JP2000505080A5 - - Google Patents

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Publication number
JP2000505080A5
JP2000505080A5 JP1997526511A JP52651197A JP2000505080A5 JP 2000505080 A5 JP2000505080 A5 JP 2000505080A5 JP 1997526511 A JP1997526511 A JP 1997526511A JP 52651197 A JP52651197 A JP 52651197A JP 2000505080 A5 JP2000505080 A5 JP 2000505080A5
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JP
Japan
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.)
Granted
Application number
JP1997526511A
Other languages
English (en)
Japanese (ja)
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JP2000505080A (ja
JP4094666B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP1997/000238 external-priority patent/WO1997027197A1/en
Publication of JP2000505080A publication Critical patent/JP2000505080A/ja
Publication of JP2000505080A5 publication Critical patent/JP2000505080A5/ja
Application granted granted Critical
Publication of JP4094666B2 publication Critical patent/JP4094666B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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JP52651197A 1996-01-26 1997-01-20 ガンシクロビル誘導体の製造方法 Expired - Lifetime JP4094666B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US59228296A 1996-01-26 1996-01-26
US592,282 1996-01-26
PCT/EP1997/000238 WO1997027197A1 (en) 1996-01-26 1997-01-20 Process for preparing ganciclovir derivatives

Publications (3)

Publication Number Publication Date
JP2000505080A JP2000505080A (ja) 2000-04-25
JP2000505080A5 true JP2000505080A5 (enExample) 2004-11-11
JP4094666B2 JP4094666B2 (ja) 2008-06-04

Family

ID=24370063

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52651197A Expired - Lifetime JP4094666B2 (ja) 1996-01-26 1997-01-20 ガンシクロビル誘導体の製造方法

Country Status (7)

Country Link
US (2) US5840890A (enExample)
EP (1) EP0885224B1 (enExample)
JP (1) JP4094666B2 (enExample)
AU (1) AU1593197A (enExample)
DE (1) DE69717974T2 (enExample)
ES (1) ES2187752T3 (enExample)
WO (1) WO1997027197A1 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6040446A (en) * 1996-01-26 2000-03-21 Syntex (U.S.A.) Inc. Process for preparing a 2-(2-amino-1,6-dihydro-6-oxo-purin-9-yl) methoxy-1,3-propanediol derivative
US5869493A (en) * 1996-02-16 1999-02-09 Medivir Ab Acyclic nucleoside derivatives
US6703394B2 (en) 1996-02-16 2004-03-09 Medivir Ab Acyclic nucleoside derivatives
AU735438B2 (en) * 1996-11-12 2001-07-05 Medivir Ab Nucleosides
EP1436295A4 (en) * 2001-09-07 2007-07-11 Teva Pharma CRISTALLINE FORMS OF VALACYCLOVIR HYDROCHLORIDE
US20050043329A1 (en) * 2002-09-06 2005-02-24 Shlomit Wizel Crystalline forms of valacyclovir hydrochloride
US20050059684A1 (en) * 2002-10-16 2005-03-17 Ben-Zion Dolitzky Method for reducing residual alcohols in crystalline valacyclovir hydrochloride
CN1860120A (zh) * 2003-08-28 2006-11-08 兰贝克赛实验室有限公司 无定形盐酸缬更昔洛韦
CN101068814A (zh) 2004-09-04 2007-11-07 特瓦制药工业有限公司 分离的伐昔洛韦杂质,制备伐昔洛韦杂质的方法及其作为参比标准物的应用
CA2594688A1 (en) * 2005-01-25 2006-08-03 Sigma Coatings B.V. A binder composition
ZA200702234B (en) * 2006-03-21 2008-07-30 Cipla Ltd Preparation of ester of purine derivatives
EP1870411B1 (en) * 2006-06-21 2016-03-16 Fidia Farmaceutici S.p.A. Process for the preparation and purification of valgancyclovir
NZ577179A (en) 2006-12-13 2011-12-22 Hoffmann La Roche Powder formulation for valganciclovir
US20090076040A1 (en) * 2007-09-15 2009-03-19 Protia, Llc Deuterium-enriched valganciclovir
WO2010036904A2 (en) * 2008-09-26 2010-04-01 Dr. Reddy's Laboratories Ltd. Preparation of valganciclovir and its salts
IT1397233B1 (it) * 2010-01-08 2013-01-04 Fidia Farmaceutici Procedimento migliorativo per la sintesi del mono-acetil ganciclovir, intermedio chiave per la sintesi del valganciclovir.
CN101955481B (zh) * 2010-10-09 2016-04-20 广东肇庆星湖生物科技股份有限公司 一种盐酸缬更昔洛韦的制备方法
CN103562207B (zh) * 2011-05-31 2016-08-17 法尔玛赞公司 用于制备缬更昔洛韦的2-氨基-9-((2-苯基-1,3-二噁烷-5-基氧基)甲基)-1h-嘌呤-6(9h)-酮化合物的制备方法
CN105693722B (zh) * 2016-04-20 2018-07-20 安徽海康药业有限责任公司 一种cbz-缬更昔洛韦的制备方法
CN105693724B (zh) * 2016-04-20 2017-08-11 安徽海康药业有限责任公司 一种cbz‑缬更昔洛韦的制备方法
CN105732630B (zh) * 2016-04-20 2018-11-30 安徽海康药业有限责任公司 一种cbz-缬更昔洛韦的制备方法
CN112409359A (zh) * 2020-11-30 2021-02-26 沃德药业(安徽)股份有限公司 一种盐酸缬更昔洛韦制备方法
CN113880838B (zh) * 2021-11-15 2024-03-19 仁合益康集团有限公司 一种微通道反应器合成盐酸缬更昔洛韦的方法
CN115286632B (zh) * 2022-09-16 2023-05-09 河北医科大学 一种盐酸缬更昔洛韦的制备工艺

