EA026089B1 - Способ и промежуточные соединения для получения ингибиторов интегразы - Google Patents
Способ и промежуточные соединения для получения ингибиторов интегразы Download PDFInfo
- Publication number
- EA026089B1 EA026089B1 EA201590018A EA201590018A EA026089B1 EA 026089 B1 EA026089 B1 EA 026089B1 EA 201590018 A EA201590018 A EA 201590018A EA 201590018 A EA201590018 A EA 201590018A EA 026089 B1 EA026089 B1 EA 026089B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compound
- formula
- salt
- mixture
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/30—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with halogen containing compounds, e.g. hypohalogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/12—Preparation of carboxylic acid esters from asymmetrical anhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Quinoline Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261679475P | 2012-08-03 | 2012-08-03 | |
| PCT/US2013/053295 WO2014022707A1 (en) | 2012-08-03 | 2013-08-01 | Process and intermediates for preparing integrase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA201590018A1 EA201590018A1 (ru) | 2015-05-29 |
| EA026089B1 true EA026089B1 (ru) | 2017-02-28 |
Family
ID=48980354
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201590018A EA026089B1 (ru) | 2012-08-03 | 2013-08-01 | Способ и промежуточные соединения для получения ингибиторов интегразы |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US8877931B2 (forum.php) |
| EP (1) | EP2880017B1 (forum.php) |
| JP (1) | JP6147856B2 (forum.php) |
| KR (1) | KR20150040340A (forum.php) |
| CN (1) | CN104520275B (forum.php) |
| AU (1) | AU2013296289B2 (forum.php) |
| BR (1) | BR112015002275A2 (forum.php) |
| CA (1) | CA2878699C (forum.php) |
| EA (1) | EA026089B1 (forum.php) |
| ES (1) | ES2608860T3 (forum.php) |
| IL (1) | IL236618A (forum.php) |
| IN (1) | IN2015DN01688A (forum.php) |
| MX (1) | MX337094B (forum.php) |
| NZ (1) | NZ630199A (forum.php) |
| PT (1) | PT2880017T (forum.php) |
| SG (1) | SG11201500812QA (forum.php) |
| WO (1) | WO2014022707A1 (forum.php) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT3608325T (pt) | 2012-12-21 | 2022-10-17 | Gilead Sciences Inc | Compostos carbamoílpiridona policíclicos e sua utilização farmacêutica |
| NO2865735T3 (forum.php) | 2013-07-12 | 2018-07-21 | ||
| JP6411491B2 (ja) | 2013-07-12 | 2018-10-24 | ギリアード サイエンシス インコーポレーテッド | 多環式カルバモイルピリドン化合物およびｈｉｖ感染症を処置するためのその使用 |
| TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
| TWI677489B (zh) | 2014-06-20 | 2019-11-21 | 美商基利科學股份有限公司 | 多環型胺甲醯基吡啶酮化合物之合成 |
| NO2717902T3 (forum.php) | 2014-06-20 | 2018-06-23 | ||
| TWI738321B (zh) | 2014-12-23 | 2021-09-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
| JP6402259B2 (ja) | 2015-04-02 | 2018-10-10 | ギリアード サイエンシーズ， インコーポレイテッド | 多環式カルバモイルピリドン化合物およびそれらの薬学的使用 |
| WO2021056193A1 (zh) * | 2019-09-24 | 2021-04-01 | 凯莱英医药集团（天津）股份有限公司 | 一种苄基卤化锌及其衍生物的连续制备方法 |
| CN112661698A (zh) * | 2021-01-14 | 2021-04-16 | 浙江海森药业股份有限公司 | 一种艾维雷韦的制备方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009036161A1 (en) * | 2007-09-11 | 2009-03-19 | Gilead Sciences, Inc. | Process and intermediates for preparing integrase inhibitors |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE9904108D0 (sv) * | 1999-11-15 | 1999-11-15 | New Pharma Research Ab | Nya föreningar |
