SG106657A1 - Nycleotide analog composition and sythesis method - Google Patents

Nycleotide analog composition and sythesis method

Info

Publication number
SG106657A1
SG106657A1 SG200200487A SG200200487A SG106657A1 SG 106657 A1 SG106657 A1 SG 106657A1 SG 200200487 A SG200200487 A SG 200200487A SG 200200487 A SG200200487 A SG 200200487A SG 106657 A1 SG106657 A1 SG 106657A1
Authority
SG
Singapore
Prior art keywords
pmpa
composition
diethyl
useful
nycleotide
Prior art date
Application number
SG200200487A
Other languages
English (en)
Inventor
John D Munger Jr
John C Rohloff
Lisa M Schultze
Original Assignee
Gilead Sciences Inc
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=26732232&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG106657(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from US08/900,752 external-priority patent/US5935946A/en
Application filed by Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of SG106657A1 publication Critical patent/SG106657A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C07F9/65616—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/20—Antivirals for DNA viruses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32—Nitrogen atom
    • C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
SG200200487A 1997-07-25 1998-07-23 Nycleotide analog composition and sythesis method SG106657A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US5377797P 1997-07-25 1997-07-25
US08/900,752 US5935946A (en) 1997-07-25 1997-07-25 Nucleotide analog composition and synthesis method

Publications (1)

Publication Number Publication Date
SG106657A1 true SG106657A1 (en) 2004-10-29

Family

ID=26732232

Family Applications (2)

Application Number Title Priority Date Filing Date
SG200200487A SG106657A1 (en) 1997-07-25 1998-07-23 Nycleotide analog composition and sythesis method
SG200200438A SG106656A1 (en) 1997-07-25 1998-07-23 Nucleotide analog composition and synthesis method

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG200200438A SG106656A1 (en) 1997-07-25 1998-07-23 Nucleotide analog composition and synthesis method

Country Status (19)

