JP2005515172A - Hcv阻害剤としての4−(6−員)−ヘテロアリールアシルピロリジン誘導体 - Google Patents
Hcv阻害剤としての4−(6−員)−ヘテロアリールアシルピロリジン誘導体 Download PDFInfo
- Publication number
- JP2005515172A JP2005515172A JP2003540176A JP2003540176A JP2005515172A JP 2005515172 A JP2005515172 A JP 2005515172A JP 2003540176 A JP2003540176 A JP 2003540176A JP 2003540176 A JP2003540176 A JP 2003540176A JP 2005515172 A JP2005515172 A JP 2005515172A
- Authority
- JP
- Japan
- Prior art keywords
- tert
- pyrrolidine
- rel
- carboxylic acid
- isobutyl
- 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.)
- Ceased
Links
- 0 C*(C([C@@](C1N)(C=C)N)N)C1(C(P)=O)N Chemical compound C*(C([C@@](C1N)(C=C)N)N)C1(C(P)=O)N 0.000 description 6
- QYMGRIFMUQCAJW-UHFFFAOYSA-N C1NC=CN=C1 Chemical compound C1NC=CN=C1 QYMGRIFMUQCAJW-UHFFFAOYSA-N 0.000 description 1
- SIYFIZUOZWDFSF-NTUHNPAUSA-N CC(C(OC(C)(C)C)=O)/N=C/c1ncc[s]1 Chemical compound CC(C(OC(C)(C)C)=O)/N=C/c1ncc[s]1 SIYFIZUOZWDFSF-NTUHNPAUSA-N 0.000 description 1
- ZOLIVRFPHHXEIK-OCGXGRQSSA-N CC(C)C[C@@](C[C@H]([C@@H](C1)c2ncc[s]2)C2NC=C(C(F)(F)F)C=C2)(C1C(c1ccc(C(C)(C)C)cc1)=O)N Chemical compound CC(C)C[C@@](C[C@H]([C@@H](C1)c2ncc[s]2)C2NC=C(C(F)(F)F)C=C2)(C1C(c1ccc(C(C)(C)C)cc1)=O)N ZOLIVRFPHHXEIK-OCGXGRQSSA-N 0.000 description 1
- YCADWLANWUNTGP-BTYIYWSLSA-N CC(C)C[C@](C1)(C(OC(C)(C)C)=O)NC[C@H]1c1cnc(cccc2)c2n1 Chemical compound CC(C)C[C@](C1)(C(OC(C)(C)C)=O)NC[C@H]1c1cnc(cccc2)c2n1 YCADWLANWUNTGP-BTYIYWSLSA-N 0.000 description 1
- ZWWXGBBPWDOBIP-HXUWFJFHSA-N CC(C)C[C@](CCc1cnccn1)(N)NCc(cc1)ccc1N(C)C Chemical compound CC(C)C[C@](CCc1cnccn1)(N)NCc(cc1)ccc1N(C)C ZWWXGBBPWDOBIP-HXUWFJFHSA-N 0.000 description 1
- WCIJZKBEXNTWDT-QVNGGLPSSA-N CC(C)C[C@](C[C@@H]([C@@H]1c2ccccc2)c2cnccn2)(C(O)=O)N1C(c1ccc(C(C)(C)C)cc1)=O Chemical compound CC(C)C[C@](C[C@@H]([C@@H]1c2ccccc2)c2cnccn2)(C(O)=O)N1C(c1ccc(C(C)(C)C)cc1)=O WCIJZKBEXNTWDT-QVNGGLPSSA-N 0.000 description 1
- UJKGRLOTZKJWST-CEQIKUNHSA-N CC(C)C[C@](C[C@@H]1c2ccccn2)(C(OC(C)(C)C)=O)N[C@H]1c1ncc[s]1 Chemical compound CC(C)C[C@](C[C@@H]1c2ccccn2)(C(OC(C)(C)C)=O)N[C@H]1c1ncc[s]1 UJKGRLOTZKJWST-CEQIKUNHSA-N 0.000 description 1
- TYKXESJFRDZFGC-MYRUOYEDSA-N CC(C)C[C@](C[C@@H]1c2cnccn2)(C(OC(C)(C)C)=O)N[C@H]1c1nc(cccc2)c2[s]1 Chemical compound CC(C)C[C@](C[C@@H]1c2cnccn2)(C(OC(C)(C)C)=O)N[C@H]1c1nc(cccc2)c2[s]1 TYKXESJFRDZFGC-MYRUOYEDSA-N 0.000 description 1
- FLFZLWNBSOBVJZ-LSBZLQRGSA-N CC(C)C[C@](C[C@@H]1c2cnccn2)(NOC(C)(C)C)N[C@H]1c1csc[nH]1 Chemical compound CC(C)C[C@](C[C@@H]1c2cnccn2)(NOC(C)(C)C)N[C@H]1c1csc[nH]1 FLFZLWNBSOBVJZ-LSBZLQRGSA-N 0.000 description 1
- PIVLWTMLEJJTQM-UHFFFAOYSA-N CCOc1cc(C(O)=O)ccc1C(C)(C)C Chemical compound CCOc1cc(C(O)=O)ccc1C(C)(C)C PIVLWTMLEJJTQM-UHFFFAOYSA-N 0.000 description 1
