Pharmaceutical compositions comprising a macrocyclic quinoxaline compound which is an hcv ns3 protease inhibitor

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DESCRIPTION

Combinations of a macrocyclic quinoxaline compound that is an inhibitor of HCV NS3 protease with other HCV agents 5

Field of the Invention

The present invention relates to macrocyclic compounds that are useful as inhibitors of the hepatitis C virus NS3 protease (HCV), the synthesis of said compounds and the use of said compounds to treat

10 HCV infection and / or reduce the probability or severity of HCV infection

Background of the invention

Hepatitis C virus (HCV) infection is a major health problem that leads to disease

fifteen chronic liver disease, such as cirrhosis and hepatocellular carcinoma in a significant number of infected individuals. Current treatments for HCV infection include immunotherapy with recombinant interferon-α alone or in combination with the nucleoside analogue ribavirin.

Several virus-encoded enzymes are supposed targets for therapeutic intervention, including a

twenty metalloprotease (NS2-3), a serine protease (NS3), a helicase (NS3) and an RNA-dependent RNA polymerase (NS5B). The NS3 protease is located in the N-terminal domain of the NS3 protein. NS4A provides a cofactor for NS3 activity.

Possible treatments for HCV infection have been treated in the different references, including

25 Balsano, Mini Rev. Med. Chem. 8 (4): 307-318, 2008, Rönn et al., Current Topics in Medicinal Chemistry 8: 533-562, 2008, Sheldon et al., Expert Opin. Investig. Drugs 16 (8): 1171-1181, 2007, and De Francesco et al., Antiviral Research 58: 1-16, 2003.

Summary of the invention

30 The present invention relates to a macrocyclic compound of formula (I) and / or pharmaceutically salts thereof. The compound and its salts are inhibitors of HCV NS3 protease. The compound and its salts have therapeutic and research applications.

35 Therefore, a first aspect of the present invention describes a compound of formula (I) or a pharmaceutically acceptable salt thereof:

<figref>image 1</figref>

40 The present invention also relates to pharmaceutical compositions containing a compound of the present invention and methods for preparing said pharmaceutical compositions. In addition, the present invention describes methods for treating or reducing the probability or severity of HCV infection.

Other embodiments, aspects and features of the present invention are further described or will be apparent from the following description, examples and appended claims.

Detailed description of the invention

The present invention relates to a compound of formula (I) and / or pharmaceutically acceptable salts thereof. The compound and its pharmaceutically acceptable salts are useful in the inhibition of HCV NS3 protease, the treatment of HCV infection and / or the reduction of the probability or severity of HCV infection.

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Prophylactic applications include, for example, treatment after suspected exposure to HCV by means such as blood transfusion, exchange of body fluids, bites, accidental needle punctures

or exposure to a patient's blood during surgery.

As ingredients of the pharmaceutical composition, the compounds and salts may be the primary therapeutic agent. When appropriate, it can be combined with other therapeutic agents, including, among others, HCV antivirals, anti-infectives, immunomodulators, antibiotics or vaccines.

NS3 inhibitors are also useful in the preparation and execution of screening tests for antiviral compounds. For example, such compounds can be used to isolate enzyme mutants, which are excellent screening tools for more potent antiviral compounds. In addition, the compounds can be used to establish or determine the binding site of other antiviral compounds against HCV, for example, by competitive inhibition.

As described in Example 2, the compound of formula (I) was compared with the compound of Examples 110 and 118 of WO 2008/057209 and has several advantages.

I. Compositions and Methods

The different embodiments include the following:

<dl><dt>(to) </dt><dd>A pharmaceutical composition comprising an effective amount of a compound of formula (I) and a pharmaceutically acceptable carrier. </dd></dl>

<dl><dt>(b) </dt><dd>The pharmaceutical composition of (a), further comprising a second therapeutic agent selected from the group consisting of HCV antiviral agents, immunomodulators and anti-infective agents. </dd></dl>

<dl><dt>(c) </dt><dd>The pharmaceutical composition of (b), wherein the HCV antiviral agent is an antiviral selected from the group consisting of HCV protease inhibitors and HCV NS5B polymerase inhibitors. </dd></dl>

<dl><dt>(d) </dt><dd>A pharmaceutical combination which is (i) a compound of formula I and (ii) a second therapeutic agent selected from the group consisting of HCV antiviral agents, immunomodulators and anti-infective agents; wherein the compound of formula I and the second therapeutic agent are each employed in an amount that makes the combination effective to inhibit NS3 HCV protease or to treat and / or prevent and / or reduce the probability or severity of infection. by HCV.</dd></dl>

<dl><dt>(and) </dt><dd>The composition of (d), wherein the HCV antiviral agent is an antiviral selected from the group consisting of HCV protease inhibitors and HCV NS5B polymerase inhibitors. </dd></dl>

<dl><dt>(F) </dt><dd>A pharmaceutical composition for use in a method for inhibiting HCV NS3 protease in a subject in need thereof comprising administering to the subject an effective amount of a compound of formula I. </dd></dl>

<dl><dt>(g) </dt><dd>A pharmaceutical composition for use in a method for treating an HCV infection and / or reducing the probability or severity of HCV infection in a subject in need thereof comprising administering to the subject an effective amount of a compound of formula (I). </dd></dl>

<dl><dt>(h) </dt><dd>A pharmaceutical composition for use in a method of (g), wherein the compound of formula (I) is administered in combination with an effective amount of at least a second therapeutic agent selected from the group consisting of HCV antiviral agents, immunomodulators and anti-infective agents. </dd></dl>

<dl><dt>(i) </dt><dd>A pharmaceutical composition for use in a method of (h), wherein the HCV antiviral agent is an antiviral selected from the group consisting of HCV protease inhibitors and HCV NS5B polymerase inhibitors. </dd></dl>

<dl><dt>(j) </dt><dd>A pharmaceutical composition for use in a method for inhibiting HCV NS3 protease in a subject in need thereof comprising administering to the subject the pharmaceutical composition of (a), (b) or (c) or the combination of </dd></dl>

<dl><dt>(d) </dt><dd>or (e). </dd></dl>

<dl><dt>(k) </dt><dd>A pharmaceutical composition for use in a method of treating an HCV infection and / or reducing the probability or severity of HCV infection in a subject in need that comprises administering to the subject the pharmaceutical composition of (a), (b) or (c) or the combination of (d) or (e). </dd></dl>

<dl><dt>(l) </dt><dd>A pharmaceutical composition comprising a compound of formula (I) for use as a medicament, for use in the prevention or treatment of HCV infection or for use (i) in, (ii) as a medicament for, or (iii ) for use in the preparation of a medicament for: (a) inhibiting HCV NS3 protease, or (b) treating an HCV infection and / or reducing the likelihood or severity of HCV infection. In these uses, the compounds of the present invention may optionally be used in combination with one or more second therapeutic agents selected from HCV antiviral agents, anti-infective agents and immunomodulators. </dd></dl>

In all these reactions, the compound may optionally be used in the form of a pharmaceutically acceptable salt.

As used herein, the term "or" indicates alternatives that, when appropriate, may be combined. Therefore, the term "or" includes each alternative indicated separately in addition to its combination if the combination is not mutually exclusive. .

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A reference to a compound also includes stable complexes of the compound, such as a stable hydrate. A "stable" compound is a compound that can be prepared and isolated and whose structure and properties remain or can be caused to remain essentially unchanged for a period of time sufficient to allow the use of the compound for the purposes described herein (by example, therapeutic or prophylactic administration to a subject).

