ACYLAMINOHETEROARYL HEPATITIS C VIRUS PROTEASE INHIBITORS

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit of US application 11/503,502 filed August

11 ^th , 2006, the entire content of which is herein incorporated by reference.

TECHNICAL FIELD

The present invention relates to acylaminoheteroaryl hepatitis C virus (HCV) protease compounds having antiviral activity against HCV and useful in the treatment of HCV infections. More particularly, the invention relates to acylaminoheteroaryl HCV protease inhibitor compounds, compositions containing such compounds and methods for using the same, as well as processes for making such compounds.

BACKGROUND OF THE INVENTION

HCV is the principal cause of non-A, non-B hepatitis and is an increasingly severe public health problem both in the developed and developing world. It is estimated that the virus infects over 200 million people worldwide, surpassing the number of individuals infected with the human immunodeficiency virus (HIV) by nearly five fold. HCV infected patients, due to the high percentage of individuals inflicted with chronic infections, are at an elevated risk of developing cirrhosis of the liver, subsequent hepatocellular carcinoma and terminal liver disease. HCV is the most prevalent cause of hepatocellular cancer and cause of patients requiring liver transplantations in the western world.

There are considerable barriers to the development of anti-HCV therapeutics, which include, but are not limited to, the persistence of the virus, the genetic diversity of the virus during replication in the host, the high incident rate of the virus developing drug-resistant mutants, and the lack of reproducible infectious culture systems and small-animal models for HCV replication and pathogenesis. In a majority of cases, given the mild course of the infection and the complex biology

of the liver, careful consideration must be given to antiviral drugs, which are likely to have significant side effects.

Only two approved therapies for HCV infection are currently available. The original treatment regimen generally involves a 3-12 month course of intravenous interferon-α (IFN-α), while a new approved second-generation treatment involves co-treatment with IFN-α and the general antiviral nucleoside mimics like ribavirin. Both of these treatments suffer from interferon-related side effects as well as low efficacy against HCV infections. There exists a need for the development of effective antiviral agents for treatment of HCV infection due to the poor tolerability and disappointing efficacy of existing therapies.

In a patient population where the majority of individuals are chronically infected and asymptomatic and the prognoses are unknown, an effective drug preferably possesses significantly fewer side effects than the currently available treatments. The hepatitis C non-structural protein-3 (NS3) is a proteolytic enzyme required for processing of the viral polyprotein and consequently viral replication. Despite the huge number of viral variants associated with HCV infection, the active site of the NS3 protease remains highly conserved thus making its inhibition an attractive mode of intervention. Recent success in the treatment of HIV with protease inhibitors supports the concept that the inhibition of NS3 is a key target in the battle against HCV.

HCV is a flaviridae type RNA virus. The HCV genome is enveloped and contains a single strand RNA molecule composed of circa 9600 base pairs. It encodes a polypeptide comprised of approximately 3010 amino acids.

The HCV polyprotein is processed by viral and host peptidase into 10 discreet peptides which serve a variety of functions. There are three structural proteins, C, El and E2. The P7 protein is of unknown function and is comprised of a highly variable sequence. There are six non-structural proteins. NS2 is a zinc- dependent metalloproteinase that functions in conjunction with a portion of the NS3 protein. NS3 incorporates two catalytic functions (separate from its association with NS2): a serine protease at the N-terminal end, which requires

NS4A as a cofactor, and an ATP-ase-dependent helicase function at the carboxyl terminus. NS4A is a tightly associated but non-covalent cofactor of the serine protease.

The NS3-NS4A protease is responsible for cleaving four sites on the viral polyprotein. The NS3-NS4A cleavage is autocatalytic, occurring in cis. The remaining three hydrolyses, NS4A-NS4B, NS4B-NS5A and NS5A-NS5B all occur in trans. NS3 is a serine protease which is structurally classified as a chymotrypsin- like protease. While the NS serine protease possesses proteolytic activity by itself, the HCV protease enzyme is not an efficient enzyme in terms of catalyzing polyprotein cleavage. It has been shown that a central hydrophobic region of the NS4A protein is required for this enhancement. The complex formation of the NS3 protein with NS4A seems necessary to the processing events, enhancing the proteolytic efficacy at all of the sites.

A general strategy for the development of antiviral agents is to inactivate virally encoded enzymes, including NS3, that are essential for the replication of the virus. Current efforts directed toward the discovery of NS3 protease inhibitors were reviewed by S. Tan, A. Pause, Y. Shi, N. Sonenberg, Hepatitis C Therapeutics: Current Status and Emerging Strategies, Nature Rev. Drug Discov., 1, 867-881 (2002). Patent disclosures describing the synthesis of HCV protease inhibitors are: WO 00/59929 (2000); WO 99/07733 (1999); WO 00/09543 (2000); WO 99/50230 (1999); US5861297 (1999); US publications 20050153877, 20050261200 and 20050065073.

SUMMARY OF THE INVENTION

The present invention relates to acylaminoheteroaryl HCV protease compounds including pharmaceutically acceptable salts, esters, or prodrugs thereof which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the compounds of the present invention interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HCV infection. The present invention further features pharmaceutical compositions comprising a compound of the present invention (or a pharmaceutically acceptable salt, ester or prodrug thereof) and another anti-HCV agent, such as alpha-interferon, beta-interferon, ribavirin, amantadine, another HCV protease inhibitor, or an HCV polymerase, helicase or internal ribosome

entry site inhibitor. The invention also relates to methods of treating an HCV infection in a subject by administering a pharmaceutical composition of the present invention.

In one embodiment of the present invention there are disclosed compounds represented by Formulae I and II, or pharmaceutically acceptable salts, esters, or prodrugs thereof:

wherein A is selected from H, -(C=O)-O-Ri, -(C=O)-R ₂ , -C(O)-NH-R ₂ , or

-S(O) ₂ -Ri, -S(O) ₂ NHR ₂ ;

each Ri is independently selected from the group consisting of:

(i) aryl; (ii) substituted aryl;

(iii) heteroaryl;

(iv) substituted heteroaryl;

(v) heterocycloalkyl or substituted heterocycloalkyl;

(vi) -Ci-Cs alkyl, -C ₂ -Cs alkenyl, -C ₂ -Cs alkynyl each containing O, 1, 2, or 3 heteroatoms selected from O, S, or N;

(vii) substituted -Ci-C ₈ alkyl, substituted -C ₂ -C ₈ alkenyl, substituted -C ₂ -C ₈ alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;

(viii) -C ₃ -C ₁₂ cycloalkyl; (ix) substituted -C3-C ₁₂ cycloalkyl;

(x) -C3-C ₁₂ cycloalkenyl; and

(xi) substituted -C3-C ₁₂ cycloalkenyl;

each R ₂ is independently selected from the group consisting of: (i) hydrogen;

(ii) aryl;

(iii) substituted aryl;

(iv) heteroaryl;

(v) substituted heteroaryl; (vi) heterocycloalkyl or

(vii) substituted heterocycloalkyl;

(viii) -Ci-C ₈ alkyl, -C2-C ₈ alkenyl, -C ₂ -C ₈ alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;

(ix) substituted -Ci-C ₈ alkyl, substituted -C2-C ₈ alkenyl, substituted -C ₂ -C ₈ alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;

(x) -C ₃ -C ₁₂ cycloalkyl, or

(xi) substituted -C ₃ -C ₁₂ cycloalkyl;

(xii) -C ₃ -Ci ₂ cycloalkenyl, or ( ^χ iϋ) substituted -C ₃ -C ₁₂ cycloalkenyl;

R ₀ is H, Me, Et, -OH, or -C(O)NH ₂ ;

Ui, U ₂ , and U3 are independently selected from -CR ₃ and N, wherein R ₃ is independently selected from: (i) hydrogen; (ii) halogen; (iii) -NO ₂ ;

(iv) -CN;

(v) -M-R ₄ , Wherein M is absent, or O, S, NH, NR ₅ ;

(vi) aryl; substituted aryl; heteroaryl; substituted heteroaryl; and

(vii) heterocycloalkyl or substituted heterocycloalkyl;

Each R ₄ , R ₅ is independently selected from:

(i) hydrogen;

(ii) aryl;

(iii) substituted aryl; (iv) heteroaryl;

(v) substituted heteroaryl;

(vi) heterocycloalkyl;

(vii) substituted heterocycloalkyl;

(viii) -Ci-Cg alkyl, -C ₂ -Cg alkenyl, -C ₂ -C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S, or N;

(ix) substituted -Ci-Cg alkyl, substituted -C ₂ -Cg alkenyl, substituted -C ₂ -Cg alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N;

(x) -C3-C ₁₂ cycloalkyl; (xi) substituted -C3-C ₁₂ cycloalkyl;

(xii) -C ₃ -C ₁₂ cycloalkenyl; and

(xiii) substituted -C ₃ -C ₁₂ cycloalkenyl;

L is selected from -CH ₂ -, -O-, -S-, -S(O) ₂ -, -CO-, -C(O)O-, -C(O)NH-, - CHF-, -CF ₂ -, aryl, substituted aryl, heteroaryl, and substituted heteroaryl;

W and V are independently selected from the group consisting of:

(i) hydrogen;

(ii) aryl; (iii) substituted aryl;

(iv) heteroaryl;

(v) substituted heteroaryl;

(vi) heterocyclic or;

(vii) substituted heterocyclic;

(viii) -Ci-Cg alkyl, -C ₂ -C8 alkenyl, -C ₂ -C8 alkynyl each containing 0,

1, 2, or 3 heteroatoms selected from O, S or N;

(ix) substituted -Ci-Cg alkyl, substituted -C ₂ -C8 alkenyl, substituted -C2-C8 alkynyl each containing 0, 1, 2, or 3 heteroatoms selected from O, S or N; (x) -C3-C ₁₂ cycloalkyl; (xi) substituted -C3-C12 cycloalkyl; (xii) -C ₃ -C ₁₂ cycloalkenyl; and ( ^χm ) substituted -C ₃ -C ₁₂ cycloalkenyl;

X is absent or is selected from the group consisting of: (i) oxygen; (ii) sulfur; and (iii) NR ₄ ; where R ₄ is as previously defined above;

Y is absent or is selected from the group consisting of:

(i) -Ci-C ₆ alkyl containing 0, 1, 2, or 3 heteroatoms selected from O,

S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl; (ii) -C ₂ -C ₆ alkenyl containing 0, 1, 2, or 3 heteroatoms selected from

O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl;

(iii) -C ₂ -C ₆ alkynyl containing 0, 1 , 2, or 3 heteroatoms selected from

O, S, or N, optionally substituted with one or more substituent selected from halogen, aryl, substituted aryl, heteroaryl, or substituted heteroaryl; (iv) -C ₃ -C ₁₂ cycloalkyl;

(v) substituted -C3-C 12 cycloalkyl; (vi) heterocycloalkyl; and

(vii) substituted heterocycloalkyl;

Z is selected from aryl, substituted aryl, heteroaryl, and substituted heteroaryl;

J = O, 1, 2, 3, or 4; k=l, 2, or 3; m = 0, I, or 2; n = 1 , or 2; and

== denotes a carbon-carbon single or double bond.