- LGBPDTUTHQVNLR-LJQANCHMSA-N CC[C@@](CC(C)C)(N)N(C)C(c1cc(Br)c(C(C)(C)C)cc1)=O Chemical compound CC[C@@](CC(C)C)(N)N(C)C(c1cc(Br)c(C(C)(C)C)cc1)=O LGBPDTUTHQVNLR-LJQANCHMSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0126440A GB0126440D0 (en) | 2001-11-02 | 2001-11-02 | Compounds |
| GB0203900A GB0203900D0 (en) | 2002-02-19 | 2002-02-19 | Compounds |
| GB0219321A GB0219321D0 (en) | 2002-08-19 | 2002-08-19 | Compounds |
| PCT/EP2002/012176 WO2003037895A1 (en) | 2001-11-02 | 2002-10-30 | 4-(6-membered)-heteroaryl acyl pyrrolidine derivatives as hcv inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005515172A true JP2005515172A (ja) | 2005-05-26 |
| JP2005515172A5 JP2005515172A5 (enExample) | 2006-01-05 |
Family
ID=27256312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003540176A Ceased JP2005515172A (ja) | 2001-11-02 | 2002-10-30 | Hcv阻害剤としての4−(6−員)−ヘテロアリールアシルピロリジン誘導体 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7259163B2 (enExample) |
| EP (1) | EP1440069B1 (enExample) |
| JP (1) | JP2005515172A (enExample) |
| AR (1) | AR037182A1 (enExample) |
| AT (1) | ATE370137T1 (enExample) |
| DE (1) | DE60221875T2 (enExample) |
| ES (1) | ES2289161T3 (enExample) |
| TW (1) | TW200302823A (enExample) |
| WO (1) | WO2003037895A1 (enExample) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0211418D0 (en) * | 2002-05-17 | 2002-06-26 | Glaxo Group Ltd | Compounds |
| EP2033654B1 (en) | 2003-04-16 | 2012-05-16 | Bristol-Myers Squibb Company | Process for resolving a mixture of alkyl ester enantiomers using an enzyme |
| SG184700A1 (en) | 2004-02-20 | 2012-10-30 | Boehringer Ingelheim Int | Viral polymerase inhibitors |
| JP2007530516A (ja) * | 2004-03-26 | 2007-11-01 | スミスクライン・ビーチャム・コーポレイション | 抗ウイルス剤として有用な4−カルボキシピラゾール誘導体 |
| GB0423672D0 (en) * | 2004-10-25 | 2004-11-24 | Glaxo Group Ltd | Compounds |
| GB0519486D0 (en) * | 2005-09-23 | 2005-11-02 | Glaxo Group Ltd | Compounds |
| GB0519485D0 (en) * | 2005-09-23 | 2005-11-02 | Glaxo Group Ltd | Compounds |
| GB0519478D0 (en) * | 2005-09-23 | 2005-11-02 | Glaxo Group Ltd | Compounds |
| WO2007039146A1 (en) * | 2005-09-23 | 2007-04-12 | Smithkline Beecham Corporation | 4-carboxy pyrazole derivatives as anti-viral agents |
| US7964580B2 (en) | 2007-03-30 | 2011-06-21 | Pharmasset, Inc. | Nucleoside phosphoramidate prodrugs |
| US20090004140A1 (en) * | 2007-06-26 | 2009-01-01 | Yao-Ling Qiu | 4-substituted pyrrolidine as anti-infectives |
| US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
| BRPI0922366B8 (pt) | 2008-12-03 | 2021-05-25 | Presidio Pharmaceuticals Inc | composto, composição farmacêutica e uso de um composto |
| SG171890A1 (en) | 2008-12-03 | 2011-07-28 | Presidio Pharmaceuticals Inc | Inhibitors of hcv ns5a |
| BRPI0923815A2 (pt) | 2008-12-23 | 2015-07-14 | Pharmasset Inc | Síntese de nucleosídeos de purina |
