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IS3873A - Hliðstæð aðferð til framleiðslu á kristölluðum oxaþíólan afleiðum - Google Patents

Hliðstæð aðferð til framleiðslu á kristölluðum oxaþíólan afleiðum

Info

Publication number
IS3873A
IS3873A IS3873A IS3873A IS3873A IS 3873 A IS3873 A IS 3873A IS 3873 A IS3873 A IS 3873A IS 3873 A IS3873 A IS 3873A IS 3873 A IS3873 A IS 3873A
Authority
IS
Iceland
Prior art keywords
oxathiol
crystalline
derivatives
production
analogous method
Prior art date
Application number
IS3873A
Other languages
English (en)
Other versions
IS1867B (is
Inventor
Ravenscroft Paul
Evans Paul
Original Assignee
Glaxo Group Limited
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10696001&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IS3873(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glaxo Group Limited filed Critical Glaxo Group Limited
Publication of IS3873A publication Critical patent/IS3873A/is
Publication of IS1867B publication Critical patent/IS1867B/is

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D411/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D411/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D411/04Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Secondary Cells (AREA)
IS3873A 1991-06-03 1992-06-02 Hliðstæð aðferð til framleiðslu á kristölluðum oxaþíólan afleiðum IS1867B (is)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB919111902A GB9111902D0 (en) 1991-06-03 1991-06-03 Chemical compounds

Publications (2)

Publication Number Publication Date
IS3873A true IS3873A (is) 1992-12-04
IS1867B IS1867B (is) 2003-05-02

Family

ID=10696001

Family Applications (2)

Application Number Title Priority Date Filing Date
IS3873A IS1867B (is) 1991-06-03 1992-06-02 Hliðstæð aðferð til framleiðslu á kristölluðum oxaþíólan afleiðum
IS4268A IS4268A (is) 1991-06-03 1992-12-04 Kristallaðar oxathiolane afleiður

Family Applications After (1)

Application Number Title Priority Date Filing Date
IS4268A IS4268A (is) 1991-06-03 1992-12-04 Kristallaðar oxathiolane afleiður

Country Status (30)

Country Link
US (1) US5905082A (is)
EP (2) EP0517145B1 (is)
JP (1) JP2851480B2 (is)
KR (1) KR100244008B1 (is)
AP (1) AP300A (is)
AT (1) ATE212630T1 (is)
AU (2) AU656379B2 (is)
BG (1) BG60914B1 (is)
CA (2) CA2311988C (is)
CZ (1) CZ284513B6 (is)
DE (1) DE69232387T2 (is)
DK (1) DK0517145T3 (is)
ES (1) ES2171158T3 (is)
GB (1) GB9111902D0 (is)
GE (1) GEP19991834B (is)
IE (2) IE921780A1 (is)
IL (1) IL102073A (is)
IS (2) IS1867B (is)
MX (1) MX9202619A (is)
NO (1) NO301713B1 (is)
NZ (1) NZ242981A (is)
OA (1) OA09913A (is)
PT (1) PT517145E (is)
RU (1) RU2102393C1 (is)
SG (1) SG52455A1 (is)
SK (1) SK281249B6 (is)
TW (1) TW254939B (is)
UA (1) UA41265C2 (is)
WO (1) WO1992021676A1 (is)
ZA (1) ZA924007B (is)

