CN102209717B - 治疗丙型肝炎的化合物 - Google Patents
治疗丙型肝炎的化合物 Download PDFInfo
- Publication number
- CN102209717B CN102209717B CN200980144912.3A CN200980144912A CN102209717B CN 102209717 B CN102209717 B CN 102209717B CN 200980144912 A CN200980144912 A CN 200980144912A CN 102209717 B CN102209717 B CN 102209717B
- Authority
- CN
- China
- Prior art keywords
- solvent
- phenyl
- minutes
- fluorophenyl
- column
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CCC(CCC(C)(C)N=C)C*C Chemical compound CCC(CCC(C)(C)N=C)C*C 0.000 description 3
- COTPWXWBAZHKAT-UHFFFAOYSA-N CC(C)(C(O)=O)NC(c1cccc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1)=O Chemical compound CC(C)(C(O)=O)NC(c1cccc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1)=O COTPWXWBAZHKAT-UHFFFAOYSA-N 0.000 description 1
- BTCDHBMCIQJLRL-UHFFFAOYSA-N CC(C)(C)NC(c1cccc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1)=O Chemical compound CC(C)(C)NC(c1cccc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1)=O BTCDHBMCIQJLRL-UHFFFAOYSA-N 0.000 description 1
- CYDUCSXBOFPHPP-UHFFFAOYSA-N CC(C)(CN1CCOCC1)NC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c(C)cc1)=O Chemical compound CC(C)(CN1CCOCC1)NC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c(C)cc1)=O CYDUCSXBOFPHPP-UHFFFAOYSA-N 0.000 description 1
- HOHDPNIPWLVVFK-UHFFFAOYSA-N CC(C)(c(cc1)ccc1F)NC(c1cc(-c(cc2c(C(NC)=O)c(-c(cc3)ccc3F)[o]c2c2)c2N(CCO)S(C)(=O)=O)ccc1)=O Chemical compound CC(C)(c(cc1)ccc1F)NC(c1cc(-c(cc2c(C(NC)=O)c(-c(cc3)ccc3F)[o]c2c2)c2N(CCO)S(C)(=O)=O)ccc1)=O HOHDPNIPWLVVFK-UHFFFAOYSA-N 0.000 description 1
- MELOVSWSWSKMEN-UHFFFAOYSA-N CC(C)CN(C)C(c1cccc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1)=O Chemical compound CC(C)CN(C)C(c1cccc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1)=O MELOVSWSWSKMEN-UHFFFAOYSA-N 0.000 description 1
- JWNDOSPRZHPEIT-UHFFFAOYSA-N CC(C)CNC(c(cc1)cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1OC(F)F)=O Chemical compound CC(C)CNC(c(cc1)cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1OC(F)F)=O JWNDOSPRZHPEIT-UHFFFAOYSA-N 0.000 description 1
- OCQAXGMOWZVKMC-UHFFFAOYSA-N CC(C)CNC(c(cc1)cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1OCCN(Cc1ccccc1)Cc1ccccc1)=O Chemical compound CC(C)CNC(c(cc1)cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1OCCN(Cc1ccccc1)Cc1ccccc1)=O OCQAXGMOWZVKMC-UHFFFAOYSA-N 0.000 description 1
- XPJUVIURUQICIO-UHFFFAOYSA-N CC(C)CNC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1OC(C)C)=O Chemical compound CC(C)CNC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1OC(C)C)=O XPJUVIURUQICIO-UHFFFAOYSA-N 0.000 description 1
- VWJRZRCCGKTAQJ-UHFFFAOYSA-N CC(C)CNC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1OC)=O Chemical compound CC(C)CNC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1OC)=O VWJRZRCCGKTAQJ-UHFFFAOYSA-N 0.000 description 1
- PKJQFSQREIYTLR-UHFFFAOYSA-N CC(C)CNC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1OCCNC(N)=O)=O Chemical compound CC(C)CNC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1OCCNC(N)=O)=O PKJQFSQREIYTLR-UHFFFAOYSA-N 0.000 description 1
