JP2014524442A5 - - Google Patents

Download PDF

Info

Publication number
JP2014524442A5
JP2014524442A5 JP2014526215A JP2014526215A JP2014524442A5 JP 2014524442 A5 JP2014524442 A5 JP 2014524442A5 JP 2014526215 A JP2014526215 A JP 2014526215A JP 2014526215 A JP2014526215 A JP 2014526215A JP 2014524442 A5 JP2014524442 A5 JP 2014524442A5
Authority
JP
Japan
Prior art keywords
radiation
degrees
copper
values
diffraction pattern
Prior art date
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.)
Pending
Application number
JP2014526215A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014524442A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/051168 external-priority patent/WO2013028465A1/en
Publication of JP2014524442A publication Critical patent/JP2014524442A/ja
Publication of JP2014524442A5 publication Critical patent/JP2014524442A5/ja
Pending legal-status Critical Current

Links

JP2014526215A 2011-08-19 2012-08-16 Hcvプロテアーゼ阻害剤の結晶形態 Pending JP2014524442A (ja)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US201161525462P 2011-08-19 2011-08-19
US61/525,462 2011-08-19
US201161533439P 2011-09-12 2011-09-12
US61/533,439 2011-09-12
US201161533915P 2011-09-13 2011-09-13
US61/533,915 2011-09-13
US201161539540P 2011-09-27 2011-09-27
US61/539,540 2011-09-27
PCT/US2012/051168 WO2013028465A1 (en) 2011-08-19 2012-08-16 Crystal forms of a hcv protease inhibitor

Publications (2)

Publication Number Publication Date
JP2014524442A JP2014524442A (ja) 2014-09-22
JP2014524442A5 true JP2014524442A5 (enExample) 2015-10-15

Family

ID=47746773

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2014526217A Pending JP2014521750A (ja) 2011-08-19 2012-08-16 マクロラクタムを調製するための方法および中間体
JP2014526215A Pending JP2014524442A (ja) 2011-08-19 2012-08-16 Hcvプロテアーゼ阻害剤の結晶形態

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2014526217A Pending JP2014521750A (ja) 2011-08-19 2012-08-16 マクロラクタムを調製するための方法および中間体

Country Status (11)

