SG11201408011SA - Synthesis of antiviral compound - Google Patents
Synthesis of antiviral compoundInfo
- Publication number
- SG11201408011SA SG11201408011SA SG11201408011SA SG11201408011SA SG11201408011SA SG 11201408011S A SG11201408011S A SG 11201408011SA SG 11201408011S A SG11201408011S A SG 11201408011SA SG 11201408011S A SG11201408011S A SG 11201408011SA SG 11201408011S A SG11201408011S A SG 11201408011SA
- Authority
- SG
- Singapore
- Prior art keywords
- california
- foster city
- gilead
- international
- lakeside drive
- Prior art date
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyrane Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261655935P | 2012-06-05 | 2012-06-05 | |
| US13/800,202 US9056860B2 (en) | 2012-06-05 | 2013-03-13 | Synthesis of antiviral compound |
| PCT/US2013/044148 WO2013184702A1 (en) | 2012-06-05 | 2013-06-04 | Synthesis of antiviral compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG11201408011SA true SG11201408011SA (en) | 2015-01-29 |
Family
ID=49671039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201408011SA SG11201408011SA (en) | 2012-06-05 | 2013-06-04 | Synthesis of antiviral compound |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US9056860B2 (de) |
| EP (1) | EP2855454B1 (de) |
| JP (3) | JP6181169B2 (de) |
| KR (2) | KR20200066376A (de) |
| CN (2) | CN107266428A (de) |
| AU (1) | AU2013271772B2 (de) |
| BR (1) | BR112014030365A2 (de) |
| CA (1) | CA2875508C (de) |
| ES (1) | ES2587782T3 (de) |
| HK (3) | HK1208670A1 (de) |
| IL (2) | IL235941B (de) |
| IN (1) | IN2014MN02496A (de) |
| MX (1) | MX350892B (de) |
| PT (1) | PT2855454T (de) |
| RU (1) | RU2636943C2 (de) |
| SG (1) | SG11201408011SA (de) |
| WO (1) | WO2013184702A1 (de) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005003147A2 (en) | 2003-05-30 | 2005-01-13 | Pharmasset, Inc. | Modified fluorinated nucleoside analogues |
| UA116087C2 (uk) | 2011-09-16 | 2018-02-12 | Гіліад Фармассет Елелсі | Композиція для лікування вірусу гепатиту c |
| US9056860B2 (en) * | 2012-06-05 | 2015-06-16 | Gilead Pharmasset Llc | Synthesis of antiviral compound |
| US8969588B2 (en) | 2012-06-05 | 2015-03-03 | Gilead Pharmasset Llc | Solid forms of an antiviral compound |
| KR20140119012A (ko) | 2013-01-31 | 2014-10-08 | 길리어드 파마셋 엘엘씨 | 두 항바이러스 화합물의 병용 제형물 |
| CN104211565A (zh) * | 2013-05-31 | 2014-12-17 | 浙江九洲药业股份有限公司 | 一种抗丙型肝炎药物中间体的制备方法 |
| ES2900570T3 (es) | 2013-08-27 | 2022-03-17 | Gilead Pharmasset Llc | Formulación de combinación de dos compuestos antivirales |
| EP2883876A1 (de) * | 2013-12-16 | 2015-06-17 | Actelion Pharmaceuticals Ltd. | Stereoselektive Synthese von substituierten Pyrrolidinen |
| TWI679203B (zh) * | 2014-06-11 | 2019-12-11 | 美商基利法瑪席特有限責任公司 | 製備抗病毒化合物之方法 |
| CN104513223B (zh) * | 2014-11-20 | 2017-07-14 | 上海众强药业有限公司 | 芴乙酮衍生物的制备方法 |
| CN104513147B (zh) * | 2014-11-20 | 2016-05-11 | 上海众强药业有限公司 | 芴乙酮衍生物的制备方法 |
| WO2016103232A1 (en) * | 2014-12-24 | 2016-06-30 | Granules India Limited | An improved process for the preparation of hcv inhibitor |
| CN104530016A (zh) * | 2014-12-25 | 2015-04-22 | 上海泓博智源医药技术有限公司 | 一种雷迪帕韦的制备方法及其中间体 |
| US20180008624A1 (en) | 2015-02-13 | 2018-01-11 | Sandoz Ag | Pharmaceutical Compositions Comprising Ledipasvir And Sofosbuvir |
| WO2016145269A1 (en) | 2015-03-12 | 2016-09-15 | Teva Pharmaceuticals International Gmbh | Solid state forms ledipasvir and processes for preparation of ledipasvir |