II. Administration and compositions

The term "administration" and variants thereof (for example, "administering" a compound) means providing the compound or a prodrug of the compound to the individual in need of treatment. When a compound of the invention or a prodrug thereof is provided in combination with another or more active agents (eg, antiviral agents useful for treating HCV infection), it is understood that "administration" and its variants each include the concurrent and sequential supply of the compound or salt and other agents

The compounds of the present invention can be administered in the form of pharmaceutically acceptable salts. The term "pharmaceutically acceptable salt" refers to a salt of the parental compound that has activity and is not undesirable either biologically or otherwise (for example, it is not toxic or otherwise harmful to the recipient thereof). Suitable salts include acid addition salts which, for example, can be formed by mixing a solution of the compound with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, acetic acid, trifluoroacetic acid or benzoic acid. Compounds that carry an acid moiety can be mixed with pharmaceutically acceptable salts suitable to provide, for example, alkali metal salts (e.g., sodium or potassium salts), alkaline earth metal salts (e.g., calcium or calcium salts). magnesium) and salts formed with suitable organic ligands such as quaternary ammonium salts. In addition, in the event that an acid group (-COOH) or alcohol is present, pharmaceutically acceptable esters can be used to modify the solubility or hydrolysis characteristics of the compound.

As used herein, the term "prodrug" is intended to include an inactive form or compound of the drug that is converted into the active form or compound by the action of enzymes, chemical agents or metabolic processes in the body of an individual to whom It is administered.

As used herein, the term "composition" is intended to include a product comprising the specified ingredients as well as any product that is the result, directly or indirectly, of combining the specified ingredients.

By "pharmaceutically acceptable" it is meant that the ingredients of the pharmaceutical composition must be compatible with each other and not harmful to the recipient thereof.

"The term" subject "(alternatively referred to herein as" patient ") as used herein refers to an animal, preferably a mammal, more preferably a human being, which has been the object of a treatment, an observation. or an experiment

The term "effective amount" indicates an amount that exerts a prophylactic or therapeutic effect. For an HCV infected patient, an effective amount is sufficient to achieve one or more of the following effects: reduce the ability of HCV to replicate, reduce the burden of HCV and increase viral clearance. For a patient not infected with HCV, an effective amount is sufficient to achieve one or more of the following: a lower susceptibility to HCV infection and a lower ability for the infectious virus to establish persistent infection for chronic disease.

For the purpose of inhibiting HCV NS3 protease and treating an HCV infection and / or reducing the likelihood or severity of the symptoms of HCV infection, the compounds of the present invention, optionally in the form of a salt, can be administer by any means that produces contact of the active agent with the agent's site of action. They can be administered by any conventional means available for use in conjunction with pharmaceutical compounds, as individual therapeutic agents or in a combination of therapeutic agents. They can be administered alone, but are usually administered with a selected pharmaceutical vehicle based on the selected route of administration and conventional pharmaceutical practice.

The compounds of the invention can be administered, for example, by one or more of the following routes: oral, parenteral (including subcutaneous, intravenous, intramuscular injections, intrasternal injection or infusion techniques), inhalation (such as by spraying) or rectally, in the form of a unit dosage of a pharmaceutical composition containing an effective amount of the compound and conventional non-toxic pharmaceutically acceptable carriers, adjuvants and excipients. Liquid preparations suitable for oral administration (eg, suspensions, syrups, elixirs and the like) can be prepared according to procedures known in the art and can employ any of the usual means such as water, glycols, oils, alcohols and the like. Solid preparations suitable for oral administration (eg, powders, pills, capsules and tablets) can be prepared according to procedures known in the

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technique and can use solid excipients such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like. Parenteral compositions can be prepared according to procedures known in the art and usually employ sterile water as a carrier and, optionally, other ingredients such as solubility adjuvants. Injectable solutions can be prepared according to procedures known in the art in which the vehicle comprises a saline solution, a glucose solution or a solution containing a mixture of saline solution and glucose. Additional guidance for procedures suitable for use in the preparation of pharmaceutical compositions of the present invention and ingredients suitable for use in such compositions is provided in Remington's Pharmaceutical Sciences, 20th edition (ed. A. R Gennaro, Mack Publishing Co., 2000 ).

The compounds of the present invention can be administered orally in a dosage range of 0.001 to 1000 mg / kg of mammalian body weight (eg, human) per day in a single dose or in divided doses. A preferred dosage range is 0.01 to 500 mg / kg body weight per day orally in a single dose or in divided doses. Another dosage range is 0.1 to 100 mg / kg body weight per day orally in individual or divided doses. For oral administration, the compositions may be provided in the form of tablets or capsules containing 1.0 to 500 milligrams of the active ingredient, particularly 1, 5, 10, 15, 20, 25, 50, 75, 100, 150, 200 , 250, 300, 400 and 500 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. The specific dose level and dosage frequency for any particular patient may vary and will depend on various factors including the activity of the specific compound employed, metabolic stability and duration of action of that compound, age, body weight, general condition. , sex, diet, mode and timing of administration, rate of excretion, pharmacological combination, the severity of the particular condition and the host undergoing therapy.

III. Combination treatment

The quinoxaline macrocyclic compounds described herein can be used in a combination treatment with one or more additional therapeutic agents. Additional therapeutic agents include those directed to HCV, directed at a different causative agent or immune system enhancers. Agents that boost the immune system include those that generally boost the immune system and those that produce a specific immune response against HCV. Additional therapeutic agents directed against HCV include agents directed against NS3 and agents directed at other HCV activities such as NS5A and NS5B and agents directed at host cell activities involved in HCV replication.

Different HCV inhibitors are described in different publications. Macrocyclic compounds useful as inhibitors, inhibitors of HCV protease are described in WO06 / 119061, WO7 / 015785, WO7 / 016441, WO07 / 148135, WO08 / 051475, WO 08 / 051477, WO 08/051514, WO 08/057209. Other HCV NS3 protease inhibitors are disclosed in international patent application publications WO 98/22496, WO 98/46630, WO 99/07733, WO 99/07734, WO 99/38888, WO 99/50230, WO 99 / 64442, WO 00/09543, WO 00/59929, WO 02/48116, WO 02/48172, British Patent No. GB ​​2 337 262, and United States Patent No. 6,323,180.

Additional examples of therapeutic agents that may be present in a combination include ribavirin, levovirin, viramidine, thymosin alpha-1, interferon-β, interferon-α, pegylated interferon-α (peginterferon-a), a combination of interferon-α and ribavirin , a combination of peginterferon-α and ribavirin, a combination of interferon-α and levovirin and a combination of peginterferon-α and levovirin. Interferon-α includes, but is not limited to, recombinant interferon-α2a (such as Roferon interferon available in Hoffmann-LaRoche, Nutley, NJ), pegylated interferonα-2a (Pegasys), interferon-α2b (such as Intron-A interferon available in Schering Corp., Kenilworth, NJ), pegylated interferon-α-2b (Peglntron), a recombinant consensus interferon (such as interferon alphacon-1), and a purified interferon-α product. Amgen's recombinant consensus interferon has the trade name Infergen®. Levovirin is the L-enantiomer of ribavirin that has demonstrated an immunomodulatory activity similar to ribavirin. Viramidine represents a ribavirin analog described in WO 01/60379. The individual components of the combination can be administered separately at different times during the course of therapy or simultaneously in divided or individual combination forms.

Ribavirin, levovirin and viramidine can exert their anti-HCV effects by modulating intracellular combinations of guanine nucleotides by inhibiting the intracellular enzyme inosine monophosphate dehydrogenase (IMPDH). IMPDH is the speed-limiting enzyme in the biosynthetic pathway in the de novo guanine nucleotide biosynthesis. Ribavirin is easily phosphorylated intracellularly and the monophosphate derivative is an IMPDH inhibitor. Therefore, inhibition of IMPDH represents another useful target for the discovery of inhibitors of HCV replication. Therefore, the compounds of the present invention can also be administered in combination with the IMPDH inhibitor, such as VX-497, which is described in WO 97/41211 and WO 01/00622; another IMPDH inhibitor such as that described in WO 00/25780; or mycophenolate mofetil [see AC Allison and EM Eugui, Agents Action, 44 (Suppl.): 165 (1993)].

