Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
  • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
  • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
  • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D333/40—Thiophene-2-carboxylic acid
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
  • A61P31/14—Antivirals for RNA viruses
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
  • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

• the present invention relates to novel compounds and a method for the treatment or prevention of Flavivirus infections using novel compounds.
• Hepatitis is a disease occurring throughout the world. It is generally of viral nature, although there are other causes known. Viral hepatitis is by far the most common form of hepatitis. Nearly 750,000 Americans are affected by hepatitis each year, and out of those, more than 150,000 are infected with the hepatitis C virus ("HCV”) .
• HCV hepatitis C virus
• HCV is a positive-stranded RNA virus belonging to the Flaviviridae family and has closest relationship to the pestiviruses that include hog cholera virus and bovine viral diarrhea virus (BVDV) . HCV is believed to replicate through the production of a complementary negative-strand RNA template. Due to the lack of efficient culture replication system for the virus, HCV particles were isolated from pooled human plasma and shown, by electron microscopy, to have a diameter of about 50-60 nm.
• BVDV bovine viral diarrhea virus
• the HCV genome is a single-stranded, positive-sense RNA of about 9,600 bp coding for a polyprotein of 3009-3030 amino-acids, which is cleaved co and post-translationally by cellular and two viral proteinases into mature viral proteins (core, El, E2, p7, NS2, NS3, NS4A, NS4B, NS5A, NS5B) . It is believed that the structural proteins, El and E2, the major glycoproteins are embedded into a viral lipid envelope and form stable heterodimers . It is also believed that the structural core protein interacts with the viral RNA genome to form the nucleocapsid.
• the nonstructural proteins designated NS2 to NS5 include proteins with enzymatic functions involved in virus replication and protein processing including a polymerase, protease and helicase.
• the main source of contamination with HCV is blood.
• the magnitude of the HCV infection as a health problem is illustrated by the prevalence among high-risk groups. For example, 60% to 90% of hemophiliacs and more than 80% of intravenous drug abusers in western countries are chronically infected with HCV. For intravenous drug abusers, the prevalence varies from about 28% to 70% depending on the population studied. The proportion of new HCV infections associated with post-transfusion has been markedly reduced lately due to advances in diagnostic tools used to screen blood donors.
• IFN- ⁇ interferon-
• ALT alanine aminotransferase
• RIBA ribavirin
• the present invention provides novel compounds represented by formula:
• Z is chosen from 3-7 membered heterocycle or 3 -7 membered cycloalkyl
• Y is 6-10 membered aryl
• X is 3-10 membered cycloalkyl
• n is an integer from 0-1; provided that when Y is unsubstituted phenyl then X is other than 4-methylcyclohexane.
• a method for treating or preventing a Flaviviridae viral infection in a host comprising administering to the subject a therapeutically effective amount of a compound, composition or combination of the invention.
• a combination comprising a compound of the invention and one or more additionnal agent chosen from viral serine protease inhibitor, viral polymerase inhibitor and viral helicase inhibitor, immunomudulating agent, antioxydant agent, antibacterial agent or antisense agent.
• composition comprising at least one compound of the invention and at least one pharmaceutically acceptable carrier or excipient .
• a compound of the invention for inhibiting or reducing the activity of viral polymerase in a host.
• a compound of the invention for the manufacture of a medicament for treating or preventing a viral Flaviridae infection in a host .
• compounds of the present invention comprise those wherein the following embodiments are present, either independently or in combination.
• Z is chosen from 3-7 membered heterocycle or 3-7 membered cycloalkyl .
• Z is:
• n is 0-2;
• Ra is H, hydroxyl or C ⁇ - 6 alkyl
• R12 is H, C ⁇ -6 alkyl, c s - ⁇ 4 aryl, C 3 - ⁇ 2 heterocycle,
• R1 3 is one or more optional substituent each of which is independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf, P0 3 RcRd, CONRgRh, Ci- 6 alkyl, C 2 - 6 alkenyl, C 2 - 6 alkynyl, C 6 - ⁇ 2 aralkyl, C 6 _i2 aryl, C ⁇ - 6 alkyloxy, C 2 - 6 alkenyloxy, C 2 - 6 alkynyloxy, C 6 - ⁇ aryloxy, C(0)C ⁇ - 6 alkyl, C(0)C 2 - 6 alkenyl, C(0)C 2 - 6 alkynyl, C (O) C 6 _ ⁇ 2 aryl, C(0)C 6 - ⁇ 2 aralkyl, C 3 - ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)ORf, cyano, azido, amidino or guanido;
• Z is 6-7 membered heterocycle or 6-7 membered cycloalkyl.
• Z is cyclohexyl, p iperidinyl or
• Rf , Re, Rd, Rg and Rh in each case are independently H, C x - 6 alkyl, C 2 - 6 alkenyl, C 2 1 6 alkynyl, C 6 - ⁇ o aryl, C3-10 heterocycle, C3.10 heteroaralkyl or C 6 - ⁇ o aralkyl; or Re and Rd are taken together with the oxygens to form a 5 to 10 membered heterocycle; or Rg and Rh are taken together with the nit rogen to form a 3 to 10 membered heterocycle.
• Z is cyclohexyl, piperidinyl, N(C ⁇ _s alkyl) -piperidinyl, hexahydrothiopyranyl , azepanyl, methylazepanyl, N(C ⁇ - 6 alkyl) - piperidinylmethyl , tetrahydropyranyl , piperidinylmethyl, pyridin 1, pyridinyl ethyl , tetrahydrothiopyranyl, dioxolanylmethyl or dioxanylmethyl which in each case is unsubstituted or substituted by one or more substituent independently chosen from halogen, S0 2 Rf, P0 3 RcRd, CONRgRh, C ⁇ - 6 alkyl, C 6 _ ⁇ 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C 6 - ⁇ 2 aryloxy, C(0)C
• Z is cyclohexyl, piperidinyl, N(C ⁇ - 6 alkyl) -piperidinyl, hexahydrothiopyranyl , azepanyl, methylazepanyl, N(C ⁇ _ 6 alkyl) -piperidinylmethyl, tetrahydropyranyl, piperidinylmethyl, pyridinyl, 0 pyridinylmethyl , tetrahydrothiopyranyl, dioxolanylmethyl or dioxanylmethyl which in each case ⁇ is unsubstituted or substituted by one or more substituent independently chosen from halogen, S0 2 Rf, CONRgRh, C ⁇ - 6 alkyl, C 6 -: 2 aralkyl, C 6 _ ⁇ 2 aryl, C ⁇ .
• Z is cyclohexyl unsubstituted or substituted by one or more substituent independently chosen from halogen, S0 2 Rf, CONRgRh, C ⁇ - 6 alkyl, C 6 - ⁇ 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C(0)C ⁇ - 6 alkyl, C 3 - ⁇ 0 heterocycle, hydroxyl, NRgRh, C (0) Orf or cyano; 5 wherein Rf, Rg and Rh in each case are independently H or C ⁇ - 6 alkyl.
• Z is piperidinyl unsubstituted or substituted by one or more substituent independently 0 chosen from halogen, S0 2 Rf, CONRgRh, C ⁇ - 6 alkyl, C 6 -i2 aralkyl, C 6 _ ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C(0)C ! - 6 alkyl, C(0)NHRf, C 3 -1 0 heterocycle, hydroxyl, NRgRh, C (0) Orf or cyano; wherein Rf, Rg and Rh in each case are independently H or C ⁇ _ 6 alkyl.