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US6069252A (en) * 1990-02-01 2000-05-30 Emory University Method of resolution and antiviral activity of 1,3-oxathiolane nucleoside enantiomers
US5276151A (en) * 1990-02-01 1994-01-04 Emory University Method of synthesis of 1,3-dioxolane nucleosides
US5914331A (en) 1990-02-01 1999-06-22 Emory University Antiviral activity and resolution of 2-hydroxymethyl-5-(5-fluorocytosin-1-yl)-1,3-oxathiolane
US5204466A (en) * 1990-02-01 1993-04-20 Emory University Method and compositions for the synthesis of bch-189 and related compounds
US5444063A (en) * 1990-12-05 1995-08-22 Emory University Enantiomerically pure β-D-dioxolane nucleosides with selective anti-Hepatitis B virus activity
US6812233B1 (en) 1991-03-06 2004-11-02 Emory University Therapeutic nucleosides
US5817667A (en) * 1991-04-17 1998-10-06 University Of Georgia Research Foudation Compounds and methods for the treatment of cancer
GB9116601D0 (en) * 1991-08-01 1991-09-18 Iaf Biochem Int 1,3-oxathiolane nucleoside analogues
US6177435B1 (en) 1992-05-13 2001-01-23 Glaxo Wellcome Inc. Therapeutic combinations
US20020120130A1 (en) 1993-09-10 2002-08-29 Gilles Gosselin 2' or 3' -deoxy and 2', 3' -dideoxy-beta-L-pentofuranonucleo-side compounds, method of preparation and application in therapy, especially as anti- viral agents
US5587362A (en) * 1994-01-28 1996-12-24 Univ. Of Ga Research Foundation L-nucleosides
IL115156A (en) 1994-09-06 2000-07-16 Univ Georgia Pharmaceutical compositions for the treatment of cancer comprising 1-(2-hydroxymethyl-1,3-dioxolan-4-yl) cytosines
US6391859B1 (en) 1995-01-27 2002-05-21 Emory University [5-Carboxamido or 5-fluoro]-[2′,3′-unsaturated or 3′-modified]-pyrimidine nucleosides
US5703058A (en) 1995-01-27 1997-12-30 Emory University Compositions containing 5-fluoro-2',3'-didehydro-2',3'-dideoxycytidine or a mono-, di-, or triphosphate thereof and a second antiviral agent
US5808040A (en) * 1995-01-30 1998-09-15 Yale University L-nucleosides incorporated into polymeric structure for stabilization of oligonucleotides
JP4413996B2 (ja) 1995-06-07 2010-02-10 エモリー・ユニバーシティ 抗b型肝炎ウィルス活性を有するヌクレオシド
US5914332A (en) * 1995-12-13 1999-06-22 Abbott Laboratories Retroviral protease inhibiting compounds
CA2258956A1 (en) 1996-06-25 1997-12-31 Glaxo Group Limited Combinations comprising vx478, zidovudine, ftc and/or 3tc for use in the treatment of hiv
US5753789A (en) * 1996-07-26 1998-05-19 Yale University Oligonucleotides containing L-nucleosides
TW536403B (en) * 1997-03-24 2003-06-11 Glaxo Group Ltd An ethanol and ethylenediaminetetraacetic acid free pharmaceutical composition comprising lamivudine and exhibiting antimicrobial preservative efficacy
US6436948B1 (en) 2000-03-03 2002-08-20 University Of Georgia Research Foundation Inc. Method for the treatment of psoriasis and genital warts
US6723728B2 (en) * 2001-03-01 2004-04-20 Gilead Sciences, Inc. Polymorphic and other crystalline forms cis-FTC
CA2351049C (en) 2001-06-18 2007-03-13 Brantford Chemicals Inc. Process for recovery of the desired cis-1,3-oxathiolane nucleosides from their undesired trans-isomers
WO2003027106A1 (en) * 2001-09-25 2003-04-03 Cadila Healthcar Limited Process for the preparation of crystalline polymorph ii of lamivudine
EP1490090A4 (en) 2002-02-22 2006-09-20 New River Pharmaceuticals Inc SYSTEMS FOR DELIVERING ACTIVE AGENTS AND METHODS FOR PROTECTING AND DELIVERING ACTIVE AGENTS
CA2505130C (en) * 2002-11-08 2009-10-06 Glaxo Group Limited Pharmaceutical compositions
KR20080032014A (ko) 2003-01-14 2008-04-11 길리애드 사이언시즈, 인코포레이티드 복합 항바이러스 치료를 위한 조성물 및 방법
KR101330626B1 (ko) * 2004-11-10 2013-11-18 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 탈아미드화된 인터페론-베타
US20060242012A1 (en) * 2005-04-22 2006-10-26 Sumit Agarwal Determining or scoring properties to solicit to join ad network using advertiser or aggregated advertiser interest
TWI375560B (en) 2005-06-13 2012-11-01 Gilead Sciences Inc Composition comprising dry granulated emtricitabine and tenofovir df and method for making the same
TWI471145B (zh) 2005-06-13 2015-02-01 Bristol Myers Squibb & Gilead Sciences Llc 單一式藥學劑量型
AU2007237818B2 (en) * 2006-04-18 2012-09-27 Lupin Limited A novel crystalline form of lamivudine
AR068374A1 (es) * 2007-09-06 2009-11-11 Combino Pharm Sl Nuevas composiciones farmaceuticas del complejo lamivudina beta - ciclodextrina
US20100190982A1 (en) * 2007-09-17 2010-07-29 Janardhana Rao Vascuri Process for the preparation of lamivudine form i
WO2009069013A1 (en) * 2007-11-29 2009-06-04 Ranbaxy Laboratories Limited Crystalline form i of lamivudine and its preparation
SI2225232T1 (sl) * 2007-11-29 2012-12-31 Ranbaxy Laboratories Limited Postopek za pripravo substituiranih 1,3-oksatiolanov
WO2009069012A1 (en) * 2007-11-29 2009-06-04 Ranbaxy Laboratories Limited Process and intermediates for the preparation of substituted 1, 3-oxathiolanes, especially lamivudine
WO2009127996A1 (en) * 2008-04-17 2009-10-22 Ranbaxy Laboratories Limited Novel crystalline form of lamivudine
WO2010023676A2 (en) * 2008-09-01 2010-03-04 Hetero Research Foundation Process for preparing lamivudine polymorph form
US20110288298A1 (en) * 2008-11-12 2011-11-24 Lupin Limited novel polymorph of emtricitabine and a process for preparing of the same
CN101531656B (zh) * 2009-03-24 2010-12-08 福建广生堂药业有限公司 拉米夫定晶型及其制备方法
CN101993439B (zh) * 2009-03-24 2013-04-24 福建广生堂药业股份有限公司 拉米夫定晶型及其制备方法
EP2435052B1 (en) * 2009-05-27 2015-07-15 Hetero Research Foundation Solid oral dosage forms of lamivudine with isomalt
US8710218B2 (en) 2009-07-15 2014-04-29 Lupin Limited Process for preparation of Efavirenz
ES2540074T3 (es) 2009-10-14 2015-07-08 Mylan Laboratories Limited Proceso para la preparación de lamivudina y nuevas sales en la fabricación de la misma
LT3494972T (lt) 2010-01-27 2024-03-12 Viiv Healthcare Company Dolutegraviro ir lamivudino kompozicija živ infekcijai gydyti
WO2011095987A1 (en) * 2010-02-03 2011-08-11 Matrix Laboratories Ltd. Novel process for the preparation of cis-nucleoside derivative
US8796452B2 (en) 2010-02-12 2014-08-05 Merck Sharp & Dohme Corp. Preparation of lamivudine form I
CN104203275A (zh) 2010-06-09 2014-12-10 疫苗技术股份有限公司 用于增强抗逆转录病毒治疗的hiv感染者的治疗性免疫
WO2013021290A1 (en) 2011-08-05 2013-02-14 Lupin Limited A stereoselective process for preparation of 1,3-oxathiolane nucleosides
WO2013168066A1 (en) 2012-05-05 2013-11-14 Lupin Limited An improved process for the manufacture of lamivudine form i.
CN114099454B (zh) * 2020-08-31 2023-06-27 长春海悦药业股份有限公司 一种拉米夫定片及其制备方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
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US5047407A (en) * 1989-02-08 1991-09-10 Iaf Biochem International, Inc. 2-substituted-5-substituted-1,3-oxathiolanes with antiviral properties
NZ228645A (en) * 1988-04-11 1991-09-25 Iaf Biochem Int 1,3-dioxolane derivatives substituted in the 5th position by a purine or pyrimidine radical; treatment of viral infections
US5204466A (en) * 1990-02-01 1993-04-20 Emory University Method and compositions for the synthesis of bch-189 and related compounds
GB9009861D0 (en) * 1990-05-02 1990-06-27 Glaxo Group Ltd Chemical compounds
US5179104A (en) * 1990-12-05 1993-01-12 University Of Georgia Research Foundation, Inc. Process for the preparation of enantiomerically pure β-D-(-)-dioxolane-nucleosides
US5248776A (en) * 1990-12-05 1993-09-28 University Of Georgia Research Foundation, Inc. Process for enantiomerically pure β-L-1,3-oxathiolane nucleosides
JPH04358486A (ja) * 1991-06-04 1992-12-11 Toshiba Corp 高能率符号化信号処理装置

