CA2682230C - Nucleoside phosphoramidate prodrugs - Google Patents
Nucleoside phosphoramidate prodrugs Download PDFInfo
- Publication number
- CA2682230C CA2682230C CA2682230A CA2682230A CA2682230C CA 2682230 C CA2682230 C CA 2682230C CA 2682230 A CA2682230 A CA 2682230A CA 2682230 A CA2682230 A CA 2682230A CA 2682230 C CA2682230 C CA 2682230C
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- CA
- Canada
- Prior art keywords
- methyl
- fluoro
- dioxo
- hydroxy
- alkyl
- 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.)
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- -1 Nucleoside phosphoramidate Chemical class 0.000 title claims description 393
- 239000002777 nucleoside Substances 0.000 title claims description 26
- 229940002612 prodrug Drugs 0.000 title description 6
- 239000000651 prodrug Substances 0.000 title description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 1022
- 125000000217 alkyl group Chemical group 0.000 claims description 766
- 229910052739 hydrogen Inorganic materials 0.000 claims description 346
- 229910052731 fluorine Inorganic materials 0.000 claims description 300
- 229910052794 bromium Inorganic materials 0.000 claims description 290
- 239000001257 hydrogen Substances 0.000 claims description 265
- 229910052801 chlorine Inorganic materials 0.000 claims description 247
- 229910052740 iodine Inorganic materials 0.000 claims description 217
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 182
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 172
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 159
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 149
- 150000001875 compounds Chemical class 0.000 claims description 134
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 132
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 118
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 104
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 102
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 84
- 125000001188 haloalkyl group Chemical group 0.000 claims description 81
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 80
- 229920002554 vinyl polymer Polymers 0.000 claims description 80
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 78
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 61
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 54
- 125000004055 thiomethyl group Chemical group [H]SC([H])([H])* 0.000 claims description 53
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 50
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 50
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 50
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 50
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 44
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 44
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 44
- 241000711549 Hepacivirus C Species 0.000 claims description 41
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 41
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 33
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 31
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 claims description 24
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 23
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 22
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 17
- 150000003833 nucleoside derivatives Chemical class 0.000 claims description 15
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 13
- 239000003112 inhibitor Substances 0.000 claims description 12
- 239000003443 antiviral agent Substances 0.000 claims description 11
- 239000008194 pharmaceutical composition Substances 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 125000004437 phosphorous atom Chemical group 0.000 claims description 6
- 208000010710 hepatitis C virus infection Diseases 0.000 claims description 5
- 101800001014 Non-structural protein 5A Proteins 0.000 claims description 4
- XVVLESMRYHJYLT-RFQRIQSBSA-N CC(C)OC(=O)[C@H](C)N=P(=O)OC1=CC=CC=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 Chemical compound CC(C)OC(=O)[C@H](C)N=P(=O)OC1=CC=CC=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 XVVLESMRYHJYLT-RFQRIQSBSA-N 0.000 claims 3
- 125000006302 indol-3-yl methyl group Chemical group [H]N1C([H])=C(C2=C([H])C([H])=C([H])C([H])=C12)C([H])([H])* 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- NOHLZRRJRHFSTN-CDHYSNCASA-N COC(=O)[C@H](C)N=P(=O)OC1=CC=CC=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 Chemical compound COC(=O)[C@H](C)N=P(=O)OC1=CC=CC=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 NOHLZRRJRHFSTN-CDHYSNCASA-N 0.000 claims 2
- VNUWVEUIPKYTOC-LDZBRYNHSA-N COC1=CC=C(OP(=O)=N[C@@H](C)C(=O)OC(C)C)C(OC[C@@H]2[C@H]([C@@](C)(F)[C@H](N3C(NC(=O)C=C3)=O)O2)O)=C1 Chemical compound COC1=CC=C(OP(=O)=N[C@@H](C)C(=O)OC(C)C)C(OC[C@@H]2[C@H]([C@@](C)(F)[C@H](N3C(NC(=O)C=C3)=O)O2)O)=C1 VNUWVEUIPKYTOC-LDZBRYNHSA-N 0.000 claims 2