| AU2905702A (en) | 2000-12-14 | 2002-06-24 | Procter & Gamble | Cyclization process step in the making of quinolones and naphthyridines |
| TW200300349A (en) | 2001-11-19 | 2003-06-01 | Sankyo Co | A 4-oxoqinoline derivative |
| EP1510510A1 (en) | 2002-05-31 | 2005-03-02 | Banyu Pharmaceutical Co., Ltd. | Method of substituent introduction through halogen-metal exchange reaction |
| US6803469B2 (en) | 2002-08-05 | 2004-10-12 | The Procter & Gamble Company | Process for preparing quinolone antibiotic intermediates |
| TW200409759A (en) | 2002-09-25 | 2004-06-16 | Wyeth Corp | Substituted 4-(indazol-3-yl)phenols |
| CZ2004764A3 (cs) | 2002-11-20 | 2005-02-16 | Japan Tobacco Inc | 4-Oxochinolinová sloučenina a její použití jako inhibitoru HIV-integrázy |
| EP1582523A1 (en) | 2004-04-02 | 2005-10-05 | Ludwig-Maximilians-Universität München | Method of preparing organomagnesium compounds |
| EP1582524B1 (en) | 2004-04-02 | 2008-08-13 | Ludwig Maximilians Universität | Method of preparing organomagnesium compounds |
| US7531554B2 (en) | 2004-05-20 | 2009-05-12 | Japan Tobacco Inc. | 4-oxoquinoline compound and use thereof as HIV integrase inhibitor |
| MY134672A (en) | 2004-05-20 | 2007-12-31 | Japan Tobacco Inc | Stable crystal of 4-oxoquinoline compound |
| JP4629104B2 (ja) | 2004-05-21 | 2011-02-09 | 日本たばこ産業株式会社 | ４−オキソキノリン誘導体および抗ｈｉｖ剤を含む併用剤 |
| WO2007063869A1 (ja) | 2005-11-30 | 2007-06-07 | Japan Tobacco Inc. | 高純度キノロン化合物の製造方法 |
| US20090233964A1 (en) | 2005-12-30 | 2009-09-17 | Gilead Sciences, Inc. | Methods for improving the pharmacokinetics of hiv integrase inhibitors |
| CN101437801B (zh) | 2006-03-06 | 2013-02-06 | 日本烟草产业株式会社 | 制备4-氧代喹啉化合物的方法 |
| EA017861B9 (ru) | 2006-03-06 | 2014-05-30 | Джапан Тобакко Инк. | Способ получения 4-оксохинолинового соединения |
| TW200811153A (en) | 2006-06-23 | 2008-03-01 | Japan Tobacco Inc | 6-(heterocyclyl-substituted benzyl)-4-oxoquinoline compound and use thereof as HIV integrase inhibitor |
| JP5221544B2 (ja) | 2006-09-12 | 2013-06-26 | ギリアード サイエンシーズ， インコーポレイテッド | インテグラーゼ阻害剤を調製するためのプロセスおよび中間体 |
| CN101743004A (zh) | 2007-06-29 | 2010-06-16 | 吉里德科学公司 | 治疗用组合物及其用途 |
| NZ582086A (en) | 2007-06-29 | 2012-07-27 | Gilead Sciences Inc | Therapeutic compositions and the use thereof |
-
2013
- 2013-08-01 PT PT137482295T patent/PT2880017T/pt unknown
- 2013-08-01 SG SG11201500812QA patent/SG11201500812QA/en unknown
- 2013-08-01 WO PCT/US2013/053295 patent/WO2014022707A1/en active Application Filing
- 2013-08-01 EP EP13748229.5A patent/EP2880017B1/en active Active
- 2013-08-01 JP JP2015525605A patent/JP6147856B2/ja not_active Expired - Fee Related
- 2013-08-01 ES ES13748229.5T patent/ES2608860T3/es active Active
- 2013-08-01 AU AU2013296289A patent/AU2013296289B2/en not_active Ceased
- 2013-08-01 BR BR112015002275A patent/BR112015002275A2/pt not_active IP Right Cessation
- 2013-08-01 IN IN1688DEN2015 patent/IN2015DN01688A/en unknown
- 2013-08-01 CA CA2878699A patent/CA2878699C/en not_active Expired - Fee Related
- 2013-08-01 MX MX2015001506A patent/MX337094B/es active IP Right Grant
- 2013-08-01 KR KR20157005620A patent/KR20150040340A/ko not_active Abandoned
- 2013-08-01 NZ NZ630199A patent/NZ630199A/en not_active IP Right Cessation
- 2013-08-01 US US13/956,905 patent/US8877931B2/en active Active
- 2013-08-01 EA EA201590018A patent/EA026089B1/ru not_active IP Right Cessation