- FZBWTSCJLMDJOQ-UHFFFAOYSA-N CC(C)CNC(c(cc1-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1Cl)=O Chemical compound CC(C)CNC(c(cc1-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1Cl)=O FZBWTSCJLMDJOQ-UHFFFAOYSA-N 0.000 description 1
- LAIMGFOJVRJYKF-UHFFFAOYSA-N CC(C)CNC(c(cc1-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1F)=O Chemical compound CC(C)CNC(c(cc1-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1F)=O LAIMGFOJVRJYKF-UHFFFAOYSA-N 0.000 description 1
- UDHAZZAXMMMEPI-UHFFFAOYSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)cc(OCC2CC2)c1)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)cc(OCC2CC2)c1)=O UDHAZZAXMMMEPI-UHFFFAOYSA-N 0.000 description 1
- NBWSRVDWSJVCKL-UHFFFAOYSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)cc(OCCc2cccnc2)c1)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)cc(OCCc2cccnc2)c1)=O NBWSRVDWSJVCKL-UHFFFAOYSA-N 0.000 description 1
- NPNJIUGLLVSQQH-UHFFFAOYSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c(cc1)ccc1C(N)=O)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c(cc1)ccc1C(N)=O)=O NPNJIUGLLVSQQH-UHFFFAOYSA-N 0.000 description 1
- JZGDAGQROZYZAX-FRKPEAEDSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c1cccc(/C=C/C(O)=O)c1)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c1cccc(/C=C/C(O)=O)c1)=O JZGDAGQROZYZAX-FRKPEAEDSA-N 0.000 description 1
- OMOPAXVQKKMIHN-UHFFFAOYSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c1ccccc1Cl)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c1ccccc1Cl)=O OMOPAXVQKKMIHN-UHFFFAOYSA-N 0.000 description 1
- DTYUVUSLAYGSDF-UHFFFAOYSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c1cncc2c1cccc2)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)ccc1-c1cncc2c1cccc2)=O DTYUVUSLAYGSDF-UHFFFAOYSA-N 0.000 description 1
- ACSMPXULARNVFN-UHFFFAOYSA-N CC(C)[n]1nnc(-c2cc(-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)ccc2)n1 Chemical compound CC(C)[n]1nnc(-c2cc(-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)ccc2)n1 ACSMPXULARNVFN-UHFFFAOYSA-N 0.000 description 1
- IQCVONRXPUNOSZ-UHFFFAOYSA-N CC(C1CC(C2)C2C1)N Chemical compound CC(C1CC(C2)C2C1)N IQCVONRXPUNOSZ-UHFFFAOYSA-N 0.000 description 1
- SDDIOOLVZRJBMT-UHFFFAOYSA-N CCCOc1cc(C(NCC(C)C)=O)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1 Chemical compound CCCOc1cc(C(NCC(C)C)=O)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1 SDDIOOLVZRJBMT-UHFFFAOYSA-N 0.000 description 1
- DFOHOLFLHMIYCU-UHFFFAOYSA-N CCNC(c1cc(-c(c(C(NCC(C)C)=O)c2)ccc2-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)ccc1)=O Chemical compound CCNC(c1cc(-c(c(C(NCC(C)C)=O)c2)ccc2-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)ccc1)=O DFOHOLFLHMIYCU-UHFFFAOYSA-N 0.000 description 1
- LCNNAKNMRLZSCZ-UHFFFAOYSA-N CCOC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc(N(C)S(C)(=O)=O)c2-c1cccc(C(O)=O)c1)=O Chemical compound CCOC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc(N(C)S(C)(=O)=O)c2-c1cccc(C(O)=O)c1)=O LCNNAKNMRLZSCZ-UHFFFAOYSA-N 0.000 description 1
- TVJAATHIDLAWME-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc(N(CCO)S(C)(=O)=O)c2-c1cccc(C(NC2(CC2)c2ccccc2)=O)c1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc(N(CCO)S(C)(=O)=O)c2-c1cccc(C(NC2(CC2)c2ccccc2)=O)c1)=O TVJAATHIDLAWME-UHFFFAOYSA-N 0.000 description 1
