.omega.-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors

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69676-7 ω-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS

Field of the Invention

This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases and proteolytic enzyme mediated diseases, and pharmaceutical compositions for use in such therapy.

Background of the Invention

W Two classes of effector molecules which are critical for the progression of rheumatoid arthritis are pro-inflammatory cytokines and tissue degrading proteases. Recently, a family of kinases was described which is instrumental in controlling the transcription and translation of the structural genes coding for these effector molecules.

The mitogen-activated protein (MAP) kinase family is made up of a series of structurally related proline-directed serine/threonine kinases which are activated either by growth factors (such as EGF) and phorbol esters (ERK), or by IL-1, TNFa or stress (p38, JNK). The MAP kinases are responsible for the activation of a wide variety of transcription factors and proteins involved in transcriptional control of

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PCT/US00/00768 cytokine production. A pair of novel protein kinases involved in the regulation of cytokine synthesis was recently described by a group from SmithKline Beecham (Lee et al. Nature 1994, 372, 739). These enzymes were isolated based on their affinity to bond to a class of compounds, named CSAIDSs (cytokine suppressive anti-inflammatory drugs) by SKB. The CSAIDs, bicyclic pyridinyl imidazoles, have been shown to have cytokine inhibitory activity both in vitro and in vivo. The isolated enzymes, CSBP-1 and -2 (CSAID binding protein 1 and 2) have been cloned and expressed. A murine homologue for CSBP-2, p38, has also been reported (Han et al. Science 1994, 265, 808).

Early studies suggested that CSAIDs function by interfering with m-RNA translational events during cytokine biosynthesis. Inhibition of p38 has been shown to inhibit both cytokine production (eg., TNFa, IL-1, IL-6, IL-8) and proteolytic enzyme production (eg., MMP-1, MMP-3) in vitro and/or in vivo.

Clinical studies have linked TNFa production and/or signaling to a number of diseases including rheumatoid arthritis (Maini. J. Royal Coll. Physicians London 1996, 30, 344). In addition, excessive levels of TNFa have been implicated in a wide variety of inflammatory and/or immunomodulatory diseases, including acute rheumatic fever (Yegin et al. Lancet 1997, 349, 170), bone resorption (Pacifici et al. J. Clin. Endocrinol. Metabol. 1997, 82, 29), postmenopausal osteoperosis (Pacifici et al. J. Bone Mineral Res. 1996, 11, 1043), sepsis (Blackwell et al. Br. J. Anaesth. 1996, 77, 110), gram negative sepsis (Debets et al. Prog. Clin. Biol. Res. 1989, 308, 463), septic shock (Tracey et al. Nature 1987, 330, 662; Girardin et al. New England J. Med. 1988, 319, 397), endotoxic shock (Beutler et al. Science 1985, 229, 869; Ashkenasi et al. Proc. Nat’l. Acad. Sci. USA 1991, 88, 10535), toxic shock syndrome, (Saha et al. J. Immunol. 1996, 157, 3869; Lina et al. FEMS Immunol. Med. Microbiol. 1996, 13, 81), systemic inflammatory response syndrome (Anon. Crit. Care Med. 1992, 20, 864), inflammatory bowel diseases (Stokkers et al. J. Inflamm. 1995-6, 47, 97) including Crohn’s disease (van Deventer et al. Aliment. Pharmacol. Therapeu. 1996, 10 (Suppl. 2), 107; van Dullemen et al. Gastroenterology 1995, 109, 129) and ulcerative colitis (Masuda et al. J. Clin. Lab.

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Immunol. 1995, 46, 111), Jarisch-Herxheimer reactions (Fekade et al. New England J. Med. 1996, 335, 311), asthma (Amrani et al. Rev. Malad. Respir. 1996, 13, 539), adult respiratory distress syndrome (Roten et al. Am. Rev. Respir. Dis. 1991, 143, 590; Suter et al. Am. Rev. Respir. Dis. 1992, 145, 1016), acute pulmonary fibrotic diseases (Pan et al. Pathol. Int. 1996, 46, 91), pulmonary sarcoidosis (Ishioka et al. Sarcoidosis Vasculitis Diffuse Lung Dis. 1996, 13, 139), allergic respiratory diseases (Casale et al. Am. J. Respir. Cell Mol. Biol. 1996,15, 35), silicosis (Gossart et al. J. Immunol. 1996, 156, 1540; Vanhee et al. Eur. Respir. J. 1995, 8, 834), coal worker’s pneumoconiosis (Borm et al. Am. Rev. Respir. Dis. 1988, 138, 1589), alveolar injury (Horinouchi et al. Am. J. Respir. Cell Mol. Biol. 1996, 14, 1044), hepatic failure (Gantner et al. J. Pharmacol. Exp. Therap. 1997, 280, 53), liver disease during acute inflammation (Kim et al. J. Biol. Chem. 1997, 272, 1402), severe alcoholic hepatitis (Bird et al. Ann. Intern. Med. 1990, 112, 917), malaria (Grau et al. Immunol. Rev. 1989,112, 49; Taverne et al. Parasitol. Today 1996,12, 290) including Plasmodium falciparum malaria (Perlmann et al. Infect. Immunit. 1997, 65, 116) and cerebral malaria (Rudin et al. Am. J. Pathol. 1997, 150, 257), non-insulin-dependent diabetes mellitus (NIDDM; Stephens et al. J. Biol. Chem. 1997, 272, 971; Ofei et al. Diabetes 1996, 45, 881), congestive heart failure (Doyama et al. Int. J. Cardiol. 1996, 54, 217; McMurray et al. Br. Heart J. 1991, 66, 356), damage following heart disease (Malkiel et al. Mol. Med. Today 1996, 2, 336), atherosclerosis (Parums et al. J. Pathol. 1996,179, A46), Alzheimer’s disease (Fagarasan et al. Brain Res. 1996, 723, 231; Aisen et al. Gerontology 1997, 43, 143), acute encephalitis (Ichiyama et al. J. Neurol. 1996, 243, 457), brain injury (Cannon et al. Crit. Care Med. 1992, 20, 1414; Hansbrough et al. Surg. Clin. N. Am. 1987, 67, 69; Marano et al. Surg. Gynecol. Obstetr. 1990, 170, 32), multiple sclerosis (M.S.; Coyle. Adv. Neuroimmunol. 1996, 6, 143; Matusevicius et al. J. Neuroimmunol. 1996, 66, 115) including demyelation and oligiodendrocyte loss in multiple sclerosis (Brosnan et al. Brain Pathol. 1996, 6, 243), advanced cancer (MucWierzgon et al. J. Biol. Regulators Homeostatic Agents 1996, 10, 25), lymphoid malignancies (Levy et al. Crit. Rev. Immunol. 1996, 16, 31), pancreatitis

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PCT/US00/00768 (Exley et al. Gut 1992, 33, 1126) including systemic complications in acute pancreatitis (McKay et al. Br. J. Surg. 1996, 83, 919), impaired wound healing in infection inflammation and cancer (Buck et al. Am. J. Pathol. 1996, 149, 195), myelodysplastic syndromes (Raza et al. lnt. J. Hematol. 1996, 63, 265), systemic lupus erythematosus (Maury et al. Arthritis Rheum. 1989, 32, 146), biliary cirrhosis (Miller et al. Am. J. Gasteroenterolog. 1992, 87, 465), bowel necrosis (Sun et al. J. Clin. Invest. 1988, <57, 1328), psoriasis (Christophers. Austr. J. Dermatol. 1996, 37, S4), radiation injury (Redlich et al. J. Immunol. 1996, 157, 1705), and toxicity following administration of monoclonal antibodies such as OKT3 (Brod et al. Neurology 1996, 46, 1633). TNFa levels have also been related to host-versusgraft reactions (Piguet et al. Immunol. Ser. 1992, 56, 409) including ischemia reperfusion injury (Colletti et al. J. Clin. Invest. 1989, 85, 1333) and allograft rejections including those of the kidney (Maury et al. J. Exp. Med. 1987, 166, 1132), liver (Imagawa et al. Transplantation 1990, 50, 219), heart (Bolling et al. Transplantation 1992, 53, 283), and skin (Stevens et al. Transplant. Proc. 1990, 22, 1924), lung allograft rejection (Grossman et al. Immunol. Allergy Clin. N. Am. 1989, 9, 153) including chronic lung allograft rejection (obliterative bronchitis; LoCicero et al. J. Thorac. Cardiovasc. Surg. 1990, 99, 1059), as well as complications due to total hip replacement (Cirino et al. Life Sci. 1996, 59, 86). TNFa has also been linked to infectious diseases (review: Beutler et al. Crit. Care Med. 1993, 21, 5423; Degre. Biotherapy 1996, 8, 219) including tuberculosis (Rook et al. Med. Malad. Infect. 1996, 26, 904), Helicobacter pylori infection during peptic ulcer disease (Beales et al. Gastroenterology 1997, 112, 136), Chaga’s disease resulting from Trypanosoma cruzi infection (Chandrasekar et al. Biochem. Biophys. Res. Commun. 1996, 223, 365), effects of Shiga-like toxin resulting from E. coli infection (Harel et al. J. Clin. Invest. 1992, 56, 40), the effects of enterotoxin A resulting from Staphylococcus infection (Fischer et al. J. Immunol. 1990,144, 4663), meningococcal infection (Waage et al. Lancet 1987, 355; Ossege et al. J. Neurolog. Sci. 1996, 144, 1), and infections from Borrelia burgdorferi (Brandt et al. Infect. Immunol. 1990, 58, 983), Treponema pallidum (Chamberlin et

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PCT/US00/00768 al. Infect. Immunol. 1989, 57, 2872), cytomegalovirus (CMV; Geist et al. Am. J. Respir. Cell Mol. Biol. 1997, 16, 31), influenza virus (Beutler et al. Clin. Res. 1986, 34, 491a), Sendai virus (Goldfield et al. Proc. Nat’l. Acad. Sci. USA 1989, 87, 1490), Theiler’s encephalomyelitis virus (Sierra et al. Immunology 1993, 78, 399), and the human immunodeficiency virus (HIV; Poli. Proc. Nat’l. Acad. Sci. USA 1990, 87, 782; Vyakaram et al. AIDS 1990, </,21; Badley et al. J. Exp. Med. 1997, 185, 55).

Because inhibition of p38 leads to inhibition of TNFa production, p38 inhibitors will be useful in treatment of the above listed diseases.

A number of diseases are thought to be mediated by excess or undesired matrix-destroying metalloprotease (MMP) activity or by an imbalance in the ratio of the MMPs to the tissue inhibitors of metalloproteinases (TIMPs). These include osteoarthritis (Woessner et al. J. Biol. Chem. 1984, 259, 3633), rheumatoid arthritis (Mullins et al. Biochim. Biophys. Acta 1983, 695, 117; Woolley et al. Arthritis

Rheum. 1977, 20, 1231; Gravallese et al. Arthritis Rheum. 1991, 34, 1076), septic arthritis (Williams et al. Arthritis Rheum. 1990, 33, 533), tumor metastasis (Reich et al. Cancer Res. 1988, 48, 3307; Matrisian et al. Proc. Nat'l. Acad. Sci., USA 1986, 83, 9413), periodontal diseases (Overall et al. J. Periodontal Res. 1987, 22, 81), corneal ulceration (Bums et al. Invest. Opthalmol. Pis. Sci. 1989, 30, 1569), proteinuria (Baricos et al. Biochem. J. 1988, 254, 609), coronary thrombosis from atherosclerotic plaque rupture (Henney et al. Proc. Nat'l. Acad. Sci., USA 1991, 88, 8154), aneurysmal aortic disease (Vine et al. Clin. Sci. 1991, 81, 233), birth control (Woessner et al. Steroids 1989, 54, 491), dystrophobic epidermolysis bullosa (Kronberger et al. J. Invest. Dermatol. 1982, 79, 208), degenerative cartilage loss following traumatic joint injury, osteopenias mediated by MMP activity, tempero mandibular joint disease, and demyelating diseases of the nervous system (Chantry et al. J. Neurochem. 1988, 50, 688).

Because inhibition of p38 leads to inhibition of MMP production, p38 inhibitors will be useful in treatment of the above listed diseases.

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Inhibitors of p38 are active in animal models of TNFa production, including a murine lipopolysaccharide (LPS) model of TNFa production. Inhibitors of p38 are active in a number of standard animal models of inflammatory diseases, including carrageenan-induced edema in the rat paw, arachadonic acid-induced edema in the rat paw, arachadonic acid-induced peritonitis in the mouse, fetal rat long bone resorption, murine type II collagen-induced arthritis, and Fruend’s adjuvant-induced arthritis in the rat. Thus, inhibitors of p38 will be useful in treating diseases mediated by one or more of the above-mentioned cytokines and/or proteolytic enzymes.

The need for new therapies is especially important in the case of arthritic diseases. The primary disabling effect of osteoarthritis, rheumatoid arthritis and septic arthritis is the progressive loss of articular cartilage and thereby normal joint function. No marketed pharmaceutical agent is able to prevent or slow this cartilage loss, although nonsteroidal antiinflammatory drugs (NSAIDs) have been given to control pain and swelling. The end result of these diseases is total loss of joint function which is only treatable by joint replacement surgery. P38 inhibitors will halt or reverse the progression of cartilage loss and obviate or delay surgical intervention.

Several patents have appeared claiming polyarylimidazoles and/or compounds containing polyarylimidazoles as inhibitors of p38 (for example, Lee et al. WO 95/07922; Adams et al. WO 95/02591; Adams et al. WO 95/13067; Adams et al. WO 95/31451). It has been reported that arylimidazoles complex to the ferric form of cytochrome P450_caæ (Harris et al. Mol. Eng. 1995, 5, 143, and references therein), causing concern that these compounds may display structure-related toxicity (Howard-Martin et al. Toxicol. Pathol. 1987, 75, 369). Therefore, there remains a need for improved p38 inhibitors.

Summary of the Invention

This invention provides compounds, generally described as aryl ureas, including both aryl and heteroaryl analogues, which inhibit p38 mediated events and

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69676-7 thus inhibit the production of cytokines (such as TNFa, IL-1 and IL-8) and proteolytic enzymes (such as MMP-1 and MMP-3). The invention also provides a method of treating a cytokine mediated disease state in humans or mammals, wherein the cytokine is one whose production is affected by p38. Examples of such cytokines include, but are not limited to TNFa, IL-1 and EL-8. The invention also provides a method of treating a protease mediated disease state in humans or mammals, wherein the protease is one whose production is affected by p38. Examples of such proteases include, but are not limited to collagenase (MMP-1) and stromelysin (MMP-3).

Accordingly, these compounds may potentially be useful therapeutic agents for such acute and chronic inflammatory and/or immunomodulatory diseases as rheumatoid arthritis, osteoarthritis, septic arthritis, rheumatic fever, bone resorption, postmenopausal osteoperosis, sepsis, gram negative sepsis, septic shock, endotoxic shock, toxic shock syndrome, systemic inflammatory response syndrome, inflammatory bowel diseases including Crohn’s disease and ulcerative colitis,

Jarisch-Herxheimer reactions, asthma, adult respiratory distress syndrome, acute pulmonary fibrotic diseases, pulmonary sarcoidosis, allergic respiratory diseases, silicosis, coal worker’s pneumoconiosis, alveolar injury, hepatic failure, liver disease during acute ' inflammation, severe alcoholic hepatitis, malaria including

Plasmodium falciparum malaria and cerebral malariaj non-insulin-dependent diabetes mellitus (NIDDM), congestive heart failure, damage following heart disease, atherosclerosis, Alzheimer’s disease, acute encephalitis, brain injury, multiple. sclerosis including demyelation and oligiodendrocyte loss in multiple sclerosis, advanced cancer, lymphoid malignancies, tumor metastasis, pancreatitis, including systemic complications.in acute pancreatitis, impaired wound healing in infection, inflammation and cancer, periodontal diseases, corneal ulceration, proteinuria, myelodysplastic syndromes, systemic lupus erythematosus, biliary cirrhosis, bowel necrosis, psoriasis, radiation injury, toxicity following administration of monoclonal antibodies such as OKT3, host-versus-graft reactions including ischemia reperfusion injury and allograft rejections including kidney,

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69676-7 liver, heart, and skin allograft rejections, lung allograft rejection including chronic lung allograft rejection (obliterative bronchitis) as well as complications due to total hip replacement, and infectious diseases including tuberculosis, Helicobacter pylori infection during peptic ulcer disease, Chaga’s disease resulting from Trypanosoma cruzi infection, effects of Shiga-like toxin resulting from E. coli infection, effects of enterotoxin A resulting from Staphylococcus infection, meningococcal infection, and infections from Borrelia burgdorferi, Treponema pallidum, cytomegalovirus, influenza virus, Theiler’s encephalomyelitis virus, and the human immunodeficiency virus (HIV).

The present invention, therefore, provides compounds generally described as aryl ureas, including both aryl and heteroaryl analogues, which inhibit the p38 pathway. The invention also provides a method for treatment of p38-mediated disease states in humans or mammals, e.g., disease states mediated by one or more cytokines or proteolytic enzymes produced and/or activated by a p38 mediated process. Thus, the invention is directed to compounds, compositions and methods for the treatment of a disease mediated by p38 kinase wherein a compound of Formula I is administered or a pharmaceutically acceptable salt thereof.

A-D-B (I)

In formula I, D is -NH-C(O)-NH-,

A is a substituted moiety of up to 40 carbon atoms of the formula: -L-(ML¹ )_q , where L is a 5 or 6 membered cyclic structure bound directly to D, I? comprises a substituted cyclic moiety having at least 5 members, M is a bridging group having at least one atom, q is an integer of from 1-3; and each cyclic structure of L and L¹ contains 0-4 members of the group consisting of nitrogen, oxygen and sulfur, and

B is a substituted or unsubstituted, up to tricyclic aryl or heteroaryl moiety of up to 30 carbon atoms with at least one 6-member cyclic structure bound

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PCT/US00/00768 directly to D containing 0-4 members of the group consisting of nitrogen, oxygen and sulfur, wherein L¹ is substituted by at least one substituent selected from the group consisting of -SC^Rx, -C(O)R_X and -C(NR_y) R_z,

R_y is hydrogen or a carbon based moiety of up to 24 carbon atoms optionally containing heteroatoms selected from N, S and O and optionally halosubstituted, up to per halo,

R_z is hydrogen or a carbon based moiety of up to 30 carbon atoms optionally containing heteroatoms selected from N, S and O and optionally substituted by halogen, hydroxy and carbon based substituents of up to 24 carbon atoms, which optionally contain heteroatoms selected from N, S and O and are optionally substituted by halogen;

R_x is R_z or NR_aRb where R_a and Rb are

a) independently hydrogen, a carbon based moiety of up to 30 carbon atoms optionally containing heteroatoms selected from N, S and O and optionally substituted by halogen, hydroxy and carbon based substituents of up to 24 carbon atoms, which optionally contain heteroatoms selected from N, S and O and are optionally substituted by halogen, or

-OSi(Rf)3 where Rf is hydrogen or a carbon based moiety of up to carbon atoms optionally containing heteroatoms selected from N, S and O and optionally substituted by halogen, hydroxy and carbon based substituents of up to 24 carbon atoms, which optionally contain heteroatoms selected from N, S and O and are optionally substituted by halogen; or

b) R_a and Rb together form a 5-7 member heterocyclic structure of 1-3 heteroatoms selected from N, S and O, or a substituted 5-7 member heterocyclic structure of 1-3 heteroatoms selected from N, S and O substituted by halogen,

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PCT/US00/00768 hydroxy or carbon based substituents of up to 24 carbon atoms, which optionally contain heteroatoms selected from N, S and O and are optionally substituted by halogen; or

c) one of R_a or R_b is -C(O)-, a C1-C5 divalent alkylene group or a 5 substituted C1-C5 divalent alkylene group bound to the moiety L to form a cyclic structure with at least 5 members, wherein the substituents of the substituted C1-C5 divalent alkylene group are selected from the group consisting of halogen, hydroxy, and carbon based substituents of up to 24 carbon atoms, which optionally contain heteroatoms selected from N, S and O and are optionally substituted by halogen;

where B is substituted, L is substituted or L¹ is additionally substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3;

wherein each W is independently selected from the group consisting of CN, -CO₂R⁷, -C(O)NR⁷R⁷, -C(O)-R⁷, -NO2, -OR⁷, -SR⁷, -NR⁷R⁷, -NR⁷C(O)OR⁷, 15 NR⁷C(O)R⁷, -Q-Ar, and carbon based moieties of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O and optionally substituted by one or more substituents independently selected from the group consisting of -CN, CO2R⁷, -C(O)R⁷, -C(O)NR⁷R⁷, -OR⁷, -SR⁷, -NR⁷R⁷, -NO2, -NR⁷C(O)R⁷, NR⁷C(O)0R⁷ and halogen up to per-halo; with each R⁷ independently selected from

H or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O and optionally substituted by halogen, wherein Q is -O-, -S-, -N(R⁷)-, -(CH2)m-, -C(O)-, -CH(OH)-, -(CH2)mO-, (CH2)mS-, -(CH2)mN(R⁷)-, -O(CH2)_m- CHX^a-, -CX^a2-, -S-(CH₂)_m- and N(R⁷)(CH₂)_m-, where m= 1-3, and X^a is halogen; and

Ar is a 5- or 6-member aromatic structure containing 0-2 members selected from the group consisting of nitrogen, oxygen and sulfur, which is optionally substituted by halogen, up to per-halo, and optionally substituted by Z_ni, wherein nl is 0 to 3 and each Z is independently selected from the group consisting of -CN, 10

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CO₂R⁷, -C(O)R⁷, -C(O)NR⁷R⁷, -NO2, -OR⁷, -SR⁷ -NR⁷R⁷, -NR⁷C(O)OR⁷, NR⁷C(O)R⁷, and a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O and optionally substituted by one or more substituents selected from the group consisting of -CN, -CO2R , -COR , 5 C(O)NR⁷R⁷, -OR⁷, -SR⁷, -NO₂, -NR⁷R⁷, -NR⁷C(O)R⁷, and -NR⁷C(O)OR⁷, with R⁷as defined above.

In formula I, suitable hetaryl groups include, but are not limited to, 5-12 carbon-atom aromatic rings or ring systems containing 1-3 rings, at least one of which is aromatic, in which one or more, e.g., 1-4 carbon atoms in one or more of the rings can be replaced by oxygen, nitrogen or sulfur atoms. Each ring typically has 3-7 atoms. For example, B can be 2- or 3-furyl, 2- or 3-thienyl, 2- or 4-triazinyl,

1- , 2- or 3-pyrrolyl, 1-, 2-, 4- or 5-imidazolyl, 1-, 3-, 4- or 5-pyrazolyl, 2-, 4- or 5oxazolyl, 3-, 4- or 5-isoxazolyl, 2-, 4- or 5-thiazolyl, 3-, 4- or 5-isothiazolyl, 2-, 3or 4-pyridyl, 2-, 4-, 5- or 6-pyrimidinyl, 1,2,3-triazol-l-, -4- or —5-yl, 1,2,4-triazol15 1-, -3- or-5-yl, 1- or 5-tetrazolyl, l,2,3-oxadiazol-4- or-5-yl, l,2,4-oxadiazol-3- or

-5-yl, l,3,4-thiadiazol-2- or-5-yl, l,2,4-oxadiazol-3- or-5-yl, l,3,4-thiadiazol-2-or -5-yl, l,3,4-thiadiazol-3- or -5-yl, l,2,3-thiadiazol-4- or -5-yl, 2-, 3-, 4-, 5- or 62H-thiopyranyl, 2-, 3- or 4-4H-thiopyranyl, 3- or 4-pyridazinyl, pyrazinyl, 2-, 3-, 4-, 5-, 6- or 7-benzofuryl, 2-, 3-, 4-, 5-, 6- or 7-benzothienyl, 1-, 2-, 3-, 4-, 5-, 6- or 720 indolyl, 1-, 2-, 4- or 5-benzimidazolyl, 1-, 3-, 4-, 5-, 6- or 7-benzopyrazolyl, 2-, 4-, 5-, 6- or 7-benzoxazolyl, 3-, 4-, 5- 6- or 7-benzisoxazolyl, 1-, 3-, 4-, 5-, 6- or 7benzothiazolyl, 2-, 4-, 5-, 6- or 7-benzisothiazolyl, 2-, 4-, 5-, 6- or 7-benz-l,3oxadiazolyl, 2-, 3-, 4-, 5-, 6-, 7- or 8-quinolinyl, 1-, 3-, 4-, 5-, 6-, 7-, 8isoquinolinyl, 1-, 2-, 3-, 4- or 9-carbazolyl, 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-acridinyl, or 2-, 4-, 5-, 6-, 7- or 8-quinazolinyl, or additionally optionally substituted phenyl,

2- or 3-thienyl, 1,3,4-thiadiazolyl, 3-pyrryl, 3-pyrazolyl, 2-thiazolyl or 5-thiazolyl, etc. For example, B can be 4-methyI-phenyl, 5-methyl-2-thienyl, 4-methyl-2thienyl, l-methyl-3-pyrryl, 1-methyl-3-pyrazolyl, 5-methyl-2-thiazolyl or 5-methyll,2,4-thiadiazol-2-yl.

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Suitable alkyl groups and alkyl portions of groups, e.g., alkoxy, etc. throughout include methyl, ethyl, propyl, butyl, etc., including all straight-chain and branched isomers such as isopropyl, isobutyl, jec-butyl, Ze/7-butyl, etc.

Suitable aryl groups which do not contain heteroatoms include, for example, 5 phenyl and 1- and 2-naphthyI.

The term “cycloalkyl”, as used herein, refers to cyclic structures with or without alkyl substituents such that, for example, “C4 cycloakyl” includes methyl substituted cyclopropyl groups as well as cyclobutyl groups. The term “cycloalkyl”, as used herein also includes saturated heterocyclic groups.

Suitable halogen groups include F, Cl, Br, and/or I, from one to persubstitution (i.e. all H atoms on a group replaced by a halogen atom) being possible where an alkyl group is substituted by halogen, mixed substitution of halogen atom types also being possible on a given moiety.

The invention also relates to compounds per se, of formula I.