Country Link
US (3) US9242917B2 (enExample)
EP (3) EP2744507A4 (enExample)
JP (2) JP2014521750A (enExample)
KR (2) KR20140059236A (enExample)
CN (2) CN103889439A (enExample)
AU (2) AU2012299218A1 (enExample)
BR (2) BR112014003802A2 (enExample)
CA (2) CA2844386A1 (enExample)
MX (2) MX2014001945A (enExample)
RU (2) RU2014110400A (enExample)
WO (3) WO2013028471A1 (enExample)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2459582B1 (en) 2009-07-30 2015-05-27 Merck Sharp & Dohme Corp. Hepatitis c virus ns3 protease inhibitors
US8957203B2 (en) 2011-05-05 2015-02-17 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
AU2012299218A1 (en) * 2011-08-19 2014-02-20 Merck Sharp & Dohme Corp. Crystal forms of a HCV protease inhibitor
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
BR112015007879A2 (pt) 2012-10-19 2017-07-04 Bristol Myers Squibb Co inibidores do vírus da hepatite c
US9334279B2 (en) 2012-11-02 2016-05-10 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US9643999B2 (en) 2012-11-02 2017-05-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2914613B1 (en) 2012-11-02 2017-11-22 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
US9409943B2 (en) 2012-11-05 2016-08-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2764866A1 (en) 2013-02-07 2014-08-13 IP Gesellschaft für Management mbH Inhibitors of nedd8-activating enzyme
EP2964664B1 (en) 2013-03-07 2017-01-11 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
CN105073758B (zh) 2013-03-15 2017-08-11 吉利德科学公司 丙型肝炎病毒抑制剂
US9873707B2 (en) 2013-10-18 2018-01-23 Merck Sharp & Dohme Corp. Methods and intermediates for preparing macrolactams
WO2015095437A1 (en) * 2013-12-20 2015-06-25 Merck Sharp & Dohme Corp. Methods and intermediates for the preparation of macrolactams
HRP20191283T1 (hr) * 2014-01-24 2019-10-18 Turning Point Therapeutics, Inc. Diaril makrocikli kao modulatori protein kinaze
CN106413736A (zh) * 2014-06-06 2017-02-15 艾伯维公司 晶型
AU2016287568B2 (en) 2015-07-02 2020-08-20 Turning Point Therapeutics, Inc. Chiral diaryl macrocycles as modulators of protein kinases
EP4397665A3 (en) * 2015-07-06 2024-08-21 Turning Point Therapeutics, Inc. Diaryl macrocycle polymorph
DK3325488T3 (da) * 2015-07-21 2020-09-14 Turning Point Therapeutics Inc Chiral diaryl-makrocyklus og anvendelse deraf til behandling af cancer
WO2017197051A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Amine-linked c3-glutarimide degronimers for target protein degradation
WO2017197046A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. C3-carbon linked glutarimide degronimers for target protein degradation
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
ES2989988T3 (es) 2016-05-10 2024-11-28 C4 Therapeutics Inc Degronímeros heterorocíclicos para la degradación de proteínas diana
TW201815799A (zh) 2016-07-28 2018-05-01 美商Tp生物醫藥公司 巨環激酶抑制劑
TWI808958B (zh) 2017-01-25 2023-07-21 美商特普醫葯公司 涉及二芳基巨環化合物之組合療法
CN110769822A (zh) 2017-06-20 2020-02-07 C4医药公司 用于蛋白降解的n/o-连接的降解决定子和降解决定子体
BR112020001695A2 (pt) 2017-07-28 2020-07-21 Turning Point Therapeutics, Inc. compostos macrocíclicos e usos dos mesmos
CN111511746B (zh) 2017-12-19 2024-01-09 特普医药公司 用于治疗疾病的巨环化合物
CN111057045A (zh) * 2019-12-18 2020-04-24 安徽红杉生物医药科技有限公司 Hcv ns3/4a蛋白酶抑制剂中间体及其合成方法、应用
CN112174982A (zh) * 2020-09-10 2021-01-05 上海希迈医药科技有限公司 一种洛普替尼晶型及其制备方法