- 2013-08-01 CN CN201380041287.6A patent/CN104520275B/zh not_active Expired - Fee Related
-
2015
- 2015-01-11 IL IL236618A patent/IL236618A/en not_active IP Right Cessation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009036161A1 (en) * | 2007-09-11 | 2009-03-19 | Gilead Sciences, Inc. | Process and intermediates for preparing integrase inhibitors |
Non-Patent Citations (2)
| Title |
|---|
| SATO M ET AL: "Novel HIV-1 integrase inhibitors derived from quinolone antibiotics", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY, US, vol. 49, no. 5, 5 March 2006 (2006-03-05), US, pages 1506 - 1508, XP002507281, ISSN: 0022-2623, DOI: 10.1021/JM0600139 * |
| SORBERA, L. A.; SERRADELL, N.: "GS-9137: anti-HIV agent HIV integrase inhibitor", DRUGS OF THE FUTURE, PROUS SCIENCE, ES, vol. 31, no. 4, 1 January 2006 (2006-01-01), ES, pages 310 - 313, XP009095707, ISSN: 0377-8282, DOI: 10.1358/dof.2006.031.04.982081 * |
Also Published As
| Publication number | Publication date |
|---|---|
| MX337094B (es) | 2016-02-10 |
| KR20150040340A (ko) | 2015-04-14 |
| ES2608860T3 (es) | 2017-04-17 |
| JP2015524822A (ja) | 2015-08-27 |
| EP2880017A1 (en) | 2015-06-10 |
| EA201590018A1 (ru) | 2015-05-29 |
| EP2880017B1 (en) | 2016-10-05 |
| HK1209748A1 (en) | 2016-04-08 |
| IL236618A (en) | 2017-04-30 |
| NZ630199A (en) | 2016-12-23 |
| CA2878699C (en) | 2018-09-11 |
| SG11201500812QA (en) | 2015-04-29 |
| AU2013296289B2 (en) | 2017-10-05 |
| CA2878699A1 (en) | 2014-02-06 |
| US8877931B2 (en) | 2014-11-04 |
| CN104520275A (zh) | 2015-04-15 |
| BR112015002275A2 (pt) | 2017-07-04 |
| MX2015001506A (es) | 2015-04-08 |
| JP6147856B2 (ja) | 2017-06-14 |
| IN2015DN01688A (forum.php) | 2015-07-03 |
| AU2013296289A1 (en) | 2015-02-19 |
| CN104520275B (zh) | 2016-11-02 |
| PT2880017T (pt) | 2016-12-14 |
| HK1209415A1 (en) | 2016-04-01 |
| WO2014022707A1 (en) | 2014-02-06 |
| IL236618A0 (en) | 2015-02-26 |
| US20140039194A1 (en) | 2014-02-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2013296289B2 (en) | Process and intermediates for preparing integrase inhibitors | |
| AU2008298943B2 (en) | Process and intermediates for preparing integrase inhibitors | |
| EP2069280B1 (en) | Process and intermediates for preparing HIV integrase inhibitors | |
| CN111448192B (zh) | 用于制备驱蠕虫的4-氨基-喹啉-3-甲酰胺衍生物的方法 | |
| CN114790151B (zh) | 一种2-氰基-2-丙戊酸甲酯的复合催化制备方法 | |
| KR100492054B1 (ko) | Ｎ,Ｎ,6-트리메틸-2-(4-메틸페닐)-이미다조-[1,2-ａ]-피리딘-3-아세트아미드 및 이의 염의 제조방법 | |
| CN107286202B (zh) | 手性Ugi’s胺和其衍生物及光学异构体的合成方法和应用 | |
| JP5023683B2 (ja) | ベンゾフルオレン誘導体の製造方法およびその中間体 | |
| HK1209748B (en) | Process and intermediates for preparing integrase inhibitors | |
| HK1209415B (zh) | 用於制备整合酶抑制剂的方法和中间产物 | |
| CN113816855A (zh) | 合成手性烯丙基羧酸酯的方法 | |
| WO1998043967A1 (fr) | PROCEDE DE PRODUCTION DE DERIVES D'ACIDE 2-(BENZO[b]THIOPHEN-5-YL)-2-HYDROXYACETIQUE, DE LEURS COMPOSES OPTIQUEMENT ACTIFS OU DE SELS DES DEUX | |
| WO2017125351A1 (en) | Process for preparing (( r)-3-[(-1-methylpyrrolidin-2-yl)methyl]-5-(2-phenylsulfonylethyl)-1h-indole | |
| WO2012059807A1 (en) | Chiral intermediates useful for the preparation of hydroxyphosphine ligands | |
| HK1141785B (en) | Process and intermediates for preparing integrase inhibitors | |
| KR20020010931A (ko) | 의약품 중간체 화합물의 제조 방법 | |
| JPH11255766A (ja) | 環状ハロメチルフェノール硫化物の製造法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG TJ TM RU |