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1523865A (en) * 1974-09-02 1978-09-06 Wellcome Found Purine compunds and salts thereof
US4355032B2 (en) * 1981-05-21 1990-10-30 9-(1,3-dihydroxy-2-propoxymethyl)guanine as antiviral agent
FI76086C (fi) * 1981-08-11 1988-09-09 Wellcome Found Foerfarande foer framstaellning av antivirala purinderivat.
US4816447A (en) * 1981-08-26 1989-03-28 Merck & Co., Inc. Anti-viral guanine compounds
NZ201662A (en) * 1981-08-26 1986-07-11 Merck & Co Inc 9-(1,3-(and 2,3)-dihydroxy-1-(and 2)-propoxy-methyl)guanine derivatives and methods for their preparation
US5250535A (en) * 1982-02-01 1993-10-05 Syntex Inc. Substituted 9-(1 or 3-monoacyloxy or 1,3-diacyloxy-2-propoxymethyl) purines as antiviral agent
NL8202626A (nl) * 1982-06-29 1984-01-16 Stichting Rega V Z W Derivaten van 9-(2-hydroxyethoxymethyl)guanine.
KR890001487B1 (ko) * 1982-10-14 1989-05-04 더 웰컴 파운데이숀 리미티드 푸린 유도체의 제조방법
AP55A (en) * 1987-08-15 1989-09-26 The Wellcome Foundation Ltd Therapeutic Acyclic Nucleosides
GB8829571D0 (en) 1988-12-19 1989-02-08 Wellcome Found Antiviral compounds
CA2005815C (en) * 1988-12-19 1999-08-03 Wellcome Foundation Limited (The) Antiviral acyclic nucleoside derivatives
ES2157259T3 (es) * 1993-06-10 2001-08-16 Rolabo Sl Procedimiento para preparar esteres de aminoacidos y analogos de nucleosidos.
US5543414A (en) * 1994-07-28 1996-08-06 Syntex (Usa) Inc. Achiral amino acid acyl esters of ganciclovir and its derivatives
PE32296A1 (es) * 1994-07-28 1996-08-07 Hoffmann La Roche Ester de l-monovalina derivado de 2-(2-amino-1,6-dihidro-6-oxo-purin-9-il) metoxi-1,3-propandiol y sus sales farmaceuticamente aceptables

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