• Z is N(C ⁇ - 6 alkyl) -piperidinyl unsubstituted or substituted by one or more substituent independently chosen from halogen, S0 2 Rf, CONRgRh, C ⁇ _ 6 alkyl, C 6 _ 12 aralkyl, C 6 - ⁇ 2 aryl, Ci-s alkyloxy, C(0)C ⁇ - 6 alkyl, C(0)NHRf, C 3 _ ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)0rf or cyano; wherein Rf, Rg and Rh in each case are independently H or C ⁇ - 6 alkyl.
• Z is cyclohexyl, piperidinyl or N(C ⁇ - 6 alkyl) - piperidinyl ;
• Z is cyclohexyl
• Z is piperidinyl; Z is N(Ci- 6 alkyl) -piperidinyl.
• Z is N -methyl-piperidinyl, N-ethyl- piperidinyl, N-propyl-piperidinyl, N-isopropyl - piperidinyl, N-butyl-piperidinyl, N-pentyl-piperidinyl, N-hexylpiperidinyl , N-cyclohexyl -piperidinyl, N-acetyl- piperidinyl, N-benzyl-piperidinyl, hydroxycyclohexyl , oxocyclohexyl, Hydroxyiminocyclohexyl, aminocyclohexyl, methanesulfonyl, methylcarbamoyl or methoxycyclohexyl .
• Z is N-methyl-piperidinyl or hydroxycyclohexyl; Z is N-methyl-piperidinyl; Z is from. N-methyl-4-piperidinyl; Z is hydroxycyclohexyl; Z is 4-hydroxyeye1ohexy1 ; Z is N-methyl-4-piperidinyl .
• X is 3-10 membered cycloalkyl.
• X is 6-membered cycloalkyl.
• X is cyclohexyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf, P0 3 RcRd, CONRgRh, C ⁇ - 6 alkyl, C 2 _ 6 alkenyl, C 2 : 6 alkynyl, C 6 _2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ _ 6 alkyloxy, C 2 - 6 alkenyloxy, C 2 -6 alkynyloxy, C 6 - ⁇ 2 aryloxy, C(0)C ⁇ - 6 alkyl, C (O) C 2 - 6 alkenyl, C(0)C 2 - 6 alkynyl, C(0)C 6 - ⁇ 2 aryl, C (0) C 6 _ ⁇ 2 aralkyl, C(0)NHRf, C 3 - ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)OR
• X is cyclohexyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf, P0 3 RcRd, CONRgRh, C ⁇ - 6 alkyl, C 6 _ 12 aralkyl, C 6 - ⁇ 2 aryl, Ci-s alkyloxy, C 6 - ⁇ 2 aryloxy, C(0)C 1 - 6 alkyl, C (O) C 6 - ⁇ 2 aryl, C(0)C 6 - ⁇ 2 aralkyl, C(0)NHRf, C3-10 heterocycle, hydroxyl, NRgRh, C(0)ORf, cyano, azido, amidino or 5 guanido; wherein Rf, Re, Rd, Rg and Rh in each case are independently H, C ⁇ _ 6 alkyl, C 2 . 6 alkenyl, C 2 - 6 alkynyl,
• X is cyclohexyl unsubstituted or substituted by one or more substitue nt independently chosen from halogen, S0 2 Rf, CONRgRh, C ⁇ - 6 alkyl, C 6 -i2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ _ 6 alkyloxy, C 6 - ⁇ 2 15 .
• X is cyclohexyl substituted by one or more substituent independently chosen from C ⁇ _ 6 alkyl, halogen, C 2 - 6 alkenyl, C 2 _ 6 alkynyl or C ⁇ - 6 25 alkyloxy.
• X is cyclohexyl substituted by C ⁇ - 6 alkyl; X is cyclohexyl substituted by C 1 -. 3 alkyl; 30 X is 4 -methyl-cyclohexyl or 2 -hydroxy-4-methyl- . cyclohexyl ; X is 4-methylcyclohexyl .
• Y is 6-10 membered aryl.
• Y is phenyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf, P0 3 RcRd, CONRgRh, C ⁇ - 6 alkyl, C 2 - s alkenyl, C 2 - 6 alkynyl, C 6 -i 2 aralkyl, C 6 - 12 aryl, C ⁇ - S alkyloxy, C 2 - 6 alkenyloxy, C 2 - 6 alkynyloxy, C 6 - ⁇ 2 aryloxy, C (0) C ⁇ - 6 alkyl, C (0) C 2 - 6 alkenyl, C(0)C 2 - 6 alkynyl, C(0)C 6 - ⁇ 2 aryl, C(0)C 6 - ⁇ 2 aralkyl, C(0)NHRf, C 3 . ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)0Rf
• Y is phenyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf,
• RcRd CONRgRh, C ⁇ _ 6 alkyl, C- 6 alkenyl, C 2 - 6 alkynyl, C 6 -i 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C 2 - 6 alkenyloxy, C 2 -6 alkynyloxy, C 6 - ⁇ 2 aryloxy, C(0)C ⁇ - 6 alkyl, C(0)C 2 - 6 alkenyl, C(0)C 2 - 6 alkynyl, C(0)C 6 _ 12 aryl, C(0)C 6 - ⁇ 2 aralkyl, C(0)NHRf, C 3 - ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)0Rf, cyano, azido, amidino or guanido; wherein Rf, Re, Rd, Rg and Rh in each case are independently H, C ⁇ - 6 alkyl, C 2 - 6 alkenyl, C
• Y is phenyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf, P0 3 RcRd, CONRgRh, d- 6 alkyl, C 6 - ⁇ 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C 6 _ ⁇ 2 aryloxy, C(0)C ⁇ _ 6 alkyl, C(0)C 6 - 12 aryl, C(0)C 6 - ⁇ 2 aralkyl, C(0)NHRf, C 3 - 10 heterocycle, hydroxyl, NRgRh, C(0)0Rf, cyano, azido, amidino or guanido; wherein Rf, Re, Rd, Rg and Rh in each case are independently H, C x .
• Y is phenyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, S0 2 Rf, CONRgRh, C ⁇ - 6 alkyl, C 6 - 12 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ _ 6 alkyloxy, C 6 .
• Y is phenyl substituted by one or more substituent independently chosen from halogen, nitro, S0 2 Rf, C ⁇ - 6 alkyl, C ⁇ - 6 alkyloxy, C (O) C ⁇ . 6 alkyl, C(0)Orf, cyano or azido.
• Y is phenyl substituted by one or more substituent independently chosen from halogen, nitro, Ci_ 6 alkyl, C ⁇ _ 6 alkyloxy or cyano.
• Y is phenyl substituted by one or more halogen; Y is phenyl substituted by one or more C ⁇ _ 6 alkyloxy;
• Y is phenyl substituted by one or more methyloxy
• Y is phenyl substituted by one or more C ⁇ _ 6 alkyl
• Y is phenyl substituted by one or more methyl
• Y is phenyl; Y is 3 -fluorophenyl, 4 -fluorophenyl 4-chlorophenyl, 4- cyanophenyl, 4-methoxyphenyl, 4-nitrophenyl or p-tolyl.
• P is an integer from 1-3 and q is an integer from 0-2;
• W is CR ⁇ 0 Rn, S(0)n, O or NR i2 ; wherein n, Rio, Rn and R i2 are as defined in herein.
• n is as defined in herein.
• R10 is H, C ⁇ - 6 alkyl, C 6 . 10 aryl, C 3 - ⁇ o heterocycle, C 3 - ⁇ 0 heteroaralkyl, C 6 - ⁇ o aralkyl , C(0)-C ⁇ - 6 alkyl, C ⁇ - 6 alkyloxy, hydroxyl or formyl; and Rll is H.