DETAILED DESCRIPTION OF THE INVENTION A first embodiment of the invention is a compound represented by Formula

I as described above, or a pharmaceutically acceptable salt, ester or prodrug thereof, alone or in combination with a pharmaceutically acceptable carrier or excipient.

A second embodiment of the invention is a compound represented by Formula II as described herein, or a pharmaceutically acceptable salt, ester or prodrug thereof, alone or in combination with a pharmaceutically acceptable carrier or excipient.

Certain aspects of the invention include, but are not limited to:

A compound of Formula III or IV:

where A, X, Y, Z, W, Ro, U ₁ , U ₂ and U3 are as defined in Formula I.

A compound of Formula V or VI:

where A, X, Y, and Z are as defined in Formula I.

A compound of Formula VII or VIII:

wherein R ₆ is selected from aryl, substituted aryl, heteroaryl, or substituted heteroaryl; J is absent, O, S, NR ₅ , CO, (CO)NR ₅ , (CO)O, NR ₅ (CO), NH(CO)NH, NR5SO ₂ , alkylene, alkenylene and alkynylene; wherein A and R ₅ are as defined in Formula I; each R7 ₁ , R ₇₂ , R73 and R7 ₄ is independently selected from: (i) hydrogen; (ii) halogen;

(iii) -NO ₂ ;

(iv) -CN;

(v) -M-R ₄ , wherein M is absent, or O, S, NH, NR ₅ ;

(vi) aryl;

(vii) substituted aryl;

(viii) heteroaryl;

(ix) substituted heteroaryl;

(x) heterocycloalkyl; and

(xi) substituted heterocycloalkyl; and wherein R ₄ , R5 are as defined previously in Formula I.

A compound of Formulae IX and X:

( IX) ( X) wherein each R7 ₁ , R ₇₂ , R ₇ 3, and R ₇₄ are as defined previously in Formulae VIII; and A is as defined in Formula I .

A compound of Formula XI or XII:

( XI) ( XII)

wherein each R ₆ , R7 ₁ , R7 ₂ , R73, R7 ₄ and J are as defined previously in Formula VII or VIII; and A is as defined in Formula I .

A compound of Formula XIII or XIV:

(XIII) _or (XIV) wherein A and Z are as defined previously in Formula I .

Representative compounds of the invention include, but are not limited to, compounds 2-25 of the Formula XV:

( XV)

wherein A, Q and G are delineated for each example in Table 1.

TABLE 1

Representative compounds of the invention include, but are not limited to, the compounds 26-49 of the Formula XVI:

( XVI) wherein A, Q and G are delineated for each example in Table 2.

TABLE 2

The present invention also features pharmaceutical compositions comprising a compound of the present invention, or a pharmaceutically acceptable salt, ester or prodrug thereof.

According to an alternate embodiment, the pharmaceutical compositions of the present invention may further contain other anti-HCV agents. Examples of anti-HCV agents include, but are not limited to, interferon (e.g., alpha-interferon, beta-interferon, consensus interferon, pegylated interferon, or albumin or other conjugated interferon), ribavirin, and amantadine. For further details see S. Tan, A. Pause, Y. Shi, N. Sonenberg, Hepatitis C Therapeutics: Current Status and Emerging Strategies, Nature Rev. DrugDiscov., 1, 867-881 (2002); WO 00/59929 (2000); WO 99/07733 (1999); WO 00/09543 (2000); WO 99/50230 (1999); US5861297 (1999); and US2002/0037998 (2002) which are herein incorporated by reference in their entirety.

According to an additional embodiment, the pharmaceutical compositions of the present invention may further contain other HCV protease inhibitors.

According to yet another embodiment, the pharmaceutical compositions of the present invention may further comprise inhibitor(s) of other targets in the HCV life cycle, including, but not limited to, helicase, polymerase, metalloprotease, and internal ribosome entry site (IRES).

According to another embodiment, the pharmaceutical compositions of the present invention may further comprise another anti-viral, anti-bacterial, antifungal or anti-cancer agent, or an immune modulator, or another thearapeutic agent.

According to still another embodiment, the present invention includes methods of treating hepatitis C infections in a subject in need of such treatment by administering to said subject an anti-HCV virally effective amount of a compound of the present invention or a pharmaceutically acceptable salt, ester, or prodrug thereof.

According to a further embodiment, the present invention includes methods of treating hepatitis C infections in a subject in need of such treatment by administering to said subject an anti-HCV virally effective amount or an inhibitory amount of a pharmaceutical composition of the present invention. An additional embodiment of the present invention includes methods of treating biological samples by contacting the biological samples with the compounds of the present invention.

Yet a further aspect of the present invention is a process of making any of the compounds delineated herein employing any of the synthetic means delineated herein.

DEFINITIONS

Listed below are definitions of various terms used to describe this invention. These definitions apply to the terms as they are used throughout this specification and claims, unless otherwise limited in specific instances, either individually or as part of a larger group.

The terms "C ₁ -CO alkyl," or "Ci-Cs alkyl," as used herein, refer to saturated, straight- or branched-chain hydrocarbon radicals containing between one

and six, or one and eight carbon atoms, respectively. Examples of Ci-C ₆ alkyl radicals include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, tert-butyl, neopentyl, n-hexyl radicals; and examples of Ci-Cg alkyl radicals include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, tert-butyl, neopentyl, n-hexyl, heptyl, octyl radicals.

The terms "C ₂ -Cg alkenyl," or "C ₂ -Cs alkenyl," as used herein, denote a monovalent group derived from a hydrocarbon moiety containing from two to six, or two to eight carbon atoms having at least one carbon-carbon double bond by the removal of a single hydrogen atom. Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, l-methyl-2-buten-l-yl, heptenyl, octenyl and the like.

The term "C ₂ -C ₆ alkynyl," or "C ₂ -C ₈ alkynyl," as used herein, denote a monovalent group derived from a hydrocarbon moiety containing from two to six, or two to eight carbon atoms having at least one carbon-carbon triple bond by the removal of a single hydrogen atom. Representative alkynyl groups include, but are not limited to, for example, ethynyl, 1-propynyl, 1-butynyl, heptynyl, octynyl and the like.

The term "C ₃ -C ₈ -cycloalkyl", or "C ₃ -Ci ₂ -cycloalkyl," as used herein, denotes a monovalent group derived from a monocyclic or polycyclic saturated carbocyclic ring compound by the removal of a single hydrogen atom, respectively. Examples of C ₃ -C ₈ -CyC loalkyl include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentyl and cyclooctyl; and examples of C3-Ci ₂ -cycloalkyl include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, bicyclo [2.2.1] heptyl, and bicyclo [2.2.2] octyl. The term "C ₃ -Cg-cycloalkenyl", or "C ₃ -Ci ₂ -cycloalkenyl" as used herein, denote a monovalent group derived from a monocyclic or polycyclic carbocyclic ring compound having at least one carbon-carbon double bond by the removal of a single hydrogen atom. Examples of C ₃ -C ₈ -cycloalkenyl include, but not limited to, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, and the like; and examples of C ₃ -Ci ₂ -cycloalkenyl include, but not limited to, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, and the like.

The term "aryl," as used herein, refers to a mono- or bicyclic carbocyclic ring system having one or two aromatic rings including, but not limited to, phenyl, naphthyl, tetrahydronaphthyl, indanyl, idenyl and the like.

The term "arylalkyl," as used herein, refers to a C ₁ -C ₃ alkyl or C ₁ -C _O alkyl residue attached to an aryl ring. Examples include, but are not limited to, benzyl, phenethyl and the like.

The term "heteroaryl," as used herein, refers to a mono-, bi-, or tri-cyclic aromatic radical or ring having from five to ten ring atoms of which one ring atom is selected from S, O and N; zero, one or two ring atoms are additional heteroatoms independently selected from S, O and N; and the remaining ring atoms are carbon. Heteroaryl includes, but is not limited to, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzooxazolyl, quinoxalinyl, and the like. The term "heteroarylalkyl," as used herein, refers to a C ₁ -C ₃ alkyl or

C ₁ -Ce alkyl residue residue attached to a heteroaryl ring. Examples include, but are not limited to, pyridinylmethyl, pyrimidinylethyl and the like.

