JP2003040874A5 - - Google Patents

Download PDF

Info

Publication number
JP2003040874A5
JP2003040874A5 JP2002163198A JP2002163198A JP2003040874A5 JP 2003040874 A5 JP2003040874 A5 JP 2003040874A5 JP 2002163198 A JP2002163198 A JP 2002163198A JP 2002163198 A JP2002163198 A JP 2002163198A JP 2003040874 A5 JP2003040874 A5 JP 2003040874A5
Authority
JP
Japan
Prior art keywords
solvent
slurry
crystalline compound
antisolvent
wet cake
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.)
Withdrawn
Application number
JP2002163198A
Other languages
English (en)
Japanese (ja)
Other versions
JP2003040874A (ja
Filing date
Publication date
Priority claimed from GBGB9706046.1A external-priority patent/GB9706046D0/en
Priority claimed from GBGB9709348.8A external-priority patent/GB9709348D0/en
Application filed filed Critical
Publication of JP2003040874A publication Critical patent/JP2003040874A/ja
Publication of JP2003040874A5 publication Critical patent/JP2003040874A5/ja
Withdrawn legal-status Critical Current

Links

JP2002163198A 1997-02-05 2002-06-04 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法 Withdrawn JP2003040874A (ja)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US3738597P 1997-02-05 1997-02-05
US60/037,385 1997-02-05
GB9706046.1 1997-03-24
GBGB9706046.1A GB9706046D0 (en) 1997-03-24 1997-03-24 Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent
US4280797P 1997-04-08 1997-04-08
US60/042,807 1997-04-08
GBGB9709348.8A GB9709348D0 (en) 1997-05-07 1997-05-07 Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent
GB9709348.8 1997-05-07

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP53319098A Division JP3418626B2 (ja) 1997-02-05 1998-02-02 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2010202879A Division JP5295190B2 (ja) 1997-02-05 2010-09-10 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法

Publications (2)

Publication Number Publication Date
JP2003040874A JP2003040874A (ja) 2003-02-13
JP2003040874A5 true JP2003040874A5 (https=) 2005-08-04

Family

ID=27451618

Family Applications (6)

Application Number Title Priority Date Filing Date
JP53319098A Expired - Lifetime JP3418626B2 (ja) 1997-02-05 1998-02-02 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2002163198A Withdrawn JP2003040874A (ja) 1997-02-05 2002-06-04 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2010202879A Expired - Lifetime JP5295190B2 (ja) 1997-02-05 2010-09-10 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2013089216A Pending JP2013139484A (ja) 1997-02-05 2013-04-22 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2015146631A Expired - Lifetime JP6126172B2 (ja) 1997-02-05 2015-07-24 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2017002745A Pending JP2017061575A (ja) 1997-02-05 2017-01-11 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP53319098A Expired - Lifetime JP3418626B2 (ja) 1997-02-05 1998-02-02 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法

Family Applications After (4)

Application Number Title Priority Date Filing Date
JP2010202879A Expired - Lifetime JP5295190B2 (ja) 1997-02-05 2010-09-10 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2013089216A Pending JP2013139484A (ja) 1997-02-05 2013-04-22 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2015146631A Expired - Lifetime JP6126172B2 (ja) 1997-02-05 2015-07-24 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
JP2017002745A Pending JP2017061575A (ja) 1997-02-05 2017-01-11 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法

Country Status (18)

Country Link
EP (1) EP0975609B1 (https=)
JP (6) JP3418626B2 (https=)
KR (1) KR100573192B1 (https=)
CN (2) CN1073991C (https=)
AT (1) ATE486065T1 (https=)
AU (1) AU738545C (https=)
CA (1) CA2279198C (https=)
CZ (2) CZ297535B6 (https=)
DE (1) DE69841972D1 (https=)
EA (1) EA001805B1 (https=)
EE (1) EE03827B1 (https=)
HU (1) HU229087B1 (https=)
IL (1) IL130715A (https=)
NO (1) NO320128B1 (https=)
NZ (1) NZ336510A (https=)
PL (1) PL197740B1 (https=)
SK (1) SK284935B6 (https=)
WO (1) WO1998033782A1 (https=)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU229087B1 (en) * 1997-02-05 2013-07-29 Merck Sharp & Dohme Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent
AR011731A1 (es) * 1997-05-16 2000-08-30 Merck & Co Inc Un proceso de reaccion de adicion enantioselectiva eficiente utilizando un reactivo de organozinc.
US20010014352A1 (en) 1998-05-27 2001-08-16 Udit Batra Compressed tablet formulation
HRP990182A2 (en) * 1998-06-11 2000-02-29 Du Pont Pharm Co Crystalline efavirenz
GB9828721D0 (en) * 1998-12-24 1999-02-17 Glaxo Group Ltd Novel apparatus and process
WO2006018853A2 (en) 2004-08-19 2006-02-23 Hetero Drugs Limited Novel polymorphs of efavirenz
WO2008108630A1 (en) * 2007-03-02 2008-09-12 Ultimorphix Technologies B.V. Polymorphic forms of efavirenz
US8318930B2 (en) * 2007-12-24 2012-11-27 Matrix Laboratories Limited Process for preparing polymorphic forms of (S)-6-chloro-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one
US8383811B2 (en) 2008-12-22 2013-02-26 Hetero Research Foundation Process for preparing efavirenz polymorph
DE102009041443A1 (de) 2009-09-16 2011-03-31 Archimica Gmbh Salze des 6-Chlor-4-(cyclopropylethinyl)-1,4-dihydro-4-(trifluormethyl)-2H-3,1-benzoxazin-2-ons und deren Synthese, Aufreinigung und Anwendung als Vorstufen für Efavirenz
EP2471783A1 (en) 2010-12-23 2012-07-04 Esteve Química, S.A. Novel polymorphic form of efavirenz
CN103508973B (zh) * 2012-06-25 2016-04-27 上海迪赛诺药业有限公司 制备依非韦伦i型结晶的方法
CN105037175B (zh) * 2014-07-18 2017-02-22 盐城迪赛诺制药有限公司 一种用于提高依非韦伦中间体光学纯度的方法
US11524964B2 (en) 2015-10-16 2022-12-13 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11773106B2 (en) 2015-10-16 2023-10-03 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US10550126B2 (en) 2015-10-16 2020-02-04 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11512092B2 (en) 2015-10-16 2022-11-29 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US12365689B2 (en) 2015-10-16 2025-07-22 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
US11365198B2 (en) 2015-10-16 2022-06-21 Abbvie Inc. Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof
SG10201913990RA (en) 2015-10-16 2020-03-30 Abbvie Inc PROCESSES FOR THE PREPARATION OF (3S,4R)-3-ETHYL-4-(3H-IMIDAZO[1,2-a]PYRROLO[2,3-e]-PYRAZIN-8-YL)-N-(2,2,2-TRIFLUOROETHYL)PYRROLIDINE-1-CARBOXAMIDE AND SOLID STATE FORMS THEREOF
CN114195761B (zh) * 2021-12-23 2023-04-14 浙江普洛家园药业有限公司 一种高纯度西他沙星3/2水合物的制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1282405C (en) * 1984-05-21 1991-04-02 Michael R. Violante Method for making uniformly sized particles from water-insoluble organic compounds
US5665720A (en) * 1992-08-07 1997-09-09 Merck & Co., Inc. Benzoxazinones as inhibitors of HIV reverse transcriptase
IL106507A (en) * 1992-08-07 1997-11-20 Merck & Co Inc Pharmaceutical compositions containing benzoxazinones and some novel compounds of this type
WO1995020389A1 (en) * 1994-01-28 1995-08-03 Merck & Co., Inc. Benzoxazinones as inhibitors of hiv reverse transcriptase
US5663467A (en) * 1995-01-23 1997-09-02 Merck & Co., Inc. Synthesis of cyclopropylacetylene
US5633405A (en) * 1995-05-25 1997-05-27 Merck & Co., Inc. Asymmetric synthesis of (-)-6-chloro-4-cyclopropyl-ethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxanzin-2-one
HU229087B1 (en) * 1997-02-05 2013-07-29 Merck Sharp & Dohme Process for the crystallization of a reverse transcriptase inhibitor using an anti-solvent
AU6876898A (en) * 1997-04-07 1998-10-30 Du Pont Pharmaceuticals Company Asymmetric synthesis of benzoxazinones via new intermediates

Similar Documents

Publication Publication Date Title
JP2003040874A5 (https=)
JP5295190B2 (ja) 逆溶媒を使用する逆転写酵素阻害剤の結晶化方法
KR100377159B1 (ko) 잔류 용매가 없는 클라리스로마이신의 결정형 2의 제조 방법
JP2024001115A (ja) オキサゾール化合物結晶
TW202216675A (zh) 一種精製乙交酯的方法及其所得乙交酯
KR102427365B1 (ko) 4-하이드록시아세토페논의 정제 방법
JP2022000462A (ja) エパルレスタットを調製する方法
PT86526B (pt) Processo para a preparacao de mono-hidrato de cefadroxil cristalino e de composicoes farmaceuticas que o contem
JPH0643429B2 (ja) 高度に結晶性のナトリウムセフオペラゾンの製法
CN111732547B (zh) 一种奥拉帕利的精制方法及用途
JPH089691B2 (ja) 青色色素化合物及びその製造方法
CN105646508B (zh) 一种盐酸纳美芬一水合物的制备方法
WO2006018853A3 (en) Novel polymorphs of efavirenz
CN101724000A (zh) 一种红霉素的结晶方法
CN104628743A (zh) 头孢硫脒化合物的新晶型及其结晶制备方法
JPH06192228A (ja) 結晶性(r)−(−)−2−シクロヘプチル−n−メチルスルフオニル−[4−(2−キノリニルメトキシ)−フエニル]−アセトアミド
JP2663105B2 (ja) 14α−ヒドロキシ−4−アンドロステン−3,6,17−トリオン水和物結晶及びその製造法
KR860001495B1 (ko) 결정성 나트륨 세포페라존의 제조방법
US3947414A (en) Cefamandole derivatives
CN105237529A (zh) 高纯度无水达沙替尼的精制方法
JP2000507919A (ja) ジオキソアザビシクロヘキサン類の製造方法
US3947415A (en) Cefamandole derivatives
WO2025086317A1 (zh) 一种阿维巴坦钠中间体的纯化方法及阿维巴坦钠中间体
CA3037771C (en) Method for purification of 4-hydroxyacetophenone
TW542840B (en) Chemical acetylation of desacetyl-cephalosporins