JP2017509585A5 - - Google Patents

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Publication number
JP2017509585A5
JP2017509585A5 JP2016541595A JP2016541595A JP2017509585A5 JP 2017509585 A5 JP2017509585 A5 JP 2017509585A5 JP 2016541595 A JP2016541595 A JP 2016541595A JP 2016541595 A JP2016541595 A JP 2016541595A JP 2017509585 A5 JP2017509585 A5 JP 2017509585A5
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JP
Japan
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formula
salt
compound
providing
crystal
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JP2016541595A
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English (en)
Japanese (ja)
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JP6425727B2 (ja
JP2017509585A (ja
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Priority claimed from PCT/US2014/071319 external-priority patent/WO2015100145A1/en
Publication of JP2017509585A publication Critical patent/JP2017509585A/ja
Publication of JP2017509585A5 publication Critical patent/JP2017509585A5/ja
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Publication of JP6425727B2 publication Critical patent/JP6425727B2/ja
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JP2016541595A 2013-12-23 2014-12-18 大環状hcv ns3阻害トリペプチド Active JP6425727B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361920446P 2013-12-23 2013-12-23
US61/920,446 2013-12-23
PCT/US2014/071319 WO2015100145A1 (en) 2013-12-23 2014-12-18 Synthesis of a macrocyclic hcv ns3 inhibiting tripeptide

Publications (3)

Publication Number Publication Date
JP2017509585A JP2017509585A (ja) 2017-04-06
JP2017509585A5 true JP2017509585A5 (cg-RX-API-DMAC7.html) 2018-01-18
JP6425727B2 JP6425727B2 (ja) 2018-11-21

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ID=52278856

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016541595A Active JP6425727B2 (ja) 2013-12-23 2014-12-18 大環状hcv ns3阻害トリペプチド

Country Status (20)

Country Link
US (2) US9440991B2 (cg-RX-API-DMAC7.html)
EP (1) EP3087085B1 (cg-RX-API-DMAC7.html)
JP (1) JP6425727B2 (cg-RX-API-DMAC7.html)
KR (1) KR102366697B1 (cg-RX-API-DMAC7.html)
CN (3) CN111320610B (cg-RX-API-DMAC7.html)
AR (1) AR098959A1 (cg-RX-API-DMAC7.html)
AU (1) AU2014370125B2 (cg-RX-API-DMAC7.html)
CA (1) CA2934537C (cg-RX-API-DMAC7.html)
EA (1) EA201691031A1 (cg-RX-API-DMAC7.html)
ES (1) ES2724460T3 (cg-RX-API-DMAC7.html)
IL (1) IL246064A0 (cg-RX-API-DMAC7.html)
MX (1) MX2016008452A (cg-RX-API-DMAC7.html)
NZ (1) NZ720745A (cg-RX-API-DMAC7.html)
PL (1) PL3087085T3 (cg-RX-API-DMAC7.html)
PT (1) PT3087085T (cg-RX-API-DMAC7.html)
SG (1) SG11201604482QA (cg-RX-API-DMAC7.html)
SI (1) SI3087085T1 (cg-RX-API-DMAC7.html)
TR (1) TR201906413T4 (cg-RX-API-DMAC7.html)
TW (3) TWI671292B (cg-RX-API-DMAC7.html)
WO (1) WO2015100145A1 (cg-RX-API-DMAC7.html)