• R10 is C ⁇ - 6 alkyl, C 6 - ⁇ o aralkyl, C(0)-Ci- 6 alkyl, C ⁇ _ 6 alkyloxy, hydroxyl or formyl; and Rll is H.
• RIO is Cl-3 alkyl, C 6 _ ⁇ 0 aralkyl, C(0)-Cl-3 alkyl, C ⁇ _ 3 alkyloxy, hydroxyl or formyl; and Rll is H.
• RIO is chosen from methyl, ethyl, propyl, isopropyl benzyl, acetyl, hydroxyl or formyl; and Rll is H.
• Ra is chosen from H, hydroxyl, methyl, ethyl, propyl or isopropyl.
• R13 is one or more optional substituent each of which is independently chosen from halogen, nitro, nitroso, S0 3 Rf, S0 2 Rf, P0 3 RcRd, CONRgRh, C ⁇ _6 alkyl, C 2 - 6 alkenyl, C 2 - 6 alkynyl, C 6 - ⁇ 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C 2 - 6 alkenyloxy, C 2 - 6 alkynyloxy, C 6 _
• R i3 is one or more substituent each of which is independently chosen from hal ogen, nitro, S0Rf, CONRgRh, C ⁇ . 6 alkyl, C 3 - ⁇ 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ _ 6 alkyloxy, C(0)C ⁇ - 6 alkyl, C 3 _ 0 heterocycle, hydroxyl, NRgRh, C(0)0Rf, cyano or azido; wherein Rf, Rg and Rh are as defined herein.
• R i3 is one or more substituent each of which is independently chosen from halogen, nitro, S0 2 Rf, CONRgRh, Cl-3 alkyl, C 6 - 12 aralkyl, C6 aryl, Cl-3 alkyloxy, C(0)Cl-3 alkyl, C3-6 heterocycle, hydroxyl, NRgRh, C(0)ORf, cyano or azido; wherein Rf, Rg and Rh are as defined herein.
• R ⁇ 3 is one or more substituent each of which is independently chosen from halogen, nitro, S0 2 CH 3 , CONH 2 , CONHCH 3 , CONH(CH 3 )2, methyl, ethyl, propyl, isopropyl, benzyl, phenyl, acetyl, methoxy, ethoxy, propyloxy, isopropyloxy, piperidinyl, piperazinyl, pyrrolidinyl, azetidinyl, aziridinyl, pyridinyl, ,. dioxanyl, dioxolanyl, azepanyl, hydroxyl, NH2, N(H)CH3, NH(CH3)2, cyano or azido; wherein Rf, Rg and Rh are as defined herein.
• Ri3 may be attached to any position of the ring.
• a person of skill will also realize that the position of R13 on the ring will be dependant on the valencies of the ring atoms and will respect normal rules of chemistry.
• the present invention provides compounds represented by formula:
• Z is cyclohexyl unsubstituted or substituted by one or more substituent independently chosen from halogen, S0 2 Rf, CONRgRh, C ⁇ - 6 alkyl, C 6 - ⁇ 2 aralkyl, C 6 _ ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C(0)C ⁇ - 6 alkyl, C 3 _ ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)0Rf or cyano; wherein Rf, Rg and Rh in each case are independently H or C .
• Y is phenyl unsubstituted or substituted by one or more substituent independently chosen from halogen, nitro, S0 2 Rf, CONRgRh, C ⁇ - S alkyl, C 6 _ ⁇ aralkyl, C 6 _ ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C 6 - ⁇ 2 aryloxy, C (0) C ⁇ - 6 alkyl, C(0)C 6 - ⁇ 2 aryl, C(0)C 6 - ⁇ 2 aralkyl, C(0)NHRf, C 3 - ⁇ 0 heterocycle, hydroxyl, NRgRh, C(0)ORf, cyano, amidino or guanido; wherein Rf, Rg and Rh in each case are independently H, C ⁇ - 6 alkyl, C 6 _ ⁇ 0 aryl, C 3 . ⁇ 0 heterocycle, C 3 - ⁇ 0 heteroaralkyl or C 6 - ⁇ o aralkyl;
• X is cyclohexyl unsubstituted or substituted by one or more substituent independently chosen from halogen, S0 2 Rf, CONRgRh, x- ⁇ alkyl, C 6 - ⁇ 2 aralkyl, C 6 _ 12 aryl, C ⁇ - 6 alkyloxy, C 6 . ⁇ 2 aryloxy, C(0)C ⁇ - 6 alkyl, C (O) C 6 - ⁇ 2 aryl, C(0)C aralkyl, C(0)NHRf, C 3 - 10 heterocycle, hydroxyl, NRgRh, C(0)0Rf, cyano or azido; wherein Rf, Re, Rd, Rg and Rh in each case are independently H, C ⁇ - 6 alkyl, C 6 - ⁇ o aryl, C3-10 heterocycle, C 3 _ ⁇ 0 heteroaralkyl or C ⁇ -io aralkyl;
• n 0;
• X is other than 4 -methylcyclohexane .
• the present invention provides novel compounds including:
• the present invention provides novel compounds including: Compound 73 5- (4-FLUORO-PHENYL) - • 3- [ (4-HYDROXY-CYCLOHEXYL) - (4-METHYL- CYCLOHEXANECARBONYL) -AMINO] -THIOPHENE-2-CARBOXYLIC ACID; Compound 74 3- [ (1-METHYLCARBAMOYL-PIPERIDIN-4-YL) - (4-METHYL-CYCLOHEXANECARBONYL) -AMINO] -5-PHENYL- THIOPHENE-2-CARBOXYLIC ACID;
• Compound 90 3- [ (3 -HYDROXY-CYCLOPENTYL) - (4-METHYL- CYCLOHEXANECARBONYL) -AMINO] -5-PHENYL-THIOPHE-2- CARBOXYLIC ACID; or pharmaceutically acceptable salts thereof.
• the present invention provides novel 3- [(6-membered cycloalkyl -carbonyl) -amino] -5-phenyl- thiophene-2-carboxylic acid compounds selected from:
• the present invention provides novel 3- [ (4-methyl-cyclohexane-carbonyl) -amino] -5-phenyl- thiophene-2-carboxylic acid compounds.
• the present invention provides novel compounds having 3 -[ (unsubstituted or substituted- benzoyl) -amino] -5-phenyl-thiophene-2-carboxylic acid selected from:
• the present invention provides novel 3-[( 6-membered heterocycle -2-carbonyl) -amino] -5- phenyl-thiophene-2-carboxylie acid compounds selected from:
• the viral infection is chosen from Flavivirus infections.
• the Flavivirus infection is chosen from Hepatitis C virus (HCV) , bovine viral diarrhea virus (BVDV) , hog cholera virus, dengue fever virus, Japanese encephalitis virus and yellow fever virus.
• HCV Hepatitis C virus
• BVDV bovine viral diarrhea virus
• hog cholera virus dengue fever virus
• Japanese encephalitis virus yellow fever virus.
• the Flavivirus infection is Hepatitis C viral infection.
• the present invention provides a method for treating or preventing a Flaviviridae viral infection in a host comprising administering to the host a therapeutically effect ive amount of at least one compound according to the invention described herein.