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For the treatment of an HCV infection, the compounds of the present invention can also be administered in combination with the antiviral agent amantadine (1-aminoadamantane). For a full description of this agent, see J. Kirschbaum, 12 Anal. Profiles Drug Subs. 1-36 (1983).

For the treatment of an HCV infection, the compounds of the present invention can also be administered in combination with the polymerase inhibitor antiviral agent R7128 (Roche).

The compounds of the present invention can also be combined for the treatment of an HCV infection with antiviral 2'-C-branched ribonucleosides described in RE Harry-O'kuru, et al., J. Org. Chem., 62: 1754-1759 (1997); MS Wolfe, et al., Tetrahedron Lett, 36: 7611-7614 (1995); U.S. Patent No. 3,480,613; International Publication Number WO 01/90121, documents WO 01/92282 WO 02/32920 (April 25, 2002); WO 04/002999 and WO 04/003000 and WO 04/002422. Such 2'-C-branched ribonucleosides include, but are not limited to, 2'-Cmethyl-cytidine, 2'-C-methyl-uridine, 2'-C-methyl-adenosine, 2'-C-methyl-guanosine and 9- (2-C-methyl-β-Dribofuranosyl) -2,6-diaminopurine and the corresponding amino acid ester of C-2 ', C-3' and C-5 'hydroxyls of ribose and 1,3- esters Corresponding optionally substituted cyclic propanediol of the 5'-phosphate derivatives.

The compounds of the present invention may also be combined for the treatment of an HCV infection with other nucleosides having anti-HCV properties, such as those described in international patent application publications WO 02/51425, WO01 / 79246, WO02 / 32920, WO02 / 48165 and WO2005 / 003147 (including R1656, (2'R) -2'-deoxy-2'-fluoro-2'-C-methylcytidine, shown as compounds 3-6 on page 77); WO 01/68663; WO 99/43691; WO 02/18404 and WO2006 / 021341, and United States patent application US 2005/0038240, including 4'-azido nucleosides such as R1626, 4'-azidocytidine; United States patent application publications US 2002/0019363, US 2003/0236216, US 2004/0006007 and US 2004/0063658; and international patent application publications WO 02/100415, WO 03/026589, WO 03/026675, WO 03/093290, WO 04/011478, WO 04/013300 and WO 04/028481.

For the treatment of an HCV infection, the compounds of the present invention can also be administered in combination with an agent that is an inhibitor of HCV NS5B polymerase. Such HCV NS5B polymerase inhibitors that can be used as combination therapy include, but are not limited to, those described in international patent publications WO02 / 057287, WO02 / 057425, WO03 / 068244, WO2004 / 000858, WO04 / 003138 and WO2004 / 007512; United States Patent No. 6,777,392 and United States Patent Application Publication No. US2004 / 0067901. Other HCV polymerase inhibitors of this type include, but are not limited to, valopicitabine (NM-283; Idenix) and 2'-F-2'-beta-methylcytidine (see also WO 2005/003147.

In one embodiment, the HC5 NS5B polymerase nucleoside inhibitors that are used in combination with the present HCV NS3 protease inhibitors are selected from the following compounds: 4-amino-7- (2-Cmethyl-β-D- arabinofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3d] pyrimidine; 4-methylamino-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-dimethylamino-7- (2-C-methyl- (βD-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-cyclopropylamino-7- (2-C-methyl -_- D-ribofuranosyl) -7Hpyrrolo [2,3d] pyrimidine; 4-amino-7- (2-C-vinyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (2-C-hydroxymethyl-o-Dribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (2-C-fluoromethyl-oD-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4 amino-5-methyl-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (2-C-methyl-β-Dribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-5-carboxylic acid; 4-amino-5-bromo-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3d] pyrimidine; 4-amino-5-chloro-7- (2-C-methyl- (3-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-5-fluoro-7- (2- Cmethyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 2,4-diamino-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3d ] pyrimidine; 2-amino-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 2-amino-4-cyclopropylamino-7- (2-Cmethyl- β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 2-amino-7- (2-C-methyl-o-Dribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin4 (3H) -one; 4-amino-7- (2-C-ethyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (2-C, 2-O-dimethyl-β-Dribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-4 (3H) -one; 2 amino-5-methyl-7- (2-C, 2-O-dimethyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidin-4 (3H) -one; 4-amino-7- (3-deoxy-2-Cmethyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (3-deoxy-2-C-methyl-β-D-arabinofuranosyl) -7Hpyrrolo [2,3-d] pyrimidine; 4-amino-2-fluoro-7- (2-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (3-Cmethyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (3-C-methyl- [3-D-xylofuranosyl) -7H-pyrrolo [2,3d] pyrimidine; 4-amino-7- (2,4-di-C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; 4-amino-7- (3-deoxy-3-fluoro-2C-methyl-β-D-ribofuranosyl) -7H-pyrrolo [2,3-d] pyrimidine; and the corresponding 5'-triphosphates; or a pharmaceutically acceptable salt thereof.

The compounds of the present invention can also be combined for the treatment of an HCV infection with non-nucleoside HCV polymerase inhibitors such as those described in international patent application publications WO 01/77091; WO 01/47883; WO 02/04425; WO 02/06246; WO 02/20497; WO 2005/016927 (specifically JTK003); and VHC-796 (Viropharma Inc.).

In one embodiment, the HCV NS5B polymerase non-nucleoside inhibitors that are used in combination with the present HCV NS3 protease inhibitors are selected from the following compounds: acid 14

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cyclohexyl-6- [2- (dimethylamino) ethyl] -7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-Cyclohexyl-6- (2-morpholin-4-ylethyl) -5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-cyclohexyl-6 [2- (dimethylamino) ethyl] -3-methoxy-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-Cyclohexyl-3-methoxy-6-methyl-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; methyl ({[(14-cyclohexyl-3-methoxy-6-methyl5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-yl) carbonyl] amino} sulfonyl) acetate; ({[(14-cyclohexyl-3methoxy-6-methyl-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-yl) carbonyl] amino} sulfonyl) acetic acid; 14-cyclohexyl-N [(dimethylamino) sulfonyl] -3-methoxy-6-methyl-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxamide; 3-Chloro-14-cyclohexyl-6- [2- (dimethylamino) ethyl] -7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; bis- (11-carboxy-14-cyclohexyl-7,8-dihydro-6H indole [1,2-e] [1,5] benzoxazocin-7-yl) -N, N-dimethylethane-1,2 (trifluoroacetate) -diamine; 14-cyclohexyl-7,8-dihydro-6H-indole [1,2-e] [1,5] benzoxazocin-11-carboxylic acid; 14-cyclohexyl-6-methyl-7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-Cyclohexyl-3-methoxy6-methyl-7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-cyclohexyl-6 [2 (dimethylamino) ethyl] -3-metrioxy-7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-Cyclohexyl-6- [3- (dimethylamino) propyl] -7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; acid 14

<dl><dt>cyclohexyl-7-oxo-6- (2-piperidin-1-ylethyl) -5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; </dt><dd>acid 14</dd></dl>

<dl><dt>cyclohexyl-6- (2-morpholin-4-ylethyl) -7-oxo-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; </dt><dd>acid 14</dd></dl>

