ES2105114T3 - Procedimiento para preparar sulfonatos de 2-desoxi-2,2-difluoro-d-ribofuranosilo enriquecidos en alfa-anomero. - Google Patents

Procedimiento para preparar sulfonatos de 2-desoxi-2,2-difluoro-d-ribofuranosilo enriquecidos en alfa-anomero.

Info

Publication number
ES2105114T3
ES2105114T3 ES93304814T ES93304814T ES2105114T3 ES 2105114 T3 ES2105114 T3 ES 2105114T3 ES 93304814 T ES93304814 T ES 93304814T ES 93304814 T ES93304814 T ES 93304814T ES 2105114 T3 ES2105114 T3 ES 2105114T3
Authority
ES
Spain
Prior art keywords
alpha
enriched
anomero
ribofuranosil
desoxi
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.)
Expired - Lifetime
Application number
ES93304814T
Other languages
English (en)
Spanish (es)
Inventor
Ta-Sen Chou
Charles David Jones
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co
Application granted granted Critical
Publication of ES2105114T3 publication Critical patent/ES2105114T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
    • C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
    • C07H13/08—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals directly attached to carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H11/00—Compounds containing saccharide radicals esterified by inorganic acids; Metal salts thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Saccharide Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
ES93304814T 1992-06-22 1993-06-21 Procedimiento para preparar sulfonatos de 2-desoxi-2,2-difluoro-d-ribofuranosilo enriquecidos en alfa-anomero. Expired - Lifetime ES2105114T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/902,305 US5256798A (en) 1992-06-22 1992-06-22 Process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates

Publications (1)

Publication Number Publication Date
ES2105114T3 true ES2105114T3 (es) 1997-10-16

Family

ID=25415655

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93304814T Expired - Lifetime ES2105114T3 (es) 1992-06-22 1993-06-21 Procedimiento para preparar sulfonatos de 2-desoxi-2,2-difluoro-d-ribofuranosilo enriquecidos en alfa-anomero.

Country Status (14)