Country Link
EP (1) EP0998480B1 (ja)
JP (7) JP4173202B2 (ja)
KR (3) KR100661153B1 (ja)
CN (2) CN1251679C (ja)
AT (3) ATE305009T1 (ja)
AU (1) AU756793B2 (ja)
BR (1) BR9811045A (ja)
CA (1) CA2298059C (ja)
DE (3) DE69831694T2 (ja)
DK (2) DK0998480T3 (ja)
ES (3) ES2187989T3 (ja)
HK (3) HK1029793A1 (ja)
ID (1) ID24701A (ja)
IN (1) IN190780B (ja)
NZ (1) NZ501287A (ja)
PT (2) PT998480E (ja)
SG (2) SG106657A1 (ja)
TW (2) TWI224103B (ja)
WO (1) WO1999005150A1 (ja)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0998480B1 (en) * 1997-07-25 2002-11-27 Gilead Sciences, Inc. Nucleotide analog composition and synthesis method
GB0013407D0 (en) * 2000-06-02 2000-07-26 Astrazeneca Ab Forms of a chemical compound
HRP20160074B1 (hr) * 2000-07-21 2021-09-03 Gilead Sciences, Inc. Prolijekovi koji su fosfonatni analozi nukleotida i metode njihovog odabira te njihova priprava
UA93354C2 (ru) * 2004-07-09 2011-02-10 Гилиад Сайенсиз, Инк. Местный противовирусный препарат
TWI471145B (zh) 2005-06-13 2015-02-01 Bristol Myers Squibb & Gilead Sciences Llc 單一式藥學劑量型
CN100352823C (zh) * 2005-08-19 2007-12-05 浙江车头制药有限公司 一种腺嘌呤衍生物的制备方法
CN100396689C (zh) * 2006-03-07 2008-06-25 中国医学科学院医药生物技术研究所 一组具有抑制hiv-1/hbv病毒复制活性的替诺福韦单酯化合物
EP2046792B1 (en) 2006-07-12 2015-02-25 Mylan Laboratories Limited Process for the preparation of tenofovir
WO2008143500A1 (en) 2007-05-22 2008-11-27 Ultimorphix Technologies B.V. Tenofovir disoproxil hemi-fumaric acid co-crystal
WO2010026603A2 (en) * 2008-09-05 2010-03-11 Matrix Laboratories Limited Novel amine salts of tenofovir, process for producing the same and use thereof in production of tenofovir dioproxil
CN101906119B (zh) * 2009-06-03 2012-12-26 中国人民解放军军事医学科学院毒物药物研究所 制备替诺福韦的新方法
EP2389929A1 (en) 2010-05-30 2011-11-30 Abdi Ibrahim Ilac Sanayi ve Ticaret Anonim Sirketi Pharmaceutical formulations of tenofovir
EP2697238B1 (en) 2011-04-08 2019-03-20 Laurus Labs Limited Solid forms of antiretroviral compounds, process for the preparation and their pharmaceutical composition thereof
CN102295660A (zh) * 2011-07-04 2011-12-28 常州大学 泰诺福韦的合成工艺
UA115311C2 (uk) 2011-08-16 2017-10-25 Гіліад Сайєнсіз, Інк. Геміфумарат тенофовіру алафенаміду
CN103626803B (zh) * 2012-08-23 2017-12-15 四川海思科制药有限公司 替诺福韦二吡呋酯的固体及其制备方法和用途
CN107312039B (zh) 2012-08-30 2019-06-25 江苏豪森药业集团有限公司 一种替诺福韦前药的制备方法
CN103230404A (zh) * 2013-05-14 2013-08-07 福建广生堂药业股份有限公司 替诺福韦二吡呋酯或其药用盐的新用途
EP2860184B1 (en) 2013-10-09 2018-08-29 Zentiva, k.s. Dihydrogenphosphate salt of Tenofovir disoproxil
EP2860185A1 (en) 2013-10-09 2015-04-15 Zentiva, k.s. An improved process for the preparation of Tenofovir disoproxil and pharmaceutically acceptable salts thereof
CN103483385B (zh) * 2013-10-11 2015-11-18 福建广生堂药业股份有限公司 替诺福韦单酯富马酸盐的新晶型及其制备方法
CN104688747B (zh) * 2013-12-04 2019-04-12 重庆药友制药有限责任公司 包含富马酸替诺福韦二吡呋酯的药物组合物
CN104725423A (zh) * 2013-12-18 2015-06-24 山东新时代药业有限公司 一种富马酸替诺福韦二吡呋酯的合成方法
CN103705478B (zh) * 2013-12-23 2020-02-07 浙江华海药业股份有限公司 含有富马酸替诺福韦二吡呋酯的口服片剂
CN104744512B (zh) * 2013-12-26 2017-01-11 成都伊诺达博医药科技有限公司 一种“一锅法”制备泰诺福韦的新工艺
KR20160003532A (ko) 2014-07-01 2016-01-11 한미약품 주식회사 테노포비어 디소프록실 인산염과, 비금속염 붕해제 및 비금속염 활택제를 포함하는 약학 조성물
CN104288118A (zh) * 2014-07-08 2015-01-21 南京卡文迪许生物工程技术有限公司 富马酸替诺福韦二吡呋酯片剂及其制备方法
CN106687467A (zh) * 2014-09-30 2017-05-17 韩美精密化学株式会社 高纯度（r）‑9‑[2‑（磷酰甲氧基）丙基]腺嘌呤的制备方法
CN106046055A (zh) * 2016-05-27 2016-10-26 湖北丽益医药科技有限公司 R‑9‑(2‑膦酰甲氧基丙基)‑腺嘌呤一水合物晶体及制备、富马酸替诺福韦二吡呋酯制备
KR101909570B1 (ko) 2016-12-05 2018-10-19 (주) 성운파마코피아 고순도 테노포비어 디소프록실 제조방법
CN108358968B (zh) * 2018-04-03 2020-09-15 科兴生物制药股份有限公司 一种替诺福韦的制备方法
CN109942634A (zh) * 2019-01-24 2019-06-28 深圳科兴药业有限公司 一种富马酸替诺福韦二吡呋酯的晶型i及制备方法和应用
CN110507625A (zh) * 2019-09-19 2019-11-29 苏州东瑞制药有限公司 一种新型富马酸替诺福韦酯片及其制备方法
CN111939134B (zh) * 2020-08-24 2023-02-17 山东罗欣药业集团股份有限公司 一种抗病毒药物组合物
KR20220141457A (ko) 2021-04-13 2022-10-20 경동제약 주식회사 신규 결정형의 테노포비어 알라펜아미드 말레산염 및 이를 포함하는 약제학적 조성물

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CS263951B1 (en) * 1985-04-25 1989-05-12 Antonin Holy 9-(phosponylmethoxyalkyl)adenines and method of their preparation
US6057305A (en) * 1992-08-05 2000-05-02 Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic Antiretroviral enantiomeric nucleotide analogs
CA2126601A1 (en) * 1993-06-29 1994-12-30 Mitsubishi Chemical Corporation Phosphonate-nucleotide ester derivatives
JP4033494B2 (ja) * 1996-07-26 2008-01-16 ギリヤド サイエンシーズ， インコーポレイテッド ヌクレオチドアナログ
EP0998480B1 (en) * 1997-07-25 2002-11-27 Gilead Sciences, Inc. Nucleotide analog composition and synthesis method