- IXULLIFXFIIACL-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc([N+]([O-])=O)c2-c1cc(C(O)=O)ccc1OC)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc([N+]([O-])=O)c2-c1cc(C(O)=O)ccc1OC)=O IXULLIFXFIIACL-UHFFFAOYSA-N 0.000 description 1
- VRNRACWWGXHRGZ-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c(cc(cc1)C(NC2(CC2)c2ccccc2)=O)c1OCCN)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c(cc(cc1)C(NC2(CC2)c2ccccc2)=O)c1OCCN)=O VRNRACWWGXHRGZ-UHFFFAOYSA-N 0.000 description 1
- JWLAIYBPTJSFJI-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c(cc(cc1)C(NC2(CC2)c2ccccn2)=O)c1OCCN)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c(cc(cc1)C(NC2(CC2)c2ccccn2)=O)c1OCCN)=O JWLAIYBPTJSFJI-UHFFFAOYSA-N 0.000 description 1
- BSRDUICQYCOEEV-ZVVUMHAFSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cc(C(NC(C2)C2(CCC2)[C@@H]2c(cc2)ccc2Cl)=O)ccc1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cc(C(NC(C2)C2(CCC2)[C@@H]2c(cc2)ccc2Cl)=O)ccc1)=O BSRDUICQYCOEEV-ZVVUMHAFSA-N 0.000 description 1
- KRMRAYPDSDLHRU-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cc(C(NC2(CC2)c2cccc(OC)c2)=O)ccc1Cl)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cc(C(NC2(CC2)c2cccc(OC)c2)=O)ccc1Cl)=O KRMRAYPDSDLHRU-UHFFFAOYSA-N 0.000 description 1
- ZBPUXZUUIQFXFU-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cc(C(NS(C)(=O)=O)=O)ccc1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cc(C(NS(C)(=O)=O)=O)ccc1)=O ZBPUXZUUIQFXFU-UHFFFAOYSA-N 0.000 description 1
- XWEXWMOICFEPKX-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(-c2nc(-c3ccccc3)c[nH]2)c1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(-c2nc(-c3ccccc3)c[nH]2)c1)=O XWEXWMOICFEPKX-UHFFFAOYSA-N 0.000 description 1
- YCQXYIHXCTXZBO-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(C(N(CC2)CC2c(cc2)ccc2F)=O)c1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(C(N(CC2)CC2c(cc2)ccc2F)=O)c1)=O YCQXYIHXCTXZBO-UHFFFAOYSA-N 0.000 description 1
- BBQIYHZTFFKAJD-SANMLTNESA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(C(OC2)=N[C@@H]2c2ccccc2)c1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(C(OC2)=N[C@@H]2c2ccccc2)c1)=O BBQIYHZTFFKAJD-SANMLTNESA-N 0.000 description 1
- BBQIYHZTFFKAJD-AREMUKBSSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(C(OC2)=N[C@H]2c2ccccc2)c1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc(C(OC2)=N[C@H]2c2ccccc2)c1)=O BBQIYHZTFFKAJD-AREMUKBSSA-N 0.000 description 1
- FMIUDOCVPJOWIL-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc2c1cc[nH]2)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c1cccc2c1cc[nH]2)=O FMIUDOCVPJOWIL-UHFFFAOYSA-N 0.000 description 1
- JXNKSRTZGUKVFI-UHFFFAOYSA-N CNC(c1c(-c(cc2)ccc2F)[o]c(cc2)c1cc2-c(cc1)cc(C(O)=O)c1Cl)=O Chemical compound CNC(c1c(-c(cc2)ccc2F)[o]c(cc2)c1cc2-c(cc1)cc(C(O)=O)c1Cl)=O JXNKSRTZGUKVFI-UHFFFAOYSA-N 0.000 description 1
- RLLGLBMQWNYOAP-UHFFFAOYSA-N CNC(c1c(-c(cc2)ccc2F)[o]c(cc2)c1cc2-c1cc(C(O)=O)ccc1OC)=O Chemical compound CNC(c1c(-c(cc2)ccc2F)[o]c(cc2)c1cc2-c1cc(C(O)=O)ccc1OC)=O RLLGLBMQWNYOAP-UHFFFAOYSA-N 0.000 description 1