<dl><dt>cyclohexyl-6- [2- (diethylamino) ethyl] -7-oxo-5,6,7,8-tetrahydroindole [2,1] [2,5] benzodiazocin-11-carboxylic; </dt><dd>acid 14</dd></dl>

cyclohexyl-6- (1-methylpiperidin-4-yl) -7-oxo-5,6,7,8-tetrahydroindole [2,1a] [2,5] benzodiazocin-11-carboxylic acid; 14-cyclohexylN - [(dimethylamino) sulfonyl] -7-oxo-6- (2-piperidin-1-ylethyl) -5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin- 11carboxamide; 14-cyclohexyl-6- [2- (dimethylamino) ethyl] -N - [(dimethylamino) sulfonyl] -7-oxo-5,6,7,8-tetrahydroindole [2,1a] [2,5] benzodiazocin-11 -carboxamide; 14-cyclopentyl-6- [2- (dimethylamino) ethyl] -7-oxo-5,6,7,8-tetrahydroindole [2,1a] [2,5] benzodiazocin-11-carboxylic acid; 14-cyclohexyl-5,6,7,8-tetrahydroindo [2,1-a] [2,5] benzodiazocin-11 carboxylic acid; 6-allyl-14-cyclohexyl-3-methoxy-5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-cyclopentyl-6- [2- (dimethylamino) ethyl] -5,6,7,8-tetrahydroindole [2,1-a] [2,5] benzodiazocin-11-carboxylic acid; 14-Cyclohexyl-6- [2- (dimethylamino) ethyl] -5,6,7,8-tetrahydroiridolo [2,1a] [2,5] benzodiazocin-11-carboxylic acid; 13-cyclohexyl5-methyl-4,5,6,7-tetrahydrofuro [3 ', 2': 6.7] [1,4] diazocino [1,8-a] indole-10-carboxylic acid; 15-cyclohexyl-6- [2 (dimethylamino) ethyl] -7-oxo-6,7,8,9-tetrahydro-5H-indole [2,1a] [2,6] benzodiazonin-12-carboxylic acid; 15-cyclohexyl-8oxo-6,7,8,9-tetrahydro-5H-indole [2,1-a] [2,5] benzodiazonin-12-carboxylic acid; 13-Cyclohexyl-6-oxo-6,7-dihydro-5 Hindolo [1,2-d] [1,4] benzodiazepine-10-carboxylic acid; and pharmaceutically acceptable salts thereof.

IV. Compound Evaluation

The compounds described herein can be evaluated according to different activities, such as the ability to inhibit HCV NS3 activity, HCV replicon activity and HCV replication activity using techniques well known in the art (see, for example, Carroll et al., J. Biol. Chem. 278: 1197911984, 2003.)

One such test is the temporary resolution fluorescence assay of HCV NS3 protease (TRF) as described below and in Mao et al., Anal. Biochem 373: 1-8, 2008 and in the international patent application publication WO 2006/102087. An NS3 protease assay can be performed, for example, in a thin volume of the 100 ml assay buffer containing 50 mM HEPES, pH 7, .5, 150 mM NaCl, 15% glycerol, 0.15% TRITON X-100, 10 mM DTT, and 0.1% PEG 8000. The NS3 and NS4A protease is pre-incubated with various concentrations of inhibitors in DMSO for 30 minutes. The reaction is started by adding the TRF peptide substrate (final concentration 100 nM). The substrate hydrolysis by NS3 protease activity is quenched after 1 hour at room temperature with 100 ml of 500 mM HEPES at pH 5.5. The fluorescent product was detected using a Victor V2 or Fusion fluorimeter (Perkin Elmer Life and Analytical Sciences) with excitation at 340 nm and emission at 615 nm with a delay of 400 µs. Test concentrations of different enzyme forms were selected with a signal to background ratio of 10-30. IC50 values ​​obtained using a four parameter setting. Ki values ​​are derived from IC50 values ​​using the following formula,

in which [S] is the concentration of the peptide substrate in the reaction and Km is the Michaelis constant. See Gallinari et al., 38 BIOCHEM. 5620-32 (1999); P. Gallinari et al., 72 J. VIROL. 6758-69 (1998); M. Taliani et al., 240 ANAL. BIOCHEM 60-67 (1996); Mao et al., Analytical Biochemistry 373: 1-8, 2008.

V. Production of general compounds

The present invention also relates to processes for preparing compounds of formula (I). The compounds of the present invention can be easily prepared according to the following reaction schemes and examples or modifications thereof, using starting materials and reagents readily available in the market and conventional synthesis procedures. In these reactions, it is also possible to make use of variants that are known among those skilled in the art, but are not mentioned in more detail. In addition, other procedures for preparing the compounds of the invention will be readily apparent to a person.

10

15

20

25

30

35

40

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Specialist in the art in light of the following reaction schemes and examples. Unless otherwise indicated, all variables are as defined above. The following reaction schemes and examples only serve to illustrate the invention and its practice.

Olefin metathesis catalysts include the following ruthenium-based species: F. Miller et al., 118 J. AM. CHEM Soc. 9606 (1996); G. Kingsbury et al., 121 J. Am. Chem. Soc. 791 (1999); H. Scholl et al., 1 ORG. LETT 953 (1999); US patent application US2002 / 0107138; K. Furstner et al., 64 J. ORG. CHEM 8275 (1999). The usefulness of these catalysts in ring closure metathesis is well known in the literature (eg, Trnka and Grubbs, 4 ACC. CHEM. BEEF. 18 (2001).

The following examples only serve to illustrate the invention and its practice. The examples should not be construed as limitations on the scope of the invention.

List of abbreviations

List of abbreviations

DCM / CH2Cl2 dichloromethane

DCE 1,2 dichloroethane

DIEA diisopropylethylamine

DMF dimethylformamide

DMSO dimethylsulfoxide

Dppf diphenyl phosphoferoferrocene

Et2O diethyl ether

EtOAc ethyl acetate

HATU O- (7-Azabenzotriazol-1-yl-N, N, N ', N'-tetramethyluronium hexafluorophosphate

HCl hydrochloric acid

TMSCl Chlorotrimethylsilane

TBAF Tetra-Butyl Ammonium Fluoride

DMAP Dimethylamino pyridine

MeCN acetonitrile

MeOH methanol

Pd / C palladium on carbon

TBTU O-benzotriazol-1-yl-N, N, N ', N'-tetramethyluronium tetrafluoroborate

TFA Trifluoroacetic Acid

THF tetrahydrofuran

Flash chromatography Purification using Biotage Horizon with silica gel cartridge and specified mobile phase gradient

HPLC High performance liquid chromatography with automatic or UV-triggered mass using acidified MeCN and H2O gradients as mobile phase

MHz Megahertz

Synthesis of intermediate compounds

Intermediate Compounds A

Structure No. Name Reference

Compound

<figref>image2</figref>Wang Intermediate bibliographic

et al., (1R, 2S) -1-amino-N-A1-Hydrochloride

(cyclopropylsulfonyl) -2-United States vinylcyclopropanecarboxamide No. 6,995,174

Intermediate Compound B1: 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valine

<figref>image3</figref>

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Stage 1: [(1E) -hepta-1,6-dien-1-yloxy] (trimethyl) silane

<figref>image4</figref>

5 A solution (0.5 M) of butenyl magnesium bromide in THF (1.4 eq.) Was treated at -78 ° C with Cu (I) Br.SMe2 (0.05 eq) and HMPA (2.4 eq) . The mixture was stirred for 10 min and then a solution (1 M) of acrolein (1 eq) and TMSCI (2 eq) in THF was added for 1 hour so that the internal temperature remained below -68 ° C . The resulting mixture was stirred at -78 ° C for 2 hours and then treated with an excess of Et3N and diluted with hexanes. After reaching room temperature, the mixture was treated with a small portion of H2O and

10 filtered through CELITE. The filtrate was washed 10 times with H2O and then with brine. The organic layer was dried and the volatiles removed, giving a residue that was distilled under reduced pressure (2 kPa). The fraction collected at 8086 ° C contained the title compound (58%) as a colorless liquid. 1H NMR (400 MHz, CDCl3) δ 6.19 (d, J = 11.6 Hz, 1H), 5.85-5.75 (m, 1H), 5.02 -4.92 (m, 3H) , 2.08 -2.02 (m, 2H), 1.94 -1.88 (m, 2H), 1.46 -1.38 (m, 2H), 0.18 (s, 9H).