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4871868A (en) * 1987-03-11 1989-10-03 Takeda Chemical Industries, Ltd. Production of substituted acetylenic compounds
GB9207987D0 (en) * 1992-04-10 1992-05-27 Smithkline Beecham Plc Novel container and closure
US5716960A (en) * 1995-01-13 1998-02-10 U.S. Bioscience Inc. And Individuals Crystalline trimetrexate salts and the process for making the same
NO317155B1 (no) 1997-02-04 2004-08-30 Ono Pharmaceutical Co <omega>-cykloalkyl-prostagladin-E<N>2</N>-derivater
ZA98879B (en) * 1997-02-04 1998-08-03 Ono Pharmaceutical Co Omega-cycloalkyl-prostaglandin e2 derivatives
AU2006215041B2 (en) 2005-02-18 2012-05-31 Mitsubishi Tanabe Pharma Corporation Salt of proline derivative, solvate thereof, and production method thereof
US7834145B2 (en) 2005-03-22 2010-11-16 Merck Sharp & Dohme Corp. HCV protease substrates
AU2006242475B2 (en) 2005-05-02 2011-07-07 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
CN101228181B (zh) * 2005-07-20 2013-09-18 默沙东公司 Hcv ns3蛋白酶抑制剂
TWI387603B (zh) 2005-07-20 2013-03-01 Merck Sharp & Dohme Hcv ns3蛋白酶抑制劑
EP1913016B1 (en) 2005-08-01 2013-01-16 Merck Sharp & Dohme Corp. Macrocyclic peptides as hcv ns3 protease inhibitors
CA2645234A1 (en) * 2006-03-07 2007-09-13 The Procter & Gamble Company Compositions for oxidatively dyeing keratin fibers and methods for using such compositions
GB0609492D0 (en) 2006-05-15 2006-06-21 Angeletti P Ist Richerche Bio Therapeutic agents
GB0612423D0 (en) 2006-06-23 2006-08-02 Angeletti P Ist Richerche Bio Therapeutic agents
CN101583372A (zh) 2006-10-24 2009-11-18 默克公司 Hcv ns3蛋白酶抑制剂
AU2007309546A1 (en) 2006-10-24 2008-05-02 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. HCV NS3 protease inhibitors
US8377874B2 (en) 2006-10-27 2013-02-19 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
MY164469A (en) 2006-10-27 2017-12-15 Msd Italia Srl Hcv ns3 protease inhibitors
SG174809A1 (en) 2007-05-03 2011-10-28 Intermune Inc Macrocyclic compounds useful as inhibitors of hepatitis c virus
WO2009010804A1 (en) 2007-07-19 2009-01-22 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Macrocyclic compounds as antiviral agents
WO2009108507A1 (en) 2008-02-25 2009-09-03 Merck & Co., Inc. Therapeutic compounds
WO2009131196A1 (ja) * 2008-04-24 2009-10-29 武田薬品工業株式会社 置換ピロリジン誘導体およびその用途
US8871753B2 (en) * 2008-04-24 2014-10-28 Incyte Corporation Macrocyclic compounds and their use as kinase inhibitors
CA2720850A1 (en) 2008-04-28 2009-11-05 Merck Sharp & Dohme Corp. Hcv ns3 protease inhibitors
SI2540350T1 (sl) * 2008-07-22 2015-01-30 Merck Sharp & Dohme Corp. Kombinacije makrocikliäśnih kinoksalinske spojine, ki je hcv ns3 proteazni inhibitor z drugimi hcv uäśinkovinami
EP2459582B1 (en) 2009-07-30 2015-05-27 Merck Sharp & Dohme Corp. Hepatitis c virus ns3 protease inhibitors
CN102470158A (zh) * 2009-08-27 2012-05-23 默沙东公司 制备丙型肝炎病毒的蛋白酶抑制剂的工艺方法
AU2012299218A1 (en) 2011-08-19 2014-02-20 Merck Sharp & Dohme Corp. Crystal forms of a HCV protease inhibitor

Similar Documents

Publication Publication Date Title
JP2014524442A5 (enExample)
RU2014110399A (ru) Кристаллические формы вгс протеазного ингибитора
FI2534153T4 (fi) 8-fluori-2-{4-[(metyyliamino}metyyli]fenyyli}-1,3,4,5-tetrahydro-6h-atsepino[5,4,3-cd]indol-6-onin suoloja ja polymorfeja
JP2013543867A5 (enExample)
JP2018024682A5 (enExample)
JP2018520205A5 (enExample)
RU2017142958A (ru) Кристаллы азабициклического соединения
JP2013237682A5 (enExample)
JP2013520424A5 (enExample)
JP2009537498A5 (enExample)
JP2015145426A5 (enExample)
JP2015522037A5 (enExample)
JP2023002516A5 (enExample)
JP2018521121A5 (enExample)
NZ742200A (en) Treatment of osteoarthritis
JP2017522276A5 (enExample)
JP2013518107A5 (enExample)
JP2016006096A5 (enExample)
JP2013049690A5 (enExample)
HRP20171201T1 (hr) Postupak kristalizacije i biodostupnost
JP2012523395A5 (enExample)
JP2015522589A5 (enExample)
JP2014530818A5 (enExample)
JP2013538849A5 (enExample)
JP2015516425A5 (enExample)