS: 384 (MNa⁺).

[0480] c) Preparation of (5R)-3-methyl-5-{(lS)-l-[(tert- butoxycarbonyl)amino1-2-phenylethyl} -2,5-dihydrofuran-2-one 6.4: To a solution of 63 (8.4 g, 23.2 mmol) in MeOH (200 mL) cooled to -78 °C was added sodium borohydride (1.7 g, 46.4 mmol). The mixture was stiπed and warmed to -15 °C in 3 h, and kept at the same temperature overnight. IN aqueous HC1 (100 mL) was added to the cold reaction mixture, and the volatiles were removed by rotary evaporator. The resulted mixture was extracted with EtOAc. The combined extracts were washed with saturated aqueous NaHCO₃ and brine, and dried over MgSO₄. After removal of solvents, the residue was purified by column chromatography (silica gel, Hexane-EtOAc 3:1) to give pure product 6Λ (4.3 g, 58%&gt;) and its 5-epimer (3.0 g, 41%) both as white solids. 1H NMR (400 MHz, CDC1₃) δ ppm 1.36 (s, 9 H) 1.88 (s, 3 H) 2.80 (d, J=6.61 Hz, 2 H) 4.05 (m, 1 H) 4.68 (d, J=8.39 Hz, 1 H) 4.92 (s, 1 H) 6.91 (s, 1 H) 7.23 (m, 5 H); MS: 340 (Na⁺).

[0481] d) Preparation of (3R,5R)-3-methyl-5-{(lS)-l-[(tert- butoxycarbonyl)amino]-2-phenylethyl}-tetrahydrofuran-2-one κ5: Lactone 6Λ (3.5 g, 11.0 mmol) was dissolved in THF (300 mL), to which 10% Pd/C (350 mg) was added. The mixture was stiπed under an atmosphere of H₂ (balloon) for 5 h, followed by filtration and concentration in vacuo to provide product (κ5 (3.5 g, 99%&gt;) as white solid. 1H NMR (400 MHz, CDC1₃) δ ppm 1.26 (d, J=7.12 Hz, 3 H) 1.35 (s, 9 H) 1.71 (m, 1 H) 2.42 (m, 1 H) 2.64 (m, 1 H) 2.87 (m, 1 H) 3.01 (m, 1 H) 3.92 (m, 1 H) 4.25 (m, 1 H) 4.46 (m, 1 H) 7.24 (m, 5 H); MS: 342 (MNa⁺). [0482] e) Preparation of (2S,3R,5R)-2-tert-butoxycarbonylamino-l- phenyl-5-methylhexan-3,6-diol 6 &gt;: To a solution of &lt;^ή5 (3.5 g, 11.0 mmol) in THF (50 mL) cooled to 0 °C was added 0.5 M LiAlH₄ in DME (22.0 mL, 11.0 mmol). The mixture was stiπed at 0 °C for 0.5 h and warmed to room temperature. The mixture was stirred until TLC indicated that the reduction was completed. The mixture was cooled to 0 °C and IN NaHS0₄ (30 mL) was added slowly. After stiπing for 30 min at room temperature, the mixture was extracted with EtOAc. The combined extracts were washed with saturated aqueous NaHCO₃ and brine, and dried over MgSO . After removal of solvents, the residue was purified by column chromatography (silica gel, Hexane-EtOAc 1:1) to yield pure product 6^6 (2.7 g, 76%) as white solid. 1H NMR (400 MHz, CDC1₃) δ ppm 0.82 (d, J=6.61 Hz, 3 H) 1.19 (s, 9 H) 1.26 (m, 1 H) 1.41 (m, 1 H) 1.75 (m, J=15.13, 5.72 Hz, 1 H) 2.46 (dd, J=13.61, 10.05 Hz, 1 H) 2.93 (dd, J=13.73, 3.05 Hz, 1 H) 3.30 (m, 2 H) 3.50 (m, 2 H) 7.10 (m, 5 H); MS: 324 (MH¹-).

[0483] f) Preparation of [(lS,2R,4R)-l-Benzyl-5-(tert-butyl-dimethyl- silanyloxy)-2-hydroxy-4-methyl-pentyl] -carbamic acid tert-butyl ester 6 7: To a solution of 6 6 (1.0 g, 3.10 mmol) in CH₂C1₂ (15 mL) was added imidazole (422 mg, 6.20 mmol) and TBSCI (578 mg, 3.72 mmol) sequentially at 0 °C. After stiπing at 0 °C for 1 h, H₂O (10 mL) was added to quench the reaction. The organic layer was separated and the aqueous layer was extracted with CH₂C1₂. The combined CH₂C1₂ solution was washed with H₂0 and dried over MgSO₄. After removal of solvents, the residue was purified by column chromatography (silica gel, Hexane-EtOAc 3:1) to afford pure product 6/7 (1.34 g, 98%) as a white solid. 1H NMR (400 MHz, CDC1₃) δ ppm 0.08 (s, 6 H) 0.87 (d, J=6.87 Hz, 3 H) 0.91 (s, 9 H) 1.32 (s, 9 H) 1.49 (m, J=6.36 Hz, 2 H) 1.80 (m, 1 H) 2.77 (m, 1 H) 2.89 (m, 1 H) 3.40 (m, 1 H) 3.58 (dd, J=10.05, 4.20 Hz, 1 H) 3.68 (s, 1 H) 3.81 (s, 1 H) 4.18 (m, J=12.33, 4.96 Hz, 1 H) 4.78 (d, J=8.65 Hz, 1 H) 7.21 (m, 5 H); MS: 438 (MH*), 460 (MNa⁺).