- NEWKKEXMMFXVGW-UHFFFAOYSA-N CNC(c1c(-c(cc2)ccc2F)[o]c(cc2)c1cc2-c1cccc(C(NC2(CCC2)c2ccccc2)=O)c1)=O Chemical compound CNC(c1c(-c(cc2)ccc2F)[o]c(cc2)c1cc2-c1cccc(C(NC2(CCC2)c2ccccc2)=O)c1)=O NEWKKEXMMFXVGW-UHFFFAOYSA-N 0.000 description 1
- BYFNKPPGVJSGLX-HBXADGBSSA-N Cc(c(-c(cc1)cc2c1[o]c(-c(cc1)ccc1F)c2C(NC)=O)c1)ccc1C(NC1(CC1)C(/C=C\NC)=N)=O Chemical compound Cc(c(-c(cc1)cc2c1[o]c(-c(cc1)ccc1F)c2C(NC)=O)c1)ccc1C(NC1(CC1)C(/C=C\NC)=N)=O BYFNKPPGVJSGLX-HBXADGBSSA-N 0.000 description 1
- ODQOTXZXUSKMQQ-UHFFFAOYSA-N Cc(c(-c(cc12)ccc1[o]c(-c(ccc(F)c1)c1N1)c2C1=O)c1)cc(OC)c1C(OC)=O Chemical compound Cc(c(-c(cc12)ccc1[o]c(-c(ccc(F)c1)c1N1)c2C1=O)c1)cc(OC)c1C(OC)=O ODQOTXZXUSKMQQ-UHFFFAOYSA-N 0.000 description 1
- HPJKQKKYLQAKEC-UHFFFAOYSA-N Cc(c(-c(cc1c(C(NC)=O)c(-c(cc2)ccc2F)[o]c1c1)c1N)c1)ccc1C(NC1(CC1)c1ccccc1)=O Chemical compound Cc(c(-c(cc1c(C(NC)=O)c(-c(cc2)ccc2F)[o]c1c1)c1N)c1)ccc1C(NC1(CC1)c1ccccc1)=O HPJKQKKYLQAKEC-UHFFFAOYSA-N 0.000 description 1
- RSXQLADMDWOEOY-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nc(C2CC2)n[o]1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nc(C2CC2)n[o]1)=O RSXQLADMDWOEOY-UHFFFAOYSA-N 0.000 description 1
- GLUJCJHTWXQVRG-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c(cccc2)c2Cl)[nH]1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c(cccc2)c2Cl)[nH]1)=O GLUJCJHTWXQVRG-UHFFFAOYSA-N 0.000 description 1
- DCSBSSZFPMQIBJ-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1NC(C1(CC1)c1ccccc1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1NC(C1(CC1)c1ccccc1)=O DCSBSSZFPMQIBJ-UHFFFAOYSA-N 0.000 description 1
- QEHLUCDYDPDDGA-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)cc(C(O)=O)c1)c1OCc1ccccc1 Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)cc(C(O)=O)c1)c1OCc1ccccc1 QEHLUCDYDPDDGA-UHFFFAOYSA-N 0.000 description 1
- HRWYUZFUDWPPGO-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1F)c1)cc(OC)c1C(NC1(CC1)c1ncccn1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1F)c1)cc(OC)c1C(NC1(CC1)c1ncccn1)=O HRWYUZFUDWPPGO-UHFFFAOYSA-N 0.000 description 1
- PRSBIPAGPTZCOS-UHFFFAOYSA-N Cc1nc(C2(CC2)NC(c2ccc(C)c(-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)c2)=O)n[o]1 Chemical compound Cc1nc(C2(CC2)NC(c2ccc(C)c(-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)c2)=O)n[o]1 PRSBIPAGPTZCOS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Oncology (AREA)
- Veterinary Medicine (AREA)
- Communicable Diseases (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Furan Compounds (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9600508P | 2008-09-11 | 2008-09-11 | |
| US61/096,005 | 2008-09-11 | ||
| PCT/US2009/056166 WO2010030592A1 (en) | 2008-09-11 | 2009-09-08 | Compounds for the treatment of hepatitis c |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102209717A CN102209717A (zh) | 2011-10-05 |
| CN102209717B true CN102209717B (zh) | 2015-02-18 |
Family
ID=41226922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980144912.3A Expired - Fee Related CN102209717B (zh) | 2008-09-11 | 2009-09-08 | 治疗丙型肝炎的化合物 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US8048887B2 (enExample) |
| EP (1) | EP2326633B1 (enExample) |
| JP (1) | JP5685191B2 (enExample) |
| KR (1) | KR20110059875A (enExample) |