| CN104829599B (zh) * | 2015-03-17 | 2017-06-09 | 上海众强药业有限公司 | 雷迪帕韦及其衍生物的制备方法及用于制备雷迪帕韦的中间体化合物 |
| CN104788361B (zh) * | 2015-04-21 | 2017-06-30 | 杭州科巢生物科技有限公司 | 5‑氮杂螺[2.4]庚烷‑6‑甲酸衍生物的合成方法 |
| WO2016199049A1 (en) * | 2015-06-09 | 2016-12-15 | Hetero Research Foundation | Process for the preparation of ledipasvir |
| CN104926796A (zh) * | 2015-06-17 | 2015-09-23 | 南通常佑药业科技有限公司 | 一种新的ns5a抑制剂药物的制备方法 |
| WO2016207915A1 (en) * | 2015-06-26 | 2016-12-29 | Mylan Laboratories Limited | Process for the preparation of ledipasvir |
| CN105017228A (zh) * | 2015-07-03 | 2015-11-04 | 上海众强药业有限公司 | 一种雷迪帕韦中间体单硫酸盐、其晶型及其制备方法 |
| CN104961733B (zh) | 2015-07-06 | 2019-04-09 | 上海众强药业有限公司 | 雷迪帕韦晶型及其制备方法 |
| KR101919194B1 (ko) * | 2015-09-15 | 2018-11-15 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
| CN105237516B (zh) * | 2015-10-13 | 2018-01-02 | 厦门市蔚嘉化学科技有限公司 | 一种雷迪帕韦的制备方法 |
| CN105399657B (zh) * | 2015-10-21 | 2017-10-10 | 海门慧聚药业有限公司 | 雷迪帕韦关键中间体的制备 |
| WO2017072596A1 (en) * | 2015-10-26 | 2017-05-04 | Optimus Drugs (P) Ltd | An improved process for the preparation of ledipasvir |
| CN105237384B (zh) * | 2015-11-06 | 2017-06-30 | 上海万溯化学有限公司 | 一种多取代芴衍生物的制备方法 |
| CN106892905A (zh) * | 2015-12-17 | 2017-06-27 | 常州市勇毅生物药业有限公司 | 一种雷迪帕韦的制备方法 |
| US20190062332A1 (en) * | 2016-02-01 | 2019-02-28 | Lupin Limited | Process for the preparation of ledipasvir and intermediates thereof |
| WO2017145028A1 (en) * | 2016-02-26 | 2017-08-31 | Glenmark Pharmaceuticals Limited | Process for preparation of ledipasvir |
| EP3455218A4 (de) | 2016-05-10 | 2019-12-18 | C4 Therapeutics, Inc. | Mit c3-kohlenstoff verknüpfte glutarimiddegronimere zum zielproteinabbau |
| EP3454856B1 (de) | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Heterocyclische degronimere für zielproteinabbau |
| WO2017197036A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
| WO2017195147A1 (en) | 2016-05-12 | 2017-11-16 | Lupin Limited | Process for the preparation of ledipasvir and intermediates thereof |
| CN106008316B (zh) * | 2016-06-17 | 2018-04-27 | 成都百事兴科技实业有限公司 | 一种合成雷迪帕韦手性中间体的方法 |
| CN105968040B (zh) * | 2016-06-29 | 2019-02-05 | 爱斯特（成都）生物制药股份有限公司 | 一种雷迪帕韦中间体的制备方法 |
| CN107641081A (zh) * | 2016-07-22 | 2018-01-30 | 江苏威凯尔医药科技有限公司 | 一种药物中间体的制备方法 |
| CN106349229B (zh) * | 2016-08-25 | 2018-11-06 | 安徽华昌高科药业有限公司 | 雷迪帕韦中间体的制备方法及中间体化合物 |
| CN106632275B (zh) * | 2016-12-20 | 2018-03-06 | 上海同昌生物医药科技有限公司 | 一种雷迪帕韦的制备方法及制备雷迪帕韦的中间体 |
| US10392370B2 (en) | 2017-03-13 | 2019-08-27 | Optimus Drugs Pvt Ltd | Process for the preparation of Daclatasvir dihydrochloride and its intermediates |
| CN107488685A (zh) * | 2017-06-13 | 2017-12-19 | 南京方生和医药科技有限公司 | (s)‑5‑氮杂螺环[2.4]庚烷‑6‑羧酸及其衍生物的酶化学制备方法 |
| CN107879908A (zh) * | 2017-11-14 | 2018-04-06 | 安徽诺全药业有限公司 | 一种雷迪帕维关键中间体及其制备方法 |
| CN107954990A (zh) * | 2017-11-14 | 2018-04-24 | 安徽诺全药业有限公司 | 一种雷迪帕维的制备方法 |
| CN108753863A (zh) * | 2018-06-14 | 2018-11-06 | 慎终（上海）生物科技有限公司 | 雷迪帕韦中间体的合成工艺 |
| TWI767148B (zh) * | 2018-10-10 | 2022-06-11 | 美商弗瑪治療公司 | 抑制脂肪酸合成酶(fasn) |
| EP3636637A1 (de) * | 2018-10-10 | 2020-04-15 | Forma Therapeutics, Inc. | Hemmung der fettsäuresynthase (fasn) |
| EP3885339A1 (de) * | 2020-03-27 | 2021-09-29 | Rottapharm Biotech S.r.l. | Verfahren zur herstellung von (r)-4-(1-(6-(4-(trifluormethyl)benzyl)-6-azaspiro[2.5]octan-5-carboxamido)-cyclopropyl)benzoesäure oder eines salzes davon |