[0484] g) Preparation of Methanesulfonic acid (lR,2S,4R)-l-(l-tert- butoxycarbonyl-amino-2-phenyl-ethyl)-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl- butyl ester 6.8:To a solution of 6/7 (1.2 g, 2.75 mmol) in chloroform (10 mL) was added triethylamine (0.8 mL, 5.5 mmol) and MsCl ("mesyl chloride") (0.32 mL, 4.12 mmol) sequentially at 0 °C. After stirring at 0 °C for 1 h, 1 N HC1 (5 mL) was added to quench the reaction. The organic layer was separated and the aqueous layer was extracted with CH₂C1₂. The combined CH₂C1 solution was washed with H₂O and dried over MgSO₄. After removal of solvents, the residue was purified by column chromatography (silica gel, Hexane-EtOAc 3:1) to afford pure product 6 $ (1.34 g, 95%) as colorless oil. 1H NMR (400 MHz, CDC1₃) δ ppm 0.04 (s, 6 H) 0.88 (m, 12 H) 1.32 (s, 9 H) 1.37 (m, 1 H) 1.79 (m, 1 H) 1.95 (m, 1 H) 2.66 (dd, J=13.22, 10.68 Hz, 1 H) 2.90 (dd, J=14.24, 4.83 Hz, 1 H) 3.03 (s, 3 H) 3.40 (m, 1 H) 3.52 (m, 1 H) 4.16 (s, 1 H) 4.87 (d, J=8.65 Hz, 1 H) 4.96 (d, J-9.16 Hz, 1 H) 7.23 (m, 5 H); MS: 515 (MNa⁺).

[0485] h) Preparation of [(lS,2S,4R)-2-Azido-l-benzyl-5-(tert-butyl- dimethyl-silanyloxy)-4-methyl-pentyl] -carbamic acid tert-butyl ester 6 ): Mesylate 6.8 (1.34 g, 2.60 mmol) was dissolved in anhydrous DMF (300 mL). To this stiπed solution was added NaN₃ (2.50g, 39.0 mmol). The mixture was heated to 60 °C with an oil bath and stiπed at this temperature for 8 h. The solvent was evaporated in vacuo and then H₂O (20 mL) was added to dissolve the solid. The solution was extracted with ether, and the combined extracts were dried over MgSO . After removal of solvents, the residue was purified by column chromatography (silica gel, Hexane-EtOAc 10:1) to afford pure product &lt;ή9 (0.72 g, 60%) as colorless oil. ^!H NMR (400 MHz, CDC1₃) δ ppm -0.05 (s, 3 H) -0.03 (s, 3 H) 0.74 (d, J=6.87 Hz, 3 H) 0.84 (s, 9 H) 1.39 (s, 9 H) 1.43 (m, 1 H) 1.63 (m, 1 H) 1.73 (m, 1 H) 2.75 (dd, J=13.61, 8.77 Hz, 1 H) 2.92 (m, 1 H) 3.37 (m, 2 H) 3.53 (t, J=7.12 Hz, 1 H) 3.91 (q, J=8.22 Hz, 1 H) 4.65 (d, J=9.66 Hz, 1 H) 7.25 (m, 5 H); MS: 485 (MNa⁺). [0486] i) N-[(l S,2S,4R)-2-Azido-l -benzyl-5-hydroxy-4-methyl-pentyl]-

N',N'-dipropyl-isophthalamide (6.11): Azide ή9 (109 mg, 0.24 mmol) was treated with 4N HC1 in dioxane (5 mL). After stirring for 1 h, the mixture was concentrated in vacuo and the resulting crude product 6.10 was used for the next step without purification. To a solution of the crude compound 6.10 in DMF (1 mL) was added N,N-Dipropyl-isophthalamic acid (58 mg, 0.24 mmol), diisopropylethylamine (0.3 mL, 1.42 mmol), HOBt (54 mg, 0.35 mmol) and EDC (68 mg, 0.35 mmol) sequentially. The mixture was stirred at room temperature for 8 h. IN HC1 (2 mL) was added to the mixture, followed by addition of EtOAc (80 mL). After stirring for 10 min, the organic layer was separated, washed with brine and dried over MgSO₄. After removal of solvents, the residue was purified by column chromatography (silica gel, CH₂Cl₂-MeOH 19:1) to afford pure product 601 (113 mg, 81% starting from 6u9) as colorless oil. 1H NMR (400 MHz, CD₃OD) δ ppm 0.60 (t, J=7.12 Hz, 3 H) 0.81 (d, J=6.61 Hz, 3 H) 0.89 (t, J=7.25 Hz, 3 H) 1.32 (m, 1 H) 1.43 (m, 2 H) 1.64 (m, 3 H) 1.75 (m, 1 H) 2.84 (m, 1 H) 2.94 (m, 1 H) 3.06 (m, 2 H) 3.32 (m, 4 H) 3.61 (m, 1 H) 4.41 (m, 1 H) 7.06 (m, 1 H) 7.16 (q, J=7.46 Hz, 4 H) 7.40 (m, 2 H) 7.55 (s, 1 H) 7.67 (d, J=7.12 Hz, 1 H); MS: 480 (MH*).

[0487] j) Preparation of 6.12: To a solution of 6 1 (57 mg, 0,12 mmol) in acetone (1 mL) was added Jones' reagent (2.7M, 88 μM, 0,24 mmol). After stirring at room temperature for 20 min, iPrOH (40 μL) was added. Stirring was continued for 10 min and the reaction mixture was diluted with acetone (20 mL), followed by filtration over celite. The solution was dried (Na₂SO ) and concentrated. The resulted crude product 6.12 was used for next step without purification. [0488] k) Preparation of N-{(lS,2S,4R)-2-Azido-l-benzyl-4-[(lS)-l- benzylcarbamoyl-2-methyl-propylcarbamoyl]-pentyl}-N',N'-dipropyl-isophthalamide 6.13: To a DMF (0.5 mL) solution of the crude acid 6.12 (24 mg, 0.05 mmol), was added 2-amino-N-benzyl-3-methyl-butyramide (20 mg, 0.075 mmol), diisopropylethylamine (0.1 mL, 0.45 mmol) and HATU (38 mg, 0.10 mmol) sequentially. The mixture was stirred at room temperature for 2 h, and then purified by HPLC to provide pure product 6.13 (26 mg, 76% starting from 6.11) as white solid. 1H NMR (400 MHz, CD₃OD) δ ppm 0.57 (t, J-7.25 Hz, 3 H) 0.76 (m, 6 H) 0.87 (t, J=7.25 Hz, 4 H) 0.98 (d, J=6.61 Hz, 3 H) 1.41 (m, 3 H) 1.59 (m, 2 H) 1.90 (m, 2 H) 2.66 (m, 1 H) 2.79 (dd, J=13.73, 9.66 Hz, 1 H) 2.94 (dd, J=13.99, 5.60 Hz, 1 H) 3.03 (m, 2 H) 3.22 (s, 1 H) 3.36 (m, 3 H) 3.99 (d, J=7.63 Hz, 1 H) 4.25 (s, 2 H) 4.40 (s, 1 H) 7.10 (m, 10 H) 7.38 (q, J=7.97 Hz, 2 H) 7.53 (s, 1 H) 7.65 (d, J=6.87 Hz, 1 H); MS: 682 (Mtf).

[0489] 1) N-{(lS,2S,4R)-2-Amino-l-benzyl-4-[(lS)-l-benzylcarbamoyl-

2-methyl-propylcarbamoyl]-pentyl}-N',N'-dipropyl-isophthalamide 6.14: To a solution of compound 6 3 (19 mg, 0.0279 mmol) in MeOH (5 mL) 10% Pd-C (6 mg) was added. The mixture was stirred under an atmosphere of H₂ for 30 min, followed by filtration and concentration. The resulted crude product was purified by preparative TLC to afford pure product 6.14 (16 mg, 88%&gt;) as a white solid. 1H NMR (400 MHz, CD₃OD) δ ppm 0.61 (t, J=7.25 Hz, 3 H) 0.76 (d, J=6.61 Hz, 6 H) 0.88 (m, 4 H) 0.98 (d, J=6.87 Hz, 3 H) 1.28 (m, 1 H) 1.42 (m, 2 H) 1.62 (m, 2 H) 1.79 (m, 1 H) 1.91 (m, 1 H) 2.65 (dd, J=14.62, 6.23 Hz, 1 H) 2.75 (m, 2 H) 2.91 (m, 1 H) 3.07 (m, 2 H) 3.37 (m, 2 H) 4.00 (d, J=7.38 Hz, 1 H) 4.27 (m, 2 H) 7.05 (t, J=7.12 Hz, 1 H) 7.16 (m, 9 H) 7.40 (m, 2 H) 7.58 (s, 1 H) 7.71 (d, J=7.38 Hz, 1 H); MS: 656 (MH*).

[0490] EXAMPLE 12 [0491] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0284.tif" />

[0492] These compounds are prepared according the procedure of Example 10 or Example 11 except for using other amino acids and amino acid like compounds of

Boc OH

Boc^ ^{" '} "OH the formula ^RA as a reagent instead of (Example 10) or

<img file="WO03106405A1_D0285.tif" /> (Example 11). Illustrative examples of amino acids and amino acid like compounds and their corresponding final products are shown in Table 1

[0493] Table 1

<img file="WO03106405A1_D0286.tif" /><img file="WO03106405A1_D0287.tif" /><img file="WO03106405A1_D0288.tif" /><img file="WO03106405A1_D0289.tif" />

[0494] EXAMPLE 13

[0495] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0290.tif" /> which was prepared according to the procedure in Example 10 except for using 4- fluroanaline instead of 2-amino-N-benzyl-3-methyl-butyramide in step k. MS (M+H⁺) 527. [0496] EXAMPLE 14 [0497] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0291.tif" />

[0498] These compounds are prepared according the procedure in Example 13 except for using amino acids and amino acid like compounds of the formula

<img file="WO03106405A1_D0292.tif" /> . Illustrative examples of amino acids and amino acid like compounds and their corresponding final products are shown in Table

2.

[0499] Table 2

<img file="WO03106405A1_D0293.tif" /><img file="WO03106405A1_D0294.tif" /><img file="WO03106405A1_D0295.tif" /><img file="WO03106405A1_D0296.tif" />

[0500] EXAMPLE 15

[0501] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0297.tif" /> which was prepared according to the procedure in Example 10 except for using isobutylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k. MS (MH⁺) 489. [0502] EXAMPLE 16

[0503] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0298.tif" />

[0504] These compounds are prepared according to the procedure in Example

15 except for using amino acids and amino acid like compounds of the formula

<img file="WO03106405A1_D0299.tif" /> . Illustrative examples of amino acids and amino acid like compounds and their corresponding final products are shown in Table

3.

[0505] Table 3

<img file="WO03106405A1_D0300.tif" /><img file="WO03106405A1_D0301.tif" /><img file="WO03106405A1_D0302.tif" /><img file="WO03106405A1_D0303.tif" />

[0506] EXAMPLE 17 [0507] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0304.tif" /> which was prepared according to the procedure in Example 10 except for using cyclopropyl-methylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k.

[0508] EXAMPLE 18

[0509] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0305.tif" />

[0510] These compounds are prepared according the procedure in Example 17 except for using amino acids and amino acid like compounds of the formula

<img file="WO03106405A1_D0306.tif" /> . Illustrative examples of amino acids and amino acid like compounds and their corresponding final products are shown in Table

4.

[0511] Table 4

<img file="WO03106405A1_D0307.tif" /><img file="WO03106405A1_D0308.tif" /><img file="WO03106405A1_D0309.tif" /><img file="WO03106405A1_D0310.tif" />

[0512] EXAMPLE 19

[0513] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0311.tif" /> which was prepared according to the procedure in Example 10 except for using 2- ethyl-butylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k.

[0514] EXAMPLE 20 [0515] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0312.tif" />

[0516] These compounds are prepared according the procedure in Example 19 except for using amino acids and amino acid like compounds of the formula

H

<img file="WO03106405A1_D0313.tif" /> . Illustrative examples of amino acids and amino acid like compounds and their conesponding final products are shown in Table 5. [0517] Table 5

<img file="WO03106405A1_D0314.tif" /><img file="WO03106405A1_D0315.tif" /><img file="WO03106405A1_D0316.tif" /> [0518] EXAMPLE 21

[0519] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0317.tif" /> which was prepared according to the procedure in Example 10 except for using cyclohexyl-methylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k.

[0520] EXAMPLE 22 [0521] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0318.tif" />

[0522] These compounds are prepared according the procedure in Example 21 except for using amino acids and amino acid like compounds of the formula

H O H O _Boc.N OH

Boc" "A -OH

^RA instead of I . Illustrative examples of amino acids and amino acid like compounds and their conesponding final products are shown in Table 6.

<img file="WO03106405A1_D0319.tif" /><img file="WO03106405A1_D0320.tif" /><img file="WO03106405A1_D0321.tif" /><img file="WO03106405A1_D0322.tif" />

[0524] EXAMPLE 23 [0525] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0323.tif" /> which was prepared according to the procedure in Example 10 except for using cyclopentyl-methylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k. [0526] EXAMPLE 24

[0527] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0324.tif" />

[0528] These compounds are prepared according the procedure in Example 23 except for using amino acids and amino acid like compounds of the formula

H

H O B -oc _^N OH

.N.

BOC "OH

^RA instead of I . Illustrative examples of amino acids and amino acid like compounds and their conesponding final products are shown in Table

[0529] Table 7

<img file="WO03106405A1_D0325.tif" /><img file="WO03106405A1_D0326.tif" /><img file="WO03106405A1_D0327.tif" /><img file="WO03106405A1_D0328.tif" />

[0530] EXAMPLE 25 [0531] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0329.tif" /> which was prepared according to the procedure in Example 10 except for using 2- methyl-butylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k.

[0532] EXAMPLE 26 [0533] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0330.tif" />

[0534] These compounds are prepared according the procedure in Example 25 except for using amino acids or amino acid like compounds of the formula

<img file="WO03106405A1_D0331.tif" /> . Illustrative examples of amino acids and amino acid like compounds and their conesponding final products are shown in Table 8 [0535] Table 8

<img file="WO03106405A1_D0332.tif" /><img file="WO03106405A1_D0333.tif" /><img file="WO03106405A1_D0334.tif" /> [0536] EXAMPLE 27 [0537] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0335.tif" /> where R_B is substituted or unsubstituted aliphatic, aryl or alkylaryl. These compoxmds are prepare according the procedure in Example 10 except for using acids of the formula R_BCO₂H as reagents instead of N,N-dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 9

[0538] Table 9

<img file="WO03106405A1_D0336.tif" /><img file="WO03106405A1_D0337.tif" />

[0539] EXAMPLE 28 [0540] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0338.tif" /> where RB is as defined in Example 27. These compounds are prepared according the procedure in Example 14 except for using acids of the formula RβCO₂H as reagents instead of N,N-dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 10

[0541] Table 10

<img file="WO03106405A1_D0339.tif" /><img file="WO03106405A1_D0340.tif" /> [0542] EXAMPLE 29

[0543] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0341.tif" />

[0544] For each R_B group described in Examples 27 and 28, the conesponding

R_A compound is prepared by substituting <img file="WO03106405A1_D0342.tif" /> as a reagent instead of

<img file="WO03106405A1_D0343.tif" /> . Illustrative examples of suitable RA groups are shown in Example 14.

[0545] EXAMPLE 30

[0546] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0344.tif" />

[0547] For each R_B group described in Examples 27 and 28, the conesponding

RA compound is prepared by substituting <img file="WO03106405A1_D0345.tif" /> as a reagent instead of

<img file="WO03106405A1_D0346.tif" /> . Illustrative examples of suitable RA groups are shown in Example 16. [0548] EXAMPLE 31

[0549] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0347.tif" /> where Rc is substituted or unsubstituted aliphatic, aryl, or alkylaryl. These compounds are prepared according the procedure in Example 11 except for using conesponding 2-oxo acid esters as reagents instead of ethyl pyruvate in the step b. Illustrative examples of 2-oxo acid esters and their conesponding final products are shown in Table 11

[0550] Table 11

<img file="WO03106405A1_D0348.tif" />

[0551] EXAMPLE 32

[0552] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0349.tif" />

[0553] These compounds are prepared according the procedure in Example 11 except for using the conesponding 2-oxo acid ester instead of ethyl pyruvate in step b, and using p-fluoroaniline instead of 2-amino-N-benzyl-3-metlιyl-butyramine in step j. Illustrative examples of 2-oxo acid esters and their conesponding final products are shown in Table 12. [0554] Table 12

<img file="WO03106405A1_D0350.tif" />

[0555] EXAMPLE 33 [0556] This example describes the synthesis of the following compound.

<img file="WO03106405A1_D0351.tif" /> which is prepared according the procedure in Example 11 except for using 3- benzyloxy-2-oxo propanic acid methyl ester (which is prepared from 3-hydroxyl-2- oxo propanic acid) instead of ethyl pyruvate in the step b, and using 4-fluoroaniline instead of 2-amino-N-benzyl-3-methyl-butyramine in the step j.

[0557] EXAMPLE 34

[0558] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0352.tif" /> [0559] This compound is made by treating the final product of Example 33 with PPh₃, CBr₄ or MsCl.

[0560] EXAMPLE 35

[0561] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0353.tif" /> which is prepared according to the procedure in Example 10 except for using (2- bromo-ethoxymethyl)-benzene (that is prepared from 2-bromoethanol) instead of iodomethane in step a, and using 4-fluoroanaline instead of 2-amino-N-benzyl-3- methyl-butyramide in step k.

[0562] EXAMPLE 36

[0563] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0354.tif" />

[0564] This compound is made by treating the final product Example 35 with

PPh₃, CBr₄ or MsCl.

[0565] EXAMPLE 37

[0566] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0355.tif" /> which is prepared according to Scheme 7 and the procedure below. [0567] Scheme 7.

<img file="WO03106405A1_D0356.tif" />

Jones' reagent

<img file="WO03106405A1_D0357.tif" /><img file="WO03106405A1_D0358.tif" />

<img file="WO03106405A1_D0359.tif" />

[0568] Treatment of 6.10 to 1,2,4-benzenetricarboxylic anhydride in refluxed toluene yields 7_!_&gt; which is coupled with dipropylamine by EDC/HOBt/DIEA to afford 12. The oxidation of alcohol 12. by Jones' reagent gives conesponding acid 7.3. Coupling of 73 with p-fluoroaniline by HATU/DIEA affords IA, which is following by reduction of azide to afford 7.5.

[0569] EXAMPLE 38 [0570] This example describes the synthesis of the following compound

<img file="WO03106405A1_D0360.tif" /> which is made as described by Scheme 8 and the procedure below. [0571] Scheme 8.

<img file="WO03106405A1_D0361.tif" />

<img file="WO03106405A1_D0362.tif" />

[0572] Compound 12 is reduced by LAH, followed by the Jones' oxidation to afford the conesponding acid SΛ. Coupling of 8 with p-fluoroaniline by HATU/DIEA yield compound 8;2, which followed the reduction of azide to afford amine 8.3.

[0573] EXAMPLE 40 [0574] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0363.tif" /> which is made according to Scheme 9 and the procedure below. [0575] Scheme 9.

<img file="WO03106405A1_D0364.tif" />

[0576] Compound 9Λ is prepared by the procedure described in Example 11 except for using isobutylamine instead of 2-amino-N-benzyl-3-methyl-butyramide in step k. Treatment of Lawesson's reagent with 9Λ affords 92, followed by the reaction of 9j2, formic hydrazide and mercury (II) acetate to afford 93. Reduction of azide 93 by hydrogenation affords 9Λ.

[0577] EXAMPLE 41

[0578] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0365.tif" /> which is made according to Scheme 10 and the procedure below. [0579] Scheme 10.

<img file="WO03106405A1_D0366.tif" />

[0580] Compoxmd 6.11 (see Example 11) is mesylated by MsCl followed by azide replacement to give 10.1. The 1,3-dipolar-cycloaddition reaction of terminal azide and 4-methyl-l-pentyne affords 1,2,3-triazole 10.2. Reduction of azide to the conesponding amine gives 10.3.

[0581] EXAMPLE 42 [0582] This example describes the synthesis of the compound of structure below

<img file="WO03106405A1_D0367.tif" /> which is made according to Scheme 11 and the procedure below. [0583] Scheme 11

<img file="WO03106405A1_D0368.tif" />

[0584] Reaction of compound 11.1, phenyl chloroformate, DIEA gives 11.2 as a prodrug form of 11.1.

[0585] EXAMPLE 43

[0586] This example describes the synthesis of intermediates of the structure

<img file="WO03106405A1_D0369.tif" /> wherein R_D and R_E are each independently substituted or unsubstituted aliphatic, aryl or alkylaryl. These compounds were prepared according to Scheme 12 and the procedure below.

[0587] Scheme 12.

<img file="WO03106405A1_D0370.tif" />

[0588] The mono-alkylation of compound 12.2 is conducted by the treatment of 12.2 and NaH in DMF. Halide R_DX (1 eq) is added to the reaction mixture to afford the conesponding aryl ether 12.3. The second alkylation is performed under the some conditions with halide RβX (1 eq), followed by basic hydrolysis (LiOH, H₂O/THF) to give acid 12.1 as the intermediate for use in making compounds like those described in Example 44. Illustrative examples of suitable halides and their conesponding final products are shown in Table 13.

[0589] Table 13

<img file="WO03106405A1_D0371.tif" /><img file="WO03106405A1_D0372.tif" />

[0590] EXAMPLE 44 [0591] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0373.tif" /> where R_D and R_E are as defined in Example 43. These compounds are prepare according the procedure of Example 13 except for using acids of the formula

<img file="WO03106405A1_D0374.tif" /> as reagents instead of N,N-dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 14. [0592] Table 14

<img file="WO03106405A1_D0375.tif" /><img file="WO03106405A1_D0376.tif" /><img file="WO03106405A1_D0377.tif" />

[0593] EXAMPLE 45 [0594] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0378.tif" />

[0595] These compounds are prepared according to Example 45 except for

each <img file="WO03106405A1_D0379.tif" /> described in Example 44, the conesponding RA compound is

O

H O

II BoC OH N.

BoXX "OH prepared by substituting ^RA as a reagent instead of

Illustrative examples of suitable R_A groups are shown in Example 14

[0596] EXAMPLE 46 [0597] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0380.tif" /> where R_D and R_E are as defined in Example 43. These compounds are prepare according the procedure of Example 15 except for using acids of the formula

<img file="WO03106405A1_D0381.tif" /> as reagents instead of N,N-dipropyl-isophthalamic acid in step i. [0598] EXAMPLE 47

[0599] This example describes the synthesis of compounds of the structxire

<img file="WO03106405A1_D0382.tif" />

[0600] These compoxmds are prepared according to the procedure in Example

46 except for each <img file="WO03106405A1_D0383.tif" /> described in Example 44, the conesponding R_A

H

-N .

Boc' "OH compound is prepared by substituting ^RA as a reagent instead of

H O

M,

Boc' "OH

. Illustrative examples of suitable R_A groups are shown in Example 16.

[0601] EXAMPLE 48

[0602] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0384.tif" /> which was prepared according to Scheme 13 and the procedure below. [0603] Scheme 13. <img file="WO03106405A1_D0385.tif" />

HCI/dioxane

<img file="WO03106405A1_D0386.tif" />

<img file="WO03106405A1_D0387.tif" />

[0604] The addition of 3-methoxy-benzylamine to epoxide 13.1 affords hydroxyethylamine 13.2. Protection of amine 13.2 is conducted by t-butoxycarbonylation to give 13.3. Oxidation of alcohol 13.3 by Dess-Martin reagent yields ketone 13.4, which is followed by the reductive alkylation by NELOAc to afford amine 13.5. Protection of amino group by benzyl oxycarbonyl (Cbz) group yields 13.6. Deportection of t-butoxycarbonyl group of 13.6 affords amine 13.7. The resulting amine is then coupled with N, N-dipropyl- isophthalamic acid to give 13.8, followed by the hydrogenation to remove Cbz group to give 13.9.