fifteen Stage 2: trans-2-pent-4-en-1-ylcyclopropanol

<figref>image5</figref>

twenty A solution (0.45 M) of the above compound in hexanes was treated with a solution (15%) of Et2Zn (1.2 eq) in toluene and the resulting solution was cooled in an ice bath. Dropwise, diiodomethane (1.2 eq) was added, then the solution was stirred for 1 hour before heating to 20 ° C. Pyridine (6 eq) was added and the paste was stirred for 15 min and poured into petroleum ether. The mixture was repeatedly filtered through celite until a clear solution was obtained. This mixture was concentrated at 10 kPa and the solution that remained (containing {[(trans) -2

25 pent-4-en-1-ylcyclopropyl] oxy} silane, toluene and pyridine) was further diluted with THF. The mixture was cooled to 0 ° C and treated dropwise with a solution of TBAF (1M (1.2 eq) in THF. After 10 minutes the mixture was allowed to warm to 20 ° C and after 1 h more was poured into H2O. The aqueous phase was extracted with EtOAc and the combined organic extracts were washed with brine, then dried. Removal of volatiles gave a residue that was purified by flash chromatography (eluent 0-66% Et2O / petroleum ether) to give the title compound (71%) as

30 colorless liquid 1H NMR (400 MHz, CDCl3) δ 5.85-5.75 (m, 1H), 5.00 (dd, J = 17.1, 1.6 Hz, 1H), 4.94 (da, J = 10.4 Hz, 1H), 3.20 (apparent dt, J = 6.4, 2.5 Hz, 1H), 2.10 -2.04 (m, 2H), 1.52 -1.44 (m, 2H), 1.29 -1.19 (m, 1H), 1.15 -1.07 (m, 1H), 0.95-0.87 (m, 1H), 0.71-0 , 66 (m, 1H), 0.31 (apparent c, J = 6.0 Hz, 1H).

Stage 3: 3-methyl-N- (oxomethylene) -L-methyl valinate

<figref>image6</figref>

A solution (0.39 M) of methyl 3-methyl-L-valinate in a 2: 1 mixture of saturated NaHCO3 and CH2Cl2 was cooled in an ice bath and rapidly stirred. The mixture was treated with triphosgene (0.45 eq) in one portion and the mixture

40 resulting was stirred for 0.5 h. The reaction was diluted with CH1Cl2 and the layers were separated. The aqueous phase was extracted with CH2Cl2 and the combined organic extracts were washed with brine, then dried. Solvent removal gave the title compound as a clear oil that was maintained for 12 h under vacuum (0.01 kPa) and then used directly in the next step. 1H NMR (CDCl3) δ 3.79 (s, 3H), 3.75 (s, 1H), 1.00 (s, 9H).

Four. Five Step 4: 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-methyl valineate and 3-methyl-N - ({[ (1S, 2S) -2pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-methyl valinate

<figref>image7</figref>

fifty A solution (0.45 M) trans-2-pent-4-en-1-ylcyclopropanol in toluene was treated with methyl 3-methyl-N- (oxomethylene) -L-valinate (1.1 eq) and then DMAP (1 eq). The resulting mixture was heated at reflux for 12 hours, then cooled to 20 ° C and EtOAc was added and the organic layer was separated and washed with 1N HCl, brine, and dried. The removal of volatiles gave a residue that was purified by flash chromatography (eluent 0-30%

55 Et2O / petroleum ether). The first fractions contained 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1

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ilyclopropyl] oxy} carbonyl) -L-methyl valinate (38%) as an oil. MS (ES +, m / z) 298 (M + H) +.

The last fractions contained 3-methyl-N - ({[(1RS, 2S) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-methyl valineate (28%) as an oil. MS (ES +, m / z) 298 (M + H) +. Stage 5: 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valine

<figref>image8</figref>

10 A solution (0.1 M) of methyl 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valinate in a mixture of 2: 1 MeOH / H2O was treated with LiOH.H2O (4 eq) and then heated at 60 ° C for 4 hours. The mixture was cooled and concentrated to half the volume, then diluted with EtOAc and acidified with aqueous HCl (1N). The organic layer was separated and washed with brine and dried. The removal of volatiles gave the title compound (98%) as an oil. MS (ES +, m / z) 284 (M + H) +.

15

Intermediate Compounds C

Intermediate Compound C1: (4R) -4 - [(3-chloro-7-methoxyquinoxalin-2-yl) oxy] -L-methyl prolinate, hydrochloride

<figref>image9</figref>

Stage 1: 6-methoxyquinoxaline-2,3-diol

<figref>image10</figref>

25 A suspension of 4-methoxybenzene-1,2-diamine dihydrochloride in diethyl oxalate (8 eq) was treated with Et3N (2 eq) and then heated at 150 ° C for 2 h. The mixture was cooled and filtered, then the solid was collected and washed with H2O and EtOH. The residue was dried to provide the title compound (69%). MS (ES +, m / z) 193 (M + H) +.

30 Stage 2: 3-Chloro-6-methoxyquinoxaline-2-ol

<figref>image11</figref>

A solution (1.53 M) of 6-methoxyquinoxaline-2,3-diol in DMF was treated with SOCl2 (1 eq) and heated to 110 ° C.

35 After 1.5 h, the reaction mixture was cooled and poured into aqueous HCl (1 N). The resulting precipitate was filtered and washed with H2O and Et2O. The dried solid predominantly contained the title compound as a mixture with 6-methoxyquinoline-2,3-diol and 2,2-dichloro-6-methoxyquinoxaline. This material was used directly in the next stage. MS (ES +, m / z) 211 (M + H) +.

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Step 3: 2-Methyl (2S, 4R) -4 - [(3-chloro-7-methoxyquinoxalin-2-yl) oxy] 1-tert-butyl pyrrolidine-1,2-dicarboxylate

<figref>image12</figref>

5 A solution (0.35 M) of 3-chloro-6-methoxyquinoxaline-2-ol in NMP was treated with Cs2CO3 (1.5 eq) and 2-methyl (2S, 4S) -4 {[(4-bromophenyl) 1-tert-butyl sulfonyl] oxy} pyrrolidine-1,2-dicarboxylate (1.1 eq). The resulting mixture was stirred at 50 ° C for 18 hours, then a portion (0.1 eq) of 2-methyl (2S, 4S) -4 - {[(4-bromophenyl) sulfonyl] oxy} pyrrolidine1,2- 1-tert-butyl dicarboxylate. After stirring for 2 hours, the mixture was cooled and diluted with H2O and EtOAc. The combined organic phases were washed with aqueous HCl (1 N), saturated aqueous NaHCO3 and brine. The

10 Dry organic phase was concentrated to a residue that was purified by flash chromatography (eluent 0-6% EtOAc / petroleum ether to give the title compound (35%) as a solid. MS (ES +, m / z) 438 (M + H) +.

Stage 4: (4R) -4 - [(3-chloro-7-methoxyquinoxalin-2-yl) oxy] -L-methyl prolinate, hydrochloride

<figref>image13</figref>

A solution of (0.62 M) of 2-methyl (2S, 4R) -4 - [(3-chloro-7-methoxyquinoxalin-2-yl) oxy] pyrrolidine-1,2-dicarboxylate of 1-c-butyl in CH2Cl2 It was treated with a solution (4 M) of HCl in dioxane (5 eq). The mixture was stirred at 0 ° C for 2 hours and treated with a solution (4 M) of HCl in (2 eq). After 5 hours, the reaction was judged complete and the mixture was

twenty concentrated under reduced pressure. The residue was triturated with Et2O, to provide the title compound (95%) as a solid. MS (ES +, m / z) 338 (M + H) +.