• the present invention provides a method for treating or preventing a Flaviviridae viral infection in a host comprising administering to the host a therapeutically effective amount of at least one compound according to the invention described herein and further comprising administering at least one additional agent chosen from viral serine protease inhibitor, viral polymerase inhibitor, viral helicase inhibitor, immunomudulating agent, antioxydant agent, antibacterial agent, therapeutic vaccine, ⁇ hepatoprotectant agent or antisense agent.
• the additional agent is interferon ⁇ , ribavirin, . silybum marianum, interleukine -12, amantadine, ribozyme , thymosin, N-acetyl cysteine or cyclosporin.
• the Flaviviridea viral infection is hepatitis C viral infection (HCV) .
• the present invention provides a pharmaceutical composition
• a pharmaceutical composition comprising at least one compound according to the invention described herein and at least one pharmaceutically acceptable carrier or excipient .
• the present invention provides a pharmaceutical composition
• a pharmaceutical composition comprising at least one compound according to the invention described herein and at least one pharmaceutically acceptable carrier or excipient and further comprising at least one additional agent chosen from viral serine protease inhibitor, viral polymerase inhibitor, viral helicase inhibitor, immunomudulating agent, antioxydant agent, antibacterial agent, therapeutic vaccine, hepatoprotectant agent or antisense agent.
• the additional agent is interferon ⁇ , ribavirin, silybum marianum, interleukine-12, amantadine, ribozyme, thymosin, N- acetyl cysteine or cyclosporin.
• viral serine protease inhibitor is a flaviviridae serine protease inhibitor.
• viral polymerase inhibitor is a flaviviridae polymerase inhibitor.
• viral helicase inhibitor is a flaviviridae helicase inhibitor.
• viral serine protease inhibitor is HCV serine protease inhibitor
• viral polymerase inhibitor is HCV polymerase inhibitor
• viral helicase inhibitor is HCV helicase inhibitor.
• a method for inhibiting or reducing the activity of viral polymerase in a host comprising administering a therapeutically effective amount of a compound according to the invention described herein.
• a method for inhibiting or reducing the activity of viral polymerase in a host comprising administering a therapeutically effective amount of a compound according to the invention described herein and further comprising administering one or more viral polymerase inhibitor.
• viral polymerase is a Flaviviridae viral polymerase.
• viral polymerase is a RNA-dependant RNA-polymerase.
• viral polymerase is HCV polymerase.
• a combination comprising a least one compound according to the invention described herein and one or more additionnal agent chosen from viral serine protease inhibitor, viral polymerase inhibitor and viral helicase inhibitor, immunomudulating agent, antioxydant agent, antibacterial agent, therapeutic vaccine, hepatoprotectant agent or antisense agent.
• one or more additionnal agent chosen from viral serine protease inhibitor, viral polymerase inhibitor and viral helicase inhibitor, immunomudulating agent, antioxydant agent, antibacterial agent, therapeutic vaccine, hepatoprotectant agent or antisense agent.
• the compound and additionnal agent are administered sequentially.
• the compound and additionnal agent are administered simultaneously .
• compositions comprising a-*combination as defined above together with a pharmaceutically acceptable carrier there for comprise a further aspect of the invention.
• the individual components for use in the method of the present invention or combinations of the present invention may be administered either sequentially or simultaneously in separate or combined pharmaceuti cal formulations.
• the present . invention provides the use of a compound according to the invention described herein for treating or preventing Flaviviridae viral infection in a host.
• the present invention provides the use of a compound according to the invention described herein for the manufacture of a medicament for treating or preventing a viral Flaviridea infection in a host.
• the present invention provides the use of a compound according to the invention described herein for inhibiting or reducing the activity of viral polymerase in a host .
• the compounds in accordance with the present invention can contain a chiral centre.
• the compounds of formula may thus exist in the form of two different optical isomers (i.e. (+) or (-) enantiomers). All such enantiomers and mixtures thereof including racemic mixtures are included within the scope of the invention.
• the single optical isomer or enantiomer can be obtained by method well known in the art, such as chiral HPLC, enzymatic resolution and chiral auxiliary.
• the compounds of the present invention are provided in the form of a single enantiomer at least 95%, more preferrably at least 97% and most preferably at least 99% free of the corresponding enantiomer.
• the compound of the present invention are in the form of the (+) enantiomer at least 95% free of the corresponding (-) enantiomer.
• the compound of the present invention are in the form of the (+) enantiomer at least 97% free of the corresponding (-) enantiomer.
• the compound of the present invention are in the form of the (+) enantiomer at least 99% free of the corresponding (-) enantiomer.
• the compounds of the present invention are in the form of the ( -) enantiomer at least 95% free of the corresponding (+) enantiomer. Most preferably the compound of the present invention are in the form of the (-) enantiomer at least 97% free of the corresponding (+) enantiomer.
• the compound of the present invention are in the form of the (-) enantiomer at least 99% free of the corresponding (+) enantiomer.
• the compounds in accordance with the present invention can contain more than one chiral centres .
• the compounds of formula may thus exist in the form of different diastereomers. All such diastereomers and mixtures thereof are included within the scope of the invention.
• the single diastereomer can be obtained by method well known in the art, such as HPLC, crystalisation and chromatography.
• a pharmaceutically acceptable salts of the compounds of the present invention are meant those derived from pharmaceutically acceptable inorganic and organic acids and bases .
• suitable acids include hydrochloric, hydrobromic, sulphuric, nitric, perchloric, fumaric, maleic, phosphoric, glycollic, lactic, salicylic, succinic, toleune-p-sulphonic, tartaric, acetic, trifluoroacetic, citric, ethanesulphonic, formic, benzoic, malonic, naphthalene-2-sulphonic and benzenesulphonic acids.
• Other acids such as oxalic, while not in themselves pharmaceutically acceptable, may be useful as intermediates in obtaining the compounds of the invention and their pharmaceutically acceptable acid addition salts.
• Salts derived from appropriate bases include alkali metal (e.g. sodium, lithium, potassium), alkaline earth metal (e.g. magnesium), ammonium and NR4+ (where R is C1-. alkyl) salts.
• alkali metal e.g. sodium, lithium, potassium
• alkaline earth metal e.g. magnesium
• ammonium e.g. sodium, lithium, potassium
• NR4+ where R is C1-. alkyl
• the pharmaceutically acceptable salt is a sodium salt.
• the pharmaceutically acceptable salt is a lithium salt.
• the pharmaceutically acceptable salt is a potassium salt.
• alkyl represents a straight chain or branched chain hydrocarbon moiety which may optionally be substituted by one or more of: halogen, nitro, nitroso, S0 3 R ⁇ 2 , P0 3 RcRd, CONR ⁇ 3 R ⁇ 4 , C ⁇ - 6 alkyl, C 2 - 6 alkenyl, C 2 _ 6 alkynyl, C 6 -i2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ - 6 alkyloxy, C 2 - 6 alkenyloxy, C 2 - 6 alkynyloxy, C 6 _ ⁇ 2 aryloxy, C(0)C ⁇ - 6 alkyl, C(0)C 2 - 6 alkenyl, C(0)C 2 - 6 alkynyl, C(0)C 6 .
• R 12 aryl, C (0) C 6 - ⁇ 2 aralkyl, C 3 - ⁇ 0 heterocycle, hydroxyl, NR ⁇ 3 R ⁇ 4 , C(0)OR ⁇ 2 , cyano, azido, amidino or guanido;
• R 12 Re, Rd, R i3 and R i are each independently chosen from H, Cl-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C6-14 aryl, C3-12 heterocycle, C3-18 heteroaralkyl, C6-18 aralkyl; or Re and Rd are taken together with the oxygens to form a 5 to 10 membered heterocycle; or R i3 and R i4 are taken together with the nitrogen to form a 3 to 10 membered heterocycle.