Also Published As

Publication number Publication date
AU1881092A (en) 1993-01-08
US5905082A (en) 1999-05-18
RU2102393C1 (ru) 1998-01-20
ES2171158T3 (es) 2002-09-01
IS1867B (is) 2003-05-02
NO922182L (no) 1992-12-04
UA41265C2 (uk) 2001-09-17
NZ242981A (en) 1994-04-27
TW254939B (is) 1995-08-21
CZ284513B6 (cs) 1998-12-16
CA2311988C (en) 2005-11-15
CA2311988A1 (en) 1992-12-04
AP9200395A0 (en) 1992-07-31
ATE212630T1 (de) 2002-02-15
EP1099700A1 (en) 2001-05-16
AP300A (en) 1994-01-20
BG60914B1 (bg) 1996-06-28
OA09913A (en) 1994-09-15
IL102073A0 (en) 1993-01-14
CA2070230C (en) 2004-08-03
IE20020782A1 (en) 2003-04-02
KR930000511A (ko) 1993-01-15
CZ261293A3 (en) 1994-04-13
GEP19991834B (en) 1999-11-05
IE921780A1 (en) 1992-12-16
WO1992021676A1 (en) 1992-12-10
NO922182D0 (no) 1992-06-02
HK1009599A1 (en) 1999-06-04
JP2851480B2 (ja) 1999-01-27
DE69232387T2 (de) 2002-09-26
IL102073A (en) 1996-05-14
CA2070230A1 (en) 1992-12-04
JPH06211848A (ja) 1994-08-02
AU1736192A (en) 1993-03-11
BG98254A (bg) 1994-07-29
GB9111902D0 (en) 1991-07-24
IS4268A (is) 1995-02-27
ZA924007B (en) 1993-04-28
EP0517145A1 (en) 1992-12-09
SG52455A1 (en) 1998-09-28
EP0517145B1 (en) 2002-01-30
DE69232387D1 (de) 2002-03-14
SK281249B6 (sk) 2001-01-18
NO301713B1 (no) 1997-12-01
AU656379B2 (en) 1995-02-02
DK0517145T3 (da) 2002-05-06
SK125793A3 (en) 1994-11-09
KR100244008B1 (ko) 2000-03-02
PT517145E (pt) 2002-07-31
MX9202619A (es) 1992-12-01

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