Example 1: {[(1R, 2S) -1 - ({[(1aR, 5S, 8S.10R, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3, 4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocycloprona [18,19] [1,10,3,6] dioxadiazacyclonone25 decino [11, 12-b] quinoxalin-8-yl] carbonyl} amino) -2-vinylcyclopropyl] carbonyl} (cyclopropylsulfonyl) potassium azanide

<figref>image14</figref>

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Stage 1: 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valyl- (4R) -4 - [(3-chloro -7-methoxy-quinoxalin-2-yl) oxy] -L-methyl prolinate

<figref>image15</figref>

5 A solution (0.2 M) (4R) -4 - [(3-chloro-7-methoxyquinoxalin-2-yl) oxy] -L-prolinate methyl hydrochloride (treated with 3-methyl-N - ({[(1R , 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valine (1.1 eq), DIEA (5 eq) and HATU (1.2 eq) The resulting mixture was stirred at 0-5 ° C for 5 h and diluted with EtOAc. The organic layer was separated and washed with aqueous HCl (1 N), saturated aqueous NaHCO3 and brine. The dried organic layer was concentrated under reduced pressure to give a residue that was purified by flash chromatography (eluent 10-30% EtOAc / petroleum ether) to give the

10 title compound (96%) as an oil. MS (ES +), m / z 604 (M + H) +.

Stage 2: 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valyl- (4R) -4 - [(7-methoxy -3-vinyl-quinoxalin-2il) oxy] -L-methyl prolinate

<figref>image16</figref>

A solution (0.1 M) 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valyl-4R) 4 - [( 3-Chloro-7-methoxyquinoxalin-2-yl) oxy] -L-methyl prolinate in EtOH was treated with potassium trifluoride (vinyl) borate (1.5 eq) and triethylamine (1.5 eq). The resulting mixture was degassed, then the adduct PdCl2 (dppf) -CH2Cl2 (0.1 eq) was added.

twenty The mixture was heated at reflux for 1 hour, then cooled to room temperature with H2O and EtOAc. The organic phase was separated, washed with water and brine, then dried. The removal of volatiles gave a residue that was purified by flash chromatography (eluent 20-30% EtOAc / petroleum ether) to give the title compound as a yellow foam that was used directly in the next step. MS (ES +), m / z 595 (M + H) +.

25 Stage 3: (1aR, 5S, 8S, 10R, 18E, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3,4,5,6,9,10,20 , 21,22,22a-dodecahydro8H-7,10-methanocyclopropa [18,19] [1,10,3,6] dioxadiazacyclononedecino [11,12-b] quinoxalin-8-carboxylate methyl

<figref>image17</figref>

30 A solution (0.02 M) 3-methyl-N - ({[(1R, 2R) -2-pent-4-en-1-ylcyclopropyl] oxy} carbonyl) -L-valyl-4R) 4 - [( Methyl 7-methoxy-3-vinylquinoxalin-2-yl) oxy] -L-prolinate in DCE was heated to 80 ° C and then treated with Zhan1 catalyst (0.15 eq). The resulting mixture was stirred at 80 ° C for 1 h and then cooled to room temperature and concentrated under reduced pressure. The residue was purified by flash chromatography (eluent 20

35 50% EtOAc / petroleum ether to give the title compound (25% for 2 stages) as a foam. MS (ES +),

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m / z 567 (M + H) +.

Stage 4: (1aR, 5S, 8S, 10R, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3,4,5,6,9,10,18,19 , 20,21,22,22 -tetradecahydro-8H-7,10-methanocyclopropa [18,19] [1,10,3,6] dioxadiazacyclononedecino [11,12-b] quinoxalin-8-carboxylate methyl

<figref>image18</figref>

A solution (0.05 M) of (1aR, 5S, 8S, 10R, 18E, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3,4,5,6 ,

10 9,10,20,21,22,22a-dodecahydro-8H-7,10-methanocycloprona [18,19] [1,10,3,6] dioxadiazacycllonone-decino [1,12b] quinoxalin-8-carboxylate methyl in MeOH / dioxane (1: 1 ratio) it was treated with Pd / C (8% by weight). The resulting mixture was stirred under hydrogen atmosphere for 4 hours. The catalyst was filtered and the filtrate was concentrated under reduced pressure, to give the title compound (98%) as a solid. MS (ES +) m / z 569 (M + H) +.

fifteen Stage 5: Acid (1aR, 5S, 8S, 10R, 22aR) -5-tert-butyl-1,4-methoxy-3,6-dioxo-1,1a, 3,4,5,6,9,10, 18,19,20,21,22,22atetradecahydro-8H-7,10-methanocyclopropa [18,19] [1,10,3,6] dioxadiazacyclononedecino [11,12-b] quinoxalin-8carboxylic

<figref>image19</figref>

twenty A solution (0.1 M) of (1aR, 5S, 8S, 10R, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3,4,5,6,9 , 10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocycloprona [18,19] [1,10,3,6] dioxadiazacyclononedecine [11,12-b] quinoxalin-8- Methyl carboxylate in a 1: 1 mixture of H2O / THF was treated with LiOH.H2O (3 eq). The resulting mixture was stirred at 20 ° C for 18 h, acidified with aqueous HCl (0.2 M) and diluted with EtOAc. The phase

25 The organic was separated, washed with aqueous HCl (0.2 M) and brine, then dried. The removal of volatiles gave the title compound (98%) as a solid. MS (ES +) m / z 555 (M + H) +.

Step 6: (1aR, 5S, 8S, 10R, 22aR) -5-tert-butyl-N - ((1R, 2S) -1 - {[(cyclopropylsulfonyl) amino] carboxyl} -2-vinylcyclopropyl) 1,4- methoxy-3,6-dioxo-1,1a, 3,4,5,6,9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,1030 methanocycloprona [18,19] [ 1,10,3,6] dioxadiazacyclononedecino [11,12-b] quinoxalin-8-carboxamide

<figref>image20</figref>

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A solution (0.1 M) of acid (1aR, 5S, 8S, 10R, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3,4,5,6, 9,10,18,19,20,21,2222a-tetradecahydro-8H-7,10-methanocyclopropa [18,19] [1,10,3,6] dioxadiazacyclononedecino [11,12-b] quinoxalin-8-carboxylic in CH2Cl2 it was treated with (1R, 2S) -1 {[(cyclopropylsulfonyl) amino] carbonyl} -2-vinyl propanaminium (1.3 eq), DIEA (3 eq), DMAP (1.5 eq) and TBTU chloride (1.45 eq).

5 The resulting mixture was stirred at 0-5 ° C for 18 h and diluted with EtOAc. The solution was washed with aqueous HCl (0.2 M), saturated aqueous NaHCO3 and brine. The organic phases were dried and concentrated to a residue that was purified by flash chromatography (eluent 2.5 MeOH / CH2Cl2) to give the title compound (89%) as a solid. 13C NMR (100 MHz, d6-DMSO-d6) δ 172.32, 170.63, 169.04, 159.86, 156.95, 154.74, 148.10, 140.41, 133.55 (2 signals), 128.94, 118.21, 117.58, 105.89, 74.88, 59.75, 58.71, 55.68, 54.13, 54.01, 40.13, 34.49, 34 04

10 33.76, 32.68, 30.71, 30.43, 28.55, 27.69, 27.28, 26.38, 21.98, 18.49, 10.67, 5.69, 5, 46; MS (ES +) m / z 767 (M + H)].