• alkyls include isopropyl, ethyl, fluorohexyl or cyclopropyl .
• alkyl is also meant to include alkyls in which one or more hydrogen atoms is replaced by an oxygen, (e.g. a benzoyl) or an halogen, more preferably, the halogen is fluoro (e.g. CF3- or CF 3 CH 2 - ) .
• cycloalkyl represents a cyclic alkyl.
• cycloalkyl is also meant to include a cycloalkyl containing at least one unsaturated group.
• Useful examples of cycloalkyl include cyclopropyl, cyclobutyl, cyclohexenyl, cyclohex-dienyl and cyclohexyl.
• alkenyl and alkynyl represent an alkyl containing at least one unsaturated group (e.g. allyl, acetylene, ethylene) .
• aryl represents a carbocyclic moiety containing at least one benzenoid -type ring which may optionally be substituted by one or more of halogen, nitro, nitroso, S0 3 R ⁇ 2 , P0 3 RcRd, CONR 13 R14, C ⁇ _ 6 alkyl, C 2 - s alkenyl, C 2 - 6 alkynyl, C 6 - ⁇ 2 aralkyl, C 6 - ⁇ 2 aryl, C ⁇ _ 6 alkyloxy, C 2 - 6 alkenyloxy, C 2 - 6 alkynyloxy, C 6 - ⁇ 2 aryloxy, C(0)C ⁇ - 6 alkyl, C(0)C 2 - 6 alkenyl, C(0)C 2 _ 6 alkynyl, C(0)C6-12 aryl, C(0)C 6 - ⁇ 2 aralkyl, C 3 - ⁇ 0 heterocycle, hydroxyl, NR ⁇ 3 R 4 , C(0)OR ⁇
• R i2 , Re, Rd, R i3 and R X4 are each independently chosen from H, Cl-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C6-14 aryl, C3-12 heterocycle, C3-18 heteroaralkyl, C6-18 aralkyl; or Re and Rd are taken together with the oxygens to form a 5 to 10 membered heterocycle; or R 13 and R i are taken together with the nitrogen to form a 3 to 10 membered heterocycle.
• aryl include phenyl and naphthyl .
• aralkyl represents an aryl group attached to the adjacent atom by a C ⁇ _ 6 alkyl, C ⁇ - 6 alkenyl, or Ci- 6 alkynyl (e.g. , benzyl).
• heterocycle represents a saturated or unsaturated, cyclic moiety wherein said cyclic moeity is interrupted by at least one heteroatom, (e.g. oxygen, sulfur or nitrogen) which may optionally be substituted halogen, nitro, nitroso, SO 3 R12, P0 3 RcRd, CONR 13 R 14 , Ci- 6 alkyl, C 2 - 6 alkenyl, C 2 - 6 alkynyl, C 6 - ⁇ aralkyl, C 6 - ⁇ 2 aryl, C ⁇ _ 6 alkyloxy, C 2 - 6 alkenyloxy, C_ 6 alkynyloxy, C 6 - 12 aryloxy, C(0)C ⁇ - 6 alkyl, C(0)C 2 - 6 alkenyl, C(0)C 2 - 6 alkynyl, C(0)C 6 - ⁇ 2 aryl, C(0)C 6 - 12 aralkyl, C 3 -10 heterocycle, hydroxyl, R ⁇ 3 R ⁇
• heterocyclic ring represents a mono or polycyclic (e.g., bicyclic) ring.
• heterocyclic rings include but are not limited to epoxide; furan; benzofuran; isobenzofuran; oxathiolane; dithiolane; dioxolane; pyrrole; pyrrolidine; imidazole; pyridine; pyrimidine; indole; piperidine; morpholine; thiophene and thiomorpholine.
• heteroarylkyl represents an heterocycle group attached to the adjacent atom by a C ⁇ _ 6 alkyl, C ⁇ - 6 alkenyl, or C ⁇ - 6 alkynyl.
• sulfur atom can be at different oxidation levels, ie. S, SO, or S0 2 . All such oxidation levels are within the scope of the present invention.
• the nitrogen atom can be at different oxidation levels, ie. N or NO. All such oxidation levels are within the scope of the present invention.
• a suitable dose will be in the • range of from about 0.1 to about 750 mg/kg of body weight per day, preferably in the range of 0.5 to 60 mg/kg/day, most preferably in the range of 1 to 20 mg/kg/day.
• the desired dose may conveniently be presented in a single dose or as divided dose administered at appropriate intervals, for example as two, three, four or more doses per day.
• the compound is conveniently administered in unit dosage form; for example containing 10 to 1500 mg, conveniently 20 to 1000 mg , most conveniently 50 to 700 mg of active ingredient per unit dosage form.
• the active ingredient should be administered to achieve peak plasma concentrations of the active compound of from about 1 to about 75 ⁇ M, preferably about 2 to 50 ⁇ M, most preferably about 3 to about 30 ⁇ M. This may be achieved, for example, by the intravenous injection of a 0.1 to 5% solution of the active ingredient, optionally in saline, or orally administered as a bolus containing about 1 to about 500 mg of the active ingredient. Desirable blood levels may be maintained by a continuous infusion to provide about 0.01 to about 5.0 mg/kg/hour or by intermittent infusions containing about 0.4 to about 15 mg/kg of the active ingredient.
• each compound may be either the same as or differ from that when the compound is used alone. Appropriate doses will be readily appreciated by those skilled in the art .
• a compound of the invention may be administered as the raw chemical it is preferable to present the active ingredient as a pharmaceutical composition.
• the invention thus further provides a pharmaceutical composition comprising compounds of the present invention or a pharmaceutically acceptable derivative thereof together with one or more pharmaceutically acceptable carriers therefor and, optionall y, other therapeutic and/or prophylactic ingredients.
• the carrier (s) must be "acceptable” in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
• compositions include those suitable for oral, rectal, nasal, topical (including buccal and sub - lingual),, transdermal, vaginal or parenteral (including intramuscular, sub -cutaneous and intravenous) administration or in a form suitable for administration by inhalation or insufflation.
• the formulations may, where appropriate, be conveniently presented in discrete dosage units and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing into association the active compound with liquid carriers or finely divided solid carriers or both and then, if necessary, shaping the product into the desired formulation.
• compositions suitable for oral administration may conveniently be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution, a suspension or as an emulsion.
• the active ingredient may also be presented as a bolus, electuary or paste.
• Tablets and capsules for oral administration may contain conventional excipients such as binding agents, fillers, lubricants, disintegrants, or wetting agents.
• the tablets may be coated according to methods well known in the art.
• Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for constitution with water or other suitable vehicle before use.
• Such liquid preparations may contain conventional additives su ch as suspending agents, emulsifying agents, non -aqueous vehicles (which may include edible oils) , or preservatives .
• the compounds according to the invention may also be formulated for parenteral administration (e.g. by injection, for example bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre-filled syringes, small volume infusion or in multi-dose containers with an added preservative.
• the compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing an/or dispersing agents.
• the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilisation from solution, for constitution with a suitable vehicle, e.g. sterile, pyrogen-free water, before use.
• the compounds according to the invention may be formulated as ointments, creams or lotions, or as a transdermal patch.
• transdermal patches may contain penetration enhancers such as linalool, carvacrol, thymol, citral, menthol and t-anethole.
• Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
• Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilizing agents, dispersing agents, suspending agents, thickening agents, or colouring ' agents .