The terms "heterocyclic" and "heterocycloalkyl," can be used interchangeably and referred to a non-aromatic 3-, 4-, 5-, 6- or 7-membered ring or a bi- or tri-cyclic group fused system, where (i) each ring contains between one and three heteroatoms independently selected from oxygen, sulfur and nitrogen, (ii) each 5-membered ring has 0 to 1 double bonds and each 6-membered ring has 0 to 2 double bonds, (iii) the nitrogen and sulfur heteroatoms may optionally be oxidized, (iv) the nitrogen heteroatom may optionally be quaternized, and (iv) any of the above rings may be fused to a benzene ring. Representative heterocycloalkyl groups include, but are not limited to, [l,3]dioxolane, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, and tetrahydrofuryl. The term "substituted" as used herein, refers to independent replacement of one, two, or three or more of the hydrogen atoms thereon with substituents including, but not limited to, -F, -Cl, -Br, -I, -OH, protected hydroxy, -NO ₂ , -CN, - NH ₂ , protected amino, -NH -d-C^-alkyl, -NH -C ₂ -C ₁₂ -alkenyl, -NH -C ₂ -C ₁₂ -

alkenyl, -NH -C ₃ -Ci ₂ -cycloalkyl, -NH -aryl, -NH -heteroaryl, -NH - heterocycloalkyl, -dialkylamino, -diarylamino, -diheteroarylamino, -0-C ₁ -C ₁₂ - alkyl, -O-C ₂ -C ₁₂ -alkenyl, -O-C ₂ -C ₁₂ -alkenyl, -O-C ₃ -C ₁₂ -cycloalkyl, -O-aryl, -O- heteroaryl, -O-heterocycloalkyl, -C(O)- C _r Ci ₂ -alkyl, -C(O)- C ₂ -Ci ₂ -alkenyl, - C(O)- C ₂ -Ci ₂ -alkenyl, -C(O)-C ₃ -C ₁₂ -cycloalkyl, -C(O)-aryl, -C(O)-heteroaryl, - C(O)-heterocycloalkyl, -CONH ₂ , -CONH- Ci-Ci ₂ -alkyl, -CONH- C ₂ -Ci ₂ -alkenyl, - CONH- C ₂ -Ci ₂ -alkenyl, -CONH-C ₃ -Ci ₂ -cycloalkyl, -CONH-aryl, -CONH- heteroaryl, -CONH-heterocycloalkyl, -OCO ₂ - Ci-C ₁₂ -alkyl, -OCO ₂ - C ₂ -Ci ₂ - alkenyl, -OCO ₂ - C ₂ -C ₁₂ -alkenyl, -OCO ₂ -C ₃ -C ₁₂ -cycloalkyl, -OCO ₂ -aryl, -OCO ₂ - heteroaryl, -OCO ₂ -heterocycloalkyl, -OCONH ₂ , -OCONH- Ci-C ₁₂ -alkyl, -

OCONH- C ₂ -Ci ₂ -alkenyl, -OCONH- C ₂ -Ci ₂ -alkenyl, -OCONH- C ₃ -C ₁₂ -cycloalkyl, -OCONH- aryl, -OCONH- heteroaryl, -OCONH- heterocycloalkyl, -NHC(O)- C _r Ci ₂ -alkyl, -NHC(O)-C ₂ -Ci ₂ -alkenyl, -NHC(O)-C ₂ -Ci ₂ -alkenyl, -NHC(O)-C ₃ -Ci ₂ - cycloalkyl, -NHC(0)-aryl, -NHC(O)-heteroaryl, -NHC(O)-heterocycloalkyl, - NHCO ₂ - Ci-Ci ₂ -alkyl, -NHCO ₂ - C ₂ -Ci ₂ -alkenyl, -NHCO ₂ - C ₂ -Ci ₂ -alkenyl, - NHCO ₂ - C ₃ -Ci ₂ -cycloalkyl, -NHCO ₂ - aryl, -NHCO ₂ - heteroaryl, -NHCO ₂ - heterocycloalkyl, -NHC(O)NH ₂ , -NHC(O)NH- Ci-Ci ₂ -alkyl, -NHC(O)NH-C ₂ -Ci ₂ - alkenyl, -NHC(O)NH-C ₂ -C i ₂ -alkenyl, -NHC(O)NH-C ₃ -C i ₂ -cycloalkyl, - NHC(O)NH-aryl, -NHC(O)NH-heteroaryl, -NHC(O)NH-heterocycloalkyl, NHC(S)NH ₂ , -NHC(S)NH- Ci-Ci ₂ -alkyl, -NHC(S)NH-C ₂ -Ci ₂ -alkenyl, -

NHC(S)NH-C ₂ -Ci ₂ -alkenyl, -NHC(S)NH-C ₃ -C i ₂ -cycloalkyl, -NHC(S)NH-aryl, - NHC(S)NH-heteroaryl, -NHC(S)NH-heterocycloalkyl, -NHC(NH)NH ₂ , - NHC(NH)NH- Ci-Ci ₂ -alkyl, -NHC(NH)NH-C ₂ -Ci ₂ -alkenyl, -NHC(NH)NH-C ₂ - Ci ₂ -alkenyl, -NHC(NH)NH-C ₃ -Ci ₂ -cycloalkyl, -NHC(NH)NH-aryl, - NHC(NH)NH-heteroaryl, -NHC(NH)NH-heterocycloalkyl, -NHC(NH)-Ci-Ci ₂ - alkyl, -NHC(NH)-C ₂ -C i ₂ -alkenyl, -NHC(NH)-C ₂ -Ci ₂ -alkenyl, -NHC(NH)-C ₃ -Ci ₂ - cycloalkyl, -NHC(NH)-aryl, -NHC(NH)-heteroaryl, -NHC(NH)-heterocycloalkyl, -C(NH)NH-Ci-Ci ₂ -alkyl, -C(NH)NH-C ₂ -Ci ₂ -alkenyl, -C(NH)NH-C ₂ -C i ₂ -alkenyl, - C(NH)NH-C ₃ -C ₁₂ -cycloalkyl, -C(NH)NH-aryl, -C(NH)NH-heteroaryl, - C(NH)NH-heterocycloalkyl, -S(O)-Ci-Ci ₂ -alkyl, - S(O)-C ₂ -Ci ₂ -alkenyl, - S(O)-C ₂ - Ci ₂ -alkenyl, - S(O)-C ₃ -Ci ₂ -cycloalkyl, - S(O)-aryl, - S(O)-heteroaryl, - S(O)- heterocycloalkyl -SO ₂ NH ₂ , -SO ₂ NH- Ci-Ci ₂ -alkyl, -SO ₂ NH- C ₂ -Ci ₂ -alkenyl, - SO ₂ NH- C ₂ -Ci ₂ -alkenyl, -SO ₂ NH- C ₃ -Ci ₂ -cycloalkyl, -SO ₂ NH- aryl, -SO ₂ NH-

heteroaryl, -SO ₂ NH- heterocycloalkyl, -NHSO ₂ -C i-Ci ₂ -alkyl, -NHSO ₂ -C ₂ -Ci ₂ - alkenyl, - NHSO ₂ -C ₂ -C i ₂ -alkenyl, -NHSO ₂ -C ₃ -Ci ₂ -cycloalkyl, -NHSO ₂ -aryl, - NHSO ₂ -heteroaryl, -NHSO ₂ -heterocycloalkyl, -CH ₂ NH ₂ , -CH ₂ SO ₂ CH ₃ , -aryl, - arylalkyl, -heteroaryl, -heteroarylalkyl, -heterocycloalkyl, -CrCπ-cycloalkyl, polyalkoxyalkyl, polyalkoxy, -methoxymethoxy, -methoxyethoxy, -SH, -S-C ₁ -Ci ₂ - alkyl, -S-C ₂ -C ₁₂ -alkenyl, -S-C ₂ -C i ₂ -alkenyl, -S-C ₃ -C ₁₂ -cycloalkyl, -S-aryl, -S- heteroaryl, -S-heterocycloalkyl, or methylthiomethyl. It is understood that the aryls, heteroaryls, alkyls, and the like can be further substituted. In some cases, each substituent in a substituted moiety is additionally optionally substituted with one or more groups, each group being independently selected from -F, -Cl, -Br, -I, -OH, -NO ₂ , -CN, or -NH ₂ .

In accordance with the invention, any of the aryls, substituted aryls, heteroaryls and substituted heteroaryls described herein, can be any aromatic group. Aromatic groups can be substituted or unsubstituted. It is understood that any alkyl, alkenyl, alkynyl, cycloalkyl and cycloalkenyl moiety described herein can also be an aliphatic group, an alicyclic group or a heterocyclic group. An "aliphatic group" is non-aromatic moiety that may contain any combination of carbon atoms, hydrogen atoms, halogen atoms, oxygen, nitrogen or other atoms, and optionally contain one or more units of unsaturation, e.g., double and/or triple bonds. An aliphatic group may be straight chained, branched or cyclic and preferably contains between about 1 and about 24 carbon atoms, more typically between about 1 and about 12 carbon atoms. In addition to aliphatic hydrocarbon groups, aliphatic groups include, for example, polyalkoxyalkyls, such as polyalkylene glycols, polyamines, and polyimines, for example. Such aliphatic groups may be further substituted. It is understood that aliphatic groups may be used in place of the alkyl, alkenyl, alkynyl, alkylene, alkenylene, and alkynylene groups described herein.

The term "alicyclic," as used herein, denotes a monovalent group derived from a monocyclic or polycyclic saturated carbocyclic ring compound by the removal of a single hydrogen atom. Examples include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, bicyclo [2.2.1] heptyl, and bicyclo [2.2.2] octyl. Such alicyclic groups may be further substituted.

It will be apparent that in various embodiments of the invention that the substituted or unsubstituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkynyl, arylalkyl, heteroarylalkyl, and heterocycloalkyl are intended to be monovalent or divalent. Thus, alkylene, alkenylene, and alkynylene, cycloaklylene, cycloalkenylene, cycloalkynylene, arylalkylene, hetoerarylalkylene and heterocycloalkylene groups are to be included in the above definitions, and are applicable to provide the formulas herein with proper valency.

The term "hydroxy activating group", as used herein, refers to a labile chemical moiety which is known in the art to activate a hydroxy group so that it will depart during synthetic procedures such as in a substitution or elimination reactions. Examples of hydroxy activating group include, but not limited to, mesylate, tosylate, triflate, />nitrobenzoate, phosphonate and the like.

The term "activated hydroxy", as used herein, refers to a hydroxy group activated with a hydroxy activating group, as defined above, including mesylate, tosylate, triflate, p-nitrobenzoate, phosphonate groups, for example.

The term "protected hydroxy," as used herein, refers to a hydroxy group protected with a hydroxy protecting group, as defined above, including benzoyl, acetyl, trimethylsilyl, triethylsilyl, methoxymethyl groups.

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

The compounds described herein contain one or more asymmetric centers and thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)- , or as (D)- or (L)- for amino acids. The present invention is meant to include all such possible isomers, as well as their racemic and optically pure forms. Optical isomers may be prepared from their respective optically active precursors by the procedures described above, or by resolving the racemic mixtures. The resolution can be carried out in the presence of a resolving agent, by chromatography or by repeated crystallization or by some combination of these techniques which are known to those skilled in the art. Further details regarding resolutions can be found in Jacques, et al, Enantiomers, Racemates, and Resolutions (John Wiley & Sons, 1981). When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless specified otherwise, it is

intended that the compounds include both E and Z geometric isomers. Likewise, all tautomeric forms are also intended to be included. The configuration of any carbon-carbon double bond appearing herein is selected for convenience only and is not intended to designate a particular configuration unless the text so states; thus a carbon-carbon double bond depicted arbitrarily herein as trans may be cis, trans, or a mixture of the two in any proportion.