| AU2009329917B2 (en) | 2008-12-23 | 2016-03-31 | Gilead Pharmasset Llc | Nucleoside analogs |
| CN102695513A (zh) | 2008-12-23 | 2012-09-26 | 吉利德制药有限责任公司 | 核苷氨基磷酸酯 |
| EP2410843A4 (en) | 2009-03-27 | 2012-08-08 | Presidio Pharmaceuticals Inc | FUSIONED CORE INHIBITORS OF HEPATITIS C |
| US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
| TWI583692B (zh) | 2009-05-20 | 2017-05-21 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
| ES2655091T3 (es) | 2009-12-18 | 2018-02-16 | Ogeda Sa | Derivados del ácido pirrolidíncarboxílico como agonistas del receptor 43 acoplado a proteína G (GPR43), composición farmacéutica y métodos para su uso en el tratamiento de trastornos metabólicos |
| JP5872539B2 (ja) | 2010-03-31 | 2016-03-01 | ギリアド ファーマセット エルエルシー | プリンヌクレオシドホスホルアミダート |
| SMT201700412T1 (it) | 2010-03-31 | 2017-11-15 | Gilead Pharmasset Llc | Procedimento per la cristallizzazione di (s)-isopropil 2-(((s)-(perfluorofenossi)(fenossi)fosforil)ammino)propanoato |
| EP2575866A4 (en) | 2010-05-24 | 2013-10-16 | Presidio Pharmaceuticals Inc | HCV NS5A INHIBITORS |
| WO2012020036A1 (en) | 2010-08-13 | 2012-02-16 | F. Hoffmann-La Roche Ag | Hepatitis c virus inhibitors |
| BR112013009789A2 (pt) | 2010-10-26 | 2016-07-19 | Presidio Pharmaceuticals Inc | inibidores do vírus da hepatite c |
| PT3042910T (pt) | 2010-11-30 | 2019-04-16 | Gilead Pharmasset Llc | 2'-espiro-nucleósidos para utilização na terapia da hepatite c |
| WO2012123298A1 (en) | 2011-03-11 | 2012-09-20 | F. Hoffmann-La Roche Ag | Antiviral compounds |
| WO2012175581A1 (en) | 2011-06-24 | 2012-12-27 | F. Hoffmann-La Roche Ag | Antiviral compounds |
| EP2709613B2 (en) | 2011-09-16 | 2020-08-12 | Gilead Pharmasset LLC | Methods for treating hcv |
| BR112014008616A2 (pt) | 2011-10-10 | 2017-04-18 | Hoffmann La Roche | compostos antivirais |
| US8889159B2 (en) | 2011-11-29 | 2014-11-18 | Gilead Pharmasset Llc | Compositions and methods for treating hepatitis C virus |
| ES2564906T3 (es) | 2011-12-16 | 2016-03-29 | F. Hoffmann-La Roche Ag | Inhibidores de NS5A del VHC |
| AU2012357986B2 (en) | 2011-12-20 | 2017-02-02 | Riboscience Llc | 4'-Azido, 3'-fluoro substituted nucleoside derivatives as inhibitors of HCV RNA replication |
| EP2794629B1 (en) | 2011-12-20 | 2017-05-24 | Riboscience LLC | 2',4'-difluoro-2'-methyl substituted nucleoside derivatives as inhibitors of hcv rna replication |
| KR20140130449A (ko) | 2012-02-24 | 2014-11-10 | 에프. 호프만-라 로슈 아게 | 항바이러스 화합물 |
| US20140010783A1 (en) | 2012-07-06 | 2014-01-09 | Hoffmann-La Roche Inc. | Antiviral compounds |
| CN105073726B (zh) | 2013-01-23 | 2017-05-31 | 弗·哈夫曼-拉罗切有限公司 | 抗病毒三唑衍生物 |
| PL2950786T3 (pl) | 2013-01-31 | 2020-05-18 | Gilead Pharmasset Llc | Formulacja skojarzona dwóch związków przeciwwirusowych |
