CR20140204A - Métodos para preparar análogos nucleotídicos antivirales - Google Patents

Métodos para preparar análogos nucleotídicos antivirales

Info

Publication number
CR20140204A
CR20140204A CR20140204A CR20140204A CR20140204A CR 20140204 A CR20140204 A CR 20140204A CR 20140204 A CR20140204 A CR 20140204A CR 20140204 A CR20140204 A CR 20140204A CR 20140204 A CR20140204 A CR 20140204A
Authority
CR
Costa Rica
Prior art keywords
methods
nucleotytic
analogs
prepare antiviral
antiviral
Prior art date
Application number
CR20140204A
Other languages
English (en)
Inventor
Denise A Colby
Andrew Anthony Martins
Benjamin James Roberts
Robert William Scott
Nicole S White
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
Application filed by Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of CR20140204A publication Critical patent/CR20140204A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic 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
    • C07F9/65616Heterocyclic 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
    • 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
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6509Six-membered rings
    • C07F9/6512Six-membered rings having the nitrogen atoms in positions 1 and 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Métodos para aislar 9-{(R)-2-[((S)-{[S)-1-(isopropoxicarbonil)etil]amino]-fenoxifosfinil)metoxi]propil}adenina (compuesto 16).
CR20140204A 2011-10-07 2014-05-05 Métodos para preparar análogos nucleotídicos antivirales CR20140204A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161544950P 2011-10-07 2011-10-07

Publications (1)

Publication Number Publication Date
CR20140204A true CR20140204A (es) 2014-06-03

Family

ID=47297386

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20140204A CR20140204A (es) 2011-10-07 2014-05-05 Métodos para preparar análogos nucleotídicos antivirales

Country Status (25)

Country Link
US (4) US8664386B2 (es)
EP (2) EP2764002B1 (es)
JP (2) JP6190372B2 (es)
KR (3) KR102033802B1 (es)
CN (4) CN103842366B (es)
AR (1) AR088109A1 (es)
AU (1) AU2012319172B2 (es)
BR (1) BR112014011340A2 (es)
CA (2) CA3042169C (es)
CL (1) CL2014000827A1 (es)
CO (1) CO6940431A2 (es)
CