JP2010503694A5 - - Google Patents

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Publication number
JP2010503694A5
JP2010503694A5 JP2009528433A JP2009528433A JP2010503694A5 JP 2010503694 A5 JP2010503694 A5 JP 2010503694A5 JP 2009528433 A JP2009528433 A JP 2009528433A JP 2009528433 A JP2009528433 A JP 2009528433A JP 2010503694 A5 JP2010503694 A5 JP 2010503694A5
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JP
Japan
Prior art keywords
compound
formula
salt
lithium
converting
Prior art date
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Granted
Application number
JP2009528433A
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English (en)
Japanese (ja)
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JP2010503694A (ja
JP5221544B2 (ja
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Publication date
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Priority claimed from PCT/US2007/078157 external-priority patent/WO2008033836A2/en
Publication of JP2010503694A publication Critical patent/JP2010503694A/ja
Publication of JP2010503694A5 publication Critical patent/JP2010503694A5/ja
Application granted granted Critical
Publication of JP5221544B2 publication Critical patent/JP5221544B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2009528433A 2006-09-12 2007-09-11 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 Expired - Fee Related JP5221544B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US84402006P 2006-09-12 2006-09-12
US60/844,020 2006-09-12
US90536507P 2007-03-07 2007-03-07
US60/905,365 2007-03-07
PCT/US2007/078157 WO2008033836A2 (en) 2006-09-12 2007-09-11 Process and intermediates for preparing integrase inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2012230583A Division JP2013047248A (ja) 2006-09-12 2012-10-18 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

Publications (3)

Publication Number Publication Date
JP2010503694A JP2010503694A (ja) 2010-02-04
JP2010503694A5 true JP2010503694A5 (enExample) 2012-06-28
JP5221544B2 JP5221544B2 (ja) 2013-06-26

Family

ID=39092311

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2009528433A Expired - Fee Related JP5221544B2 (ja) 2006-09-12 2007-09-11 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
JP2012230583A Withdrawn JP2013047248A (ja) 2006-09-12 2012-10-18 インテグラーゼ阻害剤を調製するためのプロセスおよび中間体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2012230583A Withdrawn JP2013047248A (ja) 2006-09-12 2012-10-18 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

Country Status (23)

Country Link
US (3) US7825252B2 (enExample)
EP (2) EP2069280B1 (enExample)
JP (2) JP5221544B2 (enExample)
KR (2) KR101565169B1 (enExample)
CN (4) CN102766098B (enExample)
AP (1) AP3004A (enExample)
AR (1) AR063710A1 (enExample)
AU (1) AU2007296555B2 (enExample)
BR (1) BRPI0716752A2 (enExample)
CA (1) CA2661943C (enExample)
EA (1) EA022099B1 (enExample)
ES (1) ES2536923T3 (enExample)
HK (2) HK1221454A1 (enExample)
HR (1) HRP20090213B1 (enExample)
IL (2) IL197527A (enExample)
MX (1) MX2009002689A (enExample)
NO (1) NO342907B1 (enExample)
NZ (1) NZ575542A (enExample)
PT (1) PT2069280E (enExample)
SG (2) SG174787A1 (enExample)
TW (1) TWI411602B (enExample)
WO (1) WO2008033836A2 (enExample)
ZA (1) ZA200901576B (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7176220B2 (en) * 2002-11-20 2007-02-13 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as pharmaceutical agent
AP2702A (en) * 2005-12-30 2013-07-23 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
JP4669040B2 (ja) * 2006-03-06 2011-04-13 日本たばこ産業株式会社 4−オキソキノリン化合物の製造方法
AU2007296555B2 (en) * 2006-09-12 2012-07-12 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
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
AR068403A1 (es) * 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa
CN104185420B (zh) 2011-11-30 2017-06-09 埃默里大学 用于治疗或预防逆转录病毒和其它病毒感染的抗病毒jak抑制剂
CN102603499A (zh) * 2012-03-01 2012-07-25 南京药石药物研发有限公司 1-溴-4-氟-5-异丙基-2-甲氧基苯的合成方法
CN102746143A (zh) * 2012-07-24 2012-10-24 上海灏翔生物科技有限公司 L-薄荷羧酸的一种高立体选择性合成方法
AU2013296289B2 (en) * 2012-08-03 2017-10-05 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
CZ304984B6 (cs) 2012-10-12 2015-03-11 Zentiva, K.S. Zlepšený způsob výroby a nové intermediáty syntézy elvitegraviru
CZ304983B6 (cs) 2012-10-12 2015-03-11 Zentiva, K.S. Způsob výroby a nové intermediáty syntézy elvitegraviru
SI2822954T1 (sl) 2012-12-21 2016-07-29 Gilead Sciences, Inc. Policiklične karbamoilpiridonske spojine in njihova farmacevtska uporaba
CZ307255B6 (cs) 2013-07-11 2018-05-02 Zentiva, K.S. Nový způsob přípravy elvitegraviru
PT3019503T (pt) 2013-07-12 2017-11-27 Gilead Sciences Inc Compostos carbamoílpiridona- policíclicos e seu uso para o tratamento de infecções por hiv
NO2865735T3 (enExample) 2013-07-12 2018-07-21
NO2717902T3 (enExample) 2014-06-20 2018-06-23
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
TWI744723B (zh) 2014-06-20 2021-11-01 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
TWI695003B (zh) 2014-12-23 2020-06-01 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
WO2016161382A1 (en) 2015-04-02 2016-10-06 Gilead Sciences, Inc. Polycyclic-carbamoylpyridone compounds and their pharmaceutical use
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

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US93482A (en) * 1869-08-10 Improved roofing-composition
US93467A (en) * 1869-08-10 Improved machine for bending car-hooks
US36684A (en) * 1862-10-14 Improvement in tailors press-board holders
US999366A (en) * 1910-09-30 1911-08-01 John M Gilmore Device for the manufacture of dental crowns.
DE3501247A1 (de) * 1985-01-16 1986-07-17 Bayer Ag, 5090 Leverkusen Aminoacrylsaeure-derivate
BR0116229A (pt) * 2000-12-14 2003-11-04 Procter & Gamble Etapa de processo de ciclização na fabricação de quinolonas e naftiridinas
TW200300349A (en) 2001-11-19 2003-06-01 Sankyo Co A 4-oxoqinoline derivative
JPWO2003101916A1 (ja) * 2002-05-31 2005-09-29 萬有製薬株式会社 ハロゲン−金属交換反応による置換基の導入法
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
CN100375742C (zh) * 2002-11-20 2008-03-19 日本烟草产业株式会社 4-氧代喹啉化合物及其用途
US7176220B2 (en) * 2002-11-20 2007-02-13 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as pharmaceutical agent
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
MY134672A (en) 2004-05-20 2007-12-31 Japan Tobacco Inc Stable crystal of 4-oxoquinoline compound
US7531554B2 (en) * 2004-05-20 2009-05-12 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as HIV integrase inhibitor
EP1758581A1 (en) * 2004-05-21 2007-03-07 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
JP4669040B2 (ja) 2006-03-06 2011-04-13 日本たばこ産業株式会社 4−オキソキノリン化合物の製造方法
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
AU2007296555B2 (en) 2006-09-12 2012-07-12 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
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
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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