• compositions suitable for topical administration in the mouth include lozenges comprising active ingredient in a flavoured base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert base such as gelatin and glycerin or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.
• compositions suitable for rectal administration wherein the carrier is a solid are most preferably presented as unit dose suppositories.
• Suitable carriers include cocoa butter and other materials commonly used in the art, and the suppositories may be conveniently formed by admixture of the active, compound with the softened or melted carrier (s) followed by chilling and shaping in moulds.
• Compositions suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or sprays containing in addition to the active ingredient such carriers as are known in the art to be appropriate .
• the compounds of the invention may be used as a liquid spray or dispersible powder or in the form of drops .
• Drops may be formulated with an aqueous or non -aqueous base also -comprising one more dispersing agents, solubilising agents or suspending agents.
• Liquid sprays are conveniently delivered from pressurized packs.
• the compounds according to the invention are conveniently delivered from an insufflator, nebulizer or a pressurized pack or other convenient means of delivering an aerosol spray.
• Pressurized packs may comprise a suitable propellant ⁇ uch as dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas .
• the dosage unit may be determined by providing a valve to deliver a metered amount .
• the compounds according to the invention may take the form of a dry powder composition, for example a powder mix of the compound and a suitable powder base such as lactose or starch.
• the powder composition may be presented in unit dosage form in, for example, capsules or cartridges or e.g. gelatin or blister packs from which the powder may be administered with the aid of an inhalator or insufflator.
• Step II 3- [ (l-Methyl-piperidin-3-ylmethyl) -amino] -5-phenyl- thiophene-2-carboxylic acid methyl ester (162 mg, 0.348 mmol) was dissolved in 1,2 -dichloroethane (3.0 mL) and treated with trans-4-Methyl-cyclohexanecarbonyl chloride in 1,2-dichloroethane (1.0 mL, 0.43 mmol). The solution was heated at reflux for 1 day.
• Step II A solution of trans 4-methyl-cyclohexanecarboxylic acid (0.629 g, 4.42 mmol) in 1,2-dichloroethane (30 ml) at 0 °C was treated with triphenylphosphine (1.16 g, 4.42 mmol), N-chlorosuccinimide (0.59 g, 4.42 mmol) and 5- Bromo-3- (1,4-dioxa-spiro [4.5] dec-8-ylamino) -thiophene- 2 -carboxylic acid methyl ester (1.10 g, 2.92 mmol) . The resulting mixture was then stirred for 36 h at 90 °C and then concentrated.
• the reaction was stirred at room temperature for 20 hours and was then diluted with ethyl acetate (10 ml) .
• the organic layer was separated, and the aqueous phase was washed twice with ethyl acetate (2 X 10 mL) .
• the combined ethyl acetate layers were washed with brine (10 ml) , dried on Na 2 S0 4 , filtered and concentrated.
• Step IV 5-Bromo-3 -[ (4-methyl-cyclohexanecarbonyl) - (4-oxo- cyclohexyl) -amino] -thiophene-2-carboxylic acid methyl ester (473 mg, 1.04 mmol) was dissolved in methanol (10.4 ml), cooled to 0°C and treated with sodium borohydride (43 mg, 1.14 mmol) . After 30 minutes of stirring at 0 °C, the reaction was left stirring at room temperature for 30 min and quenched with a 10% solution of hydrochloric acid (20 ml) .
• Step V A degassed solution of 5-Bromo-3- [ (4-hydroxy- cyclohexyl) - (4-methyl-cyclohexanecarbonyl) -amino] - thiophene-2-carboxylic acid methyl ester (70 mg, 0.15 mmol) and 3 -fluorophenyl boronic acid (32 mg, 0.23 mmol) in a mixture of DME (2.0 mL) and 2M aqueous Na 2 C0 3 (1.0 mL) was treated with Pd(PPh 3 ) (17.6 mg, 0.015 mmol) . The reaction was heated at reflux for 18h. The reaction mixture was diluted with ethyl acetate and water. The organic layer was separated, washed with brine, dried and concentrated to a residue that was purified by preparative chromatography using
• Step II 3- [ (l-Methylcarbamoyl-piperidin-4-yl) - (4-methyl- cyclohexanecarbonyl) -amino] -5-phenyl-thiophene-2- carboxylic acid methyl ester (139 mg, 0.28 mmol) was dissolved in a 4:1 mixture of dioxane :H 2 0 (2.8 ml) and treated with LiOH.H 2 0 (35.3 mg, 0.84 mmol). After 3 hours of stirring at 55 °C, the solvents were removed and then partitioned between 5 ml of H 2 0. acidified to pH 4 and 5 ml of EtOAc.
• Step II 3- [ [1,3] Dioxolan-2-ylmethyl- (4-methyl- cyclohexanecarbonyl) -amino] -5-phenyl-thiophene-2-. carboxylic acid methyl ester using a procedure similar to the procedure described in example 32.
• Butyllithium (2.5 M, 0.9 mL, 2.280 mmol) was added to a cold solution (-78 °C) of methyltriphenylphosphonium bromide (939 mg, 2.630 mmol) in THF (10 mL) .
• the reaction mixture was stirred at room temperature for lh and then 3 ⁇ [Isopropyl- (4-oxo-cyclohexanecarbonyl) - amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester. (700 mg, 1.754) in THF (5 mL) was added at -78 °C.
• the reaction mixture was allowed to stir at room temperature for 12h.
• Step III 3- [Isopropyl- (4-methylene-cyclohexanecarbonyl) -amino] - 5-phenyl-thiophene-2-carboxylic acid methyl ester (50 mg, 0.126 mmol) was taken in a mixture of THF:MeOH:H 2 0 (3:2:1, 3 mL) and then IN aqueous solution of LiOH.H 2 0 (0.8 mL, 0.8Q0 mmol) was added. The reaction mixture was stirred at room temperature for 12 h. Solvents were removed and the residue was partitioned between water and ethyl acetate. The aqueous layer was acidified using 10 % KHSO solution.
• Step II 4-Methyl-cyclohex-3-enecarbonyl chloride was prepared according to the procedure reported in Journal of Organic Chemistry (1986) 51(23), PP4485-8;. This 4- Methyl -cyclohex-3-enecarbonyl chloride (0.121 g, 0.77 mmol) was dissolved along with 5 - (4-Fluoro-phenyl) -3- isopropylamino-thiophene-2-carboxylic acid methyl ester
• the aqueous layer was acidified using 10 % KHS0 4 solution.
• the organic layer was separated, dried (Na 2 S0 4 ) and concentrated.
• the residue was purified by preparative TLC using dicholomethane:methanol (9 : 1) to obtain 5 - (4-Fluorophenyl) -3- [isopropyl- (4-methyl-cyclohex-3-enecarbonyl) - amino] -thiophene-2-carboxylic acid (compound 53) (31 mg, 23%).
• Cis/trans- l-Fluoro-4-methyl-cyclohexanecarboxylic acid was prepared according to the procedure reported in
• Step III 3- [ (l-Fluoro-4-methyl-cyclohexanecarbonyl) -isopropyl- amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (0.049 g, 0.12 mmol) was taken in a mixture of THF:MeOH:H 2 0 (3:2:1, 10 mL) and then added IN aqueous solution of LiOH.H 2 0 (0.35 mL, 0.35 mmol). The reaction mixture was stirred at 50 °C for 3 h. Solvents were removed and the residue was partitioned between water and ethyl acetate. The aqueous layer was acidified using 10 % KHSO 4 solution.