The present invention is also directed to pharmaceutically acceptable salts of formula I. Suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of inorganic and organic acids, such as hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulfonic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, p20 toluenesulfonic acid, 1-naphthalenesulfonic acid, 2-naphthalenesulfonic acid, acetic acid, trifluoroacetic acid, malic acid, tartaric acid, citric acid, lactic acid, oxalic acid, succinic acid, fumaric acid, maleic acid, benzoic acid, salicylic acid, phenylacetic acid, and mandelic acid. In addition, pharmaceutically acceptable salts include acid salts of inorganic bases, such as salts containing alkaline cations (e.g., Li⁺ Na⁺ or

K⁺), alkaline earth cations (e.g., Mg⁺² , Ca⁺² or Ba⁺²), the ammonium cation, as well as acid salts of organic bases, including aliphatic and aromatic substituted ammonium, and quaternary ammonium cations, such as those arising from protonation or peralkylation of triethylamine, A,/V-diethy lamine, N,Ndicyclohexylamine, lysine, pyridine, W-dimethylaminopyridine (DMAP), 1,412

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69676-7 diazabicyclo [2.2.2]octane (DABCO), 1,5-diazabicyclo [4.3.0] non-5-ene (DBN) and l,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

A number of the compounds of Formula I possess asymmetric carbons and can therefore exist in racemic and optically active forms. Methods of separation of enantiomeric and diastereomeric mixtures are well known to one skilled in the art. The present invention encompasses any isolated racemic or optically active form of compounds described in Formula I which possess p38 kinase inhibitory activity.

In one embodiment, the invention relates to use of a compound for the treatment of a disease mediated by p38 kinase, wherein the compound is:

the 4-chloro-3-(trifluoromethyl)phenyl urea:

N-(4-chloro-3 -(trifluoromethyl)phenyl)-N'-(3-(2-carbamoyl-4pyridyloxy)phenyl) urea,

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(3-(2-(N-methylcarbamoyl)-4pyridyloxy)phenyl) urea,

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-carbamoyl-4pyridyloxy)phenyl) urea, or

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N-methylcarbamoyl)-4pyridyloxy)phenyl) urea;

the 4-bromo-3-(trifluoromethyl)phenyl urea:

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(3-(2-(N-rnethylcarbamoyl)-4pyridyloxy)phenyl) urea,

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N-methylcarbamoyl)-4pyridyloxy)phenyl) urea,

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69676-7

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(3-(2-(N-methylcarbamoyl)-4pyridylthio)phenyl) urea,

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(2-chloro-4-(2(N-methylcarbamoyl)(4-pyridyloxy))phenyl) urea, or

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(3-chloro-4-(2(N-methylcarbamoyl)(4-pyridyloxy))phenyl) urea; or the 2-methoxy-4-chloro-5-(trifluoromethyl)phenyl urea:

N-(2-methoxy-4-chloro-5-(trifluoromethyl)phenyl)-N'-(4-(2(N-methylcarbamoyl)-4-pyridyloxy)phenyl) urea, or

N-(2-methoxy-4-chloro-5-(trifluoromethyl)phenyl)-N'-(2-chloro-4-(2(N-methylcarbamoyl)(4-pyridyloxy))phenyl) urea, or or a pharmaceutically acceptable salt of the compound.

In a further embodiment, the invention relates to a pharmaceutical composition for the treatment of a disease within a host mediated by p38 comprising a compound, and a physiologically acceptable carrier, wherein the compound is:

the 4-chloro-3-(trifluoromethyl)phenyl urea:

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(3-(2-carbamoyl-4pyridyloxy)phenyl) urea,

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(3-(2-(N-methylcarbamoyl)-420 pyridyloxy)phenyl) urea,

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-carbamoyl-4pyridyloxy)phenyl) urea, or

N-(4-chloro-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N-methylcarbamoyl)-4pyridyloxy)phenyl) urea;

13a

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69676-7 the 4-bromo-3-(trifluoromethyl)phenyl urea:

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(3-(2-(N-methylcarbamoyl)-4pyridyloxy)phenyl) urea,

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(4-(2-(N-methylcarbamoyl)-45 pyridyloxy)phenyl) urea,

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(3-(2-(N-methylcarbamoyl)-4pyridylthio)phenyl) urea,

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(2-chloro-4-(2(N-methylcarbamoyl)(4-pyridyloxy))phenyl) urea, or

N-(4-bromo-3-(trifluoromethyl)phenyl)-N'-(3-chloro-4-(2(N-methylcarbamoyl)(4-pyridyloxy))phenyl) urea; or the 2-methoxy-4-chloro-5-(trifluoromethyl)phenyl urea:

N-(2-methoxy-4-chloro-5-(trifluoromethyl)phenyl)-N'-(4-(2(N-methylcarbamoyl)-4-pyridyloxy)phenyl) urea,

N-(2-methoxy-4-chloro-5-(trifluoromethyl)phenyl)-N'-(2-chloro-4-(2(N-methylcarbamoyl)(4-pyridyloxy))phenyl) urea, or or a pharmaceutically acceptable salt of the compound.

In exemplary use and composition embodiments, there is provided the compound:

N-(4-chloro-3-(trifluoromethyl)phenyl)-N’-(4-(2-(N-methylcarbamoyl)-4pyridyloxy)phenyl)urea of the formula X (X)

13b

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<img file="CA2359244C_D0001.tif" />

or a pharmaceutically acceptable salt thereof, such as the p-toluene sulfonic acid salt of the compound.

An exemplary use is for treatment of advanced cancer.

General Preparative Methods

The compounds of Formula I may be prepared by use of known chemical reactions and procedures, some from starting materials which are commercially available. Nevertheless, the following general preparative methods are presented to aid one of skill in the art in synthesizing these compounds, with more detailed particular examples being presented in the experimental section describing the working examples.

Substituted anilines may be generated using standard methods (March. Advanced Organic Chemistry, 3^rd Ed.; John Wiley: New York (1985). Larock. Comprehensive Organic Transformations', VCH Publishers: New York (1989)). As shown in Scheme I, aryl amines are commonly synthesized by reduction of nitroaryls using a metal catalyst, such as Ni, Pd, or Pt, and H₂ or a hydride transfer agent, such as formate, cyclohexadiene, or a borohydride (Rylander. Hydrogenation Methods·, Academic Press: London, UK (1985)). Nitroaryls may also be directly reduced using a strong hydride source, such as L1AIH4 (Seyden-Penne. Reductions by the Alumino-and Borohydrides in Organic Synthesis', VCH Publishers: New York (1991)), or using a zero valent metal, such as Fe, Sn or

Ca, often in acidic media. Many methods exist for the synthesis of nitroaryls (March. Advanced Organic Chemistry, 3^rd Ed.; John Wiley: New York (1985). Larock. Comprehensive Organic Transformations', VCH Publishers: New York (1989)).

13c

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Substituted anilines may be generated using standard methods (March. Advanced Organic Chemistry, 3^rd Ed.; John Wiley; New York (1985). Larock. Comprehensive Organic Transformations', VCH Publishers; New York (1989)). As shown in Scheme I, aryl amines are commonly synthesized by reduction of nitroaryls using a metal catalyst, such as Ni, Pd, or Pt, and H₂ or a hydride transfer agent, such as formate, cyclohexadiene, or a borohydride (Rylander. Hydrogenation Methods', Academic Press: London, UK (1985)). Nitroaryls may also be directly reduced using a strong hydride source, such as L1AIH4 (Seyden-Penne. Reductions by the Alumino- and Borohydrides in Organic Synthesis; VCH Publishers: New

York (1991)), or using a zero valent metal, such as Fe, Sn or Ca, often in acidic media. Many methods exist for the synthesis of nitroaryls (March. Advanced Organic Chemistry, 3^rd Ed.; John Wiley: New York (1985). Larock. Comprehensive Organic Transformations; VCH Publishers: New York (1989)).

H₂ / catalyst / (eg. Ni, Pd, Pt)

ArNO₂ --►- ArNH₂ \ M(0) ₁₅ (eg. Fe, Sn, Ca)

Scheme I Reduction of Nitroaryls to Aryl Amines

Nitroaryls are commonly formed by electrophilic aromatic nitration using HNO3, or an alternative NO₂⁺ source. Nitroaryls may be further elaborated prior to reduction. Thus, nitroaryls substituted with

HNO₃

Ar-H -ArNO₂ potential leaving groups (eg. F, Cl, Br, etc.) may undergo substitution reactions on treatment with nucleophiles, such as thiolate (exemplified in Scheme II) or

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PCT/US00/00768 phenoxide. Nitroaryls may also undergo Ullman-type coupling reactions (Scheme II).

<img file="CA2359244C_D0002.tif" />

Scheme II Selected Nucleophilic Aromatic Substitution using Nitroaryls

Nitroaryls may also undergo transition metal mediated cross coupling reactions. For example, nitroaryl electrophiles, such as nitroaryl bromides, iodides or inflates, undergo palladium mediated cross coupling reactions with aryl nucleophiles, such as arylboronic acids (Suzuki reactions, exemplified below), aryltins (Stille reactions) or arylzincs (Negishi reaction) to afford the biaryl (5).

<img file="CA2359244C_D0003.tif" />

ArB(ORj₂

-►

Pd(0)

<img file="CA2359244C_D0004.tif" />

Ar

Either nitroaryls or anilines may be converted into the corresponding arenesulfonyl chloride (7) on treatment with chlorosulfonic acid. Reaction of the sulfonyl chloride with a fluoride source, such as KF then affords sulfonyl fluoride (8). Reaction of sulfonyl fluoride 8 with trimethylsilyl trifluoromethane in the presence of a fluoride source, such as tris(dimethylamino)sulfonium difluorotrimethylsiliconate (TASF) leads to the corresponding trifluoromethylsulfone (9). Alternatively, sulfonyl chloride 7 may be reduced to the

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PCT/US00/00768 arenethiol (10), for example with zinc amalgum. Reaction of thiol 10 with CHCIF2 in the presence of base gives the difluoromethyl mercaptam (11), which may be oxidized to the sulfone (12) with any of a variety of oxidants, including CrCb-acetic anhydride (Sedova et al. Zh. Org. Khim. 1970, 6, 568).

<img file="CA2359244C_D0005.tif" />

CHCIF₂ base

V

SCHF₂

<img file="CA2359244C_D0006.tif" />

<img file="CA2359244C_D0007.tif" />

<img file="CA2359244C_D0008.tif" />

Scheme III Selected Methods of Fluorinated Aryl Sulfone Synthesis

As shown in Scheme IV, non-symmetrical urea formation may involve reaction of an aryl isocyanate (14) with an aryl amine (13). The heteroaryl isocyanate may be synthesized from a heteroaryl amine by treatment with phosgene or a phosgene equivalent, such as trichloromethyl chloroformate (diphosgene), bis(trichloromethyl) carbonate (triphosgene), or A,.V’-carbonyldiimidazole (CDI).

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The isocyanate may also be derived from a heterocyclic carboxylic acid derivative, such as an ester, an acid halide or an anhydride by a Curtius-type rearrangement. Thus, reaction of acid derivative 16 with an azide source, followed by rearrangement affords the isocyanate. The corresponding carboxylic acid (17) may also be subjected to Curtius-type rearrangements using diphenylphosphoryl azide (DPPA) or a similar reagent.

Ar¹—NH₂ 13

COCI₂

H₂N-Ar²

Ar¹—NCO

<img file="CA2359244C_D0009.tif" />

.,A,

Ar OH ^Αγ’'ν^Λν·^Αγ2

Η H

A

Scheme IV Selected Methods of Non-Symmetrical Urea Formation

Finally, ureas may be further manipulated using methods familiar to those skilled in the art.

The invention also includes pharmaceutical compositions including a compound of Formula I, and a physiologically acceptable carrier.

The compounds may be administered orally, topically, parenterally, by inhalation or spray, vaginally, rectally or sublingually in dosage unit formulations.

The term 'administration by injection' includes intravenous, intramuscular, subcutaneous and parenteral injections, as well as use of infusion techniques. Dermal administration may include topical application or transdermal administration. One or more compounds may be present in association with one or

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PCT/US00/00768 more non-toxic pharmaceutically acceptable carriers and if desired other active ingredients.

Compositions intended for oral use may be prepared according to any suitable method known to the art for the manufacture of pharmaceutical compositions. Such compositions may contain one or more agents selected from the group consisting of diluents, sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients may be, for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, com starch, or alginic acid; and binding agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and adsorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glyceryl distearate may be employed. These compounds may also be prepared in solid, rapidly released form.

Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil.

Aqueous suspensions containing the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions may also be used. Such excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxypropyl-methylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example, lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxyethylene

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PCT/US00/00768 stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl, y&gt;-hydroxybenzoate, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose or saccharin.

Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients, for example, sweetening, flavoring and coloring agents, may also be present.

The compounds may also be in the form of non-aqueous liquid formulations, e.g., oily suspensions which may be formulated by suspending the active ingredients in a vegetable oil, for example arachis oil, olive oil, sesame oil or peanut oil, or in a mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set forth above, and flavoring agents may be added to provide palatable oral preparations. These compositions may be preserved by the addition of an antioxidant such as ascorbic acid.

Compounds of the invention may also be administrated transdermally using methods known to those skilled in the art (see, for example: Chien; “Transdermal Controlled Systemic Medications”; Marcel Dekker, Inc.; 1987. Lipp et al. WO94/04157 3Mar94). For example, a solution or suspension of a compound of Formula I in a suitable volatile solvent optionally containing penetration enhancing agents can be combined with additional additives known to those skilled in the art, such as matrix materials and bacteriocides. After sterilization, the resulting mixture

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PCT/US00/00768 can be formulated following known procedures into dosage forms. In addition, on treatment with emulsifying agents and water, a solution or suspension of a compound of Formula I may be formulated into a lotion or salve.

Suitable solvents for processing transdermal delivery systems are known to those skilled in the art, and include lower alcohols such as ethanol or isopropyl alcohol, lower ketones such as acetone, lower carboxylic acid esters such as ethyl acetate, polar ethers such as tetrahydrofuran, lower hydrocarbons such as hexane, cyclohexane or benzene, or halogenated hydrocarbons such as dichloromethane, chloroform, trichlorotrifluoroethane, or trichlorofluoroethane. Suitable solvents may also include mixtures of one or more materials selected from lower alcohols, lower ketones, lower carboxylic acid esters, polar ethers, lower hydrocarbons, halogenated hydrocarbons.

Suitable penetration enhancing materials for transdermal delivery system are known to those skilled in the art, and include, for example, monohydroxy or polyhydroxy alcohols such as ethanol, propylene glycol or benzyl alcohol, saturated or unsaturated Cg-Cis fatty alcohols such as lauryl alcohol or cetyl alcohol, saturated or unsaturated Cg-Cis fatty acids such as stearic acid, saturated or unsaturated fatty esters with up to 24 carbons such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl isobutyl tertbutyl or monoglycerin esters of acetic acid, capronic acid, lauric acid, myristinic acid, stearic acid, or palmitic acid, or diesters of saturated or unsaturated dicarboxylic acids with a total of up to 24 carbons such as diisopropyl adipate, diisobutyl adipate, diisopropyl sebacate, diisopropyl maleate, or diisopropyl fumarate. Additional penetration enhancing materials include phosphatidyl derivatives such as lecithin or cephalin, terpenes, amides, ketones, ureas and their derivatives, and ethers such as dimethyl isosorbid and di ethyleneglycol monoethyl ether. Suitable penetration enhancing formulations may also include mixtures of one or more materials selected from monohydroxy or polyhydroxy alcohols, saturated or unsaturated Cs-Cis fatty alcohols, saturated or unsaturated Cg-Cis fatty acids, saturated or unsaturated fatty esters with up to 24 carbons, diesters of saturated or unsaturated discarboxylic acids with a total of up to

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PCT/US00/00768 carbons, phosphatidyl derivatives, terpenes, amides, ketones, ureas and their derivatives, and ethers.

Suitable binding materials for transdermal delivery systems are known to those skilled in the art and include polyacrylates, silicones, polyurethanes, block polymers, styrenebutadiene coploymers, and natural and synthetic rubbers. Cellulose ethers, derivatized polyethylenes, and silicates may also be used as matrix components. Additional additives, such as viscous resins or oils may be added to increase the viscosity of the matrix.

Pharmaceutical compositions of the invention may also be in the form of oilin-water emulsions. The oil phase may be a vegetable oil, for example olive oil or arachis oil, or a mineral oil, for example liquid paraffin or mixtures of these. Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soy bean, lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate, and condensation products of the said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavoring agents.

Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative and flavoring and coloring agents.

The compounds may also be administered in the form of suppositories for rectal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal or vaginal temperature and will therefore melt in the rectum or vagina to release the drug. Such materials include cocoa butter and polyethylene glycols.

For all regimens of use disclosed herein for compounds of Formula I, the daily oral dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion

CA 02359244 2008-05-30 '69676-7 techniques will preferably be from 0.01 to 200 rng/Kg of total body weight. The daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily rectal dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/Kg. The daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily. The daily inhalation dosage regimen will preferably be from 0.01 to 10 mg/Kg of total body weight.

It will be appreciated by those skilled in the art that the particular method of administration will depend on a variety of factors, all of which are considered routinely when administering therapeutics. It will also be understood, however, that the specific dose level lor a given patient depends on a variety of factors, including specific activity of the compound administered, the age of the patient, the body weight of the patient, the general health of the patient, the gender of the patient, the diet of the patient, time of administration, route of administration, rate of excretion, drug combination, and the severity of the condition undergoing therapy, etc. It will be further appreciated by one skilled in the art that the optimal course of treatment, i.e., the mode of treatment and the daily number of doses of a compound of Fonnula

I or a pharmaceutically acceptable salt thereof given for a defined number of days, can be ascertained bythose skilled in the art using conventional course of treatment tests.

The compounds of Formula I are producible from known compounds (or from starting materials which, in turn, are producible from known compounds), e.g., through the general preparative methods shown above. The activity of a given compound to inhibit raf kinase can be routinely assayed, e.g., according to procedures disclosed below. The following examples are for illustrative purposes only and are not intended, nor should they be construed to limit the invention in any way.

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The following examples are for illustrative purposes only and are not intended, nor should they be construed to limit the invention in any way.

EXAMPLES

All reactions were performed in flame-dried or oven-dried glassware under a 5 positive pressure of dry argon or dry nitrogen, and were stirred magnetically unless otherwise indicated. Sensitive liquids and solutions were transferred via syringe or cannula, and introduced into reaction vessels through rubber septa. Unless otherwise stated, the term ‘concentration under reduced pressure’ refers to use of a Buchi rotary evaporator at approximately 15 mmHg. Unless otherwise stated, the term ‘under high vacuum’ refers to a vacuum of 0.4 -1.0 mmHg.

All temperatures are reported uncorrected in degrees Celsius (°C). Unless otherwise indicated, all parts and percentages are by weight.

Commercial grade reagents and solvents were used without further purification. Ncyclohexyl-/7’-(methylpolystyrene)carbodiimide was purchased from CalbiochemNovabiochem Corp. 3-ZerZ-Butylaniline, 5-ZerZ-butyl-2-methoxyaniline, 4-bromo-3(trifluoromethyl)aniline, 4-chloro-3-(trifluoromethyl)aniline 2-methoxy-5(trifluoromethyl)aniline, 4-ZerZ-butyl-2-nitroaniline, 3-amino-2-naphthol, ethyl 420 isocyanatobenzoate, /V-acetyl-4-chloro-2-methoxy-5-(trifluoromethyl)aniline and 4chloro-3-(trifluoromethyl)phenyl isocyanate were purchased and used without further purification. Syntheses of 3-amino-2-methoxyquinoline (E. Cho et al. WO 98/00402; A. Cordi et al. EP 542,609; IBID Bioorg. Med. Chem.. 3, 1995, 129), 4(3-carbamoylphenoxy)-l-nitrobenzene (K. Ikawa Yakugaku Zasshi 79, 1959, 760;

Chem. Abstr. 53, 1959, 12761b), 3-ZerZ-bufylphenyl isocyanate (0. Rohr et al. DE

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2,436,108) and 2-methoxy-5-(trifluoromethyl)phenyl isocyanate (K. Inukai et al. JP 42,025,067; IBID Kogyo Kagaku Zasshi 70, 1967, 491) have previously been described.

Thin-layer chromatography (TLC) was performed using Whatman® pre-coated glass-backed silica gel 60A F-254 250 pm plates. Visualization of plates was effected by one or more of the following techniques: (a) ultraviolet illumination, (b) exposure to iodine vapor, (c) immersion of the plate in a 10% solution of phosphomolybdic acid in,ethanol followed by heating, (d) immersion of the plate in a cerium sulfate solution followed by heating, and/or (e) immersion of the plate in an acidic ethanol solution of 2,4-dinitrophenylhydrazine followed by heating. Column chromatography (flash chromatography) was performed using 230-400 mesh EM Science® silica gel.

Melting points (mp) were determined using a Thomas-Hoover melting point apparatus or a Mettler FP66 automated melting point apparatus and are uncorrected. Fourier transform infrared spectra were obtained using a Mattson 4020 Galaxy Series spectrophotometer. Proton ('H) nuclear magnetic resonance (NMR) spectra were measured with a General Electric GN-Omega 300 (300 MHz) spectrometer with either Me4Si (δ 0.00) or residual protonated solvent (CHCI3 δ 7.26; MeOH δ 3.30; DMSO δ 2.49) as standard. Carbon (¹³C) NMR spectra were measured with a General Electric GN-Omega 300 (75 MHz) spectrometer with solvent (CDCI3 δ 77.0; MeOD-d3; δ 49.0; DMSO-dô δ 39.5) as standard. Low resolution mass spectra (MS) and high resolution mass spectra (HRMS) were either obtained as electron impact (EI) mass spectra or as fast atom bombardment (FAB) mass spectra. Electron impact mass spectra (EI-MS) were obtained with a Hewlett Packard 5989A mass spectrometer equipped with a Vacumetrics Desorption Chemical Ionization Probe for sample introduction. The ion source was maintained at 250 °C. Electron impact ionization was performed with electron energy of 70 eV and a trap current of 300 μΑ. Liquid-cesium secondary ion mass spectra (FAB-MS), an updated version

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PCT/US00/00768 of fast atom bombardment were obtained using a Kratos Concept 1-H spectrometer. Chemical ionization mass spectra (CI-MS) were obtained using a Hewlett Packard MS-Engine (5989A) with methane or ammonia as the reagent gas (lxlO’⁴ torr to 2.5x1 O'⁴ torr). The direct insertion desorption chemical ionization (DCI) probe (Vaccumetrics, Inc.) was ramped from 0-1.5 amps in 10 sec and held at 10 amps until all traces of the sample disappeared ( ~l-2 min). Spectra were scanned from 50-800 amu at 2 sec per scan. HPLC - electrospray mass spectra (HPLC ES-MS) were obtained using a Hewlett-Packard 1100 HPLC equipped with a quaternary pump, a variable wavelength detector, a C-18 column, and a Finnigan LCQ ion trap mass spectrometer with electrospray ionization. Spectra were scanned from 120800 amu using a variable ion time according to the number of ions in the source. Gas chromatography - ion selective mass spectra (GC-MS) were obtained with a Hewlett Packard 5890 gas chromatograph equipped with an HP-1 methyl silicone column (0.33 mM coating; 25 m x 0.2 mm) and a Hewlett Packard 5971 Mass

Selective Detector (ionization energy 70 eV). Elemental analyses are conducted by Robertson Microlit Labs, Madison NJ.

All compounds displayed NMR spectra, LRMS and either elemental analysis or HRMS consistent with assigned structures.

List of Abbreviations and Acronyms:

<td> AcOH</td><td> acetic acid</td>

<td> anh</td><td> anhydrous</td>

<td> atm</td><td> atmosphere(s)</td>

<td> BOC</td><td> /erZ-butoxycarbonyl</td>

<td> CDI</td><td> 1,1’-carbonyl diimidazole</td>

<td> cone</td><td> concentrated</td>

<td> d</td><td> day(s)</td>

<td> dec</td><td> decomposition</td>

<td> DMAC</td><td> Λζ/V-dimethylacetamide</td>

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<td> DMPU</td><td> l,3-dimethyl-3,4,5,6-tetrahydro-2(lH)-pyrimidinone</td>

<td> DMF</td><td> A.TV-dimethylformamide</td>

<td> DMSO</td><td> dimethylsulfoxide</td>

<td> DPPA</td><td> diphenylphosphoryl azide</td>

<td> 5 EDCI</td><td> l-(3-dimethylaminopropyl)-3-ethylcarbodiimide</td>

<td> EtOAc</td><td> ethyl acetate</td>

<td> EtOH</td><td> ethanol (100%)</td>

<td> Et₂O</td><td> diethyl ether</td>

<td> Et₃N</td><td> triethylamine</td>

<td> 10 h</td><td> hour(s)</td>

<td> HOBT</td><td> 1 -hydroxybenzo tri azole</td>

<td> «-CPBA</td><td> 3-chloroperoxybenzoic acid</td>

<td> MeOH</td><td> methanol</td>

<td> pet. ether</td><td> petroleum ether (boiling range 30-60 °C)</td>

<td> 15 temp. THF</td><td> temperature tetrahydrofuran</td>

<td> TFA</td><td> trifluoroAcOH</td>

<td> Tf</td><td> trifluoromethanesulfonyl</td>

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A. General Methods for Synthesis of Substituted Anilines

Al. General Method for Aryl Amine Formation via Ether Formation

Followed by Ester Saponification, Curtius Rearrangement, and Carbamate Deprotection. Synthesis of 2-Amino-35 methoxynaphthalene.

<img file="CA2359244C_D0010.tif" />

Step 1. Methyl 3-methoxy-2-naphthoate

A slurry of methyl 3-hydroxy-2-naphthoate (10.1 g, 50.1 mmol) and K2CO3 (7.96 g, 57.6 mmol) in DMF (200 mL) was stirred at room temp, for 15 min., then treated with iodomethane (3.43 mL, 55.1 mmol). The mixture was allowed to stir at room temp, overnight, then was treated with water (200 mL). The resulting mixture was extracted with EtOAc (2 x 200 mL). The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSOQ, concentrated under reduced pressure (approximately 0.4 mmHg overnight) to give methyl 3-methoxy-215 naphthoate as an amber oil (10.30 g): ’H-NMR (DMSO-dô) δ 2.70 (s, 3H), 2.85 (s, 3H), 7.38 (app t, 7=8.09 Hz, 1H), 7.44 (s, 1H), 7.53 (app t, 7=8.09 Hz, 1H), 7.84 (d, 7=8.09 Hz, 1H), 7.90 (s, 1H), 8.21 (s, 1H).