[0605] EXAMPLE 49 [0606] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0388.tif" /> where R_B is as defined in Example 27. These compounds are prepare according the procedure of Example 50 except for using acids of the formula RβCO₂H as reagents instead of N,N-dipropyl-isophthalamic acid. Illustrative examples of acids and their conesponding final products are shown in Table 15

[0607] Table 15

<img file="WO03106405A1_D0389.tif" /><img file="WO03106405A1_D0390.tif" /><img file="WO03106405A1_D0391.tif" /> [0608] EXAMPLE 50

[0609] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0392.tif" /> which is prepared according to the procedure in Example 10 except for using cyclopropylamine instead of 2-amino-N-Benzyl-3-methyl-butyramide in step k, and for each RB group described in Examples 27, 28, and 49, the conesponding RA

compound is prepared by substituting <img file="WO03106405A1_D0393.tif" /> a reagent instead of

H J Boc-^ OH

. Illustrative examples of suitable RA groups are showin in Example 16.

[0610] EXAMPLE 51

[0611] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0394.tif" /> which is prepared according to the procedure in Example 10 except for using isopropylamine instead of 2-amino-N-Benzyl-3-methyl-butyramide in step k, and for each R_B group described in Examples 27, 28, and 49, the conesponding R_A compound

H °

H J Boc^ ^OH

Boc^/NX H is prepared by substituting ^RA as a reagent instead of

Illustrative examples of suitable R_A groups are shown in Example 16.

[0612] EXAMPLE 52

[0613] The preparation of common intermediates of the following structure is described as shown in Scheme 14, and below where R_l5 R₂ and R₃ are defined in Table 16. <img file="WO03106405A1_D0395.tif" />

&gt;614] Scheme 14.

<img file="WO03106405A1_D0396.tif" />

[0615] The alkylation of Compound 14.2 is conducted by the treatment of

14.2 and NaH in DMF, the halide (RιX,l eq) is added to the reaction mixture to afford the conesponding aryl ether 14.3. Hydrogenation of 14.3 reduces nitro group to aniline 14.4, which followed by treatment of sulfonyl chloride to give the conesponding sulfonamide 14.5. Alkylation of sulfonamide 14.5 with halide (NaH, R₂X, 1 eq) gives 14 &gt;, followed by basic hydrolysis (LiOH, H2O/THF/MeOH) to give acid 14.1 as the intermediateds for example 53.

<img file="WO03106405A1_D0397.tif" /><img file="WO03106405A1_D0398.tif" /><img file="WO03106405A1_D0399.tif" /><img file="WO03106405A1_D0400.tif" />

[0617] EXAMPLE 53 [0618] The example describes the synthesis of compounds of the structure:

<img file="WO03106405A1_D0401.tif" /> where R_B is as defined in example 52. These compounds are prepare according the procedure of example 6 except for using acids of the formula RβCO₂H as reagents instead of N,N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their corresponding final products are shown in Table 17 [0619] Table 17

<img file="WO03106405A1_D0402.tif" /><img file="WO03106405A1_D0403.tif" /><img file="WO03106405A1_D0404.tif" /><img file="WO03106405A1_D0405.tif" />

[0621] This example describes the synthesis of compounds of the structure: <img file="WO03106405A1_D0406.tif" />

[0622] For each RB group exampled in example 52, the conesponding R_A

compound can be prepared by substituting <img file="WO03106405A1_D0407.tif" /> as a reagent instead of

H

. - N

Boc" "OH

<img file="WO03106405A1_D0408.tif" /> . Illustrative examples of suitable RA groups are shown in example 14.

[0623] EXAMPLE 55

[0624] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0409.tif" />

[0625] For each RB group exampled in example 52, the conesponding R_A

H O

-N.

BoC "OH compound can be prepared by substituting ^RA as a reagent instead of

H

Boc"^"N

<img file="WO03106405A1_D0410.tif" /> . Illustrative examples of suitable R groups are shown in example 16.

[0626] EXAMPLE 56

[0627] The preparation of common intermediates of the following structure is described as shown in Scheme 15, and below where Ri are defined in Table 18.

<img file="WO03106405A1_D0411.tif" /> [0628] Scheme 15.

<img file="WO03106405A1_D0412.tif" />

[0629] Aniline 14.4 is treated which sulfonyl chloride 2 to give the conesponding sulfonamide 15.2, which is followed by the treatment of NaH to afford the cyclic sulfonamide 153. Basic hydrolysis (LiOH, H2O/THF/MeOH) of compound 15.3 gives acid 15.1 as the intermediateds for example 57.

[0630] Table 18

<img file="WO03106405A1_D0413.tif" /><img file="WO03106405A1_D0414.tif" />

[0631] EXAMPLE 57 [0632] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0415.tif" /> where RB is as defined in example 56. These compounds are prepare according the procedure of example 6 except for using acids of the formula RβCO₂H as reagents instead of N,N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 19

[0633] Table 19 <img file="WO03106405A1_D0416.tif" /><img file="WO03106405A1_D0417.tif" />

[0634] EXAMPLE 58

[0635] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0418.tif" />

[0636] For each RB group exampled in example 57, the conesponding R

H O -N.

Boc' "OH compound can be prepared by substituting ^RA as a reagent instead of

H

N BoX V "OH

<img file="WO03106405A1_D0419.tif" /> Illustrative examples of suitable R groups are shown in example

14.