Step 7: {[(1R, 2S) -1 - ({[(1aR, 5S, 8S, 10R, 22aR) -5-tert-butyl-14-methoxy-3,6-dioxo-1,1a, 3, 4,5,6, 9,10,18,19,20,21,22,22a-tetradecahydro-8H-7,10-methanocycloprona [18,19] [1,10,3,6] dioxadiazacyclonlonone-decino [11 , 12-b] quinoxalin-8-yl] carbonyl} amino) -2-vinylcyclopropyl] carbonyl} (cyclopropylsulfonyl) potassium azanide

15

<figref>image21</figref>

The above material was suspended in EtOH and the resulting solution (0.025 M) was cooled to 0 ° C. A solution (0.02 M) of tert-BuOK (1.5 eq) in EtOH 'was added, giving the formation of a precipitate. The mixture was stirred at 20 ° C.

twenty for 18 h the solid was collected by filtration. This material was washed with EtOH and dried to give the title compound (93%) as a crystalline solid. MS (ES +) m / z 767 (M + H) +.

Example 2: Comparison of different compounds

25 The compound of Example 1 was compared with the compound of Examples 110 and 118 of WO 2008/057209. The results are shown in Tables 1 and 2 below. As illustrated in the tables and the discussion of the results, the compound of formula (I) appears to have several advantageous properties compared to the compound of Example 118 of WO 2008. / 057209 and the compound of Example 110 of WO 2008/057209.

30

Table 1

<dl><dt>Example 118 of Document WO 2008/057209 </dt><dd>Example 1 Example 110 of WO 2008/057209 </dd></dl>

<dl><dt>Structure </dt><dd><figref>image22</figref><figref>image23</figref><figref>image24</figref></dd></dl>

<dl><dt>NS 3 / 4A (Ki) 1b inhibitory activity </dt><dd>&lt;0.016 nM &lt;0.016 nM &lt;0.016 nM </dd></dl>

<dl><dt>Replicon activity2 CE50 gt1b </dt><dd>3 nM 2 nM 5 nM </dd></dl>

<dl><dt>AUC in rat plasma at 25 mpk orally3 </dt><dd>38.5 µM.h 20.6 µM.h 5.8 µM.h </dd></dl>

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<dl><dt>Concentration in rat liver at 24 h (25 mpk orally) 3 </dt><dd>18.4 µM 27.9 µM 8.5 µM </dd></dl>

<dl><dt>AUC in dog plasma at 5mpk orally 3 </dt><dd>10.9 µM.h 48.6 µM.h 1.0 µM.h </dd></dl>

<dl><dt>Concentration in dog liver at 24 h (5 mpk orally) 3 </dt><dd>Not available 120 µM 3.3 µM </dd></dl>

<dl><dt>Covalent protein binding In Vivo4 </dt><dd>Rat at 6 h plasma = BLQ, liver = 30 ± 3 pmol / mg protein Rat at 6 h plasma = LOQ, liver LOQ Rat at 6 h plasma = BLQ liver = BLQ </dd></dl>

<dl><dt>Physical properties5 </dt><dd>Potassium salt is not disproportionate in solution. Potassium salt is not disproportionate in solution. Potassium salt is disproportionate in the crystalline neutral form in solution. </dd></dl>

<dl><dt>Ki: Inhibition constant, reference to &lt;0.016 nM indicates that the activity observed is less than 0.016 nM, the exact amount less than 0.016 nM was not determined in the assay; EC50: Effective concentration that reaches 50% suppression of viral replication; gt: Genotype, AUC: Area under the plasma concentration time curve; LOQ: Limit of quantification 3 pmol / mg); BLQ: Below the quantification limit.</dt><dd /></dl>

Compound of formula (I) compared to Example 110 of WO 2008/057209

The advantageous properties of the compound of formula (I) over the compound of Example 110 of WO 5 2008/057209 are the following:

1) Physical properties (there is no disproportion of salt for the Compound of formula (I)); 2) Pharmacokinetic profile in rats after administration of potassium salt; and 3) Exposure of the liver (target organ).

10 Differences in properties are particularly advantageous for the formulation and administration of the compound of formula (I) over the compound of Example 110 of WO 2008/057209. The lack of disproportion of the salt for the compound of formula (I) allows the dissolution of 1.8 mg / ml of the K + salt form of the compound of Example 1 in water. Although the salt of K + of the compound of Example 110 of the document

fifteen WO 2008/057209 has improved aqueous solubility (9.7 mg / ml), the compound thus dissolved is disproportionate to give the crystalline zwitterionic form having a low aqueous solubility (&lt;0.009 mg / ml). The absence of this behavior for the compound of Example 1 provides an unexpected advantage in its formulation for pharmaceutical administration and results in improved pharmacokinetic properties as indicated in Table 1 (AUC in plasma and liver exposure for rats and dogs). The high exposure in

twenty Plasma and liver in preclinical species is advantageous for the selection of safe and effective doses for use in the treatment of patients.

Compound of formula (I) compared to Example 118 of WO 2008/057209

25 An observed advantage of the compound of formula (I) in comparison with Example 118 of WO2008 / 057209 is its resistance profile against different enzyme mutants. Compatible with data from cynical studies with antiviral agents of related classes (eg, VH protease inhibitors) and also from studies with HCV NS3 protease inhibitors (p. eg, VX-950, telaprevir), it is expected that viral resistance may develop in response to treatment with these compounds. The compound of Example 1 showed

30 Better enzyme affinity (Ki) against different known enzyme mutants that are known to confer resistance to HCV NS3 protease inhibitors. Table 2 summarizes the activity against different enzyme mutants. Therefore, an advantage of compound 2 may be an increase in the barrier to the development of resistant viruses when administered to patients. It also provides the possible advantage of treating patients in whom other therapies have failed due to the development of resistance, since compound 1 can inhibit this virus.

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Table 2 Ki1 values ​​against enzyme mutant 1b (nM)

<dl><dt>1b SHIFT </dt><dd>D168T D168A D168E D168G D168V D168Y D168Q </dd></dl>

<dl><dt>Example 1 </dt><dd> 0,18 0,43 0,04 0,08 0,14 0,22 0,12 </dd></dl>

<dl><dt>cmp 118 </dt><dd> 0,78 0,86 0,12 0,45 0,65 1,5 0,42 </dd></dl>

<dl><dt>1b SHIFT </dt><dd>A156S A156T A156V R155K R155Q R155G R155N </dd></dl>

<dl><dt>Example 1 </dt><dd> 0,05 5,2 11 0,07 0,43 0,63 0,13 </dd></dl>

<dl><dt>cmp 118 </dt><dd> 0,1 3,4 15 0,08 1,9 2,3 0,56 </dd></dl>

<dl><dt>1 Comparative data collected from the same cycle of enzyme tests. </dt><dd /></dl>

Other expected advantageous properties of the compound of formula (I) over the compound of Example 110 of WO 2008/057209 are the following:

5 1) Low covalent binding in vivo; and 2) High exposure in plasma and liver.

It was found that the compound of formula (I) has covalent binding characteristics and properties

10 Very good pharmacokinetics Based on the covalent binding observed in vivo and the pharmacokinetic properties of the compound of Example 1 and the compound of Example 118 of WO 2008/057209, the compound of formula (I) has covalent binding characteristics and pharmacokinetic properties in vivo significantly better.

fifteen Compounds that covalently bind to proteins, or that form metabolites that then covalently bind to proteins, give rise to adverse events in patients, such as immunological toxicities mediated by antibody responses to the drug-protein conjugate, and other idiosyncratic toxicities. (See Chem. Res. Toxicol. 2004, 17, 3-16).

twenty The compound of Example 1 showed an undetectable binding to plasma proteins after oral administration of a single dose of 20 mg / kg to rats. (See Table 1). Under analogous conditions, the compound of Example 118 of WO 2008/057209 demonstrated detectable binding to rat liver proteins (see Table 1) and, therefore, can be considered a less advantageous compound for administration to human subjects that the compound of formula (I).

25 Table 3 provides some in vivo covalent binding data observed for related compounds of WO 2008/057209 containing the (R, R) -trans-2-alkylcyclopentanol moiety incorporated in Example 118.