Country Link
US (1) US5256798A (cg-RX-API-DMAC10.html)
EP (1) EP0577302B1 (cg-RX-API-DMAC10.html)
JP (1) JP3379993B2 (cg-RX-API-DMAC10.html)
AT (1) ATE155476T1 (cg-RX-API-DMAC10.html)
BR (1) BR9302429A (cg-RX-API-DMAC10.html)
CA (1) CA2098882C (cg-RX-API-DMAC10.html)
DE (1) DE69312176T2 (cg-RX-API-DMAC10.html)
DK (1) DK0577302T3 (cg-RX-API-DMAC10.html)
ES (1) ES2105114T3 (cg-RX-API-DMAC10.html)
GR (1) GR3024975T3 (cg-RX-API-DMAC10.html)
HU (1) HU216832B (cg-RX-API-DMAC10.html)
IL (1) IL106077A (cg-RX-API-DMAC10.html)
MX (1) MX9303712A (cg-RX-API-DMAC10.html)
TW (1) TW224101B (cg-RX-API-DMAC10.html)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA41261C2 (uk) * 1992-06-22 2001-09-17 Елі Ліллі Енд Компані Спосіб одержання збагачених бета-аномером нуклеозидів
RU2131880C1 (ru) * 1992-06-22 1999-06-20 Эли Лилли Энд Компани Способ получения обогащенных бета-аномером нуклеозидов
IL106075A (en) * 1992-06-22 2000-12-06 Lilly Co Eli Process for preparing alpha-anomer enriched 1-halo-2-deoxy-2,2-difluoro-alpha-D-erythropentofuranose derivatives
US5424416A (en) * 1993-08-25 1995-06-13 Eli Lilly And Company Process for preparation of 2-deoxy-2,2-difluoro-D-ribofuranosyl-3,5-hydroxy protected-1-alkyl and aryl sulfonates and their use in preparation of 2',2'-difluoro-2'-deoxy nucleosides
US7214791B2 (en) * 2004-07-01 2007-05-08 Shenzhen Hande Technology Co., Ltd. Method for preparation of 2′-deoxy-2′, 2′-difluoro-β-cytidine or pharmaceutically acceptable salts thereof by using 1,6-anhydro-β-d-glucose as raw material
CN101023094B (zh) 2004-07-21 2011-05-18 法莫赛特股份有限公司 烷基取代的2-脱氧-2-氟代-d-呋喃核糖基嘧啶和嘌呤及其衍生物的制备
AU2005285045B2 (en) 2004-09-14 2011-10-13 Gilead Sciences, Inc. Preparation of 2'fluoro-2'- alkyl- substituted or other optionally substituted ribofuranosyl pyrimidines and purines and their derivatives
AU2005328519B2 (en) * 2005-03-04 2012-03-01 Fresenius Kabi Oncology Limited Intermediate and process for preparing of beta- anomer enriched 21deoxy, 21 ,21-difluoro-D-ribofuranosyl nucleosides
AU2011202539B2 (en) * 2005-06-03 2012-07-05 Scinopharm Taiwan, Ltd. Process of making an alpha-anomer enriched 2-deoxy-2,2-difluoro-d-ribofuranosyl sulfonate and use thereof for making a beta nucleoside
JP5091126B2 (ja) * 2005-06-03 2012-12-05 シノファーム タイワン，リミテッド α−アノマーが濃厚な２−デオキシ−２，２−ジフロロ−Ｄ−リボフラノシルスルホネートの製造方法およびβヌクレオシドを製造するためのその使用
AT502221A1 (de) * 2005-07-20 2007-02-15 Pharmacon Forschung & Beratung Gmbh Homogemcitabine, verfahren zu ihrer herstellung sowie deren verwendung
WO2007092705A2 (en) * 2006-02-07 2007-08-16 Chemagis Ltd. Process for preparing gemcitabine and associated intermediates
US20070249823A1 (en) * 2006-04-20 2007-10-25 Chemagis Ltd. Process for preparing gemcitabine and associated intermediates
US7964580B2 (en) 2007-03-30 2011-06-21 Pharmasset, Inc. Nucleoside phosphoramidate prodrugs
CN101024667B (zh) * 2007-03-30 2011-01-26 湖北益泰药业有限公司 盐酸吉西他宾的合成方法
US20080262215A1 (en) * 2007-04-23 2008-10-23 Chemagis Ltd. Gemcitabine production process
US8173621B2 (en) 2008-06-11 2012-05-08 Gilead Pharmasset Llc Nucleoside cyclicphosphates
AU2009329872B2 (en) 2008-12-23 2016-07-07 Gilead Pharmasset Llc Synthesis of purine nucleosides
US8618076B2 (en) 2009-05-20 2013-12-31 Gilead Pharmasset Llc Nucleoside phosphoramidates
TWI598358B (zh) 2009-05-20 2017-09-11 基利法瑪席特有限責任公司 核苷磷醯胺
CA2794671C (en) 2010-03-31 2018-05-01 Gilead Pharmasset Llc Stereoselective synthesis of phosphorus containing actives
US8563530B2 (en) 2010-03-31 2013-10-22 Gilead Pharmassel LLC Purine nucleoside phosphoramidate
EP2646453A1 (en) 2010-11-30 2013-10-09 Gilead Pharmasset LLC Compounds
US8889159B2 (en) 2011-11-29 2014-11-18 Gilead Pharmasset Llc Compositions and methods for treating hepatitis C virus
CN102603838B (zh) * 2012-02-14 2015-02-18 江苏八巨药业有限公司 一种制备吉西他滨盐酸盐的方法
EP3650014B1 (en) 2013-08-27 2021-10-06 Gilead Pharmasset LLC Combination formulation of two antiviral compounds
CN103692332B (zh) * 2013-12-31 2015-12-09 景宁畲族自治县通用机械配件厂（普通合伙） 全自动抛光除油机
CN107793334A (zh) * 2017-09-27 2018-03-13 九江善水科技股份有限公司 芳基磺酸铵盐化合物、其制备方法及应用

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4526988A (en) * 1983-03-10 1985-07-02 Eli Lilly And Company Difluoro antivirals and intermediate therefor
ES2157289T3 (es) * 1987-08-28 2001-08-16 Lilly Co Eli Procedimiento para la preparacion de 2'-desoxi-2',2'-difluoronucleosidos.
US4965374A (en) * 1987-08-28 1990-10-23 Eli Lilly And Company Process for and intermediates of 2',2'-difluoronucleosides

Also Published As

Publication number Publication date
DK0577302T3 (da) 1997-10-06
HU9301825D0 (en) 1993-09-28
EP0577302A1 (en) 1994-01-05
DE69312176T2 (de) 1997-12-11
US5256798A (en) 1993-10-26
MX9303712A (es) 1994-05-31
EP0577302B1 (en) 1997-07-16
BR9302429A (pt) 1994-01-11
CA2098882A1 (en) 1993-12-23
DE69312176D1 (de) 1997-08-21
TW224101B (cg-RX-API-DMAC10.html) 1994-05-21
IL106077A0 (en) 1993-10-20
GR3024975T3 (en) 1998-01-30
JP3379993B2 (ja) 2003-02-24
IL106077A (en) 1998-07-15
JPH0656865A (ja) 1994-03-01
CA2098882C (en) 2004-05-04
ATE155476T1 (de) 1997-08-15
HU216832B (hu) 1999-09-28
HUT65207A (en) 1994-05-02

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