[0637] EXAMPLE 59

[0638] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0420.tif" /> [0639] For each RB group exampled in example 57, the conesponding RA

compound can be prepared by substituting <img file="WO03106405A1_D0421.tif" /> as a reagent instead of

H

-N„

Boc "OH

<img file="WO03106405A1_D0422.tif" /> Illustrative examples of suitable RA groups are shown in example 16.

[0640] EXAMPLE 60

[0641] The preparation of common intermediates of the following structure is described as shown in Scheme 16, and below where Ri, R₂ and R₃ are defined in Table 20.

<img file="WO03106405A1_D0423.tif" />

16.1

[0642] Scheme 16:

<img file="WO03106405A1_D0424.tif" />

THF 16.1

[0643] The preparation of sulfamide 16.1 is starting with commercially available, literature or readily available diamine. The treatment of diamine 16.1 with sxxlfamine a under refluxing pyridine affords sulfamine 163, which is followed by alkylation of α-halo alkyl ester to give compound 16.4. Basic hydrolysis (LiOH, H2O/THF/MeOH) of ester gives acid 16.1 as the intermediateds for example 61. 644] Table 20

<img file="WO03106405A1_D0425.tif" /><img file="WO03106405A1_D0426.tif" /><img file="WO03106405A1_D0427.tif" /><img file="WO03106405A1_D0428.tif" />

[0645] EXAMPLE 61 [0646] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0429.tif" /> where R_B is as defined in example 60. These compounds are prepare according the procedure of example 6 except for using acids of the formula RβCO₂H as reagents instead of N_.N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their corresponding final products are shown in Table 21

[0647] Table 21

<img file="WO03106405A1_D0430.tif" /><img file="WO03106405A1_D0431.tif" /><img file="WO03106405A1_D0432.tif" /><img file="WO03106405A1_D0433.tif" /><img file="WO03106405A1_D0434.tif" />

[0648] EXAMPLE 62

[0649] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0435.tif" />

[0650] For each R_B group exampled in example 60, the conesponding RA

H O

Boc" ,N, "OH compound can be prepared by substituting ^RA as a reagent instead of

Boc"

<img file="WO03106405A1_D0436.tif" /> Illustrative examples of suitable R_A groups are shown in example

14.

[0651] EXAMPLE 63

[0652] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0437.tif" /> [0653] For each R_B group exampled in example 60, the conesponding RA

H O N,

Boc" OH compound can be prepared by substituting A as a reagent instead of

H

Boc-

<img file="WO03106405A1_D0438.tif" /> Illustrative examples of suitable RA groups are shown in example

16.

[0654] EXAMPLE 64

[0655] The preparation of common intermediates of the following structure is described as shown in Scheme 17, and below where R_, R₂, R₃, t and R₅ are defined in Table 22.

<img file="WO03106405A1_D0439.tif" />

[0656] Scheme 17.

"-Ph <img file="WO03106405A1_D0440.tif" />

17.2 17.3 17.4

<img file="WO03106405A1_D0441.tif" />

Hydrogenation ^0R Hydrolysis

<img file="WO03106405A1_D0442.tif" /><img file="WO03106405A1_D0443.tif" />

17.8 ^• 1 .9 _{17 1}

[0657] Starting from commercially available, literature or readily available protected amino acids. Amino acid 17.2 is treated with benzyl amine and a coupling reagent such as HATU, to give 17.3. Compound 17.3 is reduced by a reducing reagent such as LAH to give amine 17.4. 17.4 is treated with acid to afford diamine 17.5, which follow by condensation with an oxalic acid derivative give the dioxopiperazine 17.6. Treatment of 17.6 with NaH and alkyl halide gives compound 17.7. Removal of benzyl group by hydrogenation to give 17.8, which is alkylated with an α-halo alkyl ester to give compound 17.9. Hydrolysis of 17.9 affords acid 17.1.

<img file="WO03106405A1_D0444.tif" /><img file="WO03106405A1_D0445.tif" /><img file="WO03106405A1_D0446.tif" /><img file="WO03106405A1_D0447.tif" />

[0659] EXAMPLE 65 [0660] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0448.tif" /> where R_B is as defined in example 64. These compounds are prepare according the procedure of example 6 except for using acids of the formula RβCO₂H as reagents instead of N,N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 23

[0661] Table 23

<img file="WO03106405A1_D0449.tif" /><img file="WO03106405A1_D0450.tif" /><img file="WO03106405A1_D0451.tif" /><img file="WO03106405A1_D0452.tif" /><img file="WO03106405A1_D0453.tif" />

[0662] EXAMPLE 66

[0663] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0454.tif" /> [0664] For each Rβ group exampled in example 64, the conesponding R_A

H °

Boc"^NX "OH compoxmd can be prepared by substituting ^RA as a reagent instead of

H O N Boc^ X "OH

<img file="WO03106405A1_D0455.tif" /> Illustrative examples of suitable R_A groups are shown in example

14.

[0665] EXAMPLE 67

[0666] The example describes the synthesis of compounds of the structure <img file="WO03106405A1_D0456.tif" />

[0667] For each RB group exampled in example 64, the conesponding R

compound can be prepared by substituting <img file="WO03106405A1_D0457.tif" /> as a reagent instead of

Boc

<img file="WO03106405A1_D0458.tif" /> Illustrative examples of suitable R_A groups are shown in example

16.

[0668] EXAMPLE 68

[0669] The preparation of common intermediates of the following structure is described as shown in Scheme 18, and below where R__, R₂ and R₃ are defined in Table

24.

<img file="WO03106405A1_D0459.tif" />

[0670] Scheme 18.