<img file="CA2359244C_D0011.tif" />

Step 2. 3-Methoxy-2-naphthoic acid

A solution of methyl 3-methoxy-2-naphthoate (6.28 g, 29.10 mmol) and water (10 mL) in MeOH (100 mL) at room temp, was treated with a 1 N NaOH solution (33.4 mL, 33.4 mmol). The mixture was heated at the reflux temp, for 3 h, cooled to room temp., and made acidic with a 10% citric acid solution. The resulting solution was extracted with EtOAc (2 x 100 mL). The combined organic layers were washed

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PCT/US00/00768 with a saturated NaCl solution, dried (MgSCL) and concentrated under reduced pressure. The residue was triturated with hexane then washed several times with hexane to give 3-methoxy-2-naphthoic acid as a white solid (5.40 g, 92%); 'H-NMR (DMSO-de) δ 3.88 (s, 3H), 7.34-7.41 (m, 2H), 7.49-7.54 (m, IH), 7.83 (d, 7=8.09

Hz, IH), 7.91 (d, 7=8.09 Hz, IH), 8.19 (s, IH), 12.83 (br s, IH).

<img file="CA2359244C_D0012.tif" />

Step 3. 2-(7V-(Carbobenzyloxy)ammo-3-methoxynaphthalene

A solution of 3-methoxy-2-naphthoic acid (3.36 g, 16.6 mmol) and Et₃N (2.59 mL, 18.6 mmol) in anh toluene (70 mL) was stirred at room temp, for 15 min., then treated with a solution of DPPA (5.12 g, 18.6 mmol) in toluene (10 mL) via pipette. The resulting mixture was heated at 80 °C for 2 h. After cooling the mixture to room temp., benzyl alcohol (2.06 mL, 20 mmol) was added via syringe. The mixture was then warmed to 80 °C overnight. The resulting mixture was cooled to room temp., quenched with a 10% citric acid solution, and extracted with EtOAc (2 x 100 mL).

The combined organic layers were washed with a saturated NaCl solution, dried (MgSÛ4) and concentrated under reduced pressure. The residue was purified by column chromatography (14% EtOAc/86% hexane) to give 2-(N(carbobenzyloxy)amino-3-methoxynaphthalene as a pale yellow oil (5.1 g, 100%): ’H-NMR (DMSO-dô) δ 3.89 (s, 3H), 5.17 (s, 2H), 7.27-7.44 (m, 8H), 7.72-7.75 (m,

2H), 8.20 (s, IH), 8.76 (s, IH).

<img file="CA2359244C_D0013.tif" />

OMe

Step 4. 2-Amino-3-methoxynaphthalene

A slurry of 2-(7V-(carbobenzyloxy)amino-3-methoxynaphthalene (5.0 g, 16.3 mmol) and 10% Pd/C (0.5 g) in EtOAc (70 mL) was maintained under a H₂ atm (balloon)

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PCT/USOO/00768 at room temp, overnight. The resulting mixture was filtered through Celite® and concentrated under reduced pressure to give 2-amino-3-methoxynaphthalene as a pale pink powder (2.40 g, 85%): 'H-NMR (DMSO-d₆) δ 3.86 (s, 3H), 6.86 (s, 2H), 7.04-7.16 (m, 2H), 7.43 (d, 7=8.0 Hz, IH), 7.56 (d, 7=8.0 Hz, IH); EI-MS m/z 173 (M⁺).

A2. Synthesis of ω-CarbamyI Anilines via Formation of a

Carbamylpyridine Followed by Nucleophilic Coupling with an

<td> 10</td><td> Aryl Amine. pyridyloxy)aniline</td><td> Synthesis of 4-(2-7V-MethylcarbamyI-4-</td>

<td></td><td> CK</td><td> O</td>

Step la. Synthesis of 4-chloro-/V-methyl-2-pyridinecarboxamide via the

Menisci reaction

Caution: this is a highly hazardous, potentially explosive reaction. To a stirring solution of 4-chloropyridine (10.0 g) in /V-methylformamide (250 mL) at room temp, was added cone. H2SO4 (3.55 mL) to generate an exotherm. To this mixture was added H₂O₂ (30% wt in H₂O, 17 mL) followed by FeSO4*7H₂O (0.56 g) to generate another exotherm. The resulting mixture was stirred in the dark at room temp, for 1 h, then warmed slowly over 4 h to 45 °C. When bubbling had subsided, the reaction was heated at 60 °C for 16 h. The resulting opaque brown solution was diluted with H₂O (700 mL) followed by a 10% NaOH solution (250 mL). The resulting mixture was extracted with EtOAc (3 x 500 mL). The organic phases were washed separately with a saturated NaCl solution (3 x 150 mL), then they were combined, dried (MgSO4) and filtered through a pad of silica gel with the aid of EtOAc. The resulting brown oil was purified by column chromatography (gradient from 50% EtOAc/50% hexane to 80% EtOAc/20% hexane). The resulting yellow

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PCT/USOO/0O768 oil crystallized at 0 °C over 72 h to give 4-chloro-/V-methyl-2-pyridinecarboxamide (0.61 g, 5.3%): TLC (50% EtOAc/50% hexane) RyO.50; 'H NMR (CDC1₃) δ 3.04 (d, 7=5.1 Hz, 3H), 7.43 (dd, 7=5.4, 2.4 Hz, IH), 7.96 (br s, IH), 8.21 (s, IH), 8.44 (d, 7=5.1 Hz, 1 H); CI-MS m/z 171 ((M+H)⁺).

O

<img file="CA2359244C_D0014.tif" />

Step lb. Synthesis of 4-chloropyridine-2-carbonyl chloride HCl salt via picolinic acid

Anhydrous DMF (6.0 mL) was slowly added to SOCL (180 mL) between 40° and

50 °C. The solution was stirred in that temperature range for 10 min. then picolinic acid (60.0 g, 487 mmol) was added in portions over 30 min. The resulting solution was heated at 72 °C (vigorous SO2 evolution) for 16 h to generate a yellow solid precipitate. The resulting mixture was cooled to room temp., diluted with toluene (500 mL) and concentrated to 200 mL. The toluene addition/concentration process was repeated twice. The resulting nearly dry residue was filtered and the solids were washed with toluene (2 x 200 mL) and dried under high vacuum for 4 h to afford 4-chloropyridine-2-carbonyl chloride HCl salt as a yellow-orange solid (92.0 g, 89%).

o

OMe 31

Step 2. Synthesis of methyl 4-chloropyridine-2-carboxylate HCl salt

Anh DMF (10.0 mL) was slowly added to SOCI2 (300 mL) at 40-48 °C. The solution was stirred at that temp, range for 10 min., then picolinic acid (100 g, 812 mmol) was added over 30 min. The resulting solution was heated at 72 °C (vigorous SO2 evolution) for 16 h to generate a yellow solid. The resulting mixture was cooled to room temp., diluted with toluene (500 mL) and concentrated to 200 mL. The toluene addition/concentration process was repeated twice. The resulting nearly dry residue was filtered, and the solids were washed with toluene (50 mL)

<img file="CA2359244C_D0015.tif" />

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PCT/US00/00768 and dried under high vacuum for 4 hours to afford 4-chloropyridine-2-carbonyl chloride HCl salt as an off-white solid (27.2 g, 16%). This material was set aside.

The red filtrate was added to MeOH (200 mL) at a rate which kept the internal 5 temperature below 55 °C. The contents were stirred at room temp, for 45 min., cooled to 5 °C and treated with Et2Û (200 mL) dropwise. The resulting solids were filtered, washed with Et2O (200 mL) and dried under reduced pressure at 35 °C to provide methyl 4-chloropyridine-2-carboxylate HCl salt as a white solid (110 g,

65%): mp 108-112 °C; ’H-NMR (DMSO-d₆) δ 3.88 (s, 3H); 7.82 (dd, &gt;5.5, 2.2 10 Hz, IH); 8.08 (d, 7=2.2 Hz, IH); 8.68 (d, 7=5.5 Hz, IH); 10.68 (br s, IH); HPLC

ES-MS m/z 172 ((M+H)⁺).

Cl

Y NHMe N

Step 3a. Synthesis of 4-chloro-7V-methyl-2-pyridinecarboxamide from methyl 4-chloropyridine-2-carboxylate

A suspension of methyl 4-chloropyridine-2-carboxylate HCl salt (89.0 g, 428 mmol) in MeOH (75 mL) at 0 °C was treated with a 2.0 M methylamine solution in THF (1 L) at a rate which kept the internal temp, below 5 °C. The resulting mixture was stored at 3 °C for 5 h, then concentrated under reduced pressure. The resulting solids were suspended in EtOAc (1 L) and filtered. The filtrate was washed with a saturated NaCl solution (500 mL), dried (Na2SO₄) and concentrated under reduced pressure to afford 4-chloro-A-methyl-2-pyridinecarboxamide as pale-yellow crystals (71.2 g, 97%): mp 41-43 °C; 'H-NMR (DMSO-d₆) δ 2.81 (s, 3H), 7.74 (dd, 7=5.1, 2.2 Hz, IH), 8.00 (d, 7=2.2, IH), 8.61 (d, 7=5.1 Hz, IH), 8.85 (br d, IH); CI-MS m/z 171 ((M+H)⁺).

Cl γ NHMe N

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Step 3b. Synthesis of 4-chloro- V-methyI-2-pyridinecarboxaniide from 4chloropyridine-2-carbonyI chloride

4-Chloropyridine-2-carbonyl chloride HCI salt (7.0 g, 32.95 mmol) was added in portions to a mixture of a 2.0 M methylamine solution in THF (100 mL) and MeOH (20 mL) at 0 °C. The resulting mixture was stored at 3 °C for 4 h, then concentrated under reduced pressure. The resulting nearly dry solids were suspended in EtOAc (100 mL) and filtered. The filtrate was washed with a saturated NaCl solution (2 x 100 mL), dried (Na2SÜ4) and concentrated under reduced pressure to provide 4chloroW-methyl-2-pyridinecarboxamide as a yellow, crystalline solid (4.95 g,

88%): mp 37-40 °C.

HoN

<img file="CA2359244C_D0016.tif" />

NHMe

Step 4. Synthesis of 4-(2-(7V-methylcarbamoyl)-4-pyridyIoxy)aniline

A solution of 4-aminophenol (9.60 g, 88.0 mmol) in anh. DMF (150 mL) was treated with potassium /eri-butoxide (10.29 g, 91.7 mmol), and the reddish-brown mixture was stirred at room temp, for 2 h. The contents were treated with 4-chloro(V-methyl-2-pyridinecarboxamide (15.0 g, 87.9 mmol) and K2CO3 (6.50 g, 47.0 mmol) and then heated at 80 °C for 8 h. The mixture was cooled to room temp, and separated between EtOAc (500 mL) and a saturated NaCl solution (500 mL). The aqueous phase was back-extracted with EtOAc (300 mL). The combined organic layers were washed with a saturated NaCl solution (4 x 1000 mL), dried (Na2SOzt) and concentrated under reduced pressure. The resulting solids were dried under reduced pressure at 35 °C for 3 h to afford 4-(2-((V-methylcarbamoyl)-4pyridyloxy)aniline as a light-brown solid 17.9 g, 84%): 'H-NMR (DMSO-dô) δ 2.77 (d, 7=4.8 Hz, 3H), 5.17 (br s, 2H), 6.64, 6.86 (AA’BB’ quartet, 7=8.4 Hz, 4H), 7.06 (dd, 7=5.5, 2.5 Hz, 1H), 7.33 (d, 7=2.5 Hz, 1H), 8.44 (d, 7=5.5 Hz, 1H), 8.73 (br d, 1H); HPLC ES-MS m/z 244 ((M+H)⁺).

A3.

General Method for the Synthesis of Anilines by Nucleophilic

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Aromatic Addition Followed by Nitroarene Reduction. Synthesis of 5-(4Aminophenoxy)isoindoline-l,3-dione

<img file="CA2359244C_D0017.tif" />

Step 1. Synthesis of 5-hydroxyisoindoline-l,3-dione

To a mixture of ammonium carbonate (5.28 g, 54.9 mmol) in cone. AcOH (25 mL) was slowly added 4-hydroxyphthalic acid (5.0 g, 27.45 mmol). The resulting mixture was heated at 120 °C for 45 min., then the clear, bright yellow mixture was heated at 160 °C for 2 h. The resulting mixture was maintained at 160 °C and was concentrated to approximately 15 mL, then was cooled to room temp, and adjusted pH 10 with a IN NaOH solution. This mixture was cooled to 0 °C and slowly acidified to pH 5 using a IN HC1 solution. The resultant precipitate was collected by filtration and dried under reduced pressure to yield 5-hydroxyisoindoline-l,3dione as a pale yellow powder as product (3.24 g, 72%): *H NMR (DMSO-dô) δ

7.00-7.03 (m, 2H), 7.56 (d, 7=9.3Hz, 1H).

OoN

<img file="CA2359244C_D0018.tif" />

O

Step 2. Synthesis of 5-(4-nitrophenoxy)isoindoline-l,3-dione

To a stirring slurry of NaH (1.1 g, 44.9 mmol) in DMF (40 mL) at 0 °C was added a solution of 5-hydroxyisoindoline-l,3-dione (3.2 g, 19.6 mmol) in DMF (40 mL) dropwise. The bright yellow-green mixture was allowed to return to room temp, and was stirred for 1 h, then 1-fluoro-4-nitrobenzene (2.67 g, 18.7 mmol) was added via syringe in 3-4 portions. The resulting mixture was heated at 70 °C overnight, then cooled to room temp, and diluted slowly with water (150 mL), and extracted with EtOAc (2 x 100 mL). The combined organic layers were dried (MgSÛ4) and

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PCT/US00/00768 concentrated under reduced pressure to give 5-(4-nitrophenoxy)isoindoline-l,3dione as a yellow solid (3.3 g, 62%): TLC (30% EtOAc/70% hexane) R/0.28; IH NMR (DMSO-d₆) δ 7.32 (d, /=12 Hz, 2H), 7.52-7.57 (m, 2H), 7.89(d, /=7.8 Hz, IH), 8.29 (d, /=9 Hz, 2H), 11.43 (br s, IH); CI-MS m/z 285 ((M+H)⁺, 100%).

<img file="CA2359244C_D0019.tif" />

Step 3. Synthesis of 5-(4-aminophenoxy)isoindoline-l,3-dione

A solution of 5-(4-nitrophenoxy)isoindoline-l,3-dione (0.6 g, 2.11 mmol) in cone. AcOH (12 mL) and water (0.1 mL) was stirred under stream of argon while iron powder (0.59 g, 55.9 mmol) was added slowly. This mixture stirred at room temp, for 72 h, then was diluted with water (25 mL) and extracted with EtOAc (3 x 50 mL). The combined organic layers were dried (MgSÛ4) and concentrated under reduced pressure to give 5-(4-aminophenoxy)isoindoline-l,3-dione as a brownish solid (0.4 g, 75%): TLC (50% EtOAc/50% hexane) RyO.27; ^]H NMR (DMSO-d₆) δ

5.14 (br s, 2H), 6.62 (d, /=8.7 Hz, 2H), 6.84 (d, /=8.7 Hz, 2H), 7.03 (d, /=2.1 Hz,

IH), 7.23 (dd, IH), 7.75 (d, /=8.4 Hz, IH), 11.02 (s, IH); HPLC ES-MS m/z 255 ((M+H)⁺, 100%).

A4. General Method for the Synthesis of Pyrrolylanilines. Synthesis of 5-/i'r/-Butyl-2-(2,5-dimethylpyrrolyl)aniline

<img file="CA2359244C_D0020.tif" />

Step 1. Synthesis of l-(4-/e/y-butyI-2-nitroplienyl)-2,5-dimethyIpyrrole

To a stirring solution of 2-nitro-4-/er/-butylaniline (0.5 g, 2.57 mmol) in cyclohexane (10 mL) was added AcOH (O.lmL) and acetonylacetone (0.299 g, 2.63

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PCT/US00/00768 mmol) via syringe. The reaction mixture was heated at 120 °C for 72 h with azeotropic removal of volatiles. The reaction mixture was cooled to room temp., diluted with CH2CI2 (10 mL) and sequentially washed with a IN HCI solution (15 mL), a IN NaOH solution (15 mL) and a saturated NaCl solution (15mL), dried (

MgSOQ and concentrated under reduced pressure. The resulting orange-brown solids were purified via column chromatography (60 g S1O2; gradient from 6% EtOAc/94% hexane to 25% EtOAc/75% hexane) to give 1-(4-/er/-butyl-2nitrophenyl)-2,5-dimethylpyrrole as an orange-yellow solid (0.34 g, 49%): TLC (15% EtOAc/85% hexane) R/-0.67; *H NMR (CDCI3) d 1.34 (s, 9H), 1.89 (s, 6H),

5.84 (s, 2H), 7.19-7.24 (m, IH), 7.62 (dd, IH), 7.88 (d, 7=2.4 Hz, IH); CI-MS m/z

273 ((M+H)⁺, 50%).

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<img file="CA2359244C_D0021.tif" />

Step 2. Synthesis of 5-tert—Butyl-2-(2,5-dimethylpyrrolyl)aniline

A slurry of l-(4-/er/-butyl-2-nitrophenyl)-2,5-dimethylpyrrole (0.341 g, 1.25 mmol), 5 10%Pd/C (0.056 g) and EtOAc (50 mL) under an H₂ atmosphere (balloon) was stirred for 72 h, then filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to give 5-tert—butyl-2-(2,5-dimethylpyrrolyl)aniline as yellowish solids (0.30 g, 99%): TLC (10% EtOAc/90% hexane) Ry0.43; ^!Η NMR (CDCb) δ 1.28 (s, 9H), 1.87-1.91 (m, 8H), 5.85 (br s, 2H), 6.73-6.96 (m, 3H), 7.28 io (br s, 1H).

A5. General Method for the Synthesis of Anilines from Anilines by

Nucleophilic Aromatic Substitution. Synthesis of 4-(2-(AMethyIcarbamoyl)-4-pyridyloxy)-2-methylaniIine HC1 Salt

<img file="CA2359244C_D0022.tif" />

A solution of 4-amino-3-methylphenol (5.45 g, 44.25 mmol) in dry dimethylacetamide (75 mL) was treated with potassium /er/-butoxide (10.86 g, 96.77 mmol) and the black mixture was stirred at room temp, until the flask had reached room temp. The contents were then treated with 4-chloro-A-methyl-220 pyridinecarboxamide (Method A2, Step 3b; 7.52 g, 44.2 mmol) and heated at 110 °C for 8 h. The mixture was cooled to room temp, and diluted with water (75 mL). The organic layer was extracted with EtOAc (5 x 100 mL). The combined organic layers were washed with a saturated NaCl solution (200 mL), dried (MgSO4) and

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69676-7 concentrated under reduced pressure. The residual black oil was treated with Et2Û (50 mL) and sonicated. The solution was then treated with HC1 (1 M in EtîO; 100 mL) and stirred at room temp, for 5 min. The resulting dark pink solid (7.04 g, 24.1 mmol) was removed by filtration from solution and stored under anaerobic conditions at 0 °C prior to use: ’H NMR (DMSO-dô) δ 2.41 (s, 3H), 2.78 (d, 7=4.4 Hz, 3H), 4.93 (brs, 2H), 7.19 (dd, 7=8.5, 2.6 Hz, 1H), 7.23 (dd,7=5.5, 2.6 Hz, 1H), 7.26 (d, 7=2.6 Hz, 1H), 7.55 (d, 7=2.6 Hz, 1H), 7.64 (d, 7=8.8 Hz, 1H), 8.55 (d, 7=5.9 Hz, 1H), 8.99 (q, 7=4.8 Hz, 1H).

A6. General Method for the Synthesis of Anilines from

Hydroxyanilines by TV-Protection, Nucleophilic Aromatic Substitution and Deprotection. Synthesis of 4-(2-(TV-Methylcarbamoyl)~4-pyridyIoxy)-2chloroanlline

<img file="CA2359244C_D0023.tif" />

Step 1: Synthesis of 3-Chloro-4-(2,2,2-trifIuoroacetylamino)phenol

Iron (3.24 g, 58.00 mmol) was added to stirring TFA (200 mL). To this slurry was added 2-chloro-4-nitrophenol (10.0 g, 58.0 mmol) and trifluoroacetic anhydride (20 mL). This gray slurry was stirred at room temp, for 6 d. The iron was filtered from solution and the remaining material was concentrated under reduced pressure. The resulting gray solid was dissolved in water (20 mL). To the resulting yellow solution was added a saturated NaHCOj solution (50 mL). The solid which precipitated from solution was removed. The filtrate was slowly quenched with the sodium bicarbonate solution until the product visibly separated from solution (determined was using a mini work-up vial). The slightly cloudy yellow solution was extracted with EtOAc (3 x 125 mL). The combined organic layers were washed with a saturated NaCl solution (125 mL), dried (MgSOQ and concentrated under reduced pressure. The 'H NMR (DMSO-dô) indicated a 1:1 ratio of the nitrophenol starting material and the intended product 3-chloro-4-(2,2,225

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PCT/USOO/0O768 trifluoroacetylamino)phenol. without further purification.

The crude material was taken on to the next step

<img file="CA2359244C_D0024.tif" />

NHMe

Step 2: Synthesis of 4-(2-(7V-Methylcarbamoyl)-4-pyridyloxy)-2chlorophenyl (222-trifluoro)acetamide

A solution of crude 3-chloro-4-(2,2,2-trifluoroacetylamino)phenol (5.62 g, 23.46 mmol) in dry dimethylacetamide (50 mL) was treated with potassium Ze/7-butoxide (5.16 g, 45.98 mmol) and the brownish black mixture was stirred at room temp, until the flask had cooled to room temp. The resulting mixture was treated with 4chloro-77-methyl-2-pyridinecarboxamide (Method A2, Step 3b; 1.99 g, 11.7 mmol) and heated at 100 °C under argon for 4 d. The black reaction mixture was cooled to room temp, and then poured into cold water (100 mL). The mixture was extracted with EtOAc (3 x 75 mL) and the combined organic layers were concentrated under reduced pressure. The residual brown oil was purified by column chromatography (gradient from 20% EtOAc/pet. ether to 40% EtOAc/pet. ether) to yield 4-(2-(77Methylcarbamoyl)-4-pyridyloxy)-2-chlorophenyl (222-trifluoro)acetamide as a yellow solid (8.59 g, 23.0 mmol).

<img file="CA2359244C_D0025.tif" />

Step 3. Synthesis of 4-(2-(7V-Methylcarbamoyl)-4-pyridyloxy)-2chloroaniline

A solution of crude 4-(2-(/7-Methylcarbamoyl)-4-pyridyloxy)-2-chlorophenyl (222trifluoro)acetamide (8.59 g, 23.0 mmol) in dry 4-dioxane (20 mL) was treated with a IN NaOH solution (20 mL). This brown solution was allowed to stir for 8 h. To this solution was added EtOAc (40 mL). The green organic layer was extracted with EtOAc (3 x 40 mL) and the solvent was concentrated to yield 4-(2-(7738

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Methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline as a green oil that solidified upon standing (2.86 g, 10.30 mmol): 'H NMR (DMSO-dô) δ 2.77 (d, 7=4.8 Hz, 3H), 5.51 (s, 2H), 6.60 (dd, 7=8.5, 2.6 Hz, 1H), 6.76 (d, 7=2.6 Hz, 1H), 7.03 (d, 7=8.5 Hz, 1H), 7.07 (dd, 7=5.5, 2.6, Hz, 1H), 7.27 (d, 7=2.6 Hz, 1H), 8.46 (d, 7=5.5 Hz, 1H),

8.75 (q, 7=4.8, 1 H).

A7. General Method for the Deprotection of an Acylated Aniline.

Synthesis of 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline

<img file="CA2359244C_D0026.tif" />

OMe

A suspension of 3-chIoro-6-(N-acetyl)-4-(trifluoromethyl)anisole (4.00 g,

14.95 mmol) in a 6M HCI solution (24 mL) was heated at the reflux temp, for 1 h. The resulting solution was allowed to cool to room temp, during which time it solidified slightly. The resulting mixture was diluted with water (20 mL) then treated with a combination of solid NaOH and a saturated NaHCCb solution until the solution was basic. The organic layer was extracted with CH2CI2 (3 x 50 mL). The combined organics were dried (MgSOzj) and concentrated under reduced pressure to yield 4-chloro-2methoxy-5-(trifluoromethyl)anilme as a brown oil (3.20 g, 14.2 mmol): *H NMR (DMSO-dô) δ 3.84 (s, 3H), 5.30 (s, 2H), 7.01 (s, 2H).

A8. General Method for Synthesis of tù-Alkoxy-œ-carboxyphenyl

Anilines. Synthesis of 4-(3-(2V-Methylcarbamoyl-4methoxyphenoxy)aniline.

<img file="CA2359244C_D0027.tif" />

Step 1. 4-(3-Methoxycarbonyl-4-methoxyphenoxy)-l-nitrobenzene:

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To a solution of 4-(3-carboxy-4-hydroxyphenoxy)-l -nitrobenzene (prepared from 2,5-dihydroxybenzoic acid in a manner analogous to that described in Method A13, Step 1,12 mmol) in acetone (50 mL) was added K2CO3 (5 g) and dimethyl sulfate (3.5 mL). The resulting mixture was heated at the reflux temp, overnight, then cooled to room temp, and filtered through a pad of Celite®. The resulting solution was concentrated under reduced pressure, absorbed onto S1O2, and purified by column chromatography (50% EtOAc / 50% hexane) to give 4-(3-methoxycarbonyl4-methoxyphenoxy)-l-nitrobenzene as a yellow powder (3 g): mp 115-118 °C.

<img file="CA2359244C_D0028.tif" />

to Step 2. 4-(3-Carboxy-4-methoxyphenoxy)-l-nitrobenzene:

A mixture of 4-(3-methoxycarbonyl-4-methoxyphenoxy)-l-nitrobenzene (1.2 g), KOH (0.33 g) and water (5 mL) in MeOH (45 mL) was stirred at room temp, overnight and then heated at the reflux temp, for 4 h. The resulting mixture was cooled to room temp, and concentrated under reduced pressure. The residue was dissolved in water (50 mL), and the aqueous mixture was made acidic with a IN HCI solution. The resulting mixture was extracted with EtOAc (50 mL). The organic layer was dried (MgSOQ and concentrated under reduced pressure to give 4-(3-carboxy-4-methoxyphenoxy)-1 -nitrobenzene ( 1.04 g).