| CN (1) | CN102209717B (enExample) |
| AR (1) | AR073740A1 (enExample) |
| AU (1) | AU2009291966B2 (enExample) |
| BR (1) | BRPI0918174A2 (enExample) |
| CA (1) | CA2736988A1 (enExample) |
| CL (2) | CL2011000527A1 (enExample) |
| CO (1) | CO6382110A2 (enExample) |
| EA (1) | EA019185B1 (enExample) |
| IL (1) | IL211509A0 (enExample) |
| MX (1) | MX2011002410A (enExample) |
| NZ (1) | NZ591172A (enExample) |
| PE (1) | PE20110806A1 (enExample) |
| TW (2) | TW201014836A (enExample) |
| WO (1) | WO2010030592A1 (enExample) |
| ZA (2) | ZA201101739B (enExample) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8198449B2 (en) * | 2008-09-11 | 2012-06-12 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US7994171B2 (en) * | 2008-09-11 | 2011-08-09 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| EP2361242B1 (en) | 2008-10-17 | 2018-08-01 | Oryzon Genomics, S.A. | Oxidase inhibitors and their use |
| CA2741648A1 (en) * | 2008-10-30 | 2010-05-06 | Merck Sharp & Dohme Corp. | 2,5-disubstituted phenyl carboxamide orexin receptor antagonists |
| WO2010084160A1 (en) | 2009-01-21 | 2010-07-29 | Oryzon Genomics S.A. | Phenylcyclopropylamine derivatives and their medical use |
| CA2764956A1 (en) * | 2009-06-22 | 2010-12-29 | F. Hoffmann-La Roche Ag | Novel biphenyl and phenyl-pyridine amides |
| CA2812683C (en) | 2009-09-25 | 2017-10-10 | Oryzon Genomics S.A. | Lysine specific demethylase-1 inhibitors and their use |
| US8946296B2 (en) | 2009-10-09 | 2015-02-03 | Oryzon Genomics S.A. | Substituted heteroaryl- and aryl-cyclopropylamine acetamides and their use |
| WO2011106105A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Inhibitors for antiviral use |
| WO2011106573A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with hepadnaviridae |
| US8324212B2 (en) | 2010-02-25 | 2012-12-04 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| AR080433A1 (es) * | 2010-03-02 | 2012-04-11 | Merck Sharp & Dohme | Derivados de benzofurancarboxamidas utiles para tratar o prevenir infecciones por vhc y composiciones farmaceuticas que los contienen. |
| US8354410B2 (en) * | 2010-03-11 | 2013-01-15 | Bristol-Meyers Squibb Company | Compounds for the treatment of hepatitis C |
| JP2013522192A (ja) * | 2010-03-11 | 2013-06-13 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎の処置のための化合物 |
| HUE030938T2 (en) | 2010-04-19 | 2017-06-28 | Oryzon Genomics Sa | Lysine-specific demethylase-1 inhibitors and their use |
| US8324239B2 (en) | 2010-04-21 | 2012-12-04 | Novartis Ag | Furopyridine compounds and uses thereof |
| WO2011140333A1 (en) | 2010-05-07 | 2011-11-10 | The Board Of Trustees Of The Leland Stanford Junior University | Identification of stabilizers of multimeric proteins |
| US8445497B2 (en) * | 2010-06-30 | 2013-05-21 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| MX341732B (es) | 2010-07-29 | 2016-08-30 | Oryzon Genomics S A * | Inhibidores de la demetilasa lsd1 basados en arilciclopropilamina y sus usos médicos. |
| WO2012013727A1 (en) | 2010-07-29 | 2012-02-02 | Oryzon Genomics S.A. | Cyclopropylamine derivatives useful as lsd1 inhibitors |
| EP2616461A4 (en) | 2010-08-26 | 2014-03-26 | Rfs Pharma Llc | POTENTIVE AND SELECTIVE INHIBITORS OF HEPATITIS C VIRUS |