| CN105008350B (zh) | 2013-03-05 | 2018-05-08 | 弗·哈夫曼-拉罗切有限公司 | 抗病毒化合物 |
| MA38678A1 (fr) | 2013-05-16 | 2017-07-31 | Riboscience Llc | Dérivés nucléosidiques 4'-azido, 3'désoxy-3'-fluoro substitués |
| US9895442B2 (en) | 2013-05-16 | 2018-02-20 | Riboscience Llc | 4′-fluoro-2′-methyl substituted nucleoside derivatives as inhibitors of HCV RNA replication |
| US20180200280A1 (en) | 2013-05-16 | 2018-07-19 | Riboscience Llc | 4'-Fluoro-2'-Methyl Substituted Nucleoside Derivatives as Inhibitors of HCV RNA Replication |
| PL3038601T3 (pl) | 2013-08-27 | 2020-08-24 | Gilead Pharmasset Llc | Formulacja złożona dwóch związków przeciwwirusowych |
| KR102259934B1 (ko) | 2013-11-27 | 2021-06-03 | 에픽스 테라퓨틱스 | 염증 질환의 치료에 사용되기 위한 화합물, 의약 조성물 및 방법 |
| CN111194217B (zh) | 2017-09-21 | 2024-01-12 | 里伯赛恩斯有限责任公司 | 作为hcv rna复制抑制剂的4’-氟-2’-甲基取代的核苷衍生物 |
| CN109678814B (zh) * | 2018-12-28 | 2021-03-23 | 浙江外国语学院 | 一种制备2-氯-1, 3-噻唑-5-甲醛的方法 |
| JP2023529867A (ja) | 2020-06-05 | 2023-07-12 | キネート バイオファーマ インク. | 線維芽細胞増殖因子受容体キナーゼの阻害剤 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT395007B (de) * | 1990-03-29 | 1992-08-25 | Noe Christian | Modifizierte cyclische aminosaeuren und aus diesen synthetisierte dipeptide und verfahren zu ihrer herstellung |
| AU3761393A (en) | 1992-03-20 | 1993-10-21 | Wellcome Foundation Limited, The | Indole derivatives with antiviral activity |
| US6455571B1 (en) | 1998-04-23 | 2002-09-24 | Abbott Laboratories | Inhibitors of neuraminidases |
| HUP0101224A3 (en) | 1998-04-23 | 2002-12-28 | Abbott Lab | Pyrrolidine derivatives as inhibitors of neuraminidases and pharmaceutical compositions containing them |
-
2002
- 2002-10-30 JP JP2003540176A patent/JP2005515172A/ja not_active Ceased
- 2002-10-30 US US10/494,127 patent/US7259163B2/en not_active Expired - Fee Related
- 2002-10-30 ES ES02783059T patent/ES2289161T3/es not_active Expired - Lifetime
- 2002-10-30 WO PCT/EP2002/012176 patent/WO2003037895A1/en not_active Ceased
- 2002-10-30 AT AT02783059T patent/ATE370137T1/de not_active IP Right Cessation
- 2002-10-30 EP EP02783059A patent/EP1440069B1/en not_active Expired - Lifetime
- 2002-10-30 DE DE60221875T patent/DE60221875T2/de not_active Expired - Lifetime
- 2002-10-31 TW TW091132224A patent/TW200302823A/zh unknown
- 2002-10-31 AR ARP020104160A patent/AR037182A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US7259163B2 (en) | 2007-08-21 |
| DE60221875T2 (de) | 2007-12-20 |
| EP1440069A1 (en) | 2004-07-28 |
| ES2289161T3 (es) | 2008-02-01 |
| WO2003037895A1 (en) | 2003-05-08 |
| DE60221875D1 (de) | 2007-09-27 |
| EP1440069B1 (en) | 2007-08-15 |
| US20050043390A1 (en) | 2005-02-24 |
| AR037182A1 (es) | 2004-10-27 |
| ATE370137T1 (de) | 2007-09-15 |
| TW200302823A (en) | 2003-08-16 |
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