<img file="CA2359244C_D0029.tif" />

Step 3. 4-(3-(/V-MethylcarbamoyI)-4-methoxypbenoxy)-l-nitrobenzene:

To a solution of 4-(3-carboxy-4-methoxyphenoxy)-l-nitrobenzene (0.50 g, 1.75 mmol) in CH2CI2 (12 mL) was added SOCI2 (0.64 mL, 8.77 mmol) in portions. The resulting solution was heated at the reflux temp, for 18 h, cooled to room temp., and concentrated under reduced pressure. The resulting yellow solids were dissolved in

CH2CI2 (3 mL) then the resulting solution was treated with a methylamine solution (2.0 M in THF, 3.5 mL, 7.02 mmol) in portions (CAUTION: gas evolution), and

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69676-7 stirred at room temp, for 4 h. The resulting mixture was treated with a IN NaOH solution, then extracted with CH₂C1₂ (25 mL). The organic layer was dried (Na₂SO4) and concentrated under reduced pressure to give 4-(3-(/7methylcarbamoyl)-4-methoxyphenoxy)-l-nitrobenzene as a yellow solid (0.50 g,

95%).

<img file="CA2359244C_D0030.tif" />

Step 4. 4-(3-(/V-MethylcarbamoIy)-4-methoxyphenoxy)aniIine:

A slurry of 4-(3-(/7-methylcarbamoly)-4-methoxyphenoxy)-l-nitrobenzene (0.78 g, 2.60 mmol) and 10% Pd/C (0.20 g) in EtOH (55 mL) was stirred under 1 atm of H₂ (balloon) for 2.5 d, then was filtered through a pad of Celite®. The resulting solution was concentrated under reduced pressure to afford 4-(3-(/7methylcarbamoly)-4-methoxyphenoxy)aniline as an off-white solid (0.68 g, 96%); TLC (0.1% EtjN/99.9% EtOAc) R/0.36.

A9. General Method for Preparation of ω-AIkylphthalimidecontaining Anilines. Synthesis of 5-(4-Aminophenoxy)-2methylisoindoline-l,3-dione

<img file="CA2359244C_D0031.tif" />

Step 1. Synthesis of 5-(4-Nitrophenoxy)-2-inethyIisoindoline-l,3-dione:

A slurry of 5-(4-nitrophenoxy)isoindoline-l,3-dione (A3 Step 2; 1.0 g, 3.52 mmol) and NaH (0.13 g, 5.27 mmol) in DMF (15 mL) was stirred at room temp, for 1 h, then treated with methyl iodide (0.3 mL, 4.57 mmol). The resulting mixture was stirred at room temp, overnight, then was cooled to °C and treated with water (10 mL). The resulting solids were collected and dried under reduced pressure to give

5-(4-nitrophenoxy)-2-methylisoindoline-l,3-dione as a bright yellow solid (0.87 g, 83%): TLC (35% EtOAc/65% hexane) R/0.61.

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<img file="CA2359244C_D0032.tif" />

Step 2. Synthesis of 5-(4-Aminophenoxy)-2-methylisoindoline-l,3-dione:

A slurry of nitrophenoxy)-2-methylisoindoline-l,3-dione (0.87 g, 2.78 mmol) and 10% Pd/C (0.10 g) in MeOH was stirred under 1 atm of H₂ (balloon) overnight. The resulting mixture was filtered through a pad of Celite® and concentrated under reduced pressure. The resulting yellow solids were dissolved in EtOAc (3 mL) and filtered through a plug of SiO₂ (60% EtOAc/40% hexane) to afford 5-(4aminophenoxy)-2-methylisoindoline-l,3-dione as a yellow solid (0.67 g, 86%): TLC (40% EtOAc/60% hexane) R/0.27.

A10. General Method for Synthesis of ω-Carbamoylaryl Anilines

Through Reaction of ω-Alkoxycarbonylaryl Precursors with Amines. Synthesis of 4-(2-(.V-(2-morpholin-4ylethyl)carbamoyl)pyridyloxy)aniline

O

<img file="CA2359244C_D0033.tif" />

Step 1. Synthesis of 4-Chloro-2-(;V-(2-inorpholin-4ylethyl)carb amoyl)pyridine

To a solution of methyl 4-chloropyridine-2-carboxylate HC1 salt (Method A2, Step 2; 1.01 g, 4.86 mmol) in THF (20 mL) was added 4-(2-aminoethyl)morpholine (2.55 mL, 19.4 mmol) dropwise and the resulting solution was heated at the reflux temp, for 20 h, cooled to room temp., and treated with water (50 mL). The resulting mixture was extracted with EtOAc (50 mL). The organic layer was dried (MgSO/Q and concentrated under reduced pressure to afford 4-chloro-2-(7V-(2-morpholin-4ylethyl) carbamoyl)pyridine as a yellow oil (1.25 g, 95%); TLC (10% MeOH/90%

EtOAc) R_f 0.50.

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<img file="CA2359244C_D0034.tif" />

ylethyl)carbamoyl)pyridyloxy)aniline.

A solution of 4-aminophenol (0.49 g, 4.52 mmol) and potassium Ze/7-butoxide (0.53 g, 4.75 mol) in DMF (8 mL) was stirred at room temp, for 2 h, then was sequentially treated with 4-chloro-2-(jV-(2-morpholin-4-ylethyl)carbamoyl)pyridine (1.22 g, 4.52 mmol) and K2CO3 (0.31 g, 2.26 mmol). The resulting mixture was heated at 75 °C overnight, cooled to room temp., and separated between EtOAc (25 mL) and a saturated NaCl solution (25 mL). The aqueous layer was back extracted with

EtOAc (25 mL). The combined organic layers were washed with a saturated NaCl solution (3 x 25 mL) and concentrated under reduced pressure. The resulting brown solids were purified by column chromatography (58 g; gradient from 100% EtOAc to 25% MeOH/75% EtOAc) to afford 4-(2-(A-(2-morpholin-4ylethyl)carbamoyl)pyridyloxy)aniline (1.0 g, 65%): TLC (10% MeOH/90% EtOAc)

R/0.32.

All. General Method for the Reduction of Nitroarenes to Arylamines.

Synthesis of 4-(3-Carboxyphenoxy)aniline.

O

<img file="CA2359244C_D0035.tif" />

A slurry of 4-(3-carboxyphenoxy)-l-nitrobenzene (5.38 g, 20.7 mmol) and 10% Pd/C (0.50 g) in MeOH (120 mL) was stirred under an H2 atmosphere (balloon) for 2 d. The resulting mixture was filtered through a pad of Celite®, then concentrated under reduced pressure to afford 4-(3-carboxyphenoxy)aniline as a brown solid (2.26 g, 48%): TLC (10% MeOH/90% CH₂C1₂) R_f 0.44 (streaking).

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A12.

Step 1.

General Method for the Synthesis of Isoindolinone-Containing Anilines. Synthesis of 4-(l-Oxoisoindolin-5-yloxy)aniline.

HO

<img file="CA2359244C_D0036.tif" />

O

Synthesis of 5-hydroxyisoindolin-l-one

To a solution of 5-hydroxyphthalimide (19.8 g, 121 mmol) in AcOH (500 mL) was slowly added zinc dust (47.6 g, 729 mmol) in portions, then the mixture was heated at the reflux temp, for 40 min., filtered hot, and concentrated under reduced pressure. The reaction was repeated on the same scale and the combined oily residue was purified by column chromatography (1.1 Kg SiO₂; gradient from 60%

EtOAc/40% hexane to 25% MeOH/75% EtOAc) to give 5-hydroxyisoindolin-l-one (3.77 g): TLC (100% EtOAc) R/0.17; HPLC ES-MS m/z 150 ((M+H)⁺).

<img file="CA2359244C_D0037.tif" />

O

Step 2. Synthesis of 4-(l-isoindolinon-5-yloxy)-l-nitrobenzene

To a slurry of NaH (0.39 g, 16.1 mmol) in DMF at 0 °C was added 515 hydroxyisoindolin-l-one (2.0 g, 13.4 mmol) in portions. The resulting slurry was allowed to warm to room temp, and was stirred for 45 min., then 4-fluoro-lnitrobenzene was added and then mixture was heated at 70 °C for 3 h. The mixture was cooled to 0 °C and treated with water dropwise until a precipitate formed. The resulting solids were collected to give 4-(l-isoindolinon-5-yloxy)-l -nitrobenzene as a dark yellow solid (3.23 g, 89%): TLC (100% EtOAc) Ry0.35.

Step 3. Synthesis of 4-(l-oxoisoindolin-5-yIoxy)aniline

A slurry of 4-(l-isoindolinon-5-yloxy)-l-nitrobenzene (2.12 g, 7.8 mmol) and 10% Pd/C (0.20 g) in EtOH (50 mL) was stirred under an H₂ atmosphere (balloon) for 4 h, then filtered through a pad of Celite®. The filtrate was concentrated under

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PCT/US00/00768 reduced pressure to afford 4-(l-oxoisoindolin-5-yloxy)aniline as a dark yellow solid: TLC (100% EtOAc) R_z0.15.

A13. General Method for the Synthesis of ω-Carbamoyl Anilines via

EDCI-Mediated Amide Formation Followed by Nitroarene Reduction. Synthesis of 4-(3-jVMethylcarbamoylphenoxy)aniline.

<img file="CA2359244C_D0038.tif" />

Step 1. Synthesis of 4-(3-ethoxycarbonylphenoxy)-l-nitrobenzene

A mixture of 4-fluoro-l-nitrobenzene (16 mL, 150 mmol), ethyl 3-hydroxybenzoate 25 g, 150 mmol) and K2CO3 (41 g, 300 mmol) in DMF (125 mL) was heated at the reflux temp, overnight, cooled to room temp, and treated with water (250 mL). The resulting mixture was extracted with EtOAc (3 x 150 mL). The combined organic phases were sequentially washed with water (3 x 100 mL) and a saturated NaCl solution (2 x 100 mL), dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by column chromatography (10% EtOAc/90% hexane) to afford 4-(3-ethoxycarbonylphenoxy)-l-nitrobenzene as an oil (38 g).

<img file="CA2359244C_D0039.tif" />

To a vigorously stirred mixture of 4-(3-ethoxycarbonylphenoxy)-l -nitrobenzene (5.14 g, 17.9 mmol) in a 3:1 THF/water solution (75 mL) was added a solution LiOH’INO (1.50 g, 35.8 mmol) in water (36 mL). The resulting mixture was heated at 50 °C overnight, then cooled to room temp., concentrated under reduced pressure, and adjusted to pH 2 with a 1M HCl solution. The resulting bright yellow solids were removed by filtration and washed with hexane to give 4-(3-carboxyphenoxy)1-nitrobenzene (4.40 g, 95%).

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<img file="CA2359244C_D0040.tif" />

Step 3. Synthesis of 4-(3-(A-methyIcarbamoyl)phenoxy)-l-nitrobenzene

A mixture of 4-(3-carboxyphenoxy)-l-nitrobenzene (3.72 g, 14.4 mmol), EDCI’HCl (3.63 g, 18.6 mmol), TV-methylmorpholine (1.6 mL, 14.5 mmol) and methylamine (2.0 M in THF; 8 mL, 16 mmol) in CH2CI2 (45 mL) was stirred at room temp, for 3 d, then concentrated under reduced pressure. The residue was dissolved in EtOAc (50 mL) and the resulting mixture was extracted with a 1M HCl solution (50 mL). The aqueous layer was back-extracted with EtOAc (2 x 50 mL). The combined organic phases were washed with a saturated NaCl solution (50 mL), dried (Na2SO₄), and concentrated under reduced pressure to give 4-(3-(7Vmethylcarbamoyl)phenoxy)-l-nitrobenzene as an oil (1.89 g).

NHMe

H₂N

Step 4. Synthesis of 4-(3-(/V-methylcarbamoyl)phenoxy)aniline

A slurry of 4-(3-(A-methylcarbamoyl)phenoxy)-l-nitrobenzene (1.89 g, 6.95 mmol) and 5% Pd/C (0.24 g) in EtOAc (20 mL) was stirred under an H2 atm (balloon) overnight. The resulting mixture was filtered through a pad of Celite® and concentrated under reduced pressure. The residue was purified by column chromatography (5% MeOH/95% CH2CI2). The resulting oil solidified under vacuum overnight to give 4-(3-(7V-methylcarbamoyl)phenoxy)aniline as a yellow solid (0.95 g, 56%).

A14. General Method for the Synthesis of ω-Carbamoyl Anilines via

EDCI-Mediated Amide Formation Followed by Nitroarene Reduction.

Synthesis of 4-3-(5-MethylcarbamoyI)pyridyloxy)aniline

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<img file="CA2359244C_D0041.tif" />

Step 1. Synthesis of 4-(3-(5-methoxycarbonyl)pyridyloxy)-lnitrobenzene

To a slurry of NaH (0.63 g, 26.1 mmol) in DMF (20 mL) was added a solution of methyl 5-hydroxynicotinate (2.0 g, 13.1 mmol) in DMF (10 mL). The resulting mixture was added to a solution of 4-fluoronitrobenzene (1.4 mL, 13.1 mmol) in DMF (10 mL) and the resulting mixture was heated at 70 °C overnight, cooled to room temp., and treated with MeOH (5 mL) followed by water (50 mL). The resulting mixture was extracted with EtOAc (100 mL). The organic phase was concentrated under reduced pressure. The residue was purified by column chromatography (30% EtOAc/70% hexane) to afford 4-(3-(5methoxycarbonyl)pyridyloxy)-l-nitrobenzene (0.60 g).

<img file="CA2359244C_D0042.tif" />

Step 2. Synthesis of 4-(3-(5-methoxycarbonyl)pyridyloxy)aniline

A slurry of 4-(3-(5-methoxycarbonyl)pyridyloxy)-l -nitrobenzene (0.60 g, 2.20 mmol) and 10% Pd/C in MeOH/EtOAc was stirred under an H₂ atmosphere (balloon) for 72 h. The resulting mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (gradient from 10% EtOAc/90% hexane to 30% EtOAc/70% hexane to 50% EtOAc/50% hexane) to afford 4-(3-(5methoxycarbonyl)pyridyloxy)aniline (0.28 g, 60%): ’H NMR (CDCI3) δ 3.92 (s, 3H), 6.71 (d, 2H), 6.89 (d, 2H), 7.73 (, IH), 8.51 (d, IH), 8.87 (d, IH).

A15. Synthesis of an Aniline via Electrophilic Nitration Followed by

Reduction. Synthesis of 4-(3-Methylsulfamoylphenoxy)aniline.

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<img file="CA2359244C_D0043.tif" />

Step 1. Synthesis of A-methyl-3-bromobenzenesulfonamide

To a solution of 3-bromobenzenesulfonyl chloride (2.5 g, 11.2 mmol) in THF (15 mL) at 0 °C was added methylamine (2.0 M in THF; 28 mL, 56 mmol). The resulting solution was allowed to warm to room temp, and was stirred at room temp, overnight. The resulting mixture was separated between EtOAc (25 mL) and a 1 M HCI solution (25 mL). The aqueous phase was back-extracted with EtOAc (2 x 25 mL). The combined organic phases were sequentially washed with water (2 x 25 mL) and a saturated NaCl solution (25 mL), dried (MgSO4) and concentrated under reduced pressure to give A-methyl-3-bromobenzenesulfonamide as a white solid (2.8 g, 99%).

<img file="CA2359244C_D0044.tif" />

Step 2. Synthesis of 4-(3-(7V-methylsuifamoyl)phenyloxy)benzene

To a slurry of phenol (1.9 g, 20 mmol), K2CO3 (6.0 g, 40 mmol), and Cul (4 g, 20 mmol) in DMF (25 mL) was added A-methyl-3-bromobenzenesulfonamide (2.5 g, lOmmol), and the resulting mixture was stirred at the reflux temp, overnight, cooled to room temp., and separated between EtOAc (50 mL) and a 1 N HCI solution (50 mL). The aqueous layer was back-extracted with EtOAc (2 x 50 mL). The combined organic phases were sequentially washed with water (2 x 50 mL) and a saturated NaCl solution (50 mL), dried (MgSÛ4), and concentrated under reduced pressure. The residual oil was purified by column chromatography (30% EtOAc/70% hexane) to give 4-(3-(/V-methylsulfamoyl)phenyloxy)benzene (0.30 g).

<img file="CA2359244C_D0045.tif" />

Step 3. Synthesis of 4-(3-(.V-metliylsiiIfainoyl)phenyIoxy)-l-nitrobenzene

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To a solution of 4-(3-(/V-methylsulfamoyl)phenyloxy)benzene (0.30 g, 1.14 mmol) in TFA (6 mL) at -10°C was added NaNO₂ (0.097 g, 1.14 mmol) in portions over 5 min. The resulting solution was stirred at -10 °C for 1 h, then was allowed to warm to room temp., and was concentrated under reduced pressure. The residue was separated between EtOAc (10 mL) and water (10 mL). The organic phase was sequentially washed with water (10 mL) and a saturated NaCl solution (10 mL), dried (MgSO^ and concentrated under reduced pressure to give 4-(3-(77methylsulfamoyl)phenyloxy)-l-nitrobenzene (0.20 g). This material carried on to the next step without further purification.

<img file="CA2359244C_D0046.tif" />

Step 4. Synthesis of 4-(3-(7V-methylsulfamoyl)phenyloxy)aniline

A slurry of 4-(3-(A-methylsulfamoyl)phenyloxy)-l-nitrobenzene (0.30 g) and 10% Pd/C (0.030 g) in EtOAc (20 mL) was stirred under an H₂ atmosphere (balloon) overnight. The resulting mixture was filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (30% EtOAc/70% hexane) to give 4-(3-(77methylsulfamoyl)phenyloxy)aniline (0.070 g).

A16. Modification of ω-ketones. Synthesis of 4-(4-(l-(7V20 methoxy)iminoethyl)phenoxyaniline HC1 salt.

<img file="CA2359244C_D0047.tif" />

To a slurry of 4-(4-acetylphenoxy)aniline HC1 salt (prepared in a manner analogous to Method A13, step 4; 1.0 g, 3.89 mmol) in a mixture of EtOH (10 mL) and pyridine (1.0 mL) was added û-methylhydroxylamine HC1 salt (0.65 g, 7.78 mmol,

2.0 equiv.). The resulting solution was heated at the reflux temperature for 30 min, cooled to room temperature and concentrated under reduced pressure. The resulting

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PCT/USOO/00768 solids were triturated with water (10 mL) and washed with water to give 4-(4-( 1-(Nmethoxy)iminoethyl) phenoxyaniline HCI salt as a yellow solid (0.85 g): TLC (50% EtOAc/50% pet. ether) R/0.78; 'H NMR (DMSO-d₆) δ 3.90 (s, 3H), 5.70 (s, 3H); HPLC-MS m/z 257 ((M+H)⁺).

A17.

Synthesis of A-(o-SilyloxyaIkyl)amides. Synthesis of 4-(4-(2-(7V(2-TriisopropyIsilyloxy)ethylcarbamoyl)pyridyloxyaniline.

Cl

N

<img file="CA2359244C_D0048.tif" />

Step 1. 4-Chloro-A-(2-triisopropylsilyloxy)ethylpyridine-2-carboxamide

To a solution of 4-chloro-7V-(2-hydroxyethyl)pyridine-2-carboxamide (prepared in a manner analogous to Method A2, Step 3b; 1.5 g, 7.4 mmol) in anh DMF (7 mL) was added triisopropylsilyl chloride (1.59 g, 8.2 mmol, 1.1 equiv.) and imidazole (1.12 g, 16.4 mmol, 2.2 equiv.). The resulting yellow solution was stirred for 3 h at room temp, then was concentrated under reduced pressure. The residue was separated between water (10 mL) and EtOAc (10 mL). The aqueous layer was extracted with EtOAc (3 x 10 mL). The combined organic phases were dried (MgSO^, and concentrated under reduced pressure to afford 4-chloro-2-(ZV-(2triisopropylsilyloxy)ethyl)pyridinecarboxamide as an orange oil (2.32 g, 88%). This material was used in the next step without further purification.

.0.

h₂n

N

H

<img file="CA2359244C_D0049.tif" />

'Si

Step 2. 4-(4-(2-(^-(2Triisopropylsilyloxy)ethylcarbamoyl)pyridyloxyaniline

To a solution of 4-hydroxyaniline (0.70 g, 6.0 mmol) in anh DMF (8 mL) was added potassium Zerz-butoxide (0.67 g, 6.0 mmol, 1.0 equiv.) in one portion causing an exotherm. When this mixture had cooled to room temperature, a solution of 4chloro-2-(jV-(2-triisopropylsilyloxy)ethyl)pyridinecarboxamide (2.32 g, 6 mmol, 1

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PCT/US00/00768 equiv.) in DMF (4 mL) was added followed by K₂CO₃ (0.42 g, 3.0 mmol, 0.50 equiv.). The resulting mixture was heated at 80 °C overnight. An additional portion of potassium /er/-butoxide (0.34 g, 3 mmol, 0.5 equiv.) was then added and the mixture was stirred at 80 °C an additional 4 h. The mixture was cooled to 0 °C with an ice/water bath, then water (approx. 1 mL) was slowly added dropwise. The organic layer was extracted with EtOAc (3x10 mL). The combined organic layers were washed with a saturated NaCl solution (20 mL), dried (MgSCL) and concentrated under reduced pressure. The brown oily residue was purified by column chromatography (SiO₂; 30% EtOAc/ 70% pet ether) to afford 4-(4-(2-(77-(210 triisopropylsilyloxy)ethylcarbamoyl)pyridyloxyaniline as a clear light brown oil (0.99 g, 38%).

A18. Synthesis of 2-Pryidinecarboxylate Esters via Oxidation of 2Methylpyridines. Synthesis of 4-(5-(215 methoxycarbonyl)pyridyloxy)aniline.

<img file="CA2359244C_D0050.tif" />

Step 1. 4-(5-(2-Methyl)pyridyloxy)-l-nitrobenzene.

A mixture of 5-hydroxy-2-methylpyridine (10.0 g, 91.6 mmol), l-fluoro-4nitrobenzene (9.8 mL, 91.6 mmol, 1.0 equiv.), K₂CO₃ (25 g, 183 mmol, 2.0 equiv.) in DMF (100 mL) was heated at the reflux temperature overnight. The resulting mixture was cooled to room temperature, treated with water (200 mL), and extracted with EtOAc (3 x 100 mL). The combined organic layers were sequentially washed with water (2 x 100 mL) and a saturated NaCl solution ((100 mL), dried (MgSOQ and concentrated under reduced pressure to give 4-(5-(2-methyl)pyridyloxy)-l25 nitrobenzene as a brown solid (12.3 g).

<img file="CA2359244C_D0051.tif" />

O

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Step 2. Synthesis of 4-(5-(2-MethoxycarbonyI)pyridyloxy)-lnitrobenzene.

A mixture of 4-(5-(2-methyl)pyridyloxy)-l-nitrobenzene (1.70 g, 7.39 mmol) and selenium dioxide (2.50 g, 22.2 mmol, 3.0 equiv.) in pyridine (20 mL) was heated at the reflux temperature for 5 h, then cooled to room temperature. The resulting slurry was filtered , then concentrated under reduced pressure. The residue was dissolved in MeOH (100 mL). The solution was treated with a cone HCl solution (7 mL), then heated at the reflux temperature for 3 h, cooled to room temperature and concentrated under reduced pressure. The residue was separated between EtOAc (50 mL) and a IN NaOH solution (50 mL). The aqueous layer was extracted with

EtOAc (2 x 50 mL). The combined organic layers were sequentially washed with water (2 x 50 mL) and a saturated NaCl solution (50 mL), dried (MgSO^ and concentrated under reduced pressure. The residue was purified by column chromatography (SiO₂; 50% EtOAc/50% hexane) to afford 4-(5-(215 methoxycarbonyl)pyridyloxy)-l-nitrobenzene (0.70 g).

<img file="CA2359244C_D0052.tif" />

O

Step 3. Synthesis of 4-(5-(2-MethoxycarbonyI)pyridyloxy)aniline.

A slurry of 4-(5-(2-methoxycarbonyl)pyridyloxy)-l-nitrobenzene (0.50 g) and 10% Pd/C (0.050 g) in a mixture of EtOAc (20 mL) and MeOH (5 mL) was placed under a H₂ atmosphere (balloon) overnight. The resulting mixture was filtered through a pad of Celite®, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (SiO₂; 70% EtOAc/30% hexane) to give 4-(5-(2-methoxycarbonyl)pyridyloxy)aniline (0.40 g).

A19. Synthesis of ω-Sulfonylphenyl Anilines. Synthesis of 4-(4Methylsulfonylphenyoxy)aniline.

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<img file="CA2359244C_D0053.tif" />

Step 1. 4-(4-Methylsulfonylphenoxy)-l-nitrobenzene: To a solution of 4-(4methylthiophenoxy)-l-nitrobenzene (2.0 g, 7.7 mmol) in CH2CI2 (75 mL) at 0 °C was slowly added m-CPBA (57-86%, 4.0 g), and the reaction mixture was stirred at room temperature for 5 h. The reaction mixture was treated with a IN NaOH solution (25 mL). The organic layer was sequentially washed with a IN NaOH solution (25 mL), water (25 mL) and a saturated NaCl solution (25 mL), dried (MgSOQ, and concentrated under reduced pressure to give 4-(4methylsulfonylphenoxy)-l-nitrobenzene as a solid (2.1 g).

Step 2. 4-(4-MethyIsuIfonyIphenoxy)-l-aniIine: 4-(4-Methylsulfonylphenoxy)-lnitrobenzene was reduced to the aniline in a manner analogous to that described in Method A18, step 3.

B.

BI.

Synthesis of Urea Precursors

General Method for the Synthesis of Isocyanates from Anilines Using CDI. Synthesis of 4-Bromo-3-(trifluoromethyI)phenyl Isocyanate.

