JP2010539101A5 - - Google Patents

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Publication number
JP2010539101A5
JP2010539101A5 JP2010524261A JP2010524261A JP2010539101A5 JP 2010539101 A5 JP2010539101 A5 JP 2010539101A5 JP 2010524261 A JP2010524261 A JP 2010524261A JP 2010524261 A JP2010524261 A JP 2010524261A JP 2010539101 A5 JP2010539101 A5 JP 2010539101A5
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JP
Japan
Prior art keywords
compound
formula
salt
converted
converting
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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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JP2010524261A
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English (en)
Japanese (ja)
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JP2010539101A (ja
JP5202635B2 (ja
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Priority claimed from PCT/US2008/076002 external-priority patent/WO2009036161A1/en
Publication of JP2010539101A publication Critical patent/JP2010539101A/ja
Publication of JP2010539101A5 publication Critical patent/JP2010539101A5/ja
Application granted granted Critical
Publication of JP5202635B2 publication Critical patent/JP5202635B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2010524261A 2007-09-11 2008-09-11 インテグラーゼ阻害剤の調製のためのプロセスおよび中間体 Expired - Fee Related JP5202635B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US97139507P 2007-09-11 2007-09-11
US60/971,395 2007-09-11
PCT/US2008/076002 WO2009036161A1 (en) 2007-09-11 2008-09-11 Process and intermediates for preparing integrase inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2013024589A Division JP2013129659A (ja) 2007-09-11 2013-02-12 インテグラーゼ阻害剤の調製のためのプロセスおよび中間体

Publications (3)

Publication Number Publication Date
JP2010539101A JP2010539101A (ja) 2010-12-16
JP2010539101A5 true JP2010539101A5 (en:Method) 2012-01-26
JP5202635B2 JP5202635B2 (ja) 2013-06-05

Family

ID=39887255

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2010524261A Expired - Fee Related JP5202635B2 (ja) 2007-09-11 2008-09-11 インテグラーゼ阻害剤の調製のためのプロセスおよび中間体
JP2013024589A Withdrawn JP2013129659A (ja) 2007-09-11 2013-02-12 インテグラーゼ阻害剤の調製のためのプロセスおよび中間体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2013024589A Withdrawn JP2013129659A (ja) 2007-09-11 2013-02-12 インテグラーゼ阻害剤の調製のためのプロセスおよび中間体

Country Status (20)

Country Link
US (4) US8153801B2 (en:Method)
EP (1) EP2190804B1 (en:Method)
JP (2) JP5202635B2 (en:Method)
KR (1) KR101488550B1 (en:Method)
CN (1) CN101821223B (en:Method)
AP (1) AP2785A (en:Method)
AR (1) AR068403A1 (en:Method)
AU (1) AU2008298943B2 (en:Method)
BR (1) BRPI0816694A2 (en:Method)
CA (1) CA2698245C (en:Method)
CO (1) CO6270255A2 (en:Method)
EA (1) EA019431B1 (en:Method)
ES (1) ES2562080T3 (en:Method)
MX (1) MX2010002783A (en:Method)
NZ (1) NZ583647A (en:Method)
PT (1) PT2190804E (en:Method)
TW (1) TWI419867B (en:Method)
UA (1) UA101956C2 (en:Method)
WO (1) WO2009036161A1 (en:Method)
ZA (1) ZA201002066B (en:Method)