The term "subject" as used herein refers to a mammal. A subject therefore refers to, for example, dogs, cats, horses, cows, pigs, guinea pigs, and the like. Preferably the subject is a human. When the subject is a human, the subject may be referred to herein as a patient.

As used herein, the term "pharmaceutically acceptable salt" refers to those salts of the compounds formed by the process of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art.

The term "hydroxy protecting group," as used herein, refers to a labile chemical moiety which is known in the art to protect a hydroxy group against undesired reactions during synthetic procedures. After said synthetic procedure(s) the hydroxy protecting group as described herein may be selectively removed.

Hydroxy protecting groups as known in the are described generally in T.H. Greene and P. G., S. M. Wuts, Protective Groups in Organic Synthesis. 3rd edition, John Wiley & Sons, New York (1999). Examples of hydroxy protecting groups include benzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, 4-bromobenzyloxycarbonyl, 4- methoxybenzyloxycarbonyl, methoxycarbonyl, tert-butoxycarbonyl, isopropoxycarbonyl, diphenylmethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2- (trimethylsilyl)ethoxycarbonyl, 2-furfuryloxycarbonyl, allyloxycarbonyl, acetyl, formyl, chloroacetyl, trifluoroacetyl, methoxyacetyl, phenoxyacetyl, benzoyl, methyl, t-butyl, 2,2,2-trichloroethyl, 2-trimethylsilyl ethyl, 1 , 1 -dimethyl-2- propenyl, 3 -methyl- 3 -butenyl, allyl, benzyl, para-methoxybenzyldiphenylmethyl, triphenylmethyl (trityl), tetrahydrofuryl, methoxymethyl, methylthiomethyl, benzyloxymethyl, 2,2,2-triehloroethoxymethyl, 2-(trimethylsilyl)ethoxymethyl, methanesulfonyl, para-toluenesulfonyl, trimethylsilyl, triethylsilyl,

triisopropylsilyl, and the like. Preferred hydroxy protecting groups for the present invention are acetyl (Ac or -C(O)CH ₃ ), benzoyl (Bz or -C(O)CeH ₅ ), and trimethylsilyl (TMS or-Si(CH ₃ ) ₃ ).Berge, et al. describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 66: 1-19 (1977). The salts can be prepared in situ during the final isolation and purification of the compounds of the invention, or separately by reacting the free base function with a suitable organic acid. Examples of pharmaceutically acceptable include, but are not limited to, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include, but are not limited to, adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2- naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, />toluenesulfonate, undecanoate, valerate salts, and the like. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, alkyl having from 1 to 6 carbon atoms, sulfonate and aryl sulfonate.

The term "amino protecting group," as used herein, refers to a labile chemical moiety which is known in the art to protect an amino group against undesired reactions during synthetic procedures. After said synthetic procedure(s) the amino protecting group as described herein may be selectively removed. Amino protecting groups as known in the are described generally in T.H. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3rd edition, John

Wiley & Sons, New York (1999). Examples of amino protecting groups include, but are not limited to, t-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, benzyloxycarbonyl, and the like.

As used herein, the term "pharmaceutically acceptable ester" refers to esters of the compounds formed by the process of the present invention which hydro lyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Suitable ester groups include, for example, those derived from pharmaceutically acceptable aliphatic carboxylic acids, particularly alkanoic, alkenoic, cycloalkanoic and alkanedioic acids, in which each alkyl or alkenyl moiety advantageously has not more than 6 carbon atoms.

Examples of particular esters include, but are not limited to, formates, acetates, propionates, butyrates, acrylates and ethylsuccinates.

The term "pharmaceutically acceptable prodrugs" as used herein refers to those prodrugs of the compounds formed by the process of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals with undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the present invention. "Prodrug", as used herein means a compound which is convertible in vivo by metabolic means (e.g. by hydrolysis) to afford any compound delineated by the formulae of the instant invention. Various forms of prodrugs are known in the art, for example, as discussed in Bundgaard, (ed.), Design of Prodrugs, Elsevier (1985); Widder, et al. (ed.), Methods in Enzymology, vol. 4, Academic Press (1985); Krogsgaard-Larsen, et al., (ed). "Design and Application of Prodrugs, Textbook of Drug Design and Development, Chapter 5, 113-191 (1991); Bundgaard, et al., Journal of Drug Deliver Reviews, 8:1-38(1992); Bundgaard, J. of Pharmaceutical Sciences, 77:285 et seq. (1988); Higuchi and Stella (eds.) Prodrugs as Novel Drug Delivery Systems, American Chemical Society (1975); and Bernard Testa & Joachim Mayer, "Hydrolysis In Drug And Prodrug Metabolism: Chemistry, Biochemistry And Enzymology," John Wiley and Sons, Ltd. (2002).

The term "acyl" includes residues derived from acids, including but not limited to carboxylic acids, carbamic acids, carbonic acids, sulfonic acids, and

phosphorous acids. Examples include aliphatic carbonyls, aromatic carbonyls, aliphatic sulfonyls, aromatic sulfmyls, aliphatic sulfmyls, aromatic phosphates and aliphatic phosphates. Examples of aliphatic carbonyls include, but are not limited to, acetyl, propionyl, 2-fluoroacetyl, butyryl, 2-hydroxy acetyl, and the like. The term "aprotic solvent," as used herein, refers to a solvent that is relatively inert to proton activity, i.e., not acting as a proton-donor. Examples include, but are not limited to, hydrocarbons, such as hexane and toluene, for example, halogenated hydrocarbons, such as, for example, methylene chloride, ethylene chloride, chloroform, and the like, heterocyclic compounds, such as, for example, tetrahydrofuran and N-methylpyrrolidinone, and ethers such as diethyl ether, bis-methoxymethyl ether. Such solvents are well known to those skilled in the art, and individual solvents or mixtures thereof may be preferred for specific compounds and reaction conditions, depending upon such factors as the solubility of reagents, reactivity of reagents and preferred temperature ranges, for example. Further discussions of aprotic solvents may be found in organic chemistry textbooks or in specialized monographs, for example: Organic Solvents Physical Properties and Methods of Purification, 4th ed., edited by John A. Riddick et al., Vol. II, in the Techniques of Chemistry Series, John Wiley & Sons, NY, 1986.

The terms "protogenic organic solvent," or "protic solvent" as used herein, refer to a solvent that tends to provide protons, such as an alcohol, for example, methanol, ethanol, propanol, isopropanol, butanol, t-butanol, and the like. Such solvents are well known to those skilled in the art, and individual solvents or mixtures thereof may be preferred for specific compounds and reaction conditions, depending upon such factors as the solubility of reagents, reactivity of reagents and preferred temperature ranges, for example. Further discussions of protogenic solvents may be found in organic chemistry textbooks or in specialized monographs, for example: Organic Solvents Physical Properties and Methods of Purification, 4th ed., edited by John A. Riddick et al, Vol. II, in the Techniques of Chemistry Series. John Wiley & Sons, NY, 1986. Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. The term "stable", as used herein, refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient

period of time to be useful for the purposes detailed herein (e.g., therapeutic or prophylactic administration to a subject).

The synthesized compounds can be separated from a reaction mixture and further purified by a method such as column chromatography, high pressure liquid chromatography, or recrystallization. As can be appreciated by the skilled artisan, further methods of synthesizing the compounds of the formulae herein will be evident to those of ordinary skill in the art. Additionally, the various synthetic steps may be performed in an alternate sequence or order to give the desired compounds. In addition, the solvents, temperatures, reaction durations, etc. delineated herein are for purposes of illustration only and one of ordinary skill in the art will recognize that variation of the reaction conditions can produce the desired bridged macrocyclic products of the present invention. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing the compounds described herein are known in the art and include, for example, those such as described in R. Larock, Comprehensive

Organic Transformations. VCH Publishers (1989); T.W. Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis, 2d. Ed., John Wiley and Sons (1991); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis. John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995).

The compounds of this invention may be modified by appending various functionalities via any synthetic means delineated herein to enhance selective biological properties. Such modifications are known in the art and include those which increase biological penetration into a given biological system (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.

PHARMACEUTICAL COMPOSITIONS The pharmaceutical compositions of the present invention comprise a therapeutically effective amount of a compound of the present invention formulated together with one or more pharmaceutically acceptable carriers. As used herein, the term "pharmaceutically acceptable carrier" means a non-toxic,

inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials which can serve as pharmaceutically acceptable carriers are sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols; such a propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator. The pharmaceutical compositions of this invention can be administered to humans and other animals orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments, or drops), buccally, or as an oral or nasal spray. The pharmaceutical compositions of this invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir, preferably by oral administration or administration by injection. The pharmaceutical compositions of this invention may contain any conventional non-toxic pharmaceutically-acceptable carriers, adjuvants or vehicles. In some cases, the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form. The term parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intraarterial, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert

diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifϊers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3- butylene glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents. Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S. P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables.

The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use. In order to prolong the effect of a drug, it is often desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle. Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide.

Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.

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

Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically acceptable excipient or carrier such as sodium citrate or dicalcium phosphate and/or: a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like. The active compounds can also be in micro-encapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings, release controlling coatings and other coatings well known in the

pharmaceutical formulating art. In such solid dosage forms the active compound may be admixed with at least one inert diluent such as sucrose, lactose or starch. Such dosage forms may also comprise, as is normal practice, additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such a magnesium stearate and microcrystalline cellulose. In the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes.

Dosage forms for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulation, ear drops, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.

The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to the compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants such as chlorofluorohydrocarbons.

Transdermal patches have the added advantage of providing controlled delivery of a compound to the body. Such dosage forms can be made by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.

Antiviral Activity

An inhibitory amount or dose of the compounds of the present invention may range from about 0.1 mg/kg to about 500 mg/kg, alternatively from about 1 to about 50 mg/kg. Inhibitory amounts or doses will also vary depending on route of administration, as well as the possibility of co-usage with other agents.

According to the methods of treatment of the present invention, viral infections are treated or prevented in a subject, such as a human, by administering to the subject a therapeutically effective amount of a compound of the invention, in such amounts and for such time as is necessary to achieve the desired result. An additional method of the present invention is the treatment of biological samples with an inhibitory amount of a compound of composition of the present invention in such amounts and for such time as is necessary to achieve the desired result.