| US9061966B2 (en) | 2010-10-08 | 2015-06-23 | Oryzon Genomics S.A. | Cyclopropylamine inhibitors of oxidases |
| BR112013009789A2 (pt) | 2010-10-26 | 2016-07-19 | Presidio Pharmaceuticals Inc | inibidores do vírus da hepatite c |
| WO2012072713A2 (en) | 2010-11-30 | 2012-06-07 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae |
| US8507683B2 (en) * | 2010-12-09 | 2013-08-13 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| CA2822357A1 (en) * | 2010-12-22 | 2012-06-28 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
| EP3981395A1 (en) | 2011-02-08 | 2022-04-13 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for myeloproliferative disorders |
| WO2013033901A1 (en) * | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Heterocyclic-substituted benzofuran derivatives and methods of use thereof for the treatment of viral diseases |
| WO2013033899A1 (en) * | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for the treatment of viral diseases |
| WO2013033900A1 (en) * | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases |
| WO2013057322A1 (en) | 2011-10-20 | 2013-04-25 | Oryzon Genomics, S.A. | (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors |
| BR112014009306B1 (pt) | 2011-10-20 | 2021-07-20 | Oryzon Genomics S.A. | Compostos de (hetero)aril ciclopropilamina como inibidores de lsd1 |
| US9303020B2 (en) | 2012-02-08 | 2016-04-05 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US9096580B2 (en) | 2012-03-27 | 2015-08-04 | Bristol-Myers Squibb Company | Benzofuran derivatives for the treatment of hepatitis C |
| WO2013163466A1 (en) * | 2012-04-25 | 2013-10-31 | Presidio Pharmaceuticals, Inc. | Inhibitors of hepatitis c virus |
| US9169214B2 (en) | 2012-12-21 | 2015-10-27 | The Board Of Trustees Of The Leland Stanford Junior University | Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions |
| EP2943496B1 (en) * | 2013-01-10 | 2017-09-06 | Bristol-Myers Squibb Company | Macrocyclic benzofuran and azabenzofuran compounds for the treatment of hepatitis c |
| WO2014121416A1 (en) | 2013-02-07 | 2014-08-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c |
| US8962651B2 (en) | 2013-03-13 | 2015-02-24 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US9738653B2 (en) | 2013-03-14 | 2017-08-22 | Bristol-Myers Squibb Company | Fused furans for the treatment of hepatitis C |
| WO2014205593A1 (en) * | 2013-06-24 | 2014-12-31 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for treatment of viral diseases |
| EP3080106B1 (en) | 2013-12-13 | 2018-01-31 | Bristol-Myers Squibb Company | A novel compound for the treatment of hepatitis c |
| EP3119769A1 (en) * | 2014-03-21 | 2017-01-25 | Bristol-Myers Squibb Pharma Company | Cyanoamino (aza)benzofuran compounds for the treatment of hepatitis c |
| EA201691777A1 (ru) * | 2014-03-21 | 2016-12-30 | Бристол-Маерс Сквибб Компани | Содержащие цианогруппу соединения азабензофурана для лечения гепатита с |
| JP6543342B2 (ja) | 2014-08-14 | 2019-07-10 | アルハマドシャー,マモウン,エム. | 血清半減期を延長するための、調節可能リンカーを介した薬学的活性剤とトランスサイレチンリガンドのコンジュゲーション |
| WO2016133963A1 (en) * | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Benzofurans substituted with secondary benzamide as hcv inhibitors |