<img file="WO03106405A1_D0460.tif" />

18.2 18.3 _{18 4} 18.5

Acid

<img file="WO03106405A1_D0461.tif" />

[0671] Starting from commercially available, literature or readily available protected diamine. Mono-protected diamine 18.2 is treated with sulfonyl chloride 18. A to give 183, which is allowed by the treatment of NaH affords 18.4. Compound 18.4 is treated with NaH and an alkyl halide to afford 18.5, which followed by the treatment of acid to give 18.6. Compoxmd 18.6 is alkylated with an α-halo alkyl ester to give compound 18.7. Hydrolysis of 18.7 affords acid 18.1. [0672] Table 24

<img file="WO03106405A1_D0462.tif" /><img file="WO03106405A1_D0463.tif" /><img file="WO03106405A1_D0464.tif" /><img file="WO03106405A1_D0465.tif" />

[0673] Example 69

[0674] The example describes the synthesis of compoxmds of the structure

<img file="WO03106405A1_D0466.tif" /> where R_B is as defined in example 68. These compounds are prepare according the procedure of example 6 except for using acids of the formula RβCO₂H as reagents instead of N,N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 25

[0675] Table 25

<img file="WO03106405A1_D0467.tif" /><img file="WO03106405A1_D0468.tif" /><img file="WO03106405A1_D0469.tif" /><img file="WO03106405A1_D0470.tif" /><img file="WO03106405A1_D0471.tif" />

[0676] EXAMPLE 70

[0677] This example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0472.tif" />

[0678] For each RB group exampled in example 68, the conesponding R_A

H O Nk

BoC "OH compound can be prepared by substituting ^RA as a reagent instead of

Boc OH

<img file="WO03106405A1_D0473.tif" /> Illustrative examples of suitable R_A groups are shown in example

14.

[0679] EXAMPLE 71

[0680] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0474.tif" />

[0681] For each RB group exampled in example 68, the conesponding RA

compoxmd can be prepared by substituting <img file="WO03106405A1_D0475.tif" /> as a reagent instead of <img file="WO03106405A1_D0476.tif" /> Illustrative examples of suitable R_A groups are shown in example

16.

[0682] EXAMPLE 72

[0683] The preparation of common intermediates of the following structure is described as shown in Scheme 19, and below where Ri are defined in Table 26.

<img file="WO03106405A1_D0477.tif" />

[0684] Scheme 19.

<img file="WO03106405A1_D0478.tif" />

19.4 19.1

[0685] The mitsunobu reaction of 19.2 and 19.A gives the corresponding aryl ether 193, which is followed by the alkylation with halide (NaH, R₂X, 1 eq) to afford aryl diether 19_ Basic hydrolysis (LiOH, H2O/THF/MeOH) of 19,4 gives acid 19.1 as the intermediates for example 73.

[0686] Table 26

<img file="WO03106405A1_D0479.tif" /><img file="WO03106405A1_D0480.tif" />

[0687] EXAMPLE 73 [0688] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0481.tif" /> where R_B is as defined in example 72. These compounds are prepare according the procedure of example 6 except for using acids of the formula RβCO₂H as reagents instead of N,N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their corresponding final products are shown in Table 27. [0689] Table 27

<img file="WO03106405A1_D0482.tif" />

[0690] EXAMPLE 74

[0691] This example describes the synthesis of compounds of the structure <img file="WO03106405A1_D0483.tif" />

[0692] For each R_B group exampled in example 72, the conesponding R

compound can be prepared by substituting <img file="WO03106405A1_D0484.tif" /> as a reagent instead of

H

,N„

Boc" "OH

<img file="WO03106405A1_D0485.tif" /> Illustrative examples of suitable R_A groups are shown in example 14.

[0693] EXAMPLE 75

[0694] The example describes the synthesis of compounds of the structure

<img file="WO03106405A1_D0486.tif" />

[0695] For each RB group exampled in example 72, the conesponding R_A

compound can be prepared by substituting <img file="WO03106405A1_D0487.tif" /> as a reagent instead of

H °

.N.

BoC "OH

<img file="WO03106405A1_D0488.tif" /> Illustrative examples of suitable R_A groups are shown in example 16.

[0696] EXAMPLE 76

[0697] The example describes the synthesis of compounds of the structxire

<img file="WO03106405A1_D0489.tif" />

[0698] These compoxmds are prepared according the procedure of example 6 except for using acids of the formula RβCO H as reagents, which are prepared by the preparation described above or in literature, instead of N,N-Dipropyl-isophthalamic acid in step i. Illustrative examples of acids and their conesponding final products are shown in Table 28.

[0699] Table 28

<img file="WO03106405A1_D0490.tif" /><img file="WO03106405A1_D0491.tif" />

<img file="WO03106405A1_D0492.tif" /><img file="WO03106405A1_D0493.tif" /><img file="WO03106405A1_D0494.tif" /><img file="WO03106405A1_D0495.tif" /><img file="WO03106405A1_D0496.tif" /><img file="WO03106405A1_D0497.tif" /><img file="WO03106405A1_D0498.tif" /><img file="WO03106405A1_D0499.tif" /><img file="WO03106405A1_D0500.tif" /><img file="WO03106405A1_D0501.tif" /><img file="WO03106405A1_D0502.tif" /><img file="WO03106405A1_D0503.tif" /><img file="WO03106405A1_D0504.tif" /><img file="WO03106405A1_D0505.tif" /><img file="WO03106405A1_D0506.tif" /><img file="WO03106405A1_D0507.tif" /><img file="WO03106405A1_D0508.tif" />

[0700] EXAMPLE 77

[0701] This example describes the synthesis of compounds of the structure <img file="WO03106405A1_D0509.tif" />

[0702] For each RB group exampled in example 76, the conesponding RA

H

Boc "OH compound can be prepared by substituting A as a reagent instead of

H

Boc'

<img file="WO03106405A1_D0510.tif" /> Illustrative examples of suitable R_A groups are shown in example

14.

[0703] EXAMPLE 78

[0704] The example describes the synthesis of compoxmds of the structure

<img file="WO03106405A1_D0511.tif" />

[0705] For each RB group exampled in example 76, the conesponding R_A

H ©

Boc"^NX "OH compound can be prepared by substituting ^RA as a reagent instead of

H ©

Boc"^{N -}X "OH

<img file="WO03106405A1_D0512.tif" /> Illustrative examples of suitable R_A groups are shown in example 16.