CF,

Br

NH₂’HCI

Step 1. Synthesis of 4-bromo-3-(trifluoromethyI)aniline HC1 salt

To a solution of 4-bromo-3-(trifluoromethyl)anilme (64 g, 267 mmol) in Et20 (500 mL) was added an HC1 solution (1 M in Et20; 300 mL) dropwise and the resulting mixture was stirred at room temp, for 16 h. The resulting pink-white precipitate was removed by filtration and washed with Et₂O (50 mL) and to afford 4-bromo-325 (trifluoromethyl)aniline HC1 salt (73 g , 98%).

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ÇFa

BrNCO

Step 2. Synthesis of 4-bromo-3-(trifluoromethyl)phenyI isocyanate

A suspension of 4-bromo-3-(trifluoromethyl)aniline HCI salt (36.8 g, 133 mmol) in toluene (278 mL) was treated with tri chloromethyl chloroformate dropwise and the resulting mixture was heated at the reflux temp, for 18 h. The resulting mixture was concentrated under reduced pressure. The residue was treated with toluene (500 mL), then concentrated under reduced pressure. The residue was treated with CH2CI2 (500 mL), then concentrated under reduced pressure. The CH2CI2 treatment/concentration protocol was repeated and resulting amber oil was stored at -20 °C for 16 h, to afford 4-bromo-3-(trifluoromethyl)phenyl isocyanate as a tan solid (35.1 g, 86%): GC-MS m/z 265 (M⁺).

C. Methods of Urea Formation

Cla. General Method for the Synthesis of Ureas by Reaction of an

Isocyanate with an Aniline. Synthesis of 7V-(4-Chloro-3(trifluoromethyl)phenyl)-7V’-(4-(2-(/V-methyIcarbamoyl)-4pyridyloxy)phenyi) Urea

<img file="CA2359244C_D0054.tif" />

A solution of 4-chloro-3-(trifluoromethyl)phenyl isocyanate (14.60 g, 65.90 mmol) in CH2CI2 (35 mL) was added dropwise to a suspension of 4-(2-(//methylcarbamoyl)-4-pyridyloxy)aniline (Method A2, Step 4; 16.0 g, 65.77 mmol) in CH2CI2 (35 mL) at 0 °C. The resulting mixture was stirred at room temp, for 22 h. The resulting yellow solids were removed by filtration, then washed with CH2CI2 (2 x 30 mL) and dried under reduced pressure (approximately 1 mmHg) to afford //-(4chloro-3-(trifluoromethyl)phenyl)-//’-(4-(2-(7V-methylcarbamoyl)-4pyridyloxy)phenyl) urea as an off-white solid (28.5 g, 93%): mp 207-209 °C; *H54

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NMR (DMSO-d₆) δ 2.77 (d, 7=4.8 Hz, 3H), 7.16 (m, 3H), 7.37 (d, 7=2.5 Hz, IH), 7.62 (m, 4H), 8.11 (d, 7=2.5 Hz, IH), 8.49 (d, 7=5.5 Hz, IH), 8.77 (br d, IH), 8.99 (s, IH), 9.21 (s, IH); HPLC ES-MS m/z 465 ((M+H)⁺).

Clb. General Method for the Synthesis of Ureas by Reaction of an

Isocyanate with an Aniline. Synthesis of/V-(4-Bromo-3(trifluoromethyl)phenyl)-7V’-(4-(2-(jV-niethylcarbamoyI)-4pyridyloxy)phenyl) Urea

<img file="CA2359244C_D0055.tif" />

A solution of 4-bromo-3-(trifluoromethyl)phenyl isocyanate (Method BI, Step 2; 8.0 g, 30.1 mmol) in CH2CI2 (80 mL) was added dropwise to a solution of 4-(2-(/7methylcarbamoyl)-4-pyridyloxy)aniline (Method A2, Step 4; 7.0 g, 28.8 mmol) in CH2CI2 (40 mL) at 0 °C. The resulting mixture was stirred at room temp, for 16 h. The resulting yellow solids were removed by filtration, then washed with CH2CI2 (2 x 50 mL) and dried under reduced pressure (approximately 1 mmHg) at 40 °C to afford A-(4-bromo-3-(trifluoromethyl)phenyl)-iV’-(4-(2-(/V-methylcarbamoyl)-4pyridyloxy)phenyl) urea as a pale-yellow solid (13.2 g, 90%): mp 203-205 °C; ^]HNMR (DMSO-dô) δ 2.77 (d, 7=4.8 Hz, 3H), 7.16 (m, 3H), 7.37 (d, 7=2.5 Hz, 1H), 7.58 (m, 3H), 7.77 (d, 7=8.8 Hz, 1H), 8.11 (d, 7=2.5 Hz, 1H), 8.49 (d, 7=5.5 Hz,

1H), 8.77 (br d, 1H), 8.99 (s, 1H), 9.21 (s, 1H); HPLC ES-MS m/z 509 ((M+H)⁺).

Clc. General Method for the Synthesis of Ureas by Reaction of an

Isocyanate with an Aniline. Synthesis of A-(4-Chloro-3(trifliioromethyl)phenyl)-.V’-(2-niethyI-4-(2-(N25 methylcarbamoyl)(4-pyridyloxy))phenyl) Urea

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<img file="CA2359244C_D0056.tif" />

A solution of 2-methyl-4-(2-(N-methylcarbamoyl)(4-pyridyloxy))aniline (Method A5; 0.11 g, 0.45 mmol) in CH2CI2 (1 mL) was treated with Et3N (0.16 mL) and 4chloro-3-(trifluoromethyl)phenyl isocyanate (0.10 g, 0.45 mmol). The resulting brown solution was stirred at room temp, for 6 d, then was treated with water (5 mL). The aqueous layer was back-extracted with EtOAc (3x5 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to yield A-(4-chloro-3-(trifhioromethyl)phenyl)-/V’-(2-methyl-4-(2-(Nmethylcarbamoyl)(4-pyridyloxy))phenyl) urea as a brown oil (0.11 g, 0.22 mmol): ’H NMR (DMSO-d₆) δ 2.27 (s, 3H), 2.77 (d, 7=4.8 Hz, 3H), 7.03 (dd, 7=8.5, 2.6 Hz, IH), 7.11 (d, 7=2.9 Hz, IH), 7.15 (dd, 7=5.5, 2.6, Hz, IH), 7.38 (d, 7=2.6 Hz, IH), 7.62 (app d, 7=2.6 Hz, 2H), 7.84 (d, 7=8.8 Hz, IH), 8.12 (s, IH), 8.17 (s, IH); 8.50 (d, 7=5.5 Hz, IH), 8.78 (q, 7=5.2, IH), 9.52 (s, IH); HPLC ES-MS m/z 479 ((M+H)⁺).

Cld.

General Method for the Synthesis of Ureas by Reaction of an Isocyanate with an Aniline. Synthesis of A-(4-Chloro-3(trifluoromethyl)phenyl)-A^’-(4-aminophenyl) Urea

<img file="CA2359244C_D0057.tif" />

To a solution of 4-chloro-3-(trifhioromethyl)phenyl isocyanate (2.27 g, 10.3 mmol) in CH2CI2 (308 mL) was added //-phenylenediamine (3.32 g, 30.7 mmol) in one part. The resulting mixture was stirred at room temp, for 1 h, treated with CH2CI2 (100 mL), and concentrated under reduced pressure. The resulting pink solids were dissolved in a mixture of EtOAc (110 mL) and MeOH (15mL), and the clear solution was washed with a 0.05 N HCI solution. The organic layer was

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PCT/US00/00768 concentrated under reduced pressure to afford impure A-(4-chloro-3(trifluoromethyl)phenyl)-A’-(4-aminophenyl) urea (3.3 g): TLC (100% EtOAc) R/ 0.72.

Cle. General Method for the Synthesis of Ureas by Reaction of an

Isocyanate with an Aniline. Synthesis of A-(4-ChIoro-3(trifluoromethyl)phenyI)-7V’-(4-ethoxycarbonylphenyl) Urea

<img file="CA2359244C_D0058.tif" />

To a solution of ethyl 4-isocyanatobenzoate (3.14 g, 16.4 mmol) in CH2CI2 (30 mL) was added 4-chloro-3-(trifluoromethyl)aniline (3.21 g, 16.4 mmol), and the solution was stirred at room temp, overnight. The resulting slurry was diluted with CH2CI2 (50 mL) and filtered to afford A-(4-chloro-3-(trifluoromethyl)phenyl)-A’-(4ethoxycarbonylphenyl) urea as a white solid (5.93 g, 97%): TLC (40% EtOAc/60% hexane) Ry-0.44.

Clf. General Method for the Synthesis of Ureas by Reaction of an

Isocyanate with an Aniline. Synthesis of A-(4-Chloro-3(trifluoromethyl)phenyl)-A’-(3-carhoxyphenyI) Urea

<img file="CA2359244C_D0059.tif" />

To a solution of 4-chloro-3-(trifluoromethyl)phenyl isocyanate (1.21g, 5.46 mmol) 20 in CH₂C1₂ (8 mL) was added 4-(3-carboxyphenoxy)aniline (Method All; 0.81 g,

5.76 mmol) and the resulting mixture was stirred at room temp, overnight, then treated with MeOH (8 mL), and stirred an additional 2 h. The resulting mixture was concentrated under reduced pressure. The resulting brown solids were triturated with a 1:1 EtOAc/hexane solution to give A-(4-chloro-3-(trifluoromethyl)phenyl)25 A’-(3-carboxyphenyl) urea as an off-white solid (1.21 g, 76%).

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C2a.

General Method for Urea Synthesis by Reaction of an Aniline with A;A’-Carbonyl Diimidazole Followed by Addition of a Second Aniline. Synthesis of 7V-(2-Methoxy-5(trifluoromethyl)phenyl)-N’-(4-(2-(A-methylcarbamoyl)-4pyridyloxy)phenyl) Urea CF,

O

<img file="CA2359244C_D0060.tif" />

NHMe

OMe

H H

To a solution of 2-methoxy-5-(trifluoromethyl)aniline (0.15 g) in anh CH2CI2 (15 mL) at 0 °C was added CDI (0.13 g). The resulting solution was allowed to warm to room temp, over 1 h, was stirred at room temp, for 16 h, then was treated with 410 (2-(/7-methylcarbamoyl)-4-pyridyloxy)aniline (0.18 g). The resulting yellow solution was stirred at room temp, for 72 h, then was treated with H₂O (125 mL). The resulting aqueous mixture was extracted with EtOAc (2 x 150 mL). The combined organics were washed with a saturated NaCl solution (100 mL), dried (MgSOzt) and concentrated under reduced pressure. The residue was triturated (90%

EtOAc/10% hexane). The resulting white solids were collected by filtration and washed with EtOAc. The filtrate was concentrated under reduced pressure and the residual oil purified by column chromatography (gradient from 33% EtOAc/67% hexane to 50% EtOAc/50% hexane to 100% EtOAc) to give //-(2-m ethoxy-5(trifluoromethyl)phenyl)-//’-(4-(2-(//-methylcarbamoyl)-4-pyridyloxy)phenyl) urea as a light tan solid (0.098 g, 30%): TLC (100% EtOAc) R/0.62; ^!H NMR (DMSOd₆) δ 2.76 (d, 7=4.8 Hz, 3H), 3.96 (s, 3H), 7.1-7.6 and 8.4-8.6 (m, 11H), 8.75 (d, 7=4.8 Hz, IH), 9.55 (s, 1 H); FAB-MS m/z 461 ((M+H)⁺).

C2b.

General Method for Urea Synthesis by Reaction of an Aniline with ALV’-Carbonyl Diimidazole Followed by Addition of a Second Aniline. Symmetrical Urea’s as Side Products of a N,N’~ Carbonyl Diimidazole Reaction Procedure. Synthesis of Bis(4-(2(A⁷-methylcarbamoyl)-4-pyridyloxy)phenyl) Urea

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To a stirring solution of 3-amino-2-methoxyquinoline (0.14 g) in anhydrous CH2CI2 (15 mL) at 0 C was added CDI (0.13 g). The resulting solution was allowed to warm to room temp, over 1 h then was stirred at room temp, for 16 h. The resulting mixture was treated with 4-(2-(/V-methylcarbamoyl)-4-pyridyloxy)aniline (0.18 g). The resulting yellow solution stirred at room temp, for 72 h, then was treated with water (125 mL). The resulting aqueous mixture was extracted with EtOAc (2 x 150 mL). The combined organic phases were washed with a saturated NaCl solution (100 ml), dried (MgSO4) and concentrated under reduced pressure. The residue was triturated (90% EtOAc/10% hexane). The resulting white solids were collected by filtration and washed with EtOAc to give bis(4-(2-(A⁷-methylcarbamoyl)-4pyridyloxy)phenyl) urea (0.081 g, 44%): TLC (100% EtOAc) Ry 0.50; ^]H NMR (DMSO-d₆) δ 2.76 (d, 7=5.1 Hz, 6H), 7.1-7.6 (m, 12H), 8.48 (d, 7=5.4 Hz, IH), 8.75 (d, 7=4.8 Hz, 2H), 8.86 (s, 2H); HPLC ES-MS m/z 513 ((M+H)⁺).

C2c.

General Method for the Synthesis of Ureas by Reaction of an Isocyanate with an Aniline. Synthesis of .V-(2-Methoxy-5(trifluoromethyl)phenyI-7V’-(4-(l,3-dioxoisoindolin-5yloxy)phenyl) Urea

<img file="CA2359244C_D0062.tif" />

To a stirring solution of 2-methoxy-5-(trifluoromethyl)phenyl isocyanate (0.10 g, 0.47 mmol) in CH2CI2 (1.5 mL) was added 5-(4-aminophenoxy)isoindoline-1,3dione (Method A3, Step 3; 0.12 g, 0.47 mmol) in one portion. The resulting mixture was stirred for 12 h, then was treated with CH2CI2 (10 mL) and MeOH (5 mL). The resulting mixture was sequentially washed with a IN HC1 solution (15 mL) and a

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PCT/US00/00768 saturated NaCl solution (15 mL), dried (MgSCL) and concentrated under reduced pressure to afford jV-(2-methoxy-5-(trifluoromethyl)phenyl-/V’-(4-(l,3dioxoisoindolin-5-yloxy)phenyl) urea as a white solid (0.2 g, 96%); TLC (70% EtOAc/30% hexane) R_z 0.50; ’H NMR (DMSO-d₆) δ 3.95 (s, 3H), 7.31-7.10 (m,

6H), 7.57 (d, J=9.3Hz, 2H), 7.80 (d, J=8.7 Hz, IH), 8.53 (br s, 2H), 9.57 (s, IH),

11.27 (br s, IH); HPLC ES-MS 472.0 ((M+H)⁺, 100%).

C2d

General Method for Urea Synthesis by Reaction of an Aniline with /V,/V’-Carbonyl Diimidazole Followed by Addition of a Second Aniline. Synthesis of.V-(5-(Ziv7-Bu tyl)-2-(2,5dimethyIpyrrolyl)phenyI)-ZV’-(4-(2-(7V-methylcarbamoyl)-4pyridyloxy)phenyl) Urea

<img file="CA2359244C_D0063.tif" />

To a stirring solution of CDI (0.2 lg, 1.30 mmol) in CH2CI2 (2 mL) was added 515 (ZerZ-butyl)-2-(2,5-dimethylpyrrolyl)aniline (Method A4, Step 2; 0.30 g, 1.24 mmol) in one portion. The resulting mixture was stirred at room temp, for 4 h, then 4-(2(/V-methylcarbamoyl)-4-pyridyloxy)aniline (0.065 g, 0.267mmol) was then added in one portion. The resulting mixture was heated at 36 °C overnight, then cooled to room temp, and diluted with EtOAc (5 mL). The resulting mixture was sequentially washed with water (15 mL) and a IN HC1 solution (15mL), dried (MgSOri, and filtered through a pad of silica gel (50 g) to afford /7-(5-(ZerZ-buty 1)-2(2,5-dimethylpyrrolyl)phenyl)-/7’-(4-(2-(/7-methylcarbamoyl)-4-pyridyloxy)phenyl) urea as a yellowish solid (0.033 g, 24%): TLC (40% EtOAc/60% hexane) Ry 0.24; 'H NMR (acetone-d₆) δ 1.37 (s, 9H), 1.89 (s, 6H), 2.89 (d, J=4.8Hz, 3H), 5.83 (s,

2H), 6.87-7.20 (m, 6H), 7.17 (dd, IH), 7.51-7.58 (m, 3H), 8.43 (d, 7=5.4Hz, IH),

8.57 (d, 7=2.1Hz, IH), 8.80 (br s, IH); HPLC ES-MS 512 ((M+H)⁺, 100%).

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C3. Combinatorial Method for the Synthesis of Diphenyl Ureas Using

Triphosgene

One of the anilines to be coupled was dissolved in dichloroethane (0.10 M). This solution was added to a 8 mL vial (0.5 mL) containing dichloroethane (1 mL). To this was added a bis(trichloromethyl) carbonate solution (0.12 M in di chloroethane, 0.2 mL, 0.4 equiv.), followed by diisopropylethylamine (0.35 M in dichloroethane, 0.2 mL, 1.2 equiv.). The vial was capped and heat at 80 °C for 5 h, then allowed to cool to room temp for approximately 10 h. The second aniline was added (0.10 M in dichloroethane, 0.5 mL, 1.0 equiv.), followed by diisopropylethylamine (0.35 M in dichloroethane, 0.2 mL, 1.2 equiv.). The resulting mixture was heated at 80 °C for 4 h, cooled to room temperature and treated with MeOH (0.5 mL). The resulting mixture was concentrated under reduced pressure and the products were purified by reverse phase HPLC.

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C4.

General Method for Urea Synthesis by Reaction of an Aniline with Phosgene Followed by Addition of a Second Aniline. Synthesis of 7V-(2-Methoxy-5-(trifluoromethyl)phenyl)-/V’-(4-(2(yV-methylcarbamoyl)-4-pyridyIoxy)phenyI) Urea

CF,

O

<img file="CA2359244C_D0064.tif" />

OMe

NHMe

To a stirring solution of phosgene (1.9 M in toluene; 2.07 mL0.21g, 1.30 mmol) in CH2CI2 (20 mL) at 0 °C was added anh pyridine (0.32 mL) followed by 2-methoxy5-(trifhioromethyl)aniline (0.75 g). The yellow solution was allowed to warm to room temp during which a precipitate formed. The yellow mixture was stirred for 1 h, then concentrated under reduced pressure. The resulting solids were treated with anh toluene (20 mL) followed by 4-(2-(7V-methylcarbamoyl)-4-pyridyloxy)aniline (prepared as described in Method A2; 0.30 g) and the resulting suspension was heated at 80 °C for 20 h, then allowed to cool to room temp. The resulting mixture was diluted with water (100 mL), then was made basic with a saturated NaHCCb solution (2-3 mL). The basic solution was extracted with EtOAc (2 x 250 mL). The organic layers were separately washed with a saturated NaCl solution, combined, dried (MgSOO, and concentrated under reduced pressure. The resulting pink-brown residue was dissolved in MeOH and absorbed onto SiO₂ (100 g). Column chromatography (300 g SiO₂; gradient from 1% Et3N/33% EtOAc/66% hexane to

1% Et3N/99% EtOAc to 1% EtjN/20% MeOH/79% EtOAc) followed by concentration under reduced pressure at 45 °C gave a warm concentrated EtOAc solution, which was treated with hexane (10 mL) to slowly form crystals of 7V-(2methoxy-5-(trifluoromethyl)phenyl)-jV’-(4-(2-(7V’-methylcarbamoyl)-4pyridyloxy)phenyl) urea (0.44 g): TLC (1% Et₃N/99% EtOAc) R/0.40.

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D. Interconversion of Ureas

Dla. Conversion of ω-AminophenyI Ureas into co-(Aroylamino)phenyl

Ureas. Synthesis of /V-(4-Chloro-3-((trifluoromethyl)phenyl)-/V’(4-(3-methoxycarbonylphenyl)carboxyaminophenyl) Urea

<img file="CA2359244C_D0065.tif" />

To a solution of JV-(4-chloro-3-((trifluoromethyl)phenyl)-jV'-(4-aminophenyl) urea (Method Cld; 0.050 g, 1.52 mmol), «2O«&lt;?-methyl isophthalate (0.25 g, 1.38 mmol), ΗΟΒΤ·Η₂Ο (0.41 g, 3.03 mmol) and A-methylmorpholine (0.33 mL, 3.03 mmol) in DMF (8 mL) was added EDCI *HC1 (0.29 g, 1.52 mmol). The resulting mixture was stirred at room temp, overnight, diluted with EtOAc (25 mL) and sequentially washed with water (25 mL) and a saturated NaHCO3 solution (25 mL). The organic layer was dried (Na₂SO₄) and concentrated under reduced pressure. The resulting solids were triturated with an EtOAc solution (80% EtOAc/20% hexane) to give N(4-chloro-3-((trifluoromethyl)phenyl)-A’-(4-(315 methoxycarbonylphenyl)carboxyaminophenyl) urea (0.27 g, 43%); mp 121-122; TLC (80% EtOAc/20% hexane) R/0.75.

Dlb. Conversion of ω-Carboxyphenyl Ureas into ω(Arylcarbamoyl)phenyl Ureas. Synthesis of 7V-(4-Chloro-3((trifliioroinethyl)phenyl)-/V’-(4-(3methylcarbamoylphenyl)carbamoylphenyl) Urea

<img file="CA2359244C_D0066.tif" />

To a solution of 7V-(4-chloro-3-((trifluoromethyl)phenyl)-/V'-(4-(3methylcarbamoylphenyl) carboxyaminophenyl) urea (0.14 g, 0.48 mmol), 3methylcarbamoylaniline (0.080 g, 0.53 mmol), ΗΟΒΤ·Η₂Ο (0.14 g, 1.07 mmol),

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PCT/US00/00768 and 77-methylmorpholine (0.5mL, 1.07 mmol) in DMF (3 mL) at 0 °C was added EDCI’HCl (0.10 g, 0.53 mmol). The resulting mixture was allowed to warm to room temp, and was stirred overnight. The resulting mixture was treated with water (lOmL), and extracted with EtOAc (25 mL). The organic phase was concentrated under reduced pressure. The resulting yellow solids were dissolved in EtOAc (3 mL) then filtered through a pad of silica gel (17 g, gradient from 70% EtOAc/30% hexane to 10% MeOH/90% EtOAc) to give 77-(4-chloro-3((trifluoromethyl)phenyl)-77’-(4-(3-methylcarbamoylphenyl) carbamoylphenyl) urea as a white solid (0.097 g, 41%): mp 225-229; TLC (100% EtOAc) R/0.23.

Die. Combinatorial Approach to the Conversion of ω-Carboxyphenyl

Ureas into (û-(Arylcarbamoyl)phenyl Ureas. Synthesis of A'-(4Chloro-3-((trifluoromethyl)phenyI)-7V^,-(4-(N-(3-(N-(3pyridyl)carbamoyl)phenyl)carbamoyl)phenyl) Urea

<img file="CA2359244C_D0067.tif" />

H H

A mixture of 77-(4-chloro-3-((trifluoromethyl)pheny 1)-77 ’-(3-carboxyphenyl) urea (Method Clf; 0.030 g, 0.067 mmol) and 77-cyclohexyl-77’(methylpolystyrene)carbodiimide (55 mg) in 1,2-dichloroethane (1 mL) was treated with a solution of 3-aminopyridine in CH2CI2 (1 M; 0.074 mL, 0.074 mmol). (In cases of insolubility or turbidity, a small amount of DMSO was also added.) The resulting mixture was heated at 36 °C overnight. Turbid reactions were then treated with THF (1 mL) and heating was continued for 18 h. The resulting mixtures were treated with poly(4-(isocyanatomethyl)styrene) (0.040 g) and the resulting mixture was stirred at 36 °C for 72 h, then cooled to room temp, and filtered. The resulting solution was filtered through a plug of silica gel (1 g). Concentration under reduced pressure afforded 77-(4-chloro-3-((trifluoromethyl)phenyl)-77’-(4-(N-(3-(N-(364

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PCT/US00/00768 pyridyl)carbamoyl)phenyl)carbamoyl)phenyl) urea (0.024 g, 59%): TLC (70% EtOAc/30% hexane) R/0.12.

D2. Conversion of ω-Carboalkoxyaryl Ureas into ω-Carbamoylaryl

Ureas. Synthesis of 7V-(4-Chloro-3-((trifluoromethyl)phenyl)-7V’(4-(3-methylcarbamoylphenyi)carboxyaminophenyI) Urea

<img file="CA2359244C_D0068.tif" />

To a sample of /V-(4-chloro-3-((trifluoromethyl)phenyl)-7V’-(4-(3carbomethoxyphenyl) carboxyaminophenyl) urea (0.17 g, 0.34 mmol) was added methylamine (2 M in THF; 1 mL, 1.7 mmol) and the resulting mixture was stirred at room temp, overnight, then concentrated under reduced pressure to give /7-(4chloro-3-((trifluoromethyl)phenyl)-77 ’-(4-(3 methylcarbamoylphenyl)carboxyaminophenyl) urea as a white solid: mp 247; TLC (100% EtOAc) RyO.35.

D3. Conversion of ω-Carboalkoxyaryl Ureas into ω-Carboxyaryl

Ureas. Synthesis of /V-^-Chloro-S-iitrifluoromethyOphenyO-TV’(4-carboxyphenyl) Urea

<img file="CA2359244C_D0069.tif" />

To a slurry of 77-(4-chloro-3-((trifluoromethyl)phenyl)-77’-(4-ethoxycarbonylphenyl) urea (Method Cle; 5.93 g, 15.3 mmol) in MeOH (75 mL) was added an aqueous KOH solution (2.5 N, 10 mL, 23 mmol). The resulting mixture was heated at the reflux temp, for 12 h, cooled to room temp., and concentrated under reduced pressure. The residue was diluted with water (50 mL), then treated with a 1 N HC1 solution to adjust the pH to 2 to 3. The resulting solids were collected and dried

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D4. General Method for the Conversion of ω-Alkoxy Esters into ωAlkyl Amides. Synthesis of A-(4-Chloro-3((trifluoromethyl)phenyI)-/V’-((4-(3-(5-(2dimethylaminoethyl)carbamoyl)pyridyl)oxyphenyl) Urea

<img file="CA2359244C_D0070.tif" />

Step 1. Synthesis of 7V-(4-Chloro-3-(trifluoromethyl)phenyl)-jV’-((4_(3-(5_ carboxypyridyl) oxyphenyl) Urea

A^r-(4-Chloro-3-(trif!uoromethyl)phenyl)-77’-((4-(3-(5-methoxycarbonylpyridyl) oxyphenyl) urea was synthesized from 4-chloro-3-(trifluoromethyl)phenyl isocyanate and 4-(3-(5-methoxycarbonylpyridyl) oxyaniline (Method A14, Step 2) in a manner analogous to Method Cla. A suspension of 7V-(4-chloro-3(trifluoromethyl)phenyl)-A’-((4-(3-(5-methoxycarbonylpyridyl)oxyphenyl) urea (0.26 g, 0.56 mmol) in MeOH (10 mL) was treated with a solution of KOH (0.14 g, 2.5 mmol) in water (1 mL) and was stirred at room temp, for 1 h. The resulting mixture was adjusted to pH 5 with a 1 N HCI solution. The resulting precipitate was removed by filtration and washed with water. The resulting solids were dissolved in EtOH (10 mL) and the resulting solution was concentrated under reduced pressure. The EtOH/concentration procedure was repeated twice to give N(4-chloro-3 -(trifluoromethyl)phenyl)-/V ’-((4-(3-(5 -carboxypyridyl) oxyphenyl) urea (0.18 g, 71%).