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US7176220B2 (en) * 2002-11-20 2007-02-13 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as pharmaceutical agent
CA2635468C (en) * 2005-12-30 2016-08-09 Gilead Sciences, Inc. Methods for improving the pharmacokinetics of hiv integrase inhibitors
WO2007102499A1 (ja) * 2006-03-06 2007-09-13 Japan Tobacco Inc. 4-オキソキノリン化合物の製造方法
KR101023635B1 (ko) 2006-03-06 2011-03-22 니뽄 다바코 산교 가부시키가이샤 4-옥소퀴놀린 화합물 제조 방법
TWI411602B (zh) 2006-09-12 2013-10-11 Gilead Sciences Inc 製造整合酶抑制劑的方法及彼所用的中間物
JP5547067B2 (ja) * 2007-06-29 2014-07-09 ギリアード サイエンシーズ, インコーポレイテッド 治療組成物およびその使用
EA200971093A1 (ru) * 2007-06-29 2010-08-30 Джилид Сайэнс, Инк. Терапевтические композиции и их применение
AR068403A1 (es) * 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa
WO2011004389A2 (en) 2009-06-18 2011-01-13 Matrix Laboratories Ltd An improved process for the preparation of elvitegravir
CN102212032B (zh) * 2011-04-20 2013-07-31 复旦大学 一种5-羟基喹诺酮类衍生物及其制备方法和用途
ES3018133T3 (en) 2011-11-30 2025-05-14 Univ Emory Jak inhibitors for use in the prevention or treatment of a viral disease caused by a coronaviridae
KR20150040340A (ko) * 2012-08-03 2015-04-14 길리애드 사이언시즈, 인코포레이티드 인테그라아제 저해제 제조를 위한 방법 및 중간체
CZ304983B6 (cs) * 2012-10-12 2015-03-11 Zentiva, K.S. Způsob výroby a nové intermediáty syntézy elvitegraviru
CZ304984B6 (cs) * 2012-10-12 2015-03-11 Zentiva, K.S. Zlepšený způsob výroby a nové intermediáty syntézy elvitegraviru
ME02400B (me) 2012-12-21 2016-09-20 Gilead Sciences Inc Policiklična karbamoilpiridonska jedinjenja i njihova farmaceutska upotreba
NO2865735T3 (en:Method) 2013-07-12 2018-07-21
EP3252058B1 (en) 2013-07-12 2021-01-20 Gilead Sciences, Inc. Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections
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 (en:Method) 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
ES2837383T3 (es) 2015-04-02 2021-06-30 Gilead Sciences Inc Compuestos de carbamoilpiridonas policíclicos y su utilización farmacéutica
CN111733133B (zh) * 2020-07-22 2020-12-01 华夏源(上海)生命科技有限公司 一种促进表皮干细胞分化和生长的方法
CN111944761B (zh) * 2020-08-23 2021-03-26 泉州伟业生物医学科技有限公司 促进表皮干细胞分化和生长的方法

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US1564210A (en) * 1925-12-08 Obin d
DE3501247A1 (de) * 1985-01-16 1986-07-17 Bayer Ag, 5090 Leverkusen Aminoacrylsaeure-derivate
ATE300522T1 (de) * 2000-12-14 2005-08-15 Procter & Gamble Cyclisierungsverfahrensschritt bei der herstellung von chinolonen und naphthyridinen
TW200300349A (en) 2001-11-19 2003-06-01 Sankyo Co A 4-oxoqinoline derivative
US20050104233A1 (en) * 2002-05-31 2005-05-19 Shinji Kato 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
US7176220B2 (en) * 2002-11-20 2007-02-13 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as pharmaceutical agent
EP1582524B1 (en) 2004-04-02 2008-08-13 Ludwig Maximilians Universität Method of preparing organomagnesium compounds
EP1582523A1 (en) 2004-04-02 2005-10-05 Ludwig-Maximilians-Universität München Method of preparing organomagnesium compounds
WO2005113509A1 (en) 2004-05-20 2005-12-01 Japan Tobacco Inc. Novel 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
EP2332538A1 (en) 2004-05-21 2011-06-15 Japan Tobacco, Inc. Combinations comprising a 4-isoquinolone derivative and anti-HIV agents
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
KR101023635B1 (ko) * 2006-03-06 2011-03-22 니뽄 다바코 산교 가부시키가이샤 4-옥소퀴놀린 화합물 제조 방법
WO2007102499A1 (ja) 2006-03-06 2007-09-13 Japan Tobacco Inc. 4-オキソキノリン化合物の製造方法
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
TWI411602B (zh) * 2006-09-12 2013-10-11 Gilead Sciences Inc 製造整合酶抑制劑的方法及彼所用的中間物
EA200971093A1 (ru) * 2007-06-29 2010-08-30 Джилид Сайэнс, Инк. Терапевтические композиции и их применение
JP5547067B2 (ja) * 2007-06-29 2014-07-09 ギリアード サイエンシーズ, インコーポレイテッド 治療組成物およびその使用
AR068403A1 (es) * 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa

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