The term "therapeutically effective amount" of a compound of the invention, as used herein, means a sufficient amount of the compound so as to decrease the viral load in a subject and/or decrease the subject's HCV symptoms. As is well understood in the medical arts a therapeutically effective amount of a compound of this invention will be at a reasonable benefit/risk ratio applicable to any medical treatment. The term "anti-hepatitis C virally effective amount" of a compound of the invention, as used herein, mean a sufficient amount of the compound so as to decrease the viral load in a biological sample or in a subject. As well understood in the medical arts, an anti-hepatitis C virally effective amount of a compound of this invention will be at a reasonable benefit/risk ratio applicable to any medical treatment.

It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific

compound employed; the duration of the treatment; drugs used in combination or contemporaneously with the specific compound employed; and like factors well known in the medical arts.

The total daily dose of the compounds of this invention administered to a human or other animal in single or in divided doses can be in amounts, for example, from 0.01 to 50 mg/kg body weight or more usually from 0.1 to 25 mg/kg body weight. Single dose compositions may contain such amounts or submultiples thereof to make up the daily dose. In general, treatment regimens according to the present invention comprise administration to a patient in need of such treatment from about 10 mg to about 1000 mg of the compound(s) of this invention per day in single or multiple doses.

Lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the patient's disposition to the disease, condition or symptoms, and the judgment of the treating physician.

The term "inhibitory amount" of a compound of the present invention means a sufficient amount to decrease the hepatitis C viral load in a biological sample or a subject.

It is understood that when said inhibitory amount of a compound of the present invention is administered to a subject it will be at a reasonable benefit/risk ratio applicable to any medical treatment as determined by a physician. Upon improvement of a patient's condition, a maintenance dose of a compound, composition or combination of this invention may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level. Patients may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.

An additional method of the present invention is the treatment of biological samples with an inhibitory amount of a compound of the present invention in such

amounts and for such time as is necessary to inhibit viral replication and/or reduce viral load in the biological sample. The term "inhibitory amount" means a sufficient amount to inhibit viral replication and/or decrease the hepatitis C viral load in a biological sample. The term "biological sample(s)" as used herein means a substance of biological origin intended for administration to a subject. Examples of biological samples include, but are not limited to blood and components thereof such as plasma, platelets, subpopulations of blood cells and the like; organs such as kidney, liver, heart, lung, and the like; sperm and ova; bone marrow and components thereof; or stem cells. Thus another embodiment of the present invention is a method of treating a biological sample by contacting said biological sample with an inhibitory amount of a compound or pharmaceutical composition of the present invention.

Unless otherwise defined, all technical and scientific terms used herein are accorded the meaning commonly known to one with ordinary skill in the art. All publications, patents, published patent applications, and other references mentioned herein are hereby incorporated by reference in their entirety.

ABBREVIATIONS

Abbreviations which have been used in the descriptions of the schemes and the examples that follow are:

ACN for acetonitrile;

Ac for acetyl;

Boc for ?erϊ-butoxycarbonyl;

Bz for benzoyl; Bn for benzyl;

CDI for carbonyldiimidazole; dba for dibenzylidene acetone;

CDI for l,r-carbonyldiimidizole;

DBU for l,8-diazabicyclo[5.4.0]undec-7-ene; DCM for dichloromethane;

DIAD for diisopropylazodicarboxylate;

DMAP for dimethylaminopyridine;

DMF for dimethyl formamide;

DMSO for dimethyl sulfoxide; dppb for diphenylphosphino butane;

EtOAc for ethyl acetate;

HATU for 2-(7-Aza- 1 H-benzotriazole- 1 -yl)- 1,1,3 ,3 -tetramethyluronium hexafluorophosphate; iPrOH for isopropanol;

NaHMDS for sodium bis(trimethylsilyl)amide;

NMO for N-methylmorpholine N-oxide;

MeOH for methanol; Ph for phenyl;

POPd for dihydrogen dichlorobis(di-tert-butylphosphino)palladium(II);

TBAHS for tetrabutyl ammonium hydrogen sulfate;

TEA for triethylamine;

THF for tetrahydrofuran; TPP for triphenylphosphine;

Tris for Tris(hydroxymethyl)aminomethane;

BME for 2-mercaptoethanol;

BOP for benzotriazol-l-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate; COD for cyclooctadiene;

DAST for diethylaminosulfur trifluoride;

DABCYL for 6-(N-4'-carboxy-4-(dimethylamino)azobenzene)- aminohexyl-l-O-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramid ite;

DCM for dichloromethane; DIAD for diisopropyl azodicarboxylate;

DIBAL-H for diisoburylaluminum hydride;

DIEA for diisopropyl ethylamine;

DMAP for N,N-dimethylaminopyridine;

DME for ethylene glycol dimethyl ether; DMEM for Dulbecco's Modified Eagles Media;

EDANS for 5 -(2-Amino-ethylamino)-naphthalene-l -sulfonic acid;

DMF for N,N-dimethyl formamide;

ESI for electrospray ionization;

Et DMSO for dimethylsulfoxide;

DUPHOS for

EDANS for 5 -(2-Amino-ethylammo)-naphthalene-l -sulfonic acid;

EDCI or EDC for l-(3-diethylaminopropyl)-3-ethylcarbodiimide hydrochloride;

EtOAc for ethyl acetate;

HATU for O (7-Azabenzotriazole-l-yl)-N,N,N',N' - tetramethyluronium hexafluorophosphate;

Hoveyda's Cat. for Dichloro(o-isopropoxyphenylmethylene) (tricyclohexylphosphine)ruthenium(II);

KHMDS is potassium bis(trimethylsilyl) amide;

Ms for mesyl;

NMM for N-4-methylmorpholine;

PyBrOP for Bromo-tri-pyrolidino-phosphonium hexafluorophosphate; Ph for phenyl;

RCM for ring-closing metathesis; rt for room temperature;

HATU for O-(7-Azabenzotriazole- 1 -yl)-N,N,N' ,N '-tetramethyluronium hexafluoro-phosphate; HPLC for high-performance liquid chromatography;

Ph for phenyl;

Me for methyl;

RT for reverse transcription;

RT-PCR for reverse transcription-polymerase chain reaction; TEA for triethyl amine;

TFA for trifluoroacetic acid;

THF for tetrahydrofuran;

TLC for thin layer chromatography;

TPP or PPI13 for triphenylphosphine; tBOC or Boc for tert-butyloxy carbonyl; and

Xantphos for 4,5-Bis-diphenylphosphanyl-9,9-dimethyl-9H-xanthene.

SYNTHETIC METHODS

The compounds and processes of the present invention will be better understood in connection with the following synthetic schemes that illustrate the methods by which the compounds of the invention may be prepared.

Scheme 1.

LiOH H ₂ O 83.7%, 3 steps

1-6 1-5

All of the quinoxaline analogs were prepared from the common intermediate 1.-6. The synthesis of compound 1.-6 is outlined in Scheme 1. Deprotection of commercially available Boc-hydroxyproline 1- 1 with HCl in dioxane followed by coupling with acid 1.-2 using HATU, afforded intermediate 1- 3. Other amino acid derivatives containing a terminal alkene may be used in place of 1.-2 in order to generate varied macrocyclic structures (for further details see WO/0059929). Hydrolysis of 1-3 with LiOH followed by subsequent peptide coupling with cyclopropyl-containing amine 1.-4 yielded tri-peptide 1-5. Finally, ring-closing metathesis with a ruthenium-based catalyst gave the desired key intermediate 1.-6 (for further details on ring closing metathesis see recent reviews: Grubbs et al, Ace. Chem. Res., 1995, 28, 446; Shrock et al, Tetrahedron 1999, 55,

8141; Furstner, A. Angew. Chem. Int. Ed. 2000, 39, 3012; Trnka et al, Ace. Chem. Res. 2001, 34, 18; and Hoveyda et al., Chem. Eur. J. 2001, 7, 945).

Scheme 2.

The quinoxaline analogs of the present invention were prepared via several different synthetic routes. The simplest method, shown in Scheme 2, was to condense commercially available lH-quinoxalin-2-one analogs including, but not limited to, compounds 2-2 - 2-5 with key intermediate 1-6 by using Mitsunobu conditions followed by hydrolysis with LiOH. The existing literature predicts Mistonobu product formation at the 1 position nitrogen, however attachment at the carbonyl oxygen was observed to form compound 2-1. A detailed discussion of the identification and characterization of the unexpected oxo Mitosunobu addition product appears in the examples herein. For further details on the Mitsunobu reaction, see O. Mitsunobu, Synthesis 1981, 1-28; D. L. Hughes, Org. React. 29, 1- 162 (1983); D. L. Hughes, Organic Preparations and Procedures Int. 28, 127-164 (1996); and J. A. Dodge, S. A. Jones, Recent Res. Dev. Org. Chem. 1, 273-283 (1997).

Scheme 3.

The quinoline analogs 3-1 of the present invention were prepared via a regular Mrtsunobu reaction between the commercially available or otherwise easily synthesized quinolmes 3-2 and the macrocyclic l_-6 followed by hydrolysis with LiOH (Scheme 3).

Scheme 4.

The macrocyclic starting material 4-1 was prepared following Scheme- 1 by starting with the commercially available trans-Boc-hydroxyproline. Compounds of Formula 4-3 (the carbamates) were prepared by reacting 4-1 with CDI and isoindoline derivatives 4-2 followed by hydrolysis with LiOH (Scheme 4). R71 , R72, R73 and R74 are as previously defined in Formula I.

Scheme 5.

The tetrazole or triazole analogs of the present invention (5-2 and 5-3) are prepared by one of the two methods. 1) Through the cyclic precursor mesylate 5-1: 5-1 was synthesized by forming the mesylate upon the hydroxyl of the hydroxyl proline residue of the cyclic peptide precursor l_-6 via the synthetic route generally described above in Scheme 5. The compounds of the present invention are made via the replacement of the mesylate of the macrocyclic peptide mesylate 5-1 with a 5-substituted-2H-tetrazole, or a 4,5-substituted-lη-triazole, wherein Ql, Q2 is independently selected from -J-R6, and -J-R6 is as previously defined. 2) Through a Mitsunobu reaction between the compound 1-6 and a 5-substituted-2H-tetrazole, or a 4,5-substituted-lη-triazole, wherein Ql, Q2 is independently selected from - J-R6, and -J-R6 is as previously defined. Exemplary syntheses of such tetrazoloes and triazoles and further details of the mesylate replacement method could be found in the commonly assigned patent applications U.S. Serial Nos.10/360,947 (filed Feb. 7, 2003) and 10/365,854 (filed Feb. 13, 2003).