| WO2016133972A1 (en) * | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Substituted benzofuran compounds for the treatment of hepatitis c |
| WO2016133961A1 (en) * | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Benzofurans substituted with bicyclic secondary benzamide as hcv inhibitors |
| WO2016133970A1 (en) * | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Benzofurans substituted with primary benzamide as hcv inhibitors |
| WO2016137832A1 (en) * | 2015-02-23 | 2016-09-01 | Bristol-Myers Squibb Company | Novel compounds for the treatment of hepatitis c |
| US11161837B2 (en) | 2016-03-21 | 2021-11-02 | Bristol-Myers Squibb Company | Benzofuran derivatives for the treatment of hepatitis C |
| NZ755597A (en) | 2017-02-17 | 2023-06-30 | Eidos Therapeutics Inc | Processes for preparing ag-10, its intermediates, and salts thereof |
| KR102512548B1 (ko) | 2017-12-22 | 2023-03-22 | 삼성디스플레이 주식회사 | 유기 전계 발광 소자 및 유기 전계 발광 소자용 함질소 화합물 |
| SG11202009073WA (en) | 2018-03-23 | 2020-10-29 | Eidos Therapeutics Inc | Methods of treating ttr amyloidosis using ag10 |
| MA53238A (fr) | 2018-08-17 | 2022-04-13 | Eidos Therapeutics Inc | Formules d'ag10 |
| AU2019387370A1 (en) | 2018-11-30 | 2021-06-10 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN114174283B (zh) * | 2019-07-18 | 2023-05-12 | 石药集团中奇制药技术(石家庄)有限公司 | 作为nmt抑制剂的化合物及其应用 |
| US20250214977A1 (en) * | 2024-01-03 | 2025-07-03 | Kymera Therapeutics, Inc. | Stat6 inhibitors and uses thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1731993A (zh) * | 2002-11-01 | 2006-02-08 | 维洛药品公司 | 苯并呋喃化合物、组合物以及治疗和预防丙型肝炎病毒感染及相关疾病的方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57123181A (en) | 1981-01-23 | 1982-07-31 | Mitsubishi Paper Mills Ltd | Preparation of pyrazolo (1,5-a) pyridine derivative |
| PE20020506A1 (es) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
| JP2004525150A (ja) | 2001-03-30 | 2004-08-19 | スミスクライン ビーチャム コーポレーション | 治療用化合物としてのピラゾロピリジン類の使用 |
| US7868037B2 (en) * | 2004-07-14 | 2011-01-11 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| TW200815384A (en) * | 2006-08-25 | 2008-04-01 | Viropharma Inc | Combination therapy method for treating hepatitis C virus infection and pharmaceutical compositions for use therein |
| MX2009008439A (es) * | 2007-02-12 | 2009-08-13 | Intermune Inc | Nuevos inhibidores de la replicacion del virus de hepatitis c. |
| GB0707000D0 (en) | 2007-04-12 | 2007-05-30 | Istituto Di Ricerche D Biolog | Antiviral agents |
| CN101910145A (zh) | 2008-02-14 | 2010-12-08 | 弗·哈夫曼-拉罗切有限公司 | 抗病毒的杂环化合物 |
| WO2009137493A1 (en) | 2008-05-05 | 2009-11-12 | Wyeth | 2-substituted benzofuran compounds to treat infection with hepatitis c virus |
| WO2009137500A1 (en) | 2008-05-05 | 2009-11-12 | Wyeth | 6-substituted benzofuran compounds to treat infection with hepatitis c virus |
-
2009
- 2009-09-04 US US12/554,193 patent/US8048887B2/en active Active
- 2009-09-08 NZ NZ591172A patent/NZ591172A/xx not_active IP Right Cessation
- 2009-09-08 CN CN200980144912.3A patent/CN102209717B/zh not_active Expired - Fee Related
- 2009-09-08 JP JP2011526931A patent/JP5685191B2/ja not_active Expired - Fee Related