| CN112851545B (zh) * | 2020-07-08 | 2022-09-20 | 日照巴洛特药业有限公司 | 一种雷迪帕韦中间体的合成工艺 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20020071931A (ko) * | 2000-01-07 | 2002-09-13 | 트렌스폼 파마수티컬스 인코퍼레이티드 | 다양한 고체-형태들의 고도의 자료 처리 편성, 확인 및분석 |
| GB0215676D0 (en) * | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
| US7759337B2 (en) * | 2005-03-03 | 2010-07-20 | Amgen Inc. | Phthalazine compounds and methods of use |
| TWI410422B (zh) * | 2007-01-15 | 2013-10-01 | Mitsubishi Tanabe Pharma Corp | 縮合四氫喹啉衍生物及其醫藥用途 |
| BRPI0822323A2 (pt) * | 2008-02-13 | 2015-06-16 | Bristol Myers Squibb Co | Imidazolil bifenil imidazóis como inibidores do vírus da hepatite c |
| US8232409B2 (en) * | 2008-10-15 | 2012-07-31 | Janssen Pharmaceutica N.V. | Heterocyclic benzimidazoles as TRPM8 modulators |
| NZ706236A (en) | 2009-05-13 | 2016-07-29 | Gilead Pharmasset Llc | Antiviral compounds |
| WO2011031904A1 (en) * | 2009-09-11 | 2011-03-17 | Enanta Pharmaceuticals, Inc | Hepatitis c virus inhibitors |
| WO2011063233A1 (en) * | 2009-11-23 | 2011-05-26 | Amgen Inc. | Amino heteroaryl compounds as beta-secretase modulators and methods of use |
| TW201211047A (en) | 2010-06-10 | 2012-03-16 | Gilead Sciences Inc | Methods for treating HCV |
| US8969588B2 (en) | 2012-06-05 | 2015-03-03 | Gilead Pharmasset Llc | Solid forms of an antiviral compound |
| US9056860B2 (en) * | 2012-06-05 | 2015-06-16 | Gilead Pharmasset Llc | Synthesis of antiviral compound |
-
2013
- 2013-03-13 US US13/800,202 patent/US9056860B2/en active Active
- 2013-06-04 MX MX2014014569A patent/MX350892B/es active IP Right Grant
- 2013-06-04 JP JP2015516145A patent/JP6181169B2/ja active Active
- 2013-06-04 EP EP13729208.2A patent/EP2855454B1/de active Active
- 2013-06-04 WO PCT/US2013/044148 patent/WO2013184702A1/en active Application Filing
- 2013-06-04 CN CN201710524415.2A patent/CN107266428A/zh active Pending
- 2013-06-04 KR KR1020207015492A patent/KR20200066376A/ko not_active Application Discontinuation
- 2013-06-04 AU AU2013271772A patent/AU2013271772B2/en active Active
- 2013-06-04 BR BR112014030365A patent/BR112014030365A2/pt active Search and Examination
- 2013-06-04 ES ES13729208.2T patent/ES2587782T3/es active Active
- 2013-06-04 CN CN201380029806.7A patent/CN104520293B/zh active Active
- 2013-06-04 SG SG11201408011SA patent/SG11201408011SA/en unknown
- 2013-06-04 PT PT137292082T patent/PT2855454T/pt unknown
- 2013-06-04 CA CA2875508A patent/CA2875508C/en active Active
- 2013-06-04 KR KR1020147036884A patent/KR102206434B1/ko active IP Right Grant
- 2013-06-04 RU RU2014150435A patent/RU2636943C2/ru not_active IP Right Cessation
- 2013-06-04 IN IN2496MUN2014 patent/IN2014MN02496A/en unknown
-
2014
- 2014-11-27 IL IL235941A patent/IL235941B/en not_active IP Right Cessation
-
2015
- 2015-05-05 US US14/704,627 patent/US20150232453A1/en not_active Abandoned
- 2015-09-22 HK HK15109284.9A patent/HK1208670A1/zh unknown
- 2015-10-12 HK HK15109928.1A patent/HK1209124A1/xx unknown
- 2015-10-12 HK HK18104959.1A patent/HK1245273A1/zh unknown
-
2016
- 2016-08-04 US US15/228,825 patent/US9718807B2/en active Active
-
2017
- 2017-06-14 JP JP2017116558A patent/JP6356876B2/ja active Active
-
2018
- 2018-03-25 IL IL258327A patent/IL258327A/en unknown
- 2018-06-14 JP JP2018113637A patent/JP6594487B2/ja active Active
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