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WO2015017466A1 (en) * 2013-07-30 2015-02-05 Gilead Connecticut, Inc. Formulation of syk inhibitors
EA029281B1 (ru) 2013-07-30 2018-03-30 Джилид Коннектикут, Инк. Полиморф ингибиторов syk
ES2724460T3 (es) 2013-12-23 2019-09-11 Gilead Pharmasset Llc Síntesis de un tripéptido que inhíbe el NS3 del virus de VHC macrocíclico
UY35898A (es) 2013-12-23 2015-07-31 Gilead Sciences Inc ?compuestos inhibidores de syk y composiciones que los comprenden?.
US9809576B1 (en) 2014-07-18 2017-11-07 Abbvie Inc. Synthetic route to anti-viral agents
US9809534B1 (en) * 2014-07-21 2017-11-07 Abbvie Inc. Difluoroalkylcyclopropyl amino acids and esters, and syntheses thereof
US10059969B1 (en) 2014-10-03 2018-08-28 Abbvie Inc. Process for the preparation of (S)-2-amino-non-8-enoic acid
US10316338B1 (en) 2015-01-30 2019-06-11 Abb Vie Inc. Enzymatic process for the preparation of (1S,2R)-2-(difluoromethyl)-1-(propoxycarbonyl)cyclopropanecarboxylic acid
US10450291B2 (en) 2015-06-29 2019-10-22 Central Glass Company, Limited Method for producing fluorine-containing cyclopropane carboxylic acid compound
AU2018215337A1 (en) 2017-02-01 2019-08-22 Abbvie Inc. Enzymatic processes for the preparation of (±)-2-(difluoromethyl)-1-(alkoxycarbonyl)-cyclopropanecarboxylic acid and(±)-2-(vinyl)-1-(alkoxycarbonyl)-cyclopropanecarboxylic acid
WO2019084740A1 (zh) * 2017-10-31 2019-05-09 上海同昌生物医药科技有限公司 一种Glecaprevir合成中间体及其胺盐的制备方法
CN107739319A (zh) * 2017-10-31 2018-02-27 上海同昌生物医药科技有限公司 一种Glecaprevir合成中间体及其胺盐的制备方法
CN107827748A (zh) * 2017-11-14 2018-03-23 安徽华胜医药科技有限公司 一种乙酸2‑烯丙基环丙酯消旋体的合成方法
KR102519417B1 (ko) 2018-11-28 2023-04-10 삼성디스플레이 주식회사 스트레처블 표시 장치
AU2020225455A1 (en) 2019-02-22 2021-09-09 Kronos Bio, Inc. Solid forms of condensed pyrazines as Syk inhibitors
CN116041181A (zh) * 2023-01-04 2023-05-02 广州巨元生化有限公司 一种制备4-卤代-2-甲基-2-丁烯酸烃基酯的方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA200605247B (en) * 2003-12-15 2007-10-31 Japan Tobacco Inc N-substituted-n-sulfonylaminocyclopropane compounds and pharmaceutical use thereof
CL2008003384A1 (es) * 2007-11-14 2009-12-11 Enanta Pharm Inc Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c.
US8211891B2 (en) 2008-04-30 2012-07-03 Enanta Pharmaceuticals, Inc. Difluoromethyl-containing macrocyclic compounds as hepatitis C virus inhibitors
ME02132B (me) 2008-07-22 2014-08-22 Merck Sharp & Dohme Kombinacije makrocikličnog jedinjenja hinoksalina koje je inhibitor hcv ns3 proteaze sa drugim hcv sredstvima
US8283310B2 (en) 2008-12-15 2012-10-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2289880A1 (en) * 2009-07-08 2011-03-02 Bayer CropScience AG 2-Pyridinylcyclopropylbenzamide fungicides
EA029145B1 (ru) * 2010-09-21 2018-02-28 Энанта Фармасьютикалз, Инк. Ингибиторы hcv сериновой протеазы, полученные из макроциклического пролина
EP2618665A4 (en) * 2010-09-21 2014-08-20 Merck Sharp & Dohme HCV NS3 proteinase inhibitor
AR084217A1 (es) * 2010-12-10 2013-05-02 Gilead Sciences Inc Inhibidores macrociclicos de virus flaviviridae
UA119315C2 (uk) * 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
WO2015095430A1 (en) * 2013-12-20 2015-06-25 Merck Sharp & Dohme Corp. Methods and intermediates for the preparation of macrolactams
EP3087086B1 (en) 2013-12-23 2018-11-07 Gilead Sciences, Inc. Crystalline forms of a macrocyclic hcv ns3 inhibiting tripeptide
ES2724460T3 (es) 2013-12-23 2019-09-11 Gilead Pharmasset Llc Síntesis de un tripéptido que inhíbe el NS3 del virus de VHC macrocíclico

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