Scheme 6.

Scheme 6 illustrates the modification of the C-teminal of the macrocycle. The compounds 6-3 could be prepared by the reaction sequence of: 1) activation of the acid moiety of compound 6-1 by using a commonly known condensing reagent (i.e. CDI, HATU, EDC and the like); 2) followed by treatment with appropriate heteroaryl amines or substituted heteroaryl amines 6-2 including, but not limited to aminotetrazole, aminotriazole groups. Wherein A, X, Y, Z, RO, Ul, U2 and U3 are as previously defined in Formula I.

Scheme 7.

Scheme 7 illustrates the modification of the N-terminal and C-teminal of the macrocycle. Deprotection of the boc moiety with an acid, such as, but not limited to hydrochloric acid yields compounds of formula (7-2). The amino moiety of formula (7-2) can be alkylated or acylated with appropriate alkyl halide or acyl groups to give compounds of formula (7-3). Compounds of formula (7-3) can be hydrolyzed with base such as lithium hydroxide to free up the acid moiety

of formula (7-4). Subsequent activation of the acid moiety (i.e CDI, HATU, EDC and the like) followed by treatment with appropriate heteroaryl amines or substituted heteroaryl amines including, but not limited to ammotetrazole, aminotriazole groups to provide compounds of formula (7-5), wherein A, X, Y, Z, RO, Ul, U2 and U3 are as previously defined in Formula I.

Scheme 8.

Scheme 8 outlines the general route for the preparation of acyclic derivatives of the compounds with the structure 8-6 The synthesis of compound 8-5 is analog to the synthesis of compound 1.-5 shown m Scheme 1. Coupling of the commercially available compound 8-1 with acid 8-2 using HATU, afforded intermediate 8-3. Hydrolysis of 8-3 with LiOH followed by subsequent peptide coupling with cyclopropyl-contaimng amine 1-4 yielded tri-peptide 8-5. Compound 8-5 was converted to compound 8-6 by the methods described in Schemes 2-7 by using the acyclic starting mateπal in the place of the macrocyclic cores.

All references cited herein, whether m pπnt, electronic, computer readable storage media or other form, are expressly incorporated by reference in their entirety, including but not limited to, abstracts, articles, journals, publications, texts, treatises, internet web sites, databases, patents, and patent publications.

EXAMPLES

The compounds and processes of the present invention will be better understood in connection with the following examples (example numbers correlate with numbers within table 1), which are intended as illustrations only and not to

limit the scope of the invention. Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art and such changes and modifications including, without limitation, those relating to the chemical structures, substituents, derivatives, formulations and/or methods of the invention may be made without departing from the spirit of the invention and the scope of the appended claims.

Example 1. Synthesis of the cyclic peptide precursor:

2 eq eq

IA. To a solution of Boc-L-2-amino-8-nonenoic acid Ia (1.36g, 5 mol) and the commercially available cz ^' s-L-hydroxyproline methyl ester Ib (1.09g, 6 mmol) in 15 ml DMF, DIEA (4 ml, 4eq.) and HATU (4g, 2eq) were added. The coupling was carried out at O ⁰ C over a period of 1 hour. The reaction mixture was diluted with 100 mL EtOAc, and directly washed with 5% citric acid (2x 20 ml), water (2x 20 ml), IM NaHCO ₃ (4x 20 ml) and brine

(2x 10 ml). The organic phase was dried over anhydrous Na ₂ SO ₄ , filtered, and then concentrated in vacuo, affording the dipeptide Ic (1.9Ig, 95.8%) that was identified by HPLC (Retention time = 8.9 min, 30-70%, 90%B), and MS (found 421.37, M+Na ⁺ ).

IB. Dipeptide Ic (1.9Ig) was dissolved in 15 mL of dioxane and 15 mL of 1 N LiOH aqueous solution, and the resulting mixture was stirred at room temperature for 4 hours. The reaction mixture was acidified by 5% citric acid and extracted with 100 mL EtOAc. The organic portion was then

washed with water (2x 20 ml), IM NaHCO ₃ (2x 20 ml) and brine (2x 20 ml). The organic phase was dried over anhydrous Na ₂ SO ₄ , filtered, and then concentrated in vacuo, yielding the free carboxylic acid compound Id (1.79g, 97%), which was used directly without the need for further purification.

1C. To a solution of the free acid obtained above (1.77, 4.64 mmol) in 5 ml DMF, D-β-vinyl cyclopropane amino acid ethyl ester Ie (0.95g, 5 mmol), DIEA (4 ml, 4eq.) and HATU (4g, 2eq) were added. The coupling was carried out at 0 ⁰ C over a period of 5 hours. The reaction mixture was diluted with 80 mL EtOAc, and washed with 5% citric acid (2x 20 ml), water (2x 20 ml), IM NaHCO ₃ (4x 20 ml), and brine (2x 10 ml). The organic phase was dried over anhydrous Na ₂ SO ₄ , filtered, and then concentrated in vacuo. The residue was purified by silica gel flash chromatography using gradient elution with hexanes: EtOAc

(5: 1— »3: 1— »1 : 1— »1 :2— »1 :5). The linear tripeptide If was isolated as an oil (1.59g, 65.4%) and identified by HPLC (Retention time = 11.43 min) and MS (found 544.84, M+Na ⁺ ).

ID. Ring Closing Metathesis (RCM). A solution of the linear tripeptide

If (1.51 g, 2.89 mmol) in 200 ml dry DCM was deoxygenated by N ₂ bubbling. Hoveyda's 1 ^st generation catalyst (5 mol% eq.) was then added as a solid. The reaction was refluxed under N2 atmosphere for 12 hours. The solvent was evaporated and the residue was purified by silica gel flash chromatography using gradient elution with hexanes:EtOAc

(9: 1— »5:1— »3: 1— >1 : 1— »1 :2— »1 :5). The cyclic peptide precursor 1 was isolated as a white powder (1.24g, 87%), and identified by HPLC (Retention time = 7.84 min, 30-70%, 90%B), and MS (found 516.28, M+Na ⁺ ). For further details of the synthetic methods employed to produce the cyclic peptide precursor 1, see WO 00/059929 (2000).

Example 2. Compound of Formula XV, wherein A = αx Q=

Step 2A.

(2eq) OEt

To a cooled mixture of macrocyclic precursor 1, 3-(thiophen-2-yl)-lH- quinoxalin-2-one 2a (1.1 equiv.), and triphenylphosphine (2 equiv.) in THF was added DIAD (2 equiv.) dropwise at O ⁰ C. The resulting mixture was held at O ⁰ C for 15 min. before being warmed to room temperature. After 18 hours, the mixture was concentrated under vacuum and the residue was purified by chromatography eluting with 60% EtOAc in hexanes to give 2b as a clear oil (100 mg, 99%). MS (found): 704.4 (M+H) .

H'-NMR [CDCl ₃ , δ (ppm)]: 8.6 (d, IH), 8.0 (d, IH), 7.8 (d, IH), 7.6 (m, 2H), 7.5 (d, 2H), 7.2 (t, IH), 7.0 (brs, IH), 6.0 (brt, IH), 5.5 (m, IH), 5.3 (brd, IH), 5.2 (t, IH), 5.0 (m. IH), 4.6 (brt, IH), 4.1-4.3 (m, 3H), 3.1 (m, IH), 5.3 (m, IH), 2.1-2.3 (m, 2H), 1.3 (brs, 9H), 1.2 (t, 3H).

Step 2B. Amine deprotection.

The title compound of Step 2A (82 mg, 0.116 mmol) was treated with HCl (4 M in dioxane, 3 mL, 12 mmol). The reaction mixture was stirred at room temperature for 2 h until LCMS showed the complete consumption of starting material. The solvent was removed in vacuo.

Step 2C. Chloroformate Reagent

The chloroformate reagent 2 C was prepared by dissolving 0.22mmol of cyclopentanol in THF (5 ml) and adding 0.45 mmol of phosgene in toluene (20%). The resulting reaction mixture was stirred at room temperature for 2 hours and the solvent was removed in vacuo. To the residue was added

DCM and subsequently concentrated to dryness twice in vacuo yielding chloroformate reagent 2C.

Step 2D. Carbamate formation The resulting residue from step 2B was dissolved in DCM (3 mL) then treated with cyclopentyl chloroformate prepared in step 2C (0.22mmol) and ZPr ₂ NEt (0.35 mL, 2 mmol). The reaction mixture was stirred for 2.5h. Ethyl acetate (15 mL) was added to the solution. The mixture was washed with saturated aqueous NaHCO3 solution, Water and brine consequently. The organic layer was dried over anhydrous sodium sulfate. The organic phase was then filtered, concentrated in vacuo and subsequently purified by flash chromatography (Ethyl acetate/hexanes 1 :2) to give 60.0 mg of the ester. MS (ESI) m/z 716.31 (M+H) ⁺ .

Step 2E. Hydrolysis of the ester

The ester from step 2D and lithium hydroxide (10 equiv.) in THF/MeOH/H2θ (2: 1 :0.5) was stirred at room temperature for 20 hours. The excess solvents were evaporated in vacuo, and the resulting residue was diluted with water and acidified to pH ~5. The mixture was extracted with EtOAc (2x). The combined organic extracts were washed once with brine, dried (MgSO ₄ ), filtered and concentrated in vacuo to give an oily residue, which was purified by column chromatography eluting with 2-10% methanol-chloroform to give the title compound (42.0 mg 55% for 3 steps). MS (ESI) m/z 688.37 (M+H) ⁺ .

¹³ C-NMR (125 MHz, CD ₃ OD): δ 174.6, 173.5, 173.0, 156.7, 152.9, 141.1, 140.0, 139.2, 138.8, 133.4, 130.8, 130.1, 129.3, 128.0, 127.2, 126.7, 126.3,

77.5, 76.2, 59.7, 53.3, 52.6, 40.3, 34.8, 34.4, 32.4, 32.2, 32.1, 30.8, 27.5, 27.4, 26.4, 23.6, 23.3, 23.0, 22.3.