- 2009-09-08 WO PCT/US2009/056166 patent/WO2010030592A1/en not_active Ceased
- 2009-09-08 BR BRPI0918174A patent/BRPI0918174A2/pt not_active IP Right Cessation
- 2009-09-08 EA EA201100390A patent/EA019185B1/ru not_active IP Right Cessation
- 2009-09-08 MX MX2011002410A patent/MX2011002410A/es active IP Right Grant
- 2009-09-08 KR KR1020117008085A patent/KR20110059875A/ko not_active Ceased
- 2009-09-08 PE PE2011000445A patent/PE20110806A1/es active IP Right Grant
- 2009-09-08 CA CA2736988A patent/CA2736988A1/en not_active Abandoned
- 2009-09-08 AU AU2009291966A patent/AU2009291966B2/en not_active Ceased
- 2009-09-08 EP EP09792299.1A patent/EP2326633B1/en not_active Not-in-force
- 2009-09-11 TW TW098130829A patent/TW201014836A/zh unknown
- 2009-09-11 AR ARP090103514A patent/AR073740A1/es not_active Application Discontinuation
- 2009-09-11 TW TW100113021A patent/TW201124403A/zh unknown
-
2011
- 2011-03-01 ZA ZA2011/01739A patent/ZA201101739B/en unknown
- 2011-03-01 IL IL211509A patent/IL211509A0/en unknown
- 2011-03-11 CL CL2011000527A patent/CL2011000527A1/es unknown
- 2011-04-05 CO CO11041979A patent/CO6382110A2/es not_active Application Discontinuation
- 2011-05-25 CL CL2011001224A patent/CL2011001224A1/es unknown
- 2011-08-03 ZA ZA2011/05720A patent/ZA201105720B/en unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1731993A (zh) * | 2002-11-01 | 2006-02-08 | 维洛药品公司 | 苯并呋喃化合物、组合物以及治疗和预防丙型肝炎病毒感染及相关疾病的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2326633A1 (en) | 2011-06-01 |
| CL2011000527A1 (es) | 2011-08-12 |
| TW201124403A (en) | 2011-07-16 |
| EA201100390A1 (ru) | 2011-10-31 |
| MX2011002410A (es) | 2011-04-05 |
| EP2326633B1 (en) | 2015-12-16 |
| CA2736988A1 (en) | 2010-03-18 |
| AU2009291966B2 (en) | 2014-08-28 |
| EA019185B1 (ru) | 2014-01-30 |
| NZ591172A (en) | 2012-12-21 |
| IL211509A0 (en) | 2011-07-31 |
| CN102209717A (zh) | 2011-10-05 |
| US20100093694A1 (en) | 2010-04-15 |
| ZA201101739B (en) | 2012-08-29 |
| AU2009291966A1 (en) | 2010-03-18 |
| BRPI0918174A2 (pt) | 2019-10-01 |
| ZA201105720B (en) | 2012-08-29 |
| CL2011001224A1 (es) | 2011-09-16 |
| PE20110806A1 (es) | 2011-10-31 |
| JP5685191B2 (ja) | 2015-03-18 |
| TW201014836A (en) | 2010-04-16 |
| JP2012502101A (ja) | 2012-01-26 |
| US8048887B2 (en) | 2011-11-01 |
| WO2010030592A1 (en) | 2010-03-18 |
| KR20110059875A (ko) | 2011-06-07 |
| CO6382110A2 (es) | 2012-02-15 |
| AR073740A1 (es) | 2010-12-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102209717B (zh) | 治疗丙型肝炎的化合物 | |
| US7994171B2 (en) | Compounds for the treatment of hepatitis C | |
| JP2013522192A (ja) | C型肝炎の処置のための化合物 | |
| US7265152B2 (en) | Benzofuran compounds, compositions and methods for treatment and prophylaxis of hepatitis C viral infections and associated diseases | |
| EP2086966B1 (en) | 2-carboxy thiophene derivatives as anti viral agents | |
| EP2542545A1 (en) | Inhibitors of hepatitis c virus ns5b polymerase | |
| AU2004207675A1 (en) | EP4 receptor antagonists | |
| CN105102449A (zh) | 抗病毒化合物 | |
| JP2018509401A (ja) | C型肝炎の治療のための新規化合物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20150218 Termination date: 20200908 |