<img file="CA2359244C_D0071.tif" />

Step 2. Synthesis of A-(4-chloro-3-(triiluoroniethyl)pheiiyI)-A ’-((4-(3-(5(2-dimethylaminoethyl)carbamoyl)pyridyl)oxyphenyl) urea

A mixture of 7V-(4-chloro-3-(trifluoromethyl)phenyl)-/7’-((4-(3-(5-carboxypyridyl) 25 oxyphenyl) urea (0.050 g, 0.011 mmol), MA-dimethylethylenediamine (0.22 mg,

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0.17 mmol), HOBT (0.028 g, 0.17 mmol), /V-methylmorpholine (0.035 g, 0.28 mmol), and EDCHHCl (0.032 g, 0.17 mmol) in DMF (2.5 mL) was stirred at room temp, overnight. The resulting solution was separated between EtOAc (50 mL) and water (50 mL). The organic phase was washed with water (35 mL), dried (MgSO^ and concentrated under reduced pressure. The residue was dissolved in a minimal amount of CH2CI2 (approximately 2 mL). The resulting solution was treated with Et₂O dropwise to give /V-(4-chloro-3-(trifluoromethyl)phenyl)-/V’-((4-(3-(5-(2dimethylaminoethyl)carbamoyl) pyridyl)oxyphenyl) urea as a white precipitate (0.48 g, 84%: 'H NMR (DMSO-d₆) δ 2.10 s, 6H), 3.26 (s, H), 7.03 (d, 2H), 7.52 (d,

2H), 7.60 (m, 3H), 8.05 (s, 1H), 8.43 (s, 1H), 8.58 (t, 1H), 8.69 (s, 1H), 8.90 (s, 1H),

9.14 (s, 1H); HPLC ES-MS m/z 522 ((M+H)⁺).

D5. General Method for the Deprotection of /Υ-(ω15

Silyloxyalkyl)amides. Synthesis of 7V-(4-ChIoro-3((trifluoroinethyl)phenyl)-A^r’-(4-(4-(2-(A-(2hydroxy)ethylcarbamoyl)pyridyloxyphenyl) Urea.

Cl

To a solution of A-(4-chloro-3-((trifluoromethyl)phenyl)-/V’-(4-(4-(2-(A-(2triisopropylsilyloxy) ethylcarbamoyl)pyridyloxyphenyl) urea (prepared in a manner analogous to Method Cla; 0.25 g, 0.37 mmol) in anh THF (2 mL) was tetrabutylammonium fluoride (1.0 M in THF; 2 mL). The mixture was stirred at room temperature for 5 min, then was treated with water (10 mL). The aqueous mixture was extracted with EtOAc (3x10 mL). The combined organic layers were dried (MgSÛ4) and concentrated under reduced pressure. The residue was purified by column chromatography (S1O2; gradient from 100% hexane to 40% EtOAc/60% hexane) to give A-(4-chloro-3-((trifluoromethyl)phenyl)-A^r’-(4-(4-(2-(/V-(2hydroxy)ethylcarbamoyl) pyridyloxyphenyl) urea as a white solid (0.019 g, 10%).

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Listed below are compounds listed in the Tables below which have been synthesized according to the Detailed Experimental Procedures given above:

Syntheses of Exemplified Compounds (see Tables for compound characterization)

Entry 1: 4-(3-/V-Methylcarbamoylphenoxy)aniline was prepared according to Method A13. According to Method C3, 3-/er/-butylaniline was reacted with bis(trichloromethyl)carbonate followed by 4-(3-/V-Methylcarbamoylphenoxy)aniline to afford the urea.

Entry 2: 4-Fluoro-l-nitrobenzene and p-hydroxyacetophenone were reacted according to Method A13, Step 1 to afford the 4-(4-acetylphenoxy)-l-nitrobenzene. 4-(4-Acetylphenoxy)-1 -nitrobenzene was reduced according to Method A13, Step 4 to afford 4-(4-acetylphenoxy)aniline. According to Method C3, 3-/er/-butylaniline was reacted with bis(trichloromethyl) carbonate followed by 4-(4acetylphenoxy)aniline to afford the urea.

Entry 3: According to Method C2d, 3-/er/-butylaniline was treated with CDI, followed by 4-(3-JV-methylcarbamoyl)-4-methoxyphenoxy)aniline, which had been prepared according to Method A8, to afford the urea.

Entry 4: 5-/e/7-Butyl-2-methoxyaniline was converted to 5-/er/-butyl-2methoxyphenyl isocyanate according to Method BI. 4-(3-/7Methylcarbamoylphenoxy)aniline, prepared according to Method A13, was reacted with the isocyanate according to Method Cla to afford the urea.

Entry 5: According to Method C2d, 5-ier/-butyl-2-methoxyaniline was reacted with CDI followed by 4-(3-/V-methylcarbamoyl)-4-methoxyphenoxy)aniline, which had been prepared according to Method A8, to afford the urea.

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Entry 6: 5-(4-Aminophenoxy)isoindoline-l,3-dione was prepared according to Method A3. According to Method 2d, 5-/er/-butyl-2-methoxyaniline was reacted with CDI followed by 5-(4-aminophenoxy)isoindoline-l,3-dione to afford the urea.

Entry 7: 4-(l-Oxoisoindolin-5-yloxy)aniline was synthesized according to Method A12. According to Method 2d, 5-/er/-butyl-2-methoxyaniline was reacted with CDI followed by 4-(l-oxoisoindolin-5-yloxy)aniline to afford the urea.

Entry 8: 4-(3-/V-Methylcarbamoylphenoxy)aniline was synthesized according to Method A13. According to Method C2a, 2-methoxy-5-(trifluoromethyl)aniline was reacted with CDI followed by 4-(3-/V-methylcarbamoylphenoxy)aniline to afford the urea.

Entry 9: 4-Hydroxyacetophenone was reacted with 2-chloro-5-nitropyridine to give 4-(4-acetylphenoxy)-5-nitropyridine according to Method A3, Step 2. According to Method A8, Step 4, 4-(4-acetylphenoxy)-5-nitropyridine was reduced to 4-(4acetylphenoxy)-5-aminopyridine. 2-Methoxy-5-(trifluoromethyl)aniline was converted to 2-methoxy-5-(trifluoromethyl)phenyl isocyanate according to Method

BI. The isocyanate was reacted with 4-(4-acetylphenoxy)-5-aminopyridine according to Method Cla to afford the urea.

Entry 10: 4-Fluoro-l-nitrobenzene and p-hydroxyacetophenone were reacted according to Method A13, Step 1 to afford the 4-(4-acetylphenoxy)-l-nitrobenzene.

4-(4-Acetylphenoxy)-1 -nitrobenzene was reduced according to Method A13, Step 4 to afford 4-(4-acetylphenoxy)aniline. According to Method C3, 5-(trifluoromethyl)2-methoxybutylaniline was reacted with bis(trichloromethyl) carbonate followed by 4-(4-acetylphenoxy)aniline to afford the urea.

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Entry 11: 4-Chloro-/V-methyl-2-pyridinecarboxamide, which was synthesized according to Method A2, Step 3a, was reacted with 3-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 3-(-2-(77methylcarbamoyl)-4-pyridyloxy)aniline. According to Method C4, 2-methoxy-55 (trifluoromethyl)aniline was reacted with phosgene followed by 3-(-2-(77methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 12: 4-Chloropyridine-2-carbonyl chloride HCI salt was reacted with ammonia according to Method A2, Step 3b to form 4-chloro-2-pyridinecarboxamide. 410 Chloro-2-pyridinecarboxamide was reacted with 3-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 3-(2-carbamoyl-4pyridyloxy)aniline. According to Method C2a, 2-methoxy-5(trifluoromethyl)aniline was reacted with phosgene followed by 3-(2-carbamoyl-4pyridyloxy)aniline to afford the urea.

Entry 13: 4-Chloro-A-methyl-2-pyridinecarboxamide was synthesized according to Method A2, Step 3b. 4-Chloro-/V-methyl-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 4-(2-(A-methylcarbamoyl)-4-pyridyloxy)aniline. According to Method C2a, 220 methoxy-5-(trifluoromethyl)aniline was reacted with CDI followed by 4-(2-(77methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 14: 4-Chloropyridine-2-carbonyl chloride HCI salt was reacted with ammonia according to Method A2, Step 3b to form 4-chloro-2-pyridinecarboxamide. 425 Chloro-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 4-(2-carbamoyl-4pyridyloxy)aniline. According to Method C4, 2-methoxy-5-(trifluoromethyl)aniline was reacted with phosgene followed by 4-(2-carbamoyl-4-pyridyloxy)aniline to afford the urea.

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Entry 15: According to Method C2d, 5-(trifluoromethyl)-2-methoxyaniline was reacted with CDI followed by 4-(3-/7-methylcarbamoyl)-4methoxyphenoxy)aniline, which had been prepared according to Method A8, to afford the urea.

Entry 16: 4-(2-(/7-Methylcarbamoyl)-4-pyridyloxy)-2-methylaniline was synthesized according to Method A5. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. The isocyanate was reacted with 4-(2-(77-methylcarbamoyl)-4pyridyloxy)-2-methylaniline according to Method Clc to afford the urea.

Entry 17: 4-(2-(/7-Methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline was synthesized according to Method A6. 5-(Trifiuoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5-(TrifluoromethyI)-2-methoxyphenyl isocyanate was reacted with 4(2-(?7-methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline according to Method Cla to afford the urea.

Entry 18: According to Method A2, Step 4, 5-amino-2-methylphenol was reacted with 4-chloro-A-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 3-(2-(yV-methylcarbamoyI)-4-pyridyloxy)4-methylaniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 3-(2-(77methylcarbamoyl)-4-pyridyloxy)-4-methylaniline according to Method Cla to afford the urea.

Entry 19: 4-Chloropyridine-2-carbonyl chloride was reacted with ethylamine according to Method A2, Step 3b. The resulting 4-chloro-77-ethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2,

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Step 4 to give 4-(2-(A-ethylcarbamoyl)-4-pyridyloxy)aniline. 5-(Trifluoromethyl)2- methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(2-(/V-ethylcarbamoyl)-4-pyridyloxy)aniline according to Method Cla to afford the urea.

Entry 20: According to Method A2, Step 4, 4-amino-2-chlorophenol was reacted with 4-chloro-jV-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 4-(2-(/V-methylcarbamoyl)-4-pyridyloxy)3- chloroaniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(2-(7/methylcarbamoyl)-4-pyridyloxy)-3-chloroaniline according to Method Cla to afford the urea.

Entry 21: 4-(4-Methylthiophenoxy)-l-nitrobenzene was oxidized according to Method A19, Step 1 to give 4-(4-methylsulfonylphenoxy)-l-nitrobenzene. The nitrobenzene was reduced according to Method A19, Step 2 to give 4-(4methylsulfonylphenoxy)-l-aniline. According to Method Cla, 5-(trifluoromethyl)2-methoxyphenyl isocyanate was reacted with 4-(4-methylsulfonylphenoxy)-laniline to afford the urea.

Entry 22: 4-(3-carbamoylphenoxy)-l-nitrobenzene was reduced to 4-(3carbamoylphenoxy)aniline according to Method A15, Step 4. According to Method Cla, 5-(trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(3carbamoylphenoxy)aniline to afford the urea.

Entry 23: 5-(4-Aminophenoxy)isoindoline-l,3-dione was synthesized according to Method A3. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 573

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Entry 24: 4-Chloropyridine-2-carbonyl chloride was reacted with dimethylamine according to Method A2, Step 3b. The resulting 4-chloro-A,A-dimethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(A,A-dimethylcarbamoyl)-4-pyridyloxy)aniline. 5(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 5-(Trifluoromethyl)-2methoxyphenyl isocyanate was reacted with 4-(2-(AA-dimethylcarbamoyl)-4pyridyloxy)aniline according to Method Cla to afford the urea.

Entry 25: 4-(l-Oxoisoindolin-5-yloxy)aniline was synthesized according to Method A12. 5-(Trifluoromethyl)-2-methoxyaniline was treated with CDI, followed by 4(l-oxoisoindolin-5-yloxy)aniline according to Method C2d to afford the urea.

Entry 26: 4-Hydroxyacetophenone was reacted with 4-fluoronitrobenzene according to Method A13, Step 1 to give 4-(4-acetylphenoxy)nitrobenzene. The nitrobenzene was reduced according to Method A13, Step 4 to afford 4-(4acetylphenoxy)aniline, which was converted to the 4-(4-(1-(Amethoxy)iminoethyl)phenoxyaniline HCl salt according to Method A16. 5(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 5-(Trifluoromethyl)-2methoxyphenyl isocyanate was reacted with 4-(4-(1-(Amethoxy)iminoethyl)phenoxyaniline HCl salt to Method Cla to afford the urea.

Entry 27: 4-ChIoro-A-methylpyridinecarboxamide was synthesized as described in Method A2, Step 3b. The chloropyridine was reacted with 4-aminothiophenol according to Method A2, Step 4 to give 4-(4-(2-(Amethylcarbamoyl)phenylthio)aniline. 5-(Trifluoromethyl)-2-methoxyaniline was

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PCT/US00/00768 converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4(4-(2-(/V-methylcarbamoyl)phenylthio)aniline according to Method Cla to afford the urea.

Entry 28: 5-(4-Aminophenoxy)-2-methylisoindoline-l,3-dione was synthesized according to Method A9. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 5-(410 aminophenoxy)-2-methylisoindoline-l,3-dione according to Method Cla to afford the urea.

Entry 29: 4-Chloro-/V-methylpyridinecarboxamide was synthesized as described in Method A2, Step 3b. The chloropyridine was reacted with 3-aminothiophenol according to Method A2, Step 4 to give 3-(4-(2-(//methylcarbamoyl)phenylthio)aniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 3(4-(2-(/V-methylcarbamoyl)phenylthio)aniline according to Method Cla to afford the urea.

Entry 30: 4-Chloropyridine-2-carbonyl chloride was reacted with isopropylamine according to Method A2, Step 3b. The resulting 4-chloro-//-isopropyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2,

Step 4 to give 4-(2-(A^r-isopropylcarbamoyl)-4-pyridyloxy)aniline. 5(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 5-(Trifluoromethyl)-2methoxyphenyl isocyanate was reacted with 4-(2-(//-isopropylcarbamoyl)-4pyridyloxy)aniline according to Method Cla to afford the urea.

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Entry 31: 4-(3-(5-Methoxycarbonyl)pyridyloxy)aniline was synthesized according to Method A14. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(3-(5methoxycarbonyl)pyridyloxy)aniline according to Method Cla to afford the urea. //-(5 -(Tri fluoromethyl)-2-methoxyphenyl)-// ’-(4-(3 -(5 methoxycarbonylpyridyl)oxy)phenyl) urea was saponified according to Method D4, Step 1, and the corresponding acid was coupled with 4-(2-aminoethyl)morpholine to afford the amide according to Method D4, Step 2.

Entry 32: 4-(3-(5-Methoxycarbonyl)pyridyloxy)aniline was synthesized according to Method A14. 5-(Trifhioromethyl)-2-methoxyaniline was converted into 5(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(3-(5methoxycarbonyl)pyridyloxy)aniline according to Method Cla to afford the urea. //-(5-(Trifluoromethyl)-2-methoxyphenyl)-7/’-(4-(3-(5methoxycarbonylpyridyl)oxy)phenyl) urea was saponified according to Method D4, Step 1, and the corresponding acid was coupled with methylamine according to Method D4, Step 2 to afford the amide.

Entry 33: 4-(3-(5-Methoxycarbonyl)pyridyloxy)aniline was synthesized according to Method A14. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method BI. 5(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(3-(5methoxycarbonyl)pyridyloxy)aniline according to Method Cla to afford the urea. //-(5-(Trifluoromethyl)-2-methoxyphenyl)-//’-(4-(3-(5methoxycarbonylpyridyl)oxy)phenyl) urea was saponified according to Method D4, Step 1, and the corresponding acid was coupled with N,//-dimethylethylenediamine according to Method D4, Step 2 to afford the amide.

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Entry 34: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to

Method Clf to afford A-(5-(trifluoromethyl)-2-methoxyphenyl)-A’-(3carboxyphenyl) urea, which was coupled with 3-aminopyridine according to Method Die.

Entry 35: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All.

5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method Clf to afford A-(5-(trifluoromethyl)-2-methoxyphenyl)-jV’-(3carboxyphenyl) urea, which was coupled with TV-(4-fluorophenyl)piperazine according to Method Die.

Entry 36: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method Clf to afford A-(5-(trifluoromethyl)-2-methoxyphenyl)-A’-(3carboxyphenyl) urea, which was coupled with 4-fluoroaniline according to Method Die.

Entry 37: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method Clf to afford A-(5-(trifluoromethyl)-2-methoxyphenyl)-A’-(377

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PCT/USOO/00768 carboxyphenyl) urea, which was coupled with 4-(dimethylamino)aniline according to Method Die.

Entry 38: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All.

5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method B1. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method Clf to afford A^z-(5-(trifluoromethyl)-2-methoxyphenyl)-A’-(3carboxyphenyl) urea, which was coupled with 5-amino-2-methoxypyridine according to Method Die.

Entry 39: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method Clf to afford /V-(5-(trifluoromethyl)-2-methoxyphenyl)-A’-(3carboxyphenyl) urea, which was coupled with 4-morpholinoaniline according to Method Die.

Entry 40: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method Al 1. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2methoxyphenyl isocyanate according to Method BI. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method Clf to afford A-(5-(trifluoromethyl)-2-methoxyphenyl)-A’~(325 carboxyphenyl) urea, which was coupled with 7V-(2-pyridyl)piperazine according to Method Die.

Entry 41: 4-(3-(7V-Methylcarbamoyl)phenoxy)aniline was synthesized according to Method A13. According to Method C3, 4-chloro-3-(trifluoromethyl)aniline was

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Entry 42: 4-(2-77-Methylcarbamyl-4-pyridyloxy)aniline was synthesized according to Method A2. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4(2-/V-methylcarbamyl-4-pyridyloxy)aniline according to Method Cla to afford the urea.

Entry 43: 4-Chloropyridine-2-carbonyl chloride HC1 salt was reacted with ammonia according to Method A2, Step 3b to form 4-chloro-2-pyridinecarboxamide. 4Chloro-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to form 4-(2-carbamoyl-4-pyridyloxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2carbamoyl-4-pyridyloxy)aniline to afford the urea.

Entry 44: 4-Chloropyridine-2-carbonyl chloride HC1 salt was reacted with ammonia according to Method A2, Step 3b to form 4-chloro-2-pyridinecarboxamide. 4Chloro-2-pyridinecarboxamide was reacted with 3-aminophenol according to Method A2, Step 4 to form 3-(2-carbamoyl-4-pyridyloxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(2carbamoyl-4-pyridyloxy)aniline to afford the urea.

Entry 45: 4-Chloro-7V-methyl-2-pyridinecarboxamide, which was synthesized according to Method A2, Step 3a, was reacted with 3-aminophenol according to Method A2, Step 4 to form 3-(-2-(/V-methylcarbamoyl)-4-pyridyloxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(2-(/V-methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 46: 5-(4-Aminophenoxy)isoindoline-l,3-dione was synthesized according to Method A3. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl

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PCT/USOO/00768 isocyanate was reacted with 5-(4-aminophenoxy)isoindoline-l,3-dione to afford the urea.

Entry 47: 4-(2-(/V-Methylcarbamoyl)-4-pyridyloxy)-2-methylaniline was synthesized according to Method A5. According to Method Clc, 4-chloro-3(trifluoromethyl)phenyl isocyanate was reacted with 5-(4aminophenoxy)isoindoline-l,3-dione to afford the urea.

Entry 48: 4-(3-A-Methylsulfamoyl)phenyloxy)aniline was synthesized according to 10 Method A15. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-yV-methylsulfamoyl)phenyloxy)aniline to afford the urea.

Entry 49: 4-(2-(A-MethyIcarbamoyI)-4-pyridyloxy)-2-chloroaniline was synthesized according to Method A6. According to Method Cla, 4-chloro-3(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(/V-methylcarbamoyl)-4pyridyloxy)-2-chloroaniline to afford the urea.

Entry 50: According to Method A2, Step 4, 5-amino-2-methylphenol was reacted 20 with 4-chloro-A-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 3-(2-(A-methylcarbamoyl)-4-pyridyloxy)4-methylaniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(2-(7V-methylcarbamoyl)-4-pyridyloxy)-4methylaniline to afford the urea.

Entry 51: 4-Chloropyridine-2-carbonyl chloride was reacted with ethylamine according to Method A2, Step 3b. The resulting 4-chloro-/V-ethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(TV-ethylcarbamoyl)-4-pyridyloxy)aniline. According to Method

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Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(//ethylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 52: According to Method A2, Step 4, 4-amino-2-chlorophenol was reacted with 4-chloro-/V-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 4-(2-(//-methylcarbamoyl)-4-pyridyloxy)3-chloroaniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(//-methylcarbamoyl)-4-pyridyloxy)-3chloroaniline to afford the urea.

Entry 53: 4-(4-Methylthiophenoxy)-l-nitrobenzene was oxidized according to Method A19, Step 1 to give 4-(4-methylsulfonylphenoxy)-l-nitrobenzene. The nitrobenzene was reduced according to Method A19, Step 2 to give 4-(4methylsulfonylphenoxy)-l-aniline. According to Method Cla, 4-chloro-3(trifluoromethyl)phenyl isocyanate was reacted with 4-(4-methylsulfonylphenoxy)1-aniline to afford the urea.

Entry 54: 4-Bromobenzenesulfonyl chloride was reacted with methylamine according to Method A15, Step 1 to afford A-methyl-4-bromobenzenesulfonamide. //-Methyl-4-bromobenzenesulfonamide was coupled with phenol according to Method A15, Step 2 to afford 4-(4-(//-methylsulfamoyl)phenoxy)benzene. 4-(4-(//Methylsulfamoyl)phenoxy)benzene was converted into 4-(4-(//methylsulfamoyl)phenoxy)-l-nitrobenzene according to Method A15, Step 3. 4-(4(7/-Methylsulfamoyl)phenoxy)-l -nitrobenzene was reduced to 4-(4-//methylsulfamoyl)phenyloxy)aniline according to Method A15, Step 4. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4(3-//-methylsulfamoyl)phenyloxy)aniline to afford the urea.

Entry 55: 5-Hydroxy-2-methylpyridine was coupled with l-fluoro-4-nitrobenzene according to Method A18, Step 1 to give 4-(5-(2-Methyl)pyridyloxy)-l81

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PCT/US00/00768 nitrobenzene. The methylpyridine was oxidized according to the carboxylic acid, then esterified according to Method A18, Step 2 to give 4-(5-(2methoxycarbonyl)pyridyloxy)-l-nitrobenzene. The nitrobenzene was reduced according the Method A18, Step 3 to give 4-(5-(25 methoxycarbonyl)pyridyloxy)aniline. The aniline was reacted with 4-chloro-3(trifluoromethyl)phenyl isocyanate according to Method Cla to afford the urea.

Entry 56: 5-Hydroxy-2-methylpyridine was coupled with l-fluoro-4-nitrobenzene according to Method A18, Step 1 to give 4-(5-(2-Methyl)pyridyloxy)-l10 nitrobenzene. The methylpyridine was oxidized according to the carboxylic acid, then esterified according to Method A18, Step 2 to give 4-(5-(2methoxycarbonyl)pyridyloxy)-l-nitrobenzene. The nitrobenzene was reduced according the Method A18, Step 3 to give 4-(5-(2methoxycarbonyl)pyridyloxy)aniline. The aniline was reacted with 4-chloro-315 (trifluoromethyl)phenyl isocyanate according to Method Cla to give /V-(4-chloro-3(trifluoromethyl)phenyl)-iV’-(4-(2-(methoxycarbonyl)-5-pyridyloxy)phenyl) urea. The methyl ester was reacted with methylamine according to Method D2 to afford /V-(4-chloro-3-(trifluoromethyl)phenyl)-7V'-(4-(2-(7V-methylcarbamoyl)-5pyridyloxy)phenyl) urea.

Entry 57: A-(4-Chloro-3-(trifluoromethyl)phenyl-A’-(4-aminophenyl) urea was prepared according to Method Cld. A-(4-Chloro-3-(trifluoromethyl)phenyl-/V’-(4aminophenyl) urea was coupled with mono-methyl isophthalate according to Method Dla to afford the urea.

Entry 58: A-(4-Chloro-3-(trifluoromethyl)phenyl-A’-(4-aminophenyl) urea was prepared according to Method Cld. A-(4-Chloro-3-(trifluoromethyl)phenyl-7V’-(4aminophenyl) urea was coupled with mono-methyl isophthalate according to Method Dla to afford 7V-(4-chloro-3-(trifluoromethyl)phenyl-/V’-(4-(330 methoxycarbonylphenyl)carboxyaminophenyl) urea. According to Method D2, N82

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PCT/USOO/0O768 (4-chloro-3-(trifluoromethyl)phenyl-7V-(4-(3methoxycarbonylphenyl)carboxyaminophenyl) urea was reacted with methylamine to afford the corresponding methyl amide.