Also Published As

Publication number Publication date
ATE288914T1 (de) 2005-02-15
CN100383148C (zh) 2008-04-23
JP2013213071A (ja) 2013-10-17
JP2017057233A (ja) 2017-03-23
DE69809750D1 (de) 2003-01-09
NZ501287A (en) 2001-09-28
JP2008208126A (ja) 2008-09-11
SG106656A1 (en) 2004-10-29
JP5398662B2 (ja) 2014-01-29
DE69809750T2 (de) 2003-08-21
DE69829010D1 (de) 2005-03-17
EP0998480A1 (en) 2000-05-10
HK1051360B (zh) 2005-10-14
TWI224103B (en) 2004-11-21
HK1029793A1 (en) 2001-04-12
PT1243590E (pt) 2005-05-31
CN1554350A (zh) 2004-12-15
ID24701A (id) 2000-08-03
IN190780B (ja) 2003-08-23
KR20010022067A (ko) 2001-03-15
KR100617608B1 (ko) 2006-09-01
DE69829010T2 (de) 2006-04-13
CN1251679C (zh) 2006-04-19
JP2015199773A (ja) 2015-11-12
ATE305009T1 (de) 2005-10-15
HK1051373B (zh) 2006-04-07
DK1243593T3 (da) 2005-11-14
JP2002511098A (ja) 2002-04-09
AU756793B2 (en) 2003-01-23
CN1264387A (zh) 2000-08-23
HK1051360A1 (en) 2003-08-01
AU8582798A (en) 1999-02-16
TWI242561B (en) 2005-11-01
DK0998480T3 (da) 2003-03-24
TW200510438A (en) 2005-03-16
EP0998480B1 (en) 2002-11-27
JP4628437B2 (ja) 2011-02-09
WO1999005150A1 (en) 1999-02-04
HK1051373A1 (en) 2003-08-01
ES2236389T3 (es) 2005-07-16
PT998480E (pt) 2003-03-31
DE69831694T2 (de) 2006-07-13
DE69831694D1 (de) 2005-10-27
ATE228526T1 (de) 2002-12-15
JP2018016645A (ja) 2018-02-01
JP4173202B2 (ja) 2008-10-29
KR20060038452A (ko) 2006-05-03
ES2249511T3 (es) 2006-04-01
ES2187989T3 (es) 2003-06-16
BR9811045A (pt) 2000-08-22
JP2010280694A (ja) 2010-12-16
KR100707505B1 (ko) 2007-04-16
CA2298059A1 (en) 1999-02-04
CA2298059C (en) 2008-12-30
KR100661153B1 (ko) 2006-12-26
KR20060038451A (ko) 2006-05-03

Similar Documents

Publication Publication Date Title
SG106657A1 (en) Nycleotide analog composition and sythesis method
JP4169365B2 (ja) 不能症を処置するための、ｃＧＭＰ−ホスフォジエステラーゼインヒビターの用途
ES8800157A1 (es) Un procedimiento para preparar derivados de tironina
AU7929491A (en) New 4-aminobutyric acid compunds process for the preparation thereof and pharmaceutical preparations containing them
GR3018387T3 (en) Fluorinated bile acid derivatives, processes for the preparation thereof and pharmaceutical compositions containing them.
AU1428801A (en) Novel (1,2,3)-triazolo(4,5-D)pyrimidine compounds
Murakami et al. Escherichia coli mediated biosynthesis and in vitro anti-HIV activity of lipophilic 6-halo-2', 3'-dideoxypurine nucleosides
Aoyagi et al. Deglycobleomycin: total synthesis and oxygen transfer properties of an active bleomycin analog
Jung et al. Rapid and efficient stereocontrolled synthesis of C-3′-ethynyl ribo and xylonucleosides by organocerium additions to 3′-ketonucleosides
Wojtkowski et al. . beta.-Thionolactam analogs of cephalosporins and penicillins
DE3573119D1 (en) 8-alkylthio-2-piperazino-pyrimidoû5,4-d¨pyrimidines, their preparation and medicaments containing them
MY103569A (en) Novel 2, 5-disubstituted dithianes having pesticidal activity, methods for their production and for their use
CA2605226A1 (en) Nucleotide analog composition and synthesis method
GB2084152A (en) Antiviral agents their preparation and use
AU6826700A (en) Ceramide analogs, process for their preparation and their use as antitumor agents
ATE34176T1 (de) 2'-chloropentostatin, eine diese verbindung enthaltende pharmazeutische zusammensetzung und ein mikroorganismus zur herstellung dieser verbindung.
IL89140A (en) 4-oxo-4h-pyrido(1,2-a) pyrimidine-3-carboxamides and 3-acetamides, pharmaceutical compositions containing them and process for preparing same
Bienkowski et al. Synthesis of malondialdehyde‐1, 2, 3‐14C3 via ethyl vinyl‐[1, 2‐14C2] ether
Shiue et al. 125 I-β-iodo-D-alanine-synthesis, biodistribution and antimicrobial activity
EP0301834A3 (en) Derivatives of benzoyloxyacetic acid, and preparation and formulations thereof for therapeutic use