- JIOYWNZWTJDVJP-XKNCWQHRSA-N N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)COC2=C(C3=CC=CC=C3C=C2)OP(=O)=N[C@@H](C)C(=O)OC)C=CC(=O)NC1=O Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)COC2=C(C3=CC=CC=C3C=C2)OP(=O)=N[C@@H](C)C(=O)OC)C=CC(=O)NC1=O JIOYWNZWTJDVJP-XKNCWQHRSA-N 0.000 claims 2
- JMELFAZAZNPJDW-OVRMDKARSA-N N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)COC2=CC=CC=C2OP(=O)=N[C@@H](C)C(=O)OC2CCCCC2)C=CC(=O)NC1=O Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)COC2=CC=CC=C2OP(=O)=N[C@@H](C)C(=O)OC2CCCCC2)C=CC(=O)NC1=O JMELFAZAZNPJDW-OVRMDKARSA-N 0.000 claims 2
- RJMVGAZAYOUNNR-KDFBYGIPSA-N cyclohexyl (2s)-2-[[[(2r,3r,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyloxolan-2-yl]methoxy-(4-fluorophenoxy)phosphoryl]amino]propanoate Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)CO[P@@](=O)(N[C@@H](C)C(=O)OC2CCCCC2)OC=2C=CC(F)=CC=2)C=CC(=O)NC1=O RJMVGAZAYOUNNR-KDFBYGIPSA-N 0.000 claims 2
- RJMVGAZAYOUNNR-WMHSNBSXSA-N cyclohexyl (2s)-2-[[[(2r,3r,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyloxolan-2-yl]methoxy-(4-fluorophenoxy)phosphoryl]amino]propanoate Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)CO[P@](=O)(N[C@@H](C)C(=O)OC2CCCCC2)OC=2C=CC(F)=CC=2)C=CC(=O)NC1=O RJMVGAZAYOUNNR-WMHSNBSXSA-N 0.000 claims 2
- TTZHDVOVKQGIBA-YBSJRAAASA-N propan-2-yl (2s)-2-[[[(2r,3r,4r,5r)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyloxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)CO[P@](=O)(N[C@@H](C)C(=O)OC(C)C)OC=2C=CC=CC=2)C=CC(=O)NC1=O TTZHDVOVKQGIBA-YBSJRAAASA-N 0.000 claims 2
- TTZHDVOVKQGIBA-IQWMDFIBSA-N sofosbuvir Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@]2(F)C)O)CO[P@@](=O)(N[C@@H](C)C(=O)OC(C)C)OC=2C=CC=CC=2)C=CC(=O)NC1=O TTZHDVOVKQGIBA-IQWMDFIBSA-N 0.000 claims 2
- FQESRLYGFUVGPA-WBAFMLPDSA-N CC(C)CCOC(=O)[C@H](C)N=P(=O)OC1=CC=CC=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 Chemical compound CC(C)CCOC(=O)[C@H](C)N=P(=O)OC1=CC=CC=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 FQESRLYGFUVGPA-WBAFMLPDSA-N 0.000 claims 1
- URXASQSEFNHSRL-INGMEPTHSA-N CC(C)OC(=O)[C@H](C)N=P(=O)OC([C@H]1[C@H]([C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1)O)OC1=CC=C(Br)C=C1 Chemical compound CC(C)OC(=O)[C@H](C)N=P(=O)OC([C@H]1[C@H]([C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1)O)OC1=CC=C(Br)C=C1 URXASQSEFNHSRL-INGMEPTHSA-N 0.000 claims 1
- OPMOATVQKBAMRU-INGMEPTHSA-N CC(C)OC(=O)[C@H](C)N=P(=O)OC([C@H]1[C@H]([C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1)O)OC1=CC=C(Cl)C=C1 Chemical compound CC(C)OC(=O)[C@H](C)N=P(=O)OC([C@H]1[C@H]([C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1)O)OC1=CC=C(Cl)C=C1 OPMOATVQKBAMRU-INGMEPTHSA-N 0.000 claims 1
- MBDAKGRZCKTFKV-INGMEPTHSA-N CC(C)OC(=O)[C@H](C)N=P(=O)OC([C@H]1[C@H]([C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1)O)OC1=CC=CC=C1Cl Chemical compound CC(C)OC(=O)[C@H](C)N=P(=O)OC([C@H]1[C@H]([C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1)O)OC1=CC=CC=C1Cl MBDAKGRZCKTFKV-INGMEPTHSA-N 0.000 claims 1
- RCQSIGGBMAPEGP-HVYVWJKCSA-N CC(C)OC(=O)[C@H](C)N=P(=O)OC1=CC=C(C)C(OC[C@@H]2[C@H]([C@@](C)(F)[C@H](N3C(NC(=O)C=C3)=O)O2)O)=C1 Chemical compound CC(C)OC(=O)[C@H](C)N=P(=O)OC1=CC=C(C)C(OC[C@@H]2[C@H]([C@@](C)(F)[C@H](N3C(NC(=O)C=C3)=O)O2)O)=C1 RCQSIGGBMAPEGP-HVYVWJKCSA-N 0.000 claims 1
- IFOHCQHTSSRCLU-WSOBARQNSA-N CC(C)OC(=O)[C@H](C)N=P(=O)OC1=CC=C(F)C=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 Chemical compound CC(C)OC(=O)[C@H](C)N=P(=O)OC1=CC=C(F)C=C1OC[C@@H]1[C@@H](O)[C@@](C)(F)[C@H](N2C(NC(=O)C=C2)=O)O1 IFOHCQHTSSRCLU-WSOBARQNSA-N 0.000 claims 1
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Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
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| US90931507P | 2007-03-30 | 2007-03-30 | |
| US60/909,315 | 2007-03-30 | ||
| US98230907P | 2007-10-24 | 2007-10-24 | |
| US60/982,309 | 2007-10-24 | ||
| US12/053,015 | 2008-03-21 | ||
| US12/053,015 US7964580B2 (en) | 2007-03-30 | 2008-03-21 | Nucleoside phosphoramidate prodrugs |
| PCT/US2008/058183 WO2008121634A2 (en) | 2007-03-30 | 2008-03-26 | Nucleoside phosphoramidate prodrugs |
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| CA2682230A1 CA2682230A1 (en) | 2008-10-09 |
| CA2682230C true CA2682230C (en) | 2014-04-22 |
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| CA2682230A Active CA2682230C (en) | 2007-03-30 | 2008-03-26 | Nucleoside phosphoramidate prodrugs |
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| KR101995598B1 (ko) | 2010-07-19 | 2019-07-02 | 길리애드 사이언시즈, 인코포레이티드 | 부분입체 이성질성으로 순수한 포스포라미데이트 전구약물의 제조 방법 |
| US20120107278A1 (en) | 2010-10-29 | 2012-05-03 | Pharmasset, Inc. | Abbreviated hcv therapy for hcv infected patients with il28b c/c genotype |
| US20130109647A1 (en) | 2011-10-31 | 2013-05-02 | Gilead Pharmasset Llc | Methods and compositions for treating hepatitis c virus |
| US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9549941B2 (en) | 2011-11-29 | 2017-01-24 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
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