Entry 59: 4-Chloropyridine-2-carbonyl chloride was reacted with dimethylamine according to Method A2, Step 3b. The resulting 4-chloro-777V-dimethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(77,77-dimethylcarbamoyl)-4-pyridyloxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(210 (7V,7V-dimethylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 60: 4-Hydroxyacetophenone was reacted with 4-fluoronitrobenzene according to Method A13, Step 1 to give 4-(4-acetylphenoxy)nitrobenzene. The nitrobenzene was reduced according to Method 13, Step 4 to afford 4-(4-acetylphenoxy)aniline, which was converted to the 4-(4-( l-(TV-methoxy)iminoethyl) phenoxyaniline HCI salt according to Method A16. According to Method Cla, 4-chloro-3(trifluoromethyl)phenyl isocyanate was reacted with 4-(4-acetylphenoxy)aniline to afford the urea.

Entry 61: 4-(3-Carboxyphenoxy)-l-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with 4(2-aminoethyl)morpholine according to Method A13, Step 3 to give 4-(3-(77(2morpholinylethyl)carbamoyl)phenoxy)-l-nitrobenzene. According to Method A13 Step 4, 4-(3-(7V-(2-morpholinylethyl)carbamoyl)phenoxy)-l-nitrobenzene was reduced to 4-(3-(77(2-morpholinylethyl)carbamoyl)phenoxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3(77(2-morpholinylethyl)carbamoyl)phenoxy)aniline to afford the urea.

Entry 62: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to

Method A13, Step 2. 4-(3-Carboxyphenoxy)-!-nitrobenzene was coupled with 183

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PCT/US00/00768 (2-aminoethyl)piperidine according to Method A13, Step 3 to give 4-(3-(/7-(2piperidylethyl)carbamoyl)phenoxy)-l-nitrobenzene. According to Method A13 Step 4, 4-(3-(/7-(2-piperidylethyl)carbamoyl)phenoxy)-l-nitrobenzene was reduced to 4-(3-(/7-(2-piperidylethyl)carbamoyl)phenoxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(/7-(2piperidylethyl)carbamoyl)phenoxy)aniline to afford the urea.

Entry 63: 4-(3-Carboxyphenoxy)-l -nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-l-nitrobenzene was coupled with tetrahydrofurfurylamine according to Method A13, Step 3 to give 4-(3-(77(tetrahydrofurylmethyl)carbamoyl)phenoxy)-l-nitrobenzene. According to Method A13 Step 4, 4-(3-(/7-(tetrahydrofurylmethyl)carbamoyl)phenoxy)-l-nitrobenzene was reduced to 4-(3-(77-(tetrahydro fury lmethyl)carbamoyl)phenoxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(/7-(tetrahydrofurylmethyl)carbamoyl) phenoxy)aniline to afford the urea.

Entry 64: 4-(3-Carboxyphenoxy)-l -nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-l-nitrobenzene was coupled with 2aminomethyl-l-ethylpyrrolidine according to Method A13, Step 3 to give 4-(3-(/7((l-methylpynOlidinyl)methyl)carbamoyl)phenoxy)-l-nitrobenzene. According to Method A13 Step 4, 4-(3-(77-((l-methylpyrrolidinyl)methyl)carbamoyl)phenoxy)-lnitrobenzene was reduced to 4-(3-(/7-((1methylpyrrolidinyl)methyl)carbamoyl)phenoxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(77-((1methylpyrrolidinyl)methyl)carbamoyl)phenoxy)aniline to afford the urea.

Entry 65: 4-Chloro-/7-methylpyridinecarboxamide was synthesized as described in Method A2, Step 3b. The chloropyridine was reacted with 4-aminothiophenol according to Method A2, Step 4 to give 4-(4-(2-(/784

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Entry 66: 4-Chloropyridine-2-carbonyl chloride was reacted with isopropylamine according to Method A2, Step 3b. The resulting 4-chloro-77-isopropyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(/V-isopropylcarbamoyl)-4-pyridyloxy)aniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(210 (77-isopropylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 67: 77-(4-Chloro-3-(trifluoromethyl)phenyl-77’-(4-ethoxycarbonylphenyl) urea was synthesized according to Method Cle. 77-(4-Chloro-3(trifluoromethyl)phenyl-/7’-(4-ethoxycarbonylphenyl) urea was saponified according to Method D3 to give 77-(4-chloro-3-(trifluoromethyl)phenyl-77’-(4carboxyphenyl) urea. 77-(4-Chloro-3-(trifluoromethyl)phenyl-77’-(4-carboxyphenyl) urea was coupled with 3-methylcarbamoylaniline according to Method Dlb to give /7-(4-chloro-3-(trifluoromethyl)phenyl-77’-(4-(3methylcarbamoylphenyl)carbamoylphenyl) urea.

Entry 68: 5-(4-Aminophenoxy)-2-methylisoindoline-l,3-dione was synthesized according to Method A9. According to Method Cla, 4-chloro-3(trifluoromethyl)phenyl isocyanate was reacted with 5-(4-aminophenoxy)-2methylisoindoline-l,3-dione to afford the urea.

Entry 69: 4-Chloro-/7-methylpyridinecarboxamide was synthesized as described in Method A2, Step 3b. The chloropyridine was reacted with 3-aminothiophenol according to Method A2, Step 4 to give 3-(4-(2-(77methylcarbamoyl)phenylthio)aniline. According to Method Cla, 4-chloro-385

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Entry 70: 4-(2-(77-(2-Morpholin-4-ylethyl)carbamoyl)pyridyloxy)aniline was synthesized according to Method A10. According to Method Cla, 4-chloro-3(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(77-(2-morpholin-4ylethyl)carbamoyl)pyridyloxy)aniline to afford the urea.

Entry 71: 4-(3-(5-Methoxycarbonyl)pyridyloxy)aniline was synthesized according to Method A14. 4-Chloro-3-(trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(3-(5-methoxycarbonyl)pyridyloxy)aniline according to Method Cla to afford the urea. 77-(4-Chloro-3-(trifluoromethyl)phenyl)-77’-(4-(3-(5methoxycarbonylpyridyl) oxy)phenyl) urea was saponified according to Method D4, Step 1, and the corresponding acid was coupled with 4-(2-aminoethyl)morpholine to afford the amide.

Entry 72: 4-(3-(5-Methoxycarbonyl)pyridyloxy)aniline was synthesized according to Method A14. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4(3-(5-methoxycarbonyl)pyridyloxy)aniline according to Method Cla to afford the urea. 77-(5-(Trifluoromethyl)-2-rnethoxyphenyl)-77’-(4-(3-(5methoxycarbonylpyridyl)oxy)phenyl) urea was saponified according to Method D4, Step 1, and the corresponding acid was coupled with methylamine according to Method D4, Step 2 to afford the amide.

Entry 73: 4-(3-(5-Methoxycarbonyl)pyridyloxy)aniline was synthesized according to Method A14. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4(3-(5-methoxycarbonyl)pyridyloxy)aniline according to Method Cla to afford the urea. 77-(5 -(Trifluoromethyl)-2-methoxypheny 1)-77 -(4-(3 -(5methoxycarbonylpyridyl)oxy)phenyl) urea was saponified according to Method D4,

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Step 1, and the corresponding acid was coupled with ////-dimethylethylenediamine according to Method D4, Step 2 to afford the amide.

Entry 74: 4-Chloropyridine-2-carbonyl chloride HCI salt was reacted with 25 hydroxyethylamine according to Method A2, Step 3b to form 4-chloro-7/-(2triisopropylsilyloxy)ethylpyridine-2-carboxamide. 4-Chloro-7/-(2triisopropylsilyloxy)ethylpyridine-2-carboxamide was reacted with triisopropylsilyl chloride, followed by 4-aminophenol according to Method A17 to form 4-(4-(2-(7/(2-triisopropylsilyloxy)ethylcarbamoyl)pyridyloxyaniline. According to Method

Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(4-(2-(7/-(2triisopropylsilyloxy)ethylcarbamoyl) pyridyloxyaniline to afford 7V-(4-chloro-3((trifluoromethyl)phenyl)-/V’-(4-(4-(2-(//-(2-triisopropylsilyloxy) ethylcarbamoyl)pyridyloxyphenyl) urea.

Entry 75: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(5methoxycarbonyl)pyridyloxy)aniline according to Method Clf to afford the urea, which was coupled with 3-aminopyridine according to Method Die.

Entry 76: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 7/-(4-acetylphenyl)piperazine according to Method Die.

Entry 77: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All.

4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 4-fluoroaniline according to Method Die.

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Entry 78: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 4-(dimethylamino)aniline according to Method Die.

Entry 79: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with A-phenylethylenediamine according to Method Die.

Entry 80: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethy l)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 2-methoxyethylamine according to Method Die.

Entry 81: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 5-amino-2-methoxypyridine according to Method Die.

Entry 82: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All. 4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 4-morpholinoaniline according to Method Die.

Entry 83: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method All.

4-Chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3carboxyphenoxy)aniline according to Method Clf to afford the urea, which was coupled with 77-(2-pyridyl)piperazine according to Method Die.

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Entry 84: 4-Chloropyridine-2-carbonyl chloride HCl salt was reacted with 2hydroxyethylamine according to Method A2, Step 3b to form 4-chloro-A-(2triisopropylsilyloxy)ethylpyridine-2-carboxamide. 4-Chloro-A-(2triisopropylsilyloxy)ethylpyridine-2-carboxamide was reacted with triisopropylsilyl chloride, followed by 4-aminophenol according to Method A17 to form 4-(4-(2-(7/(2-triisopropylsilyloxy)ethylcarbamoyl)pyridyloxyaniline. According to Method Cla, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(4-(2-(7/-(2triisopropylsilyloxy)ethylcarbamoyl)pyridyloxyaniline to give A-(4-chloro-3((trifluoromethyl)phenyl)-A’-(4-(4-(2-(A-(2-triisopropylsilyloxy)ethylcarbamoyl) pyridyloxyphenyl) urea. The urea was deprotected according to Method D5 to afford 7/-(4-chloro-3-((trifluoromethyl)phenyl)-7/’-(4-(4-(2-(7/-(2hydroxy)ethylcarbamoyl)pyridyloxyphenyl) urea.

Entry 85: 4-(2-(7/-Methylcarbamoyl)-4-pyridyloxy)aniline was synthesized according to Method A2. 4-Bromo-3-(trifluoromethyl)aniline was converted to 4bromo-3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2(A-methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 86: 4-(2-(A-Methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline was synthesized according to Method A6. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(7/-methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline to afford the urea.

Entry 87: According to Method A2, Step 4, 4-amino-2-chlorophenol was reacted with 4-chloro-A-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 4-(2-(7/-methylcarbamoyl)-4-pyridyloxy)3-chloroaniline. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-389

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Entry 88: 4-Chloropyridine-2-carbonyl chloride was reacted with ethylamine according to Method A2, Step 3b. The resulting 4-chloro-/7-ethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(77-ethylcarbamoyl)-4-pyridyloxy)aniline. 4-Bromo-3(trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(77-ethylcarbamoyl)-4pyridyloxy)aniline to afford the urea.

Entry 89: 4-Chloro-77-methyl-2-pyridinecarboxamide, which was synthesized according to Method A2, Step 3a, was reacted with 3-aminophenol according to Method A2, Step 4 to form 3-(-2-(77-methylcarbamoyl)-4-pyridyloxy)aniline. 4Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-3(trifluoromethyl)phenyl isocyanate according to Method B1. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(-2-(/V20 methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 90: According to Method A2, Step 4, 5-amino-2-methylphenol was reacted with 4-chloro-77-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 3-(2-(77-methylcarbamoyl)-4-pyridyloxy)25 4-methylaniline. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(2(77-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline to afford the urea.

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Entry 91: 4-Chloropyridine-2-carbonyl chloride was reacted with dimethylamine according to Method A2, Step 3b. The resulting 4-chloro-/7,/7-dimethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(77,77-dimethylcarbamoyl)-4-pyridyloxy)aniline. 4-Bromo-35 (trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(77₎77-dimethylcarbamoyl)4-pyridyloxy)aniline to afford the urea.

Entry 92: 4-Chloro-77-methylpyridinecarboxamide was synthesized as described in Method A2, Step 3b. The chloropyridine was reacted with 4-aminothiophenol according to Method A2, Step 4 to give 4-(4-(2-(77methylcarbamoyl)phenylthio)aniline. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method

BI. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(4-(2-(77-methylcarbamoyl)phenylthio)aniline to afford the urea.

Entry 93: 4-Chloro-/7-methylpyridinecarboxamide was synthesized as described in Method A2, Step 3b. The chloropyridine was reacted with 3-aminothiophenol according to Method A2, Step 4 to give 3-(4-(2-(77methylcarbamoyl)phenylthio)aniline. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(4-(2-(77-methylcarbamoyl)phenylthio)aniline to afford the urea.

Entry 94: 4-(2-(77-(2-Morpholin-4-ylethyl)carbamoyl)pyridyloxy)aniline was synthesized according to Method A10. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was

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Entry 95: 4-(2-(A-Methylcarbamoyl)-4-pyridyloxy)aniline was synthesized according to Method A2. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was synthesized according to Method A7. 4-Chloro-2-methoxy-5(trifluoromethyl)aniline was converted into 4-chloro-2-methoxy-5(trifluoromethyl)phenyl isocyanate according to Method BE According to Method Cla, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate was reacted with 410 (2-(7V-methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 96: 4-(2-(jV-Methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline was synthesized according to Method A6. 4-Chloro-2-methoxy-5(trifluoromethyl)aniline was synthesized according to Method A7. 4-Chloro-215 methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2-methoxy-5(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate was reacted with 4(2-(7V-methylcarbamoyl)-4-pyridyloxy)-2-chloroaniline afford the urea.

Entry 97: According to Method A2, Step 4, 4-amino-2-chlorophenol was reacted with 4-chloro-jV-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 4-(2-(/V-methylcarbamoyl)-4-pyridyloxy)3-chloroaniline. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was synthesized according to Method A7. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-chloro-2-methoxy-5(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(/V-methylcarbamoyl)-4pyridyloxy)-3-chloroaniline to afford the urea.

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Entry 98: 4-Chloro-/V-methyl-2-pyridinecarboxamide, which was synthesized according to Method A2, Step 3a, was reacted with 3-aminophenol according to Method A2, Step 4 to form 3-(-2-(//-methylcarbamoyl)-4-pyridyloxy)aniline. 4Chloro-2-methoxy-5-(trifluoromethyl)aniline was synthesized according to Method

A7. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2methoxy-5-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate as was reacted with 3-(-2-(/V-methylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 99: 4-Chloropyridine-2-carbonyl chloride was reacted with ethylamine according to Method A2, Step 3b. The resulting 4-chloro-A-ethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(V-ethylcarbamoyl)-4-pyridyloxy)aniline. 4-Chloro-2-methoxy5-(trifluoromethyl)aniline was synthesized according to Method A7. 4-Chloro-215 methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2-methoxy-5(trifluoromethyl)phenyl isocyanate according to Method B1. According to Method Cla, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate was reacted with 4(2-(yV-ethylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

Entry 100: 4-Chloropyridine-2-carbonyl chloride was reacted with dimethylamine according to Method A2, Step 3b. The resulting 4-chloro-V,/V-dimethyl-2pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(//,//-dimethylcarbamoyl)-4-pyridyloxy)aniline. 4-Chloro-2methoxy-5-(trifluoromethyl)aniline was synthesized according to Method A7. 425 Chloro-2-methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2methoxy-5-(trifluoromethyl)phenyl isocyanate according to Method BI. According to Method Cla, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(7V,7V-dimethylcarbamoyl)-4-pyridyloxy)aniline to afford the urea.

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Entry 101: 2-Amino-3-methoxynaphthalene was synthesized as described in Method Al. According to Method C3, 2-amino-3-methoxynaphthalene was reacted with bis(trichloromethyl) carbonate followed by an aniline to form the urea.

Entry 102: 4-(2-(//-Methylcarbamoyl)-4-pyridyIoxy)aniline was synthesized according to Method A2. 5-/er/-Butyl-2-(2,5-dimethylpyrrolyl)aniline was synthesized according to Method A4. 5-/er/-Butyl-2-(2,5-dimethylpyrrolyl)aniIine was reacted with CDI followed by 4-(2-(//-methylcarbamoyl)-4-pyridyloxy)aniline according to Method C2d to afford the urea.

Entry 103: 4-Chloro-/V-methyl-2-pyridinecarboxamide was synthesized according to Method A2, Step 3b. 4-Chloro-//-methyl-2-pyridinecarboxamide was reacted with

4-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 4-(2-(//-methylcarbamoyl)-4-pyridyloxy)aniline. According to Method C2b, reaction of 3-amino-2-methoxyquinoline with CDI followed by 4-(2-(//20 methylcarbamoyl)-4-pyridyloxy)aniline afforded bis(4-(2-(//-methylcarbamoyl)-4pyridlyoxy)phenyl)urea.

Tables

The compounds listed in Tables 1-6 below were synthesized according to the 25 general methods shown above, and the more detailed exemplary procedures are in the entry listings above and characterizations are indicated in the tables.

Table 1. 3-teri-ButylphenyI Ureas

<img file="CA2359244C_D0072.tif" />

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<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TLC R/</td><td> TLC Solvent System</td><td> Mass Spec. [Source]</td><td> Synth. Method</td>

<td> 1</td><td> 0 y- NH ^Me</td><td></td><td></td><td> 0.22</td><td> 50% EtOAc / 50% hexane</td><td> 418 (M+H)+ (HPLC ES-MS)</td><td> A13 C3</td>

<td> 2</td><td></td><td></td><td></td><td> 0.58</td><td> 50% EtOAc / 50% hexane</td><td> 403 (M+H)+ (HPLC ES-MS)</td><td> A13 C3</td>

<td> 3</td><td> 0 y—NH</td><td> 133- 135</td><td></td><td> 0.68</td><td> 100% EtOAc</td><td> 448 (M+H)+ (FAB)</td><td> A8 C2d</td>

Table 2. 5-ier/-Butyl-2-methoxyphenyl Ureas

<img file="CA2359244C_D0073.tif" />

<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TL CR_r</td><td> TLC Solvent System</td><td> Mass Spec. [Source]</td><td> Synth. Method</td>

<td> 4</td><td> O K-NH ^Me</td><td></td><td> 5.93</td><td></td><td></td><td> 448 (M+H)+ (HPLC ES-MS)</td><td> A13 Bl Cla</td>

<td> 5</td><td> 0 Vnh</td><td> 120- 122</td><td></td><td> 0.67</td><td> 100% EtOAc</td><td> 478 (M+H)+ (FAB)</td><td> A8 C2d</td>

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<td> 6</td><td> v^NH 0</td><td></td><td></td><td> 0.40</td><td> 50% EtOAc I 50% hexane</td><td> 460 (M+H)+ (HPLC ES-MS)</td><td> A3 C2d</td>

<td> 7</td><td> Vnh</td><td></td><td></td><td> 0.79</td><td> 50% EtOAc / 50% hexane</td><td> 446 (M+H)+ (HPLC ES-MS)</td><td> A12 C2d</td>

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Table 3.

5-(TrifluoromethyI)-2-methoxyphenyI Ureas

<img file="CA2359244C_D0074.tif" />

F

F

Ο

<img file="CA2359244C_D0075.tif" />

OMe

<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TLC R/</td><td> TLC Solvent System</td><td> Mass Spec. [Source^</td><td> Synth. Method</td>

<td> 8</td><td> 0 y—NH ^Me</td><td> 250 (dec)</td><td></td><td></td><td></td><td> 460 (M+H)+ (FAB)</td><td> A13 C2a</td>

<td> 9</td><td></td><td> 206- 208</td><td></td><td> 0.54</td><td> 10% MeOH/ 90% CH2C12</td><td> 446 (M+H)+ (HPLC ES-MS)</td><td> A3 step 2, A8 step 4, BI, Cla</td>

<td> 10</td><td></td><td></td><td></td><td> 0.33</td><td> 50% EtOAc/ 50% pet ether</td><td> 445 (M+H)+ (HPLC ES-MS)</td><td> A13 C3</td>

<td> 11</td><td> -/Λ Vnh Me ^ov</td><td></td><td></td><td> 0.20</td><td> 2% Et3N/ 98% EtOAc</td><td> 461 (M+H)+ (HPLC ES-MS)</td><td> A2 C4</td>

<td> 12</td><td></td><td></td><td></td><td> 0.27</td><td> 1% Et3N/ 99% EtOAc</td><td> 447 (M+H)+ (HPLC ES-MS)</td><td> A2 C4</td>

<td> 13</td><td> 0 y—NH x-o^Μθ</td><td></td><td></td><td> 0.62</td><td> 100% EtOAc</td><td> 461 (M+H)+ (FAB)</td><td> A2 C2a</td>

<td> 14</td><td> 0 y—nh₂</td><td> 114- 117</td><td></td><td> 0.40</td><td> 1% Et3N/ 99% EtOAc</td><td> 447 (M+H)+ (FAB)</td><td> A2 C4</td>

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<td> 15</td><td> -o</td><td> 0</td><td> -ΝΗ Me OMe</td><td> 232- 235</td><td></td><td> 0.54</td><td> 100% EtOAc</td><td> 490 (M+H)+ (FAB)</td><td> A8 C2d</td>

<td> 16</td><td></td><td> 0</td><td></td><td> 210-</td><td></td><td> 0.29</td><td> 5%</td><td> 475</td><td> A5</td>

<td></td><td> Me</td><td></td><td> -NH</td><td> 213</td><td></td><td></td><td> MeOH/</td><td> (M+H)+</td><td> B1</td>

<td></td><td></td><td> /=\</td><td> Me</td><td></td><td></td><td></td><td> 45%</td><td> (HPLC</td><td> Clc</td>

<td></td><td> —C V—o-</td><td></td><td></td><td></td><td></td><td></td><td> EtOAc/ 50% pet ether</td><td> ES-MS)</td><td></td>

<td> 17</td><td></td><td> 0</td><td></td><td> 187-</td><td></td><td> 0.17</td><td> 50%</td><td> 495</td><td> A6</td>

<td></td><td> Cl \_</td><td></td><td> NH</td><td> 188</td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> B1</td>

<td></td><td></td><td rowspan="2"> π</td><td> Me</td><td></td><td></td><td></td><td> 50% pet</td><td> (HPLC</td><td> Cla</td>

<td></td><td> — rara·</td><td></td><td></td><td></td><td></td><td> ether</td><td> ES-MS)</td><td></td>

<td> 18</td><td rowspan="2"> -/Vh</td><td> 0</td><td></td><td></td><td></td><td> 0.48</td><td> 100%</td><td> 475</td><td> A2 step</td>

<td></td><td colspan="2"> /le &gt;-ΝΗ₂</td><td></td><td></td><td></td><td> EtOAc</td><td> (M+H)+</td><td> 4,</td>

<td></td><td rowspan="2"> o—</td><td></td><td></td><td></td><td></td><td></td><td></td><td> (HPLC</td><td> B1</td>

<td></td><td> W</td><td></td><td></td><td></td><td></td><td></td><td> ES-MS)</td><td> Cla</td>

<td> 19</td><td></td><td> 0</td><td></td><td> 194-</td><td></td><td> 0.31</td><td> 5%</td><td> 475</td><td> A2</td>

<td></td><td></td><td></td><td rowspan="2"> -NH Et</td><td> 196</td><td></td><td></td><td> MeOH/</td><td> (M+H)+</td><td> B1</td>

<td rowspan="2"></td><td rowspan="2"> —</td><td rowspan="2"> Ό</td><td rowspan="2"></td><td rowspan="2"></td><td rowspan="2"></td><td rowspan="2"> 45% EtOAc/ 50% pet ether</td><td rowspan="2"> (HPLC ES-MS)</td><td rowspan="2"> Cla</td>

<td></td>

<td> 20</td><td></td><td> 0</td><td></td><td> 214-</td><td></td><td> 0.25</td><td> 5%</td><td> 495</td><td> A2</td>

<td></td><td> Cl _/</td><td></td><td> NH</td><td> 216</td><td></td><td></td><td> MeOH/</td><td> (M+H)+</td><td> Cla</td>

<td></td><td> O-°-</td><td> Ό</td><td> Me</td><td></td><td></td><td></td><td> 45% EtOAc/ 50% pet ether</td><td> (HPLC ES-MS)</td><td></td>

<td> 21</td><td></td><td colspan="2"> F—\ θ OJ!</td><td> 208- 210</td><td></td><td> 0.30</td><td> 50% EtOAc/ 50%</td><td> 481 (M+H)+ (HPLC</td><td> A19 C2a</td>

<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> hexane</td><td> ES-MS)</td><td></td>

<td> 22</td><td></td><td>^ΟΛ</td><td></td><td> 188-</td><td></td><td> 0.30</td><td> 70%</td><td> 447</td><td> A15,</td>

<td></td><td></td><td> y</td><td> NH₂</td><td> 190</td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> step 4,</td>

<td></td><td> -Fu-</td><td> -Ό</td><td></td><td></td><td></td><td></td><td> 50% hexane</td><td> (HPLC ES-MS)</td><td> Cla</td>

<td> 23</td><td> -QU-</td><td></td><td></td><td></td><td></td><td> 0.50</td><td> 70% EtOAc/</td><td> 472 (M+H)+</td><td> A3 B1</td>

<td></td><td></td><td> Υ</td><td> NH</td><td></td><td></td><td></td><td> 30%</td><td> (FAB)</td><td> Cla</td>

<td></td><td></td><td> II 0</td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td></td>

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<td> 24</td><td> 0 Me</td><td> 203- 205</td><td></td><td> 0.13</td><td> 100% EtOAc</td><td> 479 (M+H)+ (HPLC ES-MS)</td><td> A2 BI Cla</td>

<td> 25</td><td></td><td></td><td></td><td> 0.09</td><td> 75% EtOAc/ 25% hexane</td><td> 458 (M+H)+ (HPLC ES-MS)</td><td> A12 C2d</td>

<td> 26</td><td> MeO</td><td> 169- 171</td><td></td><td> 0.67</td><td> 50% EtOAc/ 50% pet ether</td><td> 474 (M+H)+ (HPLC ES-MS)</td><td> A13 stepl, A13 step 4, A16, BI Cla</td>