Table 3

<dl><dt>Example 108 of WO 2008/057209 </dt><dd>Example 103 of Document WO 2008/057209 Example 96 of Document WO 2008/057209 </dd></dl>

<dl><dt>Structure </dt><dd><figref>image25</figref><figref>image26</figref><figref>image27</figref></dd></dl>

<dl><dt>Covalent protein binding In Vivo4 </dt><dd>Rat plasma at 6h = 15 pmol eq./mg liver = 38 pmol eq / mg Rat plasma at 6h = 6 pmol eq./mg liver = 24 pmol eq / mg Rat plasma at 6h = 6 pmol eq./mg Liver = 63 pmol eq / mg </dd></dl>

30 It is advantageous to have a high plasma and liver exposure in preclinical species to effectively demonstrate that the potential drug candidate does not cause unwanted toxicities. It is also more likely that a compound that has high liver and plasma exposure in animals shows the same behavior in humans as one that does not. For said compound, the effective exposure required in humans can be

35 reach with a lower dose, both advantageous for the costs and the ease of manufacture of the drug, but also potentially decreases the likelihood of adverse effects. Exposure in the target organ in multiple preclinical species provides a rationale that high exposure in the target organ can be achieved for the compound in patients and that high liver exposure in dogs and rats allows

15

25

35

45

55

65

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Reliable assessment of preclinical toxicity. High liver exposure is especially advantageous for HC V, since this is the target organ for the drug.

The compound of Example 1 had a very good exposure in rat liver and plasma. The exposure in rat liver observed was at a level greater than compound 118 and compound 110 of WO 2008/057209 (see Table 1). Based on these results and the tests of different compounds of WO 2008/057209 by oral administration to rats ((25mpk) and dogs (5mpk), it is also expected that the compound of formula (I) has dog liver exposures greater than those of compound 118 and compound 110 of WO 2008/057209.

Methods

Inhibitory activity of NS 3 / 4A1 (Ki) The inhibitory activity of NS 3 / 4A was determined as described in Section IV. Evaluation of the compound ant. and Mao el al., Anal Biochem 373: 1-8, 2008.

Replicon activity2 EC50: Replicon activity was determined using the procedures described in Carroll et al., J. Biol. Chem. 278: 11979-11984, 2003 and Olsen et al., Anti Microb. Agents 48: 3944-3953, 2004.

AUC in rat plasma at 25mpk orally3: The test compounds were dissolved in a dosage vehicle suitable for iv administration (e.g., 20%: 60%: 20% DMSO: PEG400: Water) or administration by orally (e.g., 10% POLYSORBATE 80: 90% water or 100% PEG400). Administration in animals ( n = 3) was performed using a cross-study design for non-rodents. Plasma samples were collected at the time points between 2 minutes and 24 hours and the compound levels were determined by RP-HPLC. Liver samples were collected post mortem in rats and after anesthesia (0.5 h before biopsy) in dogs. The liver samples were weighed, homogenized and diluted using techniques known to the experts and the levels of the compound were determined by RP-HPLC.

Pharmacokinetic parameters were calculated based on non-compartmental analyzes (eg, using WATSON®, WINNOLIN®). Predosis concentrations below the quantification limit (BLQ) were assigned a value of 0. For the estimation of oral AUC, the first value of BL1 in the final phase was given a value equal to ½ the lower limit of quantification , while the following values ​​in the terminal phase were assigned a value of 0. The standard pharmacokinetic parameters, CLp, Vdss, half-life (only for IV),% F, Cmax, Tmax, AUC0-last, AUC0-infinity were calculated. ACU values ​​were calculated using the linear trapezoidal procedure for ascending concentrations and the trapezoidal log procedure for descending concentrations.

Covalent binding in vivo4: The test compounds were radiolabelled covalently (3H) and a dose of 20 mg / kg containing 25-75 mCi / rat (purity&gt; 98.5%) was prepared by combining the cold compound and stock solution of marked trace evaporated. This mixture was dissolved in a dosage vehicle suitable for oral administration (see above), then orally administered to the rats (n = 3 per time point, 2h, 6h, 24h). Plasma and livers were obtained and frozen / stored at -80 ° C before analysis.

Plasma sample count: Place a 200 µl aliquot in a 20 ml scintillation vial. Add 500 µl in SOLVABLE ™ and incubate for 1 h with stirring at 55 ° C. Remove, let cool before adding to a cocktail of 15 ml scintillation and count. Plasma samples (200 µl aliquot) were then processed as described below for liver proteins.

Tissue homogenization: Heavy liver samples were diluted with 2 vol of 100 mM phosphate buffer (pH 7.4) and homogenized on ice.

Hepatic homogenate count: The aliquots were placed in a 20 ml scintillation vial, diluted with 1 ml of SOLVABLE ™ and incubated for 1 h with shaking at 55 ° C. After extraction from the incubator and cooling, 15 ml of scintillation cocktail and 20% H2O2 were added and the radioactivity was counted.

Protein precipitation: Take an aliquot of 500 µl, add 1: 8 homogenate: acetonitrile (if it is suspected that the compound has a low solubility in acetonitrile, another solvent can be selected), vortex and centrifuge (3500 rpm for 29 minutes) Discard the supernatant.

Resuspension of the protein precipitate: Sonication (minimum intensity, &lt;5 s) and vortexing until the sediment is crushed in 80% MeOH: 20% water.

Protein sediment wash: 2-5 ml 80:20 MeOH: water If necessary, remove 1.0 ml of the supernatant, add 15 ml of scintillation cocktail and count. Continue washing the protein sediment until the radioactivity in the supernatant is &lt;200 DPM or DPM stops decreasing by more than 200 in consecutive washes.

Final sediment solution: 1 ml of 1 N NaOH or SOLVABLE ™, incubated at 50 ° C overnight or until completely dissolved.

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Final sediment count: 1 ml of the final sediment, 10 ml of scintillation cocktail (if another scintillation cocktail other than ULTIMA GOLD ™ is used, it may be necessary to neutralize using 1N HCl), and count.

Protein concentration of the final sediment: BCA or BIO-RAD Ki t using BSA as a standard. 5 White sample count: 15 ml of duplicate scintillation cocktail.

Dosing solution count: Count a known volume of the dosing solution in triplicate.

10 Data Analysis: Perform the average of the radioactivity counts (DPM) in the dosing solution and calculate the specific activity of the dosing solution in µCi / mol. Perform the average of the radioactivity counts of the blank samples. Subtract the average white sample counts from the counts obtained from each sediment in liver and plasma, Calculate the amount of radioactivity (µCi) per unit volume (l) for each sediment in liver and plasma. Calculate the concentration of radioactivity in each sediment

fifteen in liver and plasma by dividing the value obtained above ((µCi) by the specific activity ((µCi / mol). Calculate the amount of radioactivity covalently bound to the protein in pmol / mg protein.

White sample count: 15 ml of duplicate scintillation cocktail.

twenty Dosing solution count: Count a known volume of the dosing solution in triplicate.

Physical properties5: The crystalline test compounds (potassium salt, approx. 5 mg) were weighed into a glass vial and water or aqueous buffer (100 µl) was added. The obtained paste was stirred for 24 hours at room temperature. After centrifugation, the supernatant was analyzed by reverse phase HPLC and equilibrium solubility was determined by comparison with a calibration curve. The solid material was partially transferred to an XRPD plate, dried and analyzed by X-ray powder diffraction. The XRPD pattern was compared with positive controls for crystalline K + salt, crystalline (or acidic) crystalline zwitterionic forms and forms. Amorphous test compound. A further demonstration of the salt form was obtained from a second portion of the solid material that was analyzed by 400 MHz NMR (Bruker) after dissolution in DMSOd6. The spectra of

30 1 H NMR were compared with the positive controls described above.

Other embodiments are within the following claims. Although several embodiments have been shown and described, various modifications can be made without departing from the scope of the present invention defined with the claims.

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