Step 2F. Acyl aminotetrazole formation

Compound of step 2E (25.0 mg, 0.036 mmol), 5 -aminotetrazole (6.0 mg, 0.07 mmol), HATU (16 mg, 0.045 mmol), and DIEA (9.0 mg, 0.07 mmol) were dissolved dissolved in 0.5 ml anhydrous DMF. The mixture was stirred at RT for 1 hour and was heated to 100 ⁰ C for 10 hours. The reaction was cooled down and 10 ml ethyl acetate was added to the solution. The mixture was washed with saturated aqueous NaHCO3 solution, Water and brine consequently. The organic layer was dried over anhydrous sodium sulfate. The organic phase was then filtered, concentrated in Vacuo and subsequently purified by HPLC (40-90% Acetonitrile in water) to give 18.0 mg (60%) of the title compound.

MS (ESI) m/z 755.2 (M+H) ⁺ .

¹ H-NMR (400 MHz, CD ₃ OD): δ 9.08 (IH, s), 8.17 (IH, d, J=3.2 Hz), 7.97 (IH, d, J=6.0Hz), 7.86 (IH, d, J=6.4 Hz), 7.61-7.69 (3H, m), 7.19 (IH, t,

J=3.4 Hz), 6.18 (IH, s), 5.65 (IH, dd, J=7.2, 15.2 Hz), 5.30 (IH, t, J=7.6 Hz), 4.85 (IH, dd, J=6.0, 8.0 Hz), 4.50 (IH, m), 4.21 (IH, m), 4.08 (IH, dd, J=2.6, 9.2 Hz), 2.82 (IH, m), 2.69 (2H, m), 2.51 (IH, dd, J=6.8, 14 Hz), 1.79 (3H, m), 1.23-1.60 (17 H, m). ¹³ C-NMR (100 MHz, CD ₃ OD): δ 177.4, 173.9, 169.5, 156.6, 153.0, 141.2,

140.0, 138.8, 134.6, 130.7, 130.0, 129.3, 128.1, 128.0, 127.2, 126.7, 125.7, 77.5, 76.2, 60.2, 53.4, 52.7, 43.1, 34.9, 32.4, 32.2, 32.0, 31.0, 27.4, 26.9, 26.3, 23.4, 23.3, 22.2.

Example 3. Compound of Formula XV, wherein A = C ₀ A _/ , Q=

The title compound was prepared following the procedure described in Example 2 by starting with the corresponding Quinoline derivative in the Mitsunobu reaction. MS (ESI) m/z 842.3 (M+H) ⁺ .

I ° Example 4. Compound of Formula XV, wherein A Q=

1'0 ^R O ^T0 C' ² , ^h 1'Oh

Step 4A. The title compound of step 2A was hydrolyzed by the procedure set forth in step 2E to give the title compound (87%). MS (found): 676.3

¹ H-NMR [CD ₃ OD, δ (ppm)]: 8.14 (IH), 7.96 (IH), 7.86 (IH), 7.65 (IH), 7.62 (IH), 7.59 (IH), 7.19 (IH), 6.07 (IH), 5.53 (IH), 5.52 (IH), 4.81 (IH), 4.75 (IH), 4.23 (IH), 4.12 (IH), 2.65-2.75 (2H), 2.52 (IH), 2.21 (IH), 1.97 (IH), 1.80 (IH), 1.62 (2H), 1.54 (IH), 1.47 (2H), 1.44 (2H), 1.41 (2H), 1.09 (9H).

¹³ C-NMR [CD ₃ OD, δ (ppm)]: 176.2, 174.1, 173.4, 156.0, 152.9, 141.0, 139.6, 138.9, 138.6, 131.5, 130.6, 130.0, 129.3, 128.1, 127.8, 127.1, 126.6, 78.6, 76.1, 59.8, 53.3, 52.3, 41.4, 34.5, 32.3, 30.0, 27.5, 27.4, 27.2 (3C), 26.1, 22.6, 22.4.

Step 4B. The title compound was prepared from the compound of step 4A following the procedure described in Example 2, step 2F. MS (ESI) m/z 743.38 (M+H) ⁺ .

Example 5. Compound of Formula XV, wherein A = αx Q=

The compound from Example 2 (13.0 mg, 0.017 mmol), K2CO3 (5.0 mg, 0.035 mmol), were dissolved in 0.5 ml anhydrous DMF. To the resulting solution was added Iodomethane (5.0 mg, 0.035 mmol) at RT. The mixture was stirred at RT for 1 hour. The reaction was quenched by adding 10 ml ethyl acetate and 5 ml water. The mixture was washed with saturated aqueous NaHCO3 solution, Water and brine consequently. The organic layer was dried over anhydrous sodium

sulfate. The organic phase was then filtered, concentrated in Vacuo and subsequently purified by HPLC (40-90% Acetonitrile in water) to give 6.0 mg (50%) of the desired compound. MS (ESI) m/z 769.2 (M+H) ⁺ .

Example 6. Compound of Formula XV, wherein A G =

HN ¹

V ^

Step 6A. Compound of Formula XV, wherein A > θ- OH G =OEt.

The title compound was prepared following Example- 1 by starting with the commercially available £ra/?s-L-hydroxyproline methyl ester in step IA.

The alcohol from step 6A (200 mg, 0.40 mmol) was condensed with CDI (79 mg, 0.49 mmol) in 5 rriL dichloromethane at rt. Once this coupling was complete as confirmed by MS analysis, isoindoline (145 mg, 1.21 mmol) was added and the resulting mixture was stirred overnight. The reaction mixture was diluted with dichloromethane (20 mL) and washed with IN aq. HCl (20 mL) and brine (20 mL). The organic portion was then dried (Na ₂ SOz _I ), filtered, and concentrated in vacuo. The crude oil was purified via flash chromatography (silica

gel) using dichloromethane/EtO Ac/acetone (60:20:1) as eluent to afford the corresponding carbamate (220 mg, 85%) as a white solid.

Once the carbamate portion was installed, ester hydrolysis was carried out in standard fashion using LiOH in a THF/MeOH/water (1.5, 0.5, 0.5 mL, respectfully) solvent mixture. Upon completion, the reaction mixture was diluted with 50 mL DCM and 5 mL water, which was acidified with IN aq. HCl. The layers were separated and the aqueous portion was washed three additional times with 10 mL DCM. The organic portions were combined and washed once with brine (20 mL). Finally, the organic layer was dried (Na ₂ SOzO, filtered, and concentrated in vacuo. The crude acid was carried on to the coupling step without any further purification.

Step 6C. Compound of Formula XV, wherein A = ° / , Q= G =

Carboxylic acid from step 6B (50 mg, 0.082 mmol) was treated with CDI (16 mg, 0.098 mmol) in 2 mL DMF at 45 ⁰ C for 1 hr. The activated intermediate was then subjected to aminotetrazole (14 mg, 0.16 mmol) and DBU (19 mg, 0.12 mmol). After stirring overnight, the reaction was diluted with 50 mL EtOAc and washed with water (3x 10 mL) and brine (Ix 20 mL). The organic portion was dried (Na ₂ SO/t), filtered, and concentrated in vacuo. The crude material was purified via preparative HPLC to yield title compound (32 mg, 60%).

MS (ESI) m/z 678.19 (M+H) ⁺ .

¹ H-NMR (500 MHz, CDCl ₃ ): δ 11.49 (IH, s), 7.36 (IH, m), 7.28-7.23 (2H, m), 7.17-7.16 (2H, m), 5.70 (IH, dd, J=17.0, 9.5 Hz), 5.59 (IH, dd, J=17.0, 10.0 Hz), 5.41 (IH, bs), 5.35 (IH, t, J=9.5 Hz), 5.31-5.29 (IH, m), 5.23 (IH, t, J=9.5 Hz), 5.18 (IH, m), 4.78-4.70 (2H, m), 4.66-4.60 (IH, m), 4.44-4.40 (IH, m), 4.25-4.19 (IH, m), 4.15-4.13 (IH, m), 3.90 (IH, dd, J=I 1.5, 5.0 Hz), 3.85 (IH, dd, J=11.5, 3.5 Hz), 2.70 (IH, ddd, J=13.5, 6.0, 6.0 Hz), 2.62-2.50 (2H, m), 2.38-2.18 (4H, m), 2.10-2.02 (IH, m), 1.88-1.20.

Example 7. Compound of Formula XV, wherein A = αx ° / , Q=

The title compound was prepared from the compound of Example 2, step 2E following the procedure described in Example 2, step 2F by using aminotriazole in the place of aminotetrazole. MS (ESI) m/z 754.36 (M+H) ⁺ .

Example 8. Compound of Formula XV, wherein A = ° /, Q=

The title compound is prepared from the compound of Example 4, step 4A following the procedure described in Example 2, step 2F by using aminotriazole in the place of aminotetrazole.

Example 9. Compound of Formula XV, wherein A = ° / , Q=

The title compound is made by following Example 4 using the corresponding triazole in the Mitsunobu reaction in place of the quinoxalin-2-one.

Additional compounds (Example 10-25) of the present invention that may be prepared via methods described in step 2F using the corresponding carboxylic acids. The corresponding carboxylic acids maybe prepared via methods described in Schemes 2-8 or in Examples 2-10, or the detailed procedure of making such acids could be found in U.S. published patent application US2002/0037998; PCT published application WO 00/59929; and commonly assigned U.S. Serial Nos.

10/384,120 (filed March 7, 2003), 10/418,759 (filed April 18, 2003), 10/360,947 (filed Feb. 7, 2003) and 10/365,854 (filed Feb. 13, 2003).

( XV)

TABLE 1

Example 26. Compound of Formula XVI, wherein A Q=

Step 26A. To a solution of Boc-L-tert-leucine (4.544g, 19.65mmol), cis-L- hydroxyproline methyl ester (19.65mmol) and DIPEA (10.3ml, 59.1mmol) in

DMF (80ml) at 0 ⁰ C was added in portions HATU (7.84g, 20.6mmol). The mixture was stirred at rt for 18h, diluted with EtOAc and washed with half-sat. -aq. NaCl four times. The organic phase was dried over anhydrous MgSO ₄ , filtered, and then concentrated in vacuo. The resudue was purified by silica gel chromatography (Hexane/EtOAC = 1 : 1 to 1 : T) to afford the desired compound (7.8g). MS (ESI): m/e 359.24 (M+H).