<td> 27</td><td> 0 /—NH _/ΓΛ_ /=/ ^Μθ</td><td> 218- 219</td><td></td><td> 0.40</td><td> 50% EtOAc/ 50% pet ether</td><td> 477 (M+H)+ (HPLC ES-MS)</td><td> A2 step 3b, A2 step 4, BI, Cla</td>

<td> 28</td><td> X^NMe 0</td><td> 212- 214</td><td></td><td> 0.30</td><td> 40% EtOAc/ 60% hexane</td><td></td><td> A9 BI Cla</td>

<td> 29</td><td> -ΖΛ Vnh r={ Me ^s_w</td><td></td><td></td><td> 0.33</td><td> 50% EtOAc/ 50% pet ether</td><td> 474 (M+H)+ (HPLC ES-MS)</td><td> A2 step 3b, A2 step 4, BI, Cla</td>

<td> 30</td><td> O V- NH ^Pr</td><td> 210- 211</td><td></td><td></td><td></td><td></td><td> A2 BI Cla</td>

<td> 31</td><td> 0 &gt;NH -o°&lt;? n</td><td> 210- 204</td><td></td><td> 0.43</td><td> 10% MeOH/ CH2C12</td><td></td><td> A14 BI Cla D4</td>

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<td rowspan="3"> 32</td><td rowspan="3"> o</td><td colspan="3"> 0</td><td rowspan="3"> 247- 249</td><td rowspan="3"></td><td rowspan="3"> 0.57</td><td rowspan="3"> 10% MeOH/ CH2C12</td><td rowspan="3"></td><td rowspan="3"> A14 BI Cla D4</td>

<td rowspan="2"></td><td colspan="2"> ONH</td>

<td> /) N</td><td> Me</td>

<td> 33</td><td></td><td> 0</td><td></td><td></td><td> 217-</td><td></td><td> 0.07</td><td> 10%</td><td></td><td> A14</td>

<td></td><td></td><td></td><td> NH</td><td></td><td> 219</td><td></td><td></td><td> MeOH/</td><td></td><td> BI</td>

<td></td><td></td><td> Ό</td><td colspan="2"> N-Me Me⁷</td><td></td><td></td><td></td><td> CH2C12</td><td></td><td> Cla D4</td>

<td> 34</td><td></td><td> 0</td><td></td><td></td><td></td><td></td><td> 0.11</td><td> 70%</td><td></td><td> All</td>

<td></td><td></td><td></td><td colspan="2"> 7-NH</td><td></td><td></td><td></td><td> EtOAc/</td><td></td><td> BI</td>

<td></td><td rowspan="2"> O'</td><td> /=k</td><td colspan="2"> .</td><td></td><td></td><td></td><td> 30%</td><td></td><td> Clf</td>

<td></td><td>^&gt;VJ</td><td></td><td> N</td><td></td><td></td><td></td><td> hexane</td><td></td><td> Die</td>

<td> 35</td><td></td><td></td><td></td><td></td><td></td><td></td><td> 0.38</td><td> 70%</td><td></td><td> All</td>

<td></td><td></td><td> )=\</td><td></td><td></td><td></td><td></td><td></td><td> EtOAc/</td><td></td><td> BI</td>

<td></td><td></td><td> w</td><td></td><td></td><td></td><td></td><td></td><td> 30%</td><td></td><td> Clf</td>

<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td> Die</td>

<td></td><td></td><td> N ί</td><td> -N &gt;</td><td> =0</td><td></td><td></td><td></td><td></td><td></td><td></td>

<td></td><td> o</td><td> -°-f</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>

<td> 36</td><td></td><td rowspan="2"> o</td><td rowspan="2"> -NH</td><td></td><td></td><td></td><td> 0.77</td><td> 70%</td><td></td><td> All</td>

<td></td><td> F-</td><td></td><td></td><td></td><td></td><td> EtOAc/</td><td></td><td> BI</td>

<td></td><td></td><td></td><td> y</td><td> =0</td><td></td><td></td><td></td><td> 30%</td><td></td><td> Clf</td>

<td></td><td> -0</td><td></td><td> J</td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td> Die</td>

<td> 37</td><td> Me</td><td rowspan="2"> o</td><td></td><td></td><td></td><td></td><td> 0.58</td><td> 70%</td><td></td><td> All</td>

<td></td><td> N-</td><td> -NH</td><td></td><td></td><td></td><td></td><td> EtOAc/</td><td></td><td> BI</td>

<td></td><td> Me⁷</td><td></td><td> y</td><td> =O</td><td></td><td></td><td></td><td> 30%</td><td></td><td> Clf</td>

<td></td><td> o</td><td></td><td> 1</td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td> Die</td>

<td> 38</td><td></td><td rowspan="2"> /0</td><td></td><td></td><td></td><td></td><td> 0.58</td><td> 70%</td><td></td><td> All</td>

<td></td><td> MeO-</td><td> -NH</td><td></td><td></td><td></td><td></td><td> EtOAc/</td><td></td><td> BI</td>

<td></td><td></td><td></td><td> y</td><td> =0</td><td></td><td></td><td></td><td> 30%</td><td></td><td> Clf</td>

<td></td><td> o</td><td></td><td> 1</td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td> Die</td>

<td> 39</td><td></td><td rowspan="2"> o</td><td rowspan="2"> -NH</td><td></td><td></td><td></td><td> 0.17</td><td> 70%</td><td></td><td> All</td>

<td></td><td> 0 N-</td><td></td><td></td><td></td><td></td><td> EtOAc/</td><td></td><td> BI</td>

<td></td><td></td><td></td><td> y</td><td> =o</td><td></td><td></td><td></td><td> 30%</td><td></td><td> Clf</td>

<td></td><td> o</td><td> °-C</td><td> 1</td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td> Die</td>

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<img file="CA2359244C_D0076.tif" />

Table 4.

3-(Trifluoromethyl)-4-chlorophenyl Ureas

<img file="CA2359244C_D0077.tif" />

<img file="CA2359244C_D0078.tif" />

<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TLC R/</td><td> I TLC Solvent System</td><td> Mass Spec. [Source]</td><td> Synth. Method</td>

<td> 41</td><td> 0 Vnh</td><td> 163- 165</td><td></td><td> 0.08</td><td> 50% EtOAc/ 50% pet ether</td><td> 464 (M+H)+ (HPLC ES-MS)</td><td> A13 C3</td>

<td> 42</td><td> 0 Vnh</td><td> 215</td><td></td><td> 0.06</td><td> 50% EtOAc/ 50% pet ether</td><td> 465 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 43</td><td> 0 V nh₂ VVⁿ</td><td></td><td></td><td> 0.10</td><td> 50% EtOAc/ 50% pet ether</td><td> 451 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 44</td><td> —((( Tnh₂ °-O</td><td></td><td></td><td> 0.25</td><td> 30% EtOAc/ 70% pet ether</td><td> 451 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 45</td><td> -ZV Vnh /V Me °Λ/</td><td></td><td></td><td> 0.31</td><td> 30% EtOAc/ 70% pet ether</td><td> 465 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 46</td><td> Y^NH ο 1</td><td> 176- 179</td><td></td><td> 0.23</td><td> 40% EtOAc/ 60% hexane</td><td> 476 (M+H)+ (FAB)</td><td> A3 Cla</td>

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<td> 47</td><td> 0 Me V-NH \—. /=&lt; Me</td><td></td><td></td><td> 0.29</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 478 (M+H)+ (HPLC ES-MS)</td><td> A5 Clc</td>

<td> 48</td><td> Ox //° S-NH -o-°A </td><td> 206- 209</td><td></td><td></td><td></td><td></td><td> A15 Cla</td>

<td> 49</td><td> 0 Cl V—NH //</td><td> 147- 151</td><td></td><td> 0.22</td><td> 50% EtOAc/ 50% pet ether</td><td> 499 (M+H)+ (HPLC ES-MS)</td><td> A6 Cla</td>

<td> 50</td><td> —/ y—Me VNH r=f Me °W</td><td></td><td></td><td> 0.54</td><td> 100% EtOAc</td><td> 479 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 51</td><td> 0 V-NH -CA-w</td><td> 187- 189</td><td></td><td> 0.33</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 479 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 52</td><td> 0 Cl y- NH // “</td><td> 219</td><td></td><td> 0.18</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 499 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 53</td><td> -00¾</td><td> 246- 248</td><td></td><td> 0.30</td><td> 50% EtOAc/ 50% hexane</td><td> 485 (M+H)+ (HPLC ES-MS)</td><td> A19, Cla</td>

<td> 54</td><td> 00¾ Me</td><td> 196- 200</td><td></td><td> 0.30</td><td> 70% EtOAc/ 30% hexane)</td><td> 502 (M+H)+ (HPLC ES-MS)</td><td> A15 Cla</td>

<td> 55</td><td> 0 OO</td><td> 228- 230</td><td></td><td> 0.30</td><td> 30% EtOAc/ 70% CH2C12</td><td> 466 (M+H)+ (HPLC ES-MS)</td><td></td>

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<td> 56</td><td> Me</td><td> 238- 245</td><td></td><td></td><td></td><td></td><td></td>

<td> 57</td><td></td><td> 221- 222</td><td></td><td> 0.75</td><td> 80% EtOAc/ 20% hexane</td><td> 492 (M+H)+ (FAB)</td><td> Cld Dla</td>

<td> 58</td><td> 0 y- NH ^Me</td><td> 247</td><td></td><td> 0.35</td><td> 100% EtOAc</td><td></td><td> Cld Dla D2</td>

<td> 59</td><td> 0 Me</td><td> 198- 200</td><td></td><td> 0.09</td><td> 100% EtOAc</td><td> 479 (M+H)+ (HPLC ES-MS)</td><td> A2 Cla</td>

<td> 60</td><td> MeO</td><td> 158- 160</td><td></td><td> 0.64</td><td> 50% EtOAc/ 50% pet ether</td><td></td><td></td>

<td> 61</td><td> 0 y- NH “Cym? %o</td><td> 195- 197</td><td></td><td> 0.39</td><td> 10% MeOH/ CH2C1 2</td><td></td><td> A13 Cla</td>

<td> 62</td><td> o y- NH</td><td> ΠΟ- 172</td><td></td><td> 0.52</td><td> 10% MeOH/ CH2C1 2</td><td></td><td> A13 Cla</td>

<td> 63</td><td> 0 %NH</td><td> 168- 171</td><td></td><td> 0.39</td><td> 10% MeOH/ CH2C1 2</td><td></td><td> A13 Cla</td>

<td> 64</td><td> 0 ^Et' y—NH %</td><td> 176- 177</td><td></td><td> 0.35</td><td> 10% MeOH/ CH2C1 2</td><td></td><td> A13 Cla</td>

<td> 65</td><td> 0 y- NH ^Me</td><td> BO- 133</td><td></td><td></td><td></td><td> 487 (M+H)+ (HPLC ES-MS)</td><td> A2 BI Cla</td>

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<td> 66</td><td> -o</td><td></td><td> 0 N /J</td><td> -NH Rr-i</td><td> 155</td><td></td><td></td><td></td><td></td><td> A2 Cla</td>

<td> 67</td><td></td><td></td><td> o_x</td><td></td><td> 225-</td><td></td><td> 0.23</td><td> 100%</td><td></td><td> Cle</td>

<td></td><td></td><td></td><td></td><td> NH</td><td> 229</td><td></td><td></td><td> EtOAc</td><td></td><td> D3</td>

<td></td><td colspan="2"></td><td> d</td><td> Me</td><td></td><td></td><td></td><td></td><td></td><td> Dlb</td>

<td> 68</td><td> --Q—</td><td> -&lt;</td><td></td><td></td><td> 234- 236</td><td></td><td> 0.29</td><td> 40% EtOAc/</td><td></td><td> A9 Cla</td>

<td></td><td></td><td></td><td> V</td><td> -NMe</td><td></td><td></td><td></td><td> 60%</td><td></td><td></td>

<td></td><td></td><td></td><td> II 0</td><td></td><td></td><td></td><td></td><td> hexane</td><td></td><td></td>

<td> 69</td><td rowspan="2"> 0}</td><td></td><td> O_K</td><td></td><td></td><td></td><td> 0.48</td><td> 50%</td><td> 481</td><td></td>

<td></td><td></td><td colspan="2"> y—NH</td><td></td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td></td>

<td></td><td></td><td></td><td rowspan="2"></td><td> Me</td><td></td><td></td><td></td><td> 50% pet</td><td> (HPLC</td><td></td>

<td></td><td> s—</td><td> v</td><td></td><td></td><td></td><td></td><td> ether</td><td> ES-MS)</td><td></td>

<td> 70</td><td></td><td> 0,</td><td></td><td></td><td></td><td></td><td> 0.46</td><td> 5%</td><td> 564</td><td> A10</td>

<td></td><td></td><td></td><td> NH</td><td></td><td></td><td></td><td></td><td> MeOH/</td><td> (M+H)+</td><td> Cla</td>

<td></td><td> —dd~°~d</td><td colspan="2"> J^N</td><td> N—\ 0 \_O</td><td></td><td></td><td></td><td> 95% CH2C12</td><td> (HPLC ES-MS)</td><td></td>

<td> 71</td><td></td><td> o_x</td><td></td><td></td><td> 199-</td><td></td><td> 0.50</td><td> 10%</td><td></td><td> A14</td>

<td></td><td> -</td><td></td><td> &gt;—NH</td><td></td><td> 201</td><td></td><td></td><td> MeOH/</td><td></td><td> Cla</td>

<td></td><td> 000</td><td> // —N</td><td></td><td> N—\ Q</td><td></td><td></td><td></td><td> CH2C1 2</td><td></td><td> D4</td>

<td> 72</td><td></td><td></td><td> O</td><td></td><td> 235-</td><td></td><td> 0.55</td><td> 10%</td><td></td><td> A14</td>

<td></td><td></td><td></td><td></td><td> -NH</td><td> 237</td><td></td><td></td><td> MeOH/</td><td></td><td> Cla</td>

<td></td><td> -o°-</td><td> Λ</td><td> /) —N</td><td> Me</td><td></td><td></td><td></td><td> CH2C1 2</td><td></td><td> D4</td>

<td> 73</td><td></td><td> o_s</td><td></td><td></td><td> 200-</td><td></td><td> 0.21</td><td> 50%</td><td></td><td> A14</td>

<td></td><td></td><td></td><td> NH</td><td></td><td> 201</td><td></td><td></td><td> MeOH/</td><td></td><td> Cla</td>

<td></td><td> -(M</td><td> }/ —N</td><td colspan="2"> N-Me Me</td><td></td><td></td><td></td><td> CH2C1 2</td><td></td><td> D4</td>

<td> 74</td><td></td><td> °_x</td><td></td><td></td><td> 145-</td><td></td><td></td><td></td><td></td><td></td>

<td></td><td></td><td> λ</td><td> -NH</td><td></td><td> 148</td><td></td><td></td><td></td><td></td><td></td>

<td></td><td rowspan="2"> 04</td><td> j</td><td></td><td> OSi(Pr-i)₃</td><td></td><td></td><td></td><td></td><td></td><td></td>

<td></td><td> N</td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>

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<td> 75</td><td> \=/ \=_O</td><td></td><td></td><td> 0.12</td><td> 70% EtOAc/ 30% hexane</td><td> 527 (M+H)+ (HPLC ES-MS)</td><td> All Clf Die</td>

<td> 76</td><td> 0 Me</td><td></td><td></td><td> 0.18</td><td> 70% EtOAc/ 30% hexane</td><td></td><td> All Clf Die</td>

<td> 77</td><td> )=o</td><td></td><td></td><td> 0.74</td><td> 70% EtOAc/ 30% hexane</td><td></td><td> All Clf Die</td>

<td> 78</td><td>^Me-_N ®y_NH Me /)=°</td><td></td><td></td><td> 0.58</td><td> 70% EtOAc/ 30% hexane</td><td></td><td> All Clf Die</td>

<td> 79</td><td> 0 V—NH ~O°Tj Λη o</td><td></td><td></td><td> 0.47</td><td> 70% EtOAc/ 30% hexane</td><td> 569 (M+H)+ (HPLC ES-MS)</td><td> All Clf Die</td>

<td> 80</td><td> 0 Vnh ^0Me</td><td></td><td></td><td> 0.18</td><td> 70% EtOAc/ 30% hexane</td><td> 508 (M+H)+ (HPLC ES-MS)</td><td> All Clf Die</td>

<td> 81</td><td> MeO——NH \=/ ^=0 -£Τ°-Ο</td><td></td><td></td><td> 0.58</td><td> 70% EtOAc/ 30% hexane</td><td> 557 (M+H)+ (HPLC ES-MS)</td><td> All Clf Die</td>

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<td rowspan="2"> 82</td><td colspan="2"> °\ ^NV-</td><td rowspan="2"></td><td rowspan="2"></td><td rowspan="2"> 0.37</td><td rowspan="2"> 70% EtOAc/ 30% hexane</td><td rowspan="2"> 611 (M+H)+ (HPLC ES-MS)</td><td rowspan="2"> All Clf Die</td>

<td></td><td> -d</td>

<td> 83</td><td> c</td><td rowspan="2"> d -d</td><td></td><td></td><td> 0.19</td><td> 70% EtOAc/ 30% hexane</td><td></td><td> All Clf Die</td>

<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td>

<td> 84</td><td></td><td> 0 V—NH N OH</td><td> 179- 183</td><td></td><td></td><td></td><td></td><td> A2 A17 Cla D5</td>

Table 5. 3-(Trifluoromethyl)-4-bromophenyl Ureas

<img file="CA2359244C_D0079.tif" />

<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TLC R/</td><td> TLC Solvent System</td><td> Mass Spec. [Source]</td><td> Synth. Method</td>

<td> 85</td><td> 0 V—nh</td><td> 186- 187</td><td></td><td> 0.13</td><td> 50% EtOAc/ 50% pet ether</td><td> 509 (M+H)+ (HPLC ES-MS)</td><td> A2 BI Cla</td>

<td> 86</td><td> 0 ci Lnh</td><td> ISO- 152</td><td></td><td> 0.31</td><td> 50% EtOAc/ 50% pet ether</td><td> 545 (M+H)+ (HPLC ES-MS)</td><td> A6 BI Cla</td>

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<td rowspan="3"> 87</td><td colspan="3"> 0</td><td rowspan="3"> 217- 219</td><td rowspan="3"></td><td rowspan="3"> 0.16</td><td rowspan="3"> 50% EtOAc/ 50% pet ether</td><td rowspan="3"> 545 (M+H)+ (HPLC ES-MS)</td><td rowspan="3"> A2 Bl Cla</td>

<td colspan="2"> ci /-</td><td rowspan="2"> -NH Me</td>

<td> -0-0.</td><td> -O</td>

<td> 88</td><td></td><td> 0</td><td></td><td> 183-</td><td></td><td> 0.31</td><td> 50%</td><td> 525</td><td> A2</td>

<td></td><td></td><td></td><td> -NH</td><td> 184</td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> Bl</td>

<td></td><td> ο»</td><td> -o</td><td> Et</td><td></td><td></td><td></td><td> 50% pet ether</td><td> (HPLC ES-MS)</td><td> Cla</td>

<td> 89</td><td rowspan="2"> -n</td><td> 0</td><td></td><td></td><td></td><td> 0.21</td><td> 50%</td><td> 511</td><td> A2</td>

<td></td><td colspan="2"> /-NH</td><td></td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> Bl</td>

<td></td><td> M</td><td> /=0</td><td> Me</td><td></td><td></td><td></td><td> 50% pet</td><td> (HPLC</td><td> Cla</td>

<td></td><td> o—</td><td> V/</td><td></td><td></td><td></td><td></td><td> ether</td><td> ES-MS)</td><td></td>

<td> 90</td><td rowspan="2"> -o</td><td> 0</td><td></td><td></td><td></td><td> 0.28</td><td> 50%</td><td> 525</td><td> A2</td>

<td></td><td colspan="2"> /Ie /-NH</td><td></td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> Bl</td>

<td></td><td></td><td></td><td> Me</td><td></td><td></td><td></td><td> 50% pet</td><td> (HPLC</td><td> Cla</td>

<td></td><td> o—</td><td> w</td><td></td><td></td><td></td><td></td><td> ether</td><td> ES-MS)</td><td></td>

<td> 91</td><td></td><td> 0</td><td> Me</td><td> 214-</td><td></td><td> 0.28</td><td> 50%</td><td> 522</td><td> A2</td>

<td></td><td></td><td></td><td> -N</td><td> 216</td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> Bl</td>

<td></td><td></td><td></td><td> Me</td><td></td><td></td><td></td><td> 50% pet ether</td><td> (HPLC ES-MS)</td><td> Cla</td>

<td> 92</td><td></td><td> 0</td><td></td><td></td><td></td><td> 0.47</td><td> 50%</td><td> 527</td><td> A2 step</td>

<td></td><td></td><td></td><td> -NH</td><td></td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> 3b,</td>

<td></td><td> -O</td><td> O¹</td><td> Me</td><td></td><td></td><td></td><td> 50% pet ether</td><td> (HPLC ES-MS)</td><td> A2 step 4, Bl, Cla</td>

<td> 93</td><td rowspan="2"></td><td> o</td><td></td><td></td><td></td><td> 0.46</td><td> 50%</td><td> 527</td><td> A2 step</td>

<td></td><td colspan="2"> /-NH</td><td></td><td></td><td></td><td> EtOAc/</td><td> (M+H)+</td><td> 3b,</td>

<td></td><td> M</td><td></td><td> Me</td><td></td><td></td><td></td><td> 50% pet</td><td> (HPLC</td><td> A2 step</td>

<td></td><td> s—</td><td></td><td></td><td></td><td></td><td></td><td> ether</td><td> ES-MS)</td><td> 4,</td>

<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> Bl,</td>

<td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td></td><td> Cla</td>

<td> 94</td><td></td><td> 0</td><td></td><td> 145-</td><td></td><td> 0.41</td><td> 5%</td><td></td><td> A10</td>

<td></td><td></td><td> &gt;-NH</td><td></td><td> 150</td><td></td><td></td><td> MeOH/</td><td></td><td> Bl</td>

<td></td><td></td><td> 7ⁿ</td><td> o ^-0</td><td></td><td></td><td></td><td> 95% CH2C12</td><td></td><td> Cla</td>

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Table 6. 5-(Trifluoromethvl)-4-chloro-2-methoxyphenyl

Ureas

<img file="CA2359244C_D0080.tif" />

<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TLC R/</td><td> TLC Solvent System</td><td> Mass Spec. [Source]</td><td> Synth. Method</td>

<td> 95</td><td> 0 y- NH -O-O-0 </td><td> MO- 144</td><td></td><td> 0.29</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 495 (M+H)+ (HPLC ES-MS)</td><td> A2 A7 BI Cla</td>

<td> 96</td><td> 0 Cl y-NH -tk'AZ/'</td><td> 244- 245</td><td></td><td> 0.39</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 529 (M+H)+ (HPLC ES-MS)</td><td> A6 A7 BI Cla</td>

<td> 97</td><td> 0 Cl V—NH -ύ-C “</td><td> 220- 221</td><td></td><td> 0.25</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 529 (M+H)+ (HPLC ES-MS)</td><td> A2 A7 BI Cla</td>

<td> 98</td><td></td><td></td><td></td><td> 0.27</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 495 (M+H)+ (HPLC ES-MS)</td><td> A2 A7 BI Cla</td>

<td> 99</td><td> 0 V—NH</td><td> 180- 181</td><td></td><td> 0.52</td><td> 5% MeOH/ 45% EtOAc/ 50% pet ether</td><td> 509 (M+H)+ (HPLC ES-MS)</td><td> A2 A7 BI Cla</td>

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<img file="CA2359244C_D0081.tif" />

A2

A7

BI

Cla

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Table 7. Additional Ureas

<td> Entry</td><td> R</td><td> mp (°C)</td><td> HPLC (min.)</td><td> TLC R/</td><td> TLC Solvent System</td><td> Mass Spec. [Source]</td><td> Synth. Method</td>

<td> 101</td><td>^Me Am ^{H H} OMe</td><td> 162- 165</td><td></td><td></td><td></td><td></td><td> Al A2 C3</td>

<td> 102</td><td> σ,ί,οχΑϊ I Η H</td><td></td><td></td><td> 0.10</td><td> 50% EtOAc/ 50% hexane</td><td> 442 (M+H)+ (HPLC ES-MS)</td><td> A2 A4 C2d</td>

<td> 103</td><td> O X HN NH 0 0 0 o NH-Me Me~NH</td><td> 125- 130</td><td></td><td> 0.24</td><td> 40% EtOAc/ 60% hexane</td><td> 512 (M+H)+ (FAB)</td><td> A2 C2b</td>

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BIOLOGICAL EXAMPLES

P38 Kinase Assay:

The in vitro inhibitory properties of compounds were determined using a p38 kinase inhibition assay. P38 activity was detected using an in vitro kinase assay run in 96-well microtiter plates. Recombinant human p38 (0.5 pg/mL) was mixed with substrate (myelin basic protein, 5 pg/mL) in kinase buffer (25 mM Hepes, 20 mM MgCb and 150 mM NaCl) and compound. One pCi/well of ³³P-labeled ATP (10 pM) was added to a final volume of 100 pL. The reaction was run at 32 °C for 30 min. and stopped with a IM HC1 solution. The amount of radioactivity incorporated into the substrate was determined by trapping the labeled substrate onto negatively charged glass fiber filter paper using a 1% phosphoric acid solution and read with a scintillation counter. Negative controls include substrate plus ATP alone.

All compounds exemplified displayed p38 IC50S of between 1 nM and 10 pM.

LPS Induced TNFa Production in Mice:

The in vivo inhibitory properties of selected compounds were determined using a murine LPS induced TNFa production in vivo model. BALB/c mice (Charles River Breeding Laboratories; Kingston, NY) in groups of ten were treated with either vehicle or compound by the route noted. After one hour, endotoxin (E. coli lipopolysaccharide (LPS) 100 pg) was administered intraperitoneally (i.p.). After 90 min, animals were euthanized by carbon dioxide asphyxiation and plasma was obtained from individual animals by cardiac puncture into heparinized tubes.

The samples were clarified by centrifugation at 12,500 x g for 5 min at 4 °C. The supernatants were decanted to new tubes, which were stored as needed at -20 °C. TNFa levels in sera were measured using a commercial murine TNF ELISA kit (Genzyme).

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The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

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