• Step II 2-Azido-4-methyl-cyclohexanecarboxylic acid ethyl ester (425 mg, 2.01 mmol) was dissolved in a 4:1 mixture of dioxane :H 2 0 (20 ml) and then LiOH IN (10 ml, 10.05 mmol) was added. After 35 minutes of stirring at room temperature, solvents were removed and then partitioned between 15 ml of H0 acidified to pH 4 and 15 ml of EtOAc. The organic layer was separated and the aqueous phase was washed twice with ethyl acetate (2X10 mL) .
• Step III To a solution of the 2:1 mixture of 2 -Azido-4-methyl- cyclohexanecarboxylic acid and 4 -Methyl -cyclohex-1- enecarboxylic acid (166 mg, 0.91 mmol) in dichloromethane (9 ml) was added a 2.0 M solution of oxalyl chloride (905 ul, 1.82 mmol) followed by 1 drop of dimethylformamide. The reaction mixture was stirred for 3 hours at room temperature.
• Step V To 3- [ (2-Azido-4-methyl-cyclohexanecarbonyl) -isopropyl- amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (17.5 mg, 0.04 mmol) in methanol (400 ul) was added concentrated hydrochloric acid (15 ul) followed by 10% palladium on charcoal (4 mg, 0.004 mmol) .
• the reaction vessel was introduced with 20 psi of hydrogen and then stirred at room temperature for 17 hours. The residue was then filtered off through celite, washed with methanol and evaporated to give the crude product .
• the resulting mixture was then stirred for 18 h at 90 °C and then cooled to room temperature. It was then diluted with ethyl acetate (10 ml) and a solution of saturated NaHC0 3 (10 ml) was added. The aqueous phase was separated and washed with ethyl acetate (2 x 10 ml) and the combined organic layers were dried (Na 2 S0 4 ), filtered and concentrated.
• Step IV 3- [ (4-Methyl-cyclohexanecarbonyl) - (4-oxo-cyclohexyl) - amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (34 mg, 0.075 mmol) was dissolved in a 4:1 mixture of dioxane :H 2 0 (1 ml) and then LiOH IN (375 ul, 0.375 mmol) was added. After 3 hours of stirring at room temperature, solvents were removed and then partitioned between 5 ml of H 2 0 acidified to pH 4 and 5 ml of EtOAc .
• Example 17 3- [ (4-Methoxy-cyclohexyl) - (4-methyl- cyclohexanecarbonyl) -amino] -5-phenyl-thiophene-2- carboxylic acid Compound 46.
• Compound 25 was prepared in a similar manner.
• Step I To a stirred solution of 3 -Amino-5-phenyl-thiophene-2- carboxylic acid methyl ester (1.0 g, 4.29 mmol) in THF (1.0 ml) was added the ketone (1.0 g, 4.29 mmol) , dibutyltin dichloride (130 mg, 0.43 mmol) and phenylsilane (582 ul, 4.72 mmol) and the reaction mixture was stirred at room temperature for 2 days. The reaction was then quenched with a saturated NaHCO 3 solution, and the mixture was extracted 3 times wit h EtOAc. The combined extracts were then washed with brine and dried on Na 2 S0 , filtered and concentrated.
• Step IV 3- [ (4 -Methyl -cyclohexanecarbonyl) -piperidin-4-yl- amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (20 mg, 0.045 mmol) was dissolved in a 4:1 mixture of dioxane :H 2 0 (0.5 ml) and then LiOH IN (135 ul, 0.135 mmol) was added. After 4 hours of stirring at room temperature, the reaction mixture was acidified to pH 3-4 with a 10% solution of hydrochloric acid and then the solvents were removed.
• Step I (a) To a stirred solution of 1 -methyl-piperidin-4-one (6.0 g, 53 mmol, 6.52 mL) and Et 3 N (14.16 g, 140 mmol, 19.5 mL) in 1,4-dioxane (20 mL) was added chlorotrimethylsilane (7.6 g, 70 mmol, 8.88 mL) drop
• reaction mixture was stirred for 4 h at room temperature.
• the solvents were then removed to obtain .
• Step VI (4R) -5- (4-Fluoro-phenyl) -3- [isopropyl- (4- methyl-cyclohex-1-enecarbonyl) -amino] -thiophene-2- carboxylic acid methyl ester and (1R,2S,4R) -3-[(2- Acetoxy-4-methyl-cyclohexanecarbonyl) -isopropyl -amino] - 5- (4-fluoro-phenyl) -thiophene-2-carboxylic acid methyl ester
• step 7 furnished 3- [isopropyl- (5-methyl-3, 6-dihydro-2H-pyran- 2-carbonyl) -amino] -5-phenyl-thiophene-2-carboxylic acid
• step 4 gave separable mixture of 3 - [isopropyl- (cis-5-methyl- tetrahydro-pyran-2-carbonyl) -amino] -5-phenyl-thiophene- 2-carboxylic acid methyl ester (30 mg, 35.5%) .
• Step IV 3- [Isopropyl- ( trans-5-methyl-tetrahydro-pyran-2- carbonyl) -amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (15 mg, 0.038 mmol) was transformed into 3 - [isopropyl- (trans-5-methyl-tetrahydro-pyran-2- carbonyl) -amino] -5-phenyl-thiophene-2-carboxylic acid (Compound 27) (10 mg, 68%) as described for example 25, step 7.
• PhSiH 3 (0.476 g, 0.542 mL) was carried out as described for example 13, step 1 gave 5 -phenyl -3- (tetrahydro- thiopyran-4-ylamino) -thiophene-2-carboxylic acid methyl ester (0.753 g, ' 56.3%).
• Step VI 5 To a stirred solution of 3- [ ( trans-4-methyl- cyclohexanecarbonyl) - (tetrahydro-thiopyran-4-yl) - amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (57 mg, 0.124 mmol) in EtOH (1.2 mL) from step 2 was added magnesium monoperoxyphthalic acid (29.6 mg,
• Step II Amidation of 4 - (2 -methoxycarbonyl -thiophen-3 -ylamino) - piperidine-1-carboxylic acid benzyl ester (3.7 g, 10 mmol) and cyclochexyl chloride was carried out as described for example 19, step II gave 4 -[(2- . methoxycarbonyl-thiophen-3 -yl) - ( trans-4 -methyl - cyclohexanecarbonyl) -amino] -piperidine-1-carboxylic acid benzyl ester (3.0 g, 60%).
• Step IV To a stirred solution of 3- [ ( rans-4-methyl- cyclohexanecarbonyl) -piperidin-4-yl-amino] -thiophene-2- carboxylic acid methyl ester (1.0 g, 2.7 mmol), from step 3, in 1,2-dichloroethane (10 mL) was sequentially
• Step I 5 A solution of p-methoxybenzyl amine ( 690mg,722 ⁇ L, 8.01 mmol) in dry methanol (5 ml) , under nitrogen was ' cooled to 0° and treated drpwise with . a solution of metacrylate ( 951 ⁇ L, l.Og, 7.28mmol) in MeOH (1.0 ml) added over 2 min. After 15.5h the clear solution was
• Step V A solution of trans 4 -methylcyclohexane carboxylic acid (56mg, 0.399mmol, 1.2eq)in 1,2-dichloroethane (1ml) at 0°, under N2, was treated with oxalyl chloride (2.0M solution in CH 2 C ⁇ 2 ) (231 ⁇ l, 0.46mmol, 1.4eq) , followed by 5 dimethylformamide (8 ⁇ l, 7mg, 0. lmmol, 30mol%) .