Step 26B. To a mixture of the above compound (1.363g, 3.803mmol), 3-(thiophen- 2-yl)-lH-quinoxalin-2-one (0.868g, 3.803mmol)) and triphenylphosphine (2.Og, 7.6mmol) in THF at 0 ⁰ C was added dropwise DIAD (1.5ml, 7.6mmol). The resulting mixture was held at 0 ⁰ C for 15 min. before being warmed to room temperature. After 18 hours, the mixture was concentrated under vacuum and the residue was purified by chromatography (Hexane/EtOAC = 9: 1 to 7:3) to give the desired compound (1.8g). MS(ESI): m/e 569.27 (M+H).

Step 26C. To a solution of compound from Step 26B (1.77g, 3.1 lmmol) in THF/MeOH/EbO (36ml- 18ml- 18ml) was added lithium hydroxide mono hydrate (0.783g, 18.6mmol).The mixture was stirred at room temperature for 20 hours. Most organic solvents were evaporated in vacuo, and the resulting residue was diluted with water and acidified to pH 5 to 6. The mixture was extracted with EtOAc three times. The combined organic extracts were dried (MgSO ₄ ), filtered and concentrated in vacuo to afford the title compound (95%). MS(ESI): m/e 555.26 (M+H).

Step 26D. To a solution of compound from Step 26C (98mg, 0.177mmol), (IR, 2S)-l-Amino-2-vinyl-cyclopropanecarboxylic acid ethyl ester HCl salt (34mg, 0.177mmol) and DIPEA (0.125ml, 0.7 lmmol) in DMF (3ml) at 0 ⁰ C was added HATU (81mg, 0.212mmol). The mixture was stirred at rt for 18h, diluted with EtOAc and washed with half-sat.-aq. NaCl four times. The organic phase was dried over anhydrous MgSO ₄ , filtered, and then concentrated in vacuo. The resudue was purified by silica gel chromatography (Hexane/EtOAC = 3 : 1 to 2 : 1) to afford the title compound (86mg). MS (ESI): m/e 692.32 (M+H).

Step 26E. To a solution of compound from Step 26D (79 mg, 0.114mmol) in THF/MeOH/H ₂ O (2ml-lml-0.5ml) was added aqueous lithium hydroxide (IN, 0.6ml, 0.6mmoL).The mixture was stirred at room temperature for 20 hours. Most organic solvents were evaporated in vacuo, and the resulting residue was diluted with water and acidified to pH 5 to 6. The mixture was extracted with EtOAc three times. The combined organic extracts were dried (MgSCU), filtered and concentrated in vacuo to afford the title compound (73mg). MS(ESI): m/e 664.20 (M+H).

Step 26F. The title compound was prepared from the compound of step 26E following the procedure described in Example 2, step 2F. MS (ESI) m/z 731.44 (M+H); 689.41 (M-N ₃ ).

Additional compounds (Example 27-49) of the present invention that may be prepared via methods described in Example 26 using the corresponding proline substitutions (step 26B). The general methods for such substitution is either illustrated in Schemes 2-8 or in Examples 2-25 by substituting the macrocyclic core structures with the acyclic structure from Step 26A.

(XVI)

The compounds of the present invention exhibit potent inhibitory properties against the HCV NS3 protease. The following examples describe assays in which the compounds of the present invention can be tested for anti-HCV effects.

Example 50. NS3/NS4a Protease Enzyme Assay

HCV protease activity and inhibition is assayed using an internally quenched fluorogenic substrate. A DABCYL and an EDANS group are attached to opposite ends of a short peptide. Quenching of the EDANS fluorescence by the DABCYL group is relieved upon proteolytic cleavage. Fluorescence is measured with a Molecular Devices Fluoromax (or equivalent) using an excitation wavelength of 355 nm and an emission wavelength of 485 nm.

The assay is run in Corning white half-area 96-well plates (VWR 29444-312 [Corning 3693]) with full-length NS3 HCV protease Ib tethered with NS4A

co factor (final enzyme concentration 1 to 15 nM). The assay buffer is complemented with 10 μM NS4A cofactor Pep 4A (Anaspec 25336 or in-house, MW 1424.8). RET Sl (Ac-Asp-Glu-Asp(EDANS)-Glu-Glu-Abu- [COO] Ala-Ser- Lys-(D ABCYL)-NH _2i .AnaSpec 22991, MW 1548.6) is used as the fluorogenic peptide substrate. The assay buffer contains 50 mM Hepes at pH 7.5, 30 mM NaCl and 10 mM BME. The enzyme reaction is followed over a 30 minutes time course at room temperature in the absence and presence of inhibitors.

The peptide inhibitors HCV Inh 1 (Anaspec 25345, MW 796.8) Ac-Asp- Glu-Met-Glu-Glu-Cys-OH, [-20 ⁰ C] and HCV Inh 2 (Anaspec 25346, MW 913.1) Ac-Asp-Glu-Dif-Cha-Cys-OH, are used as reference compounds.

IC50 values are calculated using XLFit in ActivityBase (IDBS) using equation 205: y=A+((B-A)/(l+((C/x) ^λ D))).

Example 51 - Cell-Based Replicon Assay Quantification of HCV replicon RNA (HCV Cell Based Assay) is accomplished using the Huh 11-7 cell line (Lohmann, et al Science 285: 110-113, 1999). Cells are seeded at 4x10 ³ cells/well in 96 well plates and fed media containing DMEM (high glucose), 10% fetal calf serum, penicillin-streptomycin and non-essential amino acids. Cells are incubated in a 7.5% CO2 incubator at 37 ⁰ C. At the end of the incubation period, total RNA is extracted and purified from cells using Ambion RNAqueous 96 Kit (Catalog No. AM 1812). To amplify the HCV RNA so that sufficient material can be detected by an HCV specific probe (below), primers specific for HCV (below) mediate both the reverse transcription of the HCV RNA and the amplification of the cDNA by polymerase chain reaction (PCR) using the TaqMan One-Step RT-PCR Master Mix Kit (Applied Biosystems catalog no.

4309169). The nucleotide sequences of the RT-PCR primers, which are located in the NS5B region of the HCV genome, are the following:

HCV Forward primer "RBNS5bfor" 5'GCTGCGGCCTGTCGAGCT (SEQ ID NO: 1): HCV Reverse primer "RBNS5Brev" 5'CAAGGTCGTCTCCGCATAC (SEQ ID NO 2).

Detection of the RT-PCR product is accomplished using the Applied Biosystems (ABI) Prism 7500 Sequence Detection System (SDS) that detects the fluorescence that is emitted when the probe, which is labeled with a fluorescence

reporter dye and a quencher dye, is degraded during the PCR reaction. The increase in the amount of fluorescence is measured during each cycle of PCR and reflects the increasing amount of RT-PCR product. Specifically, quantification is based on the threshold cycle, where the amplification plot crosses a defined fluorescence threshold. Comparison of the threshold cycles of the sample with a known standard provides a highly sensitive measure of relative template concentration in different samples (ABI User Bulletin #2 December 11, 1997). The data is analyzed using the ABI SDS program version 1.7. The relative template concentration can be converted to RNA copy numbers by employing a standard curve of HCV RNA standards with known copy number (ABI User Bulletin #2 December 11, 1997).

The RT-PCR product was detected using the following labeled probe: 5' FAM-CGAAGCTCCAGGACTGCACGATGCT-TAMRA (SEQ ID NO: 3) FAM= Fluorescence reporter dye. TAMRA :=Quencher dye.

The RT reaction is performed at 48 ⁰ C for 30 minutes followed by PCR. Thermal cycler parameters used for the PCR reaction on the ABI Prism 7500 Sequence Detection System are: one cycle at 95 ⁰ C, 10 minutes followed by 40 cycles each of which include one incubation at 95 ⁰ C for 15 seconds and a second incubation for 60 ⁰ C for 1 minute.

To normalize the data to an internal control molecule within the cellular RNA, RT-PCR is performed on the cellular messenger RNA glyceraldehyde-3- phosphate dehydrogenase (GAPDH). The GAPDH copy number is very stable in the cell lines used. GAPDH RT-PCR is performed on the same RNA sample from which the HCV copy number is determined. The GAPDH primers and probesare contained in the ABI Pre-Developed TaqMan Assay Kit (catalog no. 4310884E). The ratio of HCV/GAPDH RNA is used to calculate the activity of compounds evaluated for inhibition of HCV RNA replication.

Activity of compounds as inhibitors of HCV replication (Cell based Assay) in replicon containing Huh-7 cell lines.

The effect of a specific anti-viral compound on HCV replicon RNA levels in Huh-1 l-7cells is determined by comparing the amount of HCV RNA normalized to GAPDH (e.g. the ratio of HCV/GAPDH) in the cells exposed to compound versus cells exposed to the DMSO vehicle (negative control). Specifically, cells are seeded at 4x 10 ³ cells/well in a 96 well plate and are incubated either with: 1) media containing 1% DMSO (0% inhibition control), or 2) media/1 %DMSO containing a fixed concentration of compound. 96 well plates as described above are then incubated at 37 ⁰ C for 4 days (EC50 determination). Percent inhibition is defined as: % Inhibition= 1OO-1OO*S/C1 where

S= the ratio of HCV RNA copy number/GAPDH RNA copy number in the sample;

Cl= the ratio of HCV RNA copy number/GAPDH RNA copy number in the 0% inhibition control (media/l%DMSO).

The dose-response curve of the inhibitor is generated by adding compound in serial, three-fold dilutions over three logs to wells starting with the highest concentration of a specific compound at 1.5 uM and ending with the lowest concentration of 0.23 nM. Further dilution series (500 nM to 0.08 nM for example) is performed if the EC50 value is not positioned well on the curve. EC50 is determined with the IDBS Activity Base program "XL Fit" using a 4-paramater, non- linear regression fit (model # 205 in version 4.2.1, build 16).

In the above assays, representative compounds are found to have activity.

Although the invention has been described with respect to various preferred embodiments, it is not intended to be limited thereto, but rather those skilled in the art will recognize that variations and modifications may be made therein which are within the spirit of the invention and the scope of the appended claims.