• Step IV was conducted in a similar manner as described in example 30. Step IV
• Step VII A solution of 3- [ (2-Azido-l-methyl-ethyl) - (4-methyl- cyclohexanecarbonyl) -amino] -5-phenyl-thiophene-2- carboxylic acid (8mg, 0.19mmol) in EtOH (0.2ml) at 21°, was treated with 10% Pd/C (4mg, 50% w/w) and stirred 5 under an atmosphere of H2 for 1.5h.
• reaction mixture was filtered through a pad of celite with hot EtOAc and the combined filtrate and washings dried and evaporated to a glass to provide 3 -[ (2-Amino-1-methyl- ethyl) - (4-methyl-cyclohexanecarbonyl) -amino] -5-phenyl-
• Step II 3- [ (l-cyano-piperidin-4-yl) - (4-methyl cyclohexanecarbonyl) -amino] -5-phenyl-thiophene-2- carboxylic acid methyl ester (150 mg, 0.32 mmol) was dissolved in a 4:1 mixture of dioxane : H 2 0 (3.2 ml) and treated with LiOH.H 2 0 (20 mg, 0.48 mmol) . After 2 hours of stirring at 50 °C, the solvents were removed and then partitioned between 5 ml of H 2 0 acidified to pH 4 and 5 ml of EtOAc.
• Step II To a solution of water (1 mL) and tetrahydrofuran (lmL) was added mercuric acetate (83.0 mg, 0.277 mmol, 1 eq) at room temperature. After stirring 10 min, the yellow solution was cooled to 0°C and a solution of 3-[(4- Methyl-cyclohexanecarbonyl) - (4-methylene-cyclohexyl) - amino] -5-phenyl-thiophene-2-carboxylic acid methyl ester (125 mg, 0.277 mmol, 1 eq) was added dropwise. The resulting mixture was stirred 1 h at 0°C.
• Aqueous phase was acidified to pH 1 and extracted with dichloromethane (3 x 30 mL) .
• Organic phases of dichloromethane were combined, dried over sodium sulfate and concentrated.
• the crude was purified by chromatography (10% methanol/dichloromethane) to give 50 mg (74%) of cis-3 - [ (4-Hydroxy-4-methyl-cyclohexyl) - (4-methyl-cyclohexanecarbonyl) -amino] -5-phenyl- thiophene-2-carboxylic acid.
• NMR 1 H (CDC1 3 , 400 MHz) : 7,60 ppm (d, 2H) ; 7,39 ppm (m, 3H) ; 7,03 ppm (s, IH) ; 4,51 ppm (bs, 2H) ; 2,00 ppm (m, IH) ; 1.80-1.20 ppm (m, 15H) ; 1,12 ppm (s, 3H) ; 0,71 ppm (d, 3H) ; 0,60 ppm (m, 2H) .
• HCV NS5B protein purified recombinant HCV RNA - dependent RNA polymerase (NS5B protein) .
• HCV NS5B was expressed in insect cells using a recombinant baculovirus as vector. The experimental procedures used for the cloning, expression and purification of the HCV NS5B protein are described below. Followings , are details of the RNA-dependent RNA polymerase assays used to test the compounds .
• HCV NS5B protein in insect cells The cDNA encoding the entire NS5B protein of HCV -Bk strain, genotype lb, was amplified by PCR using the primers NS5Nhe5' (5 ' -GCTAGCGCTAGCTCAATGTCCTACACATGG- 3') and XhoNS53' (5 ' -CTCGAGCTCGAGCGTCCATCGGTTGGGGAG- 3') and the plasmid pCD 3.8-9.4 as template (Tomei et al, 1993) .
• NS5Nhe5' and XhoNS53' contain two Nhel and Xhol sites (underlined sequences) , respectively, at their 5' end.
• the amplified DNA fragment was cloned in the bacterial expression plasmid pET-21b (Novagen) between the restriction sites Nhel and Xhol , to generate the plasmid pET/ ⁇ S5B.
• This plasmid was later used as template to PCR-amplify the NS5B coding region, using the primers NS5B-H9 (5' - ATACATATGGCTAGCATGTCAATGTCCTACACATGG-3' ) and NS5B-R4 (5' -GGATCCGGATCCCGTTCATCGGTTGGGGAG-3')- NS5B-H9 spans a region of 15 nucleotides in the plasmid pET -21b followed by the translation initiation codon (ATG) and 8 nucleotides corresponding to the 5' end of the NS5B coding region (nt.
• NS5B -R4 contains two BamEI sites (underlined) followed by 18 nucleotides corresponding to the region around the stop codon i n the HCV genome (nt . 9365-9347).
• the amplified sequence, of 1.8 kb, was digested with Nhel and BamHI and ligated to a predigested pBlueBacII plasmid (Invitrogen) .
• the resulting recombinant plasmid was designated pBac/NS5B.
• Sf9 cells were co-transfected with 3 ⁇ g of pBac/NS5B, together with 1 ⁇ g of linearized baculovirus DNA (Invitrogen) , as described in the manufacturer's protocol. Following two rounds of plaque purification, an NS5B -recombinant baculovirus, BacNS5B, was isolated. The presence of the recombinant NS5B protein was determined by western blot analysis (Harlow and Lane, 1988) of BacNS5B - infected Sf9 cells, using a rabbit polyclonal antiserum (anti-NS5B) raised against a His -tagged version of the NS5B protein expressed in E. coli . Infections of Sf9 cells with this plaque purified virus were performed in one -liter spinner flasks at a cell density of 1.2 x 10 6 cells/ml and a multiplicity of infection of 5.
• a soluble recombinant NS5B protein Sf9 cells were infected as described above. Sixty hours post-infection, cells were harvested then washed twice with phosphate buffer saline (PBS) . Total proteins were solubilized as described in Lohmann et al . (1997) with some modifications. In brief, proteins were extracted in three steps, SI, S2, S3, using lysis buffers (LB) I, LB II and LB III (Lohmann et al, 1997) . The composition of LBII was modified to contain 0.1 % triton X-100 and 150 mM NaCl to reduce the amount of solubilized NS5B protein at this step. In addition, sonication of cell extracts was avoided throughout the protocol to preserve the integrity of the protein structure.
• PBS phosphate buffer saline
• Soluble NS5B protein in the S3 fraction was diluted to lower the NaCl concentration to 300 mM, then it incubated batchwise with DEAE sepharose beads
• Bound proteins were eluted in 1 ml fractions, using a continuous NaCl gradient of 0.2 to 1 M, over a 25 ml volume.
• NS5B -containing fractions were identified by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS -PAGE) , followed by western blotting using the anti -NS5B antiserum at a dilution of 1:2000. Positive fractions were pooled and the elution buffer was exchanged against a 50 mM NaP0 pH 7.0, 20 % glycerol, 0.5 % triton X-100 and 10 M DTT, using a PD-10 column (Amersham-Pharmacia) .
• This assay consists on measuring the incorporation of [ 3 H] radiolabelled UTP in a polyrA/ biotinylated -oligo dT template-primer, captured on the surface of streptavidin-coated scintillant-embeded microtiter FlashplatesTM (NEN Life Science Products inc, MA, USA, SMP 103A) .
• a 400 ng/ ⁇ l polyrA solution (Amersham Pharmacia Biotech) was mixed volume -to- volume with 5' biotin-oligo dT ⁇ 5 at 20 pmol/ ⁇ l.
• the template and primers were denatured at 95 C for 5 minutes then incubated at 37 C for 10 minutes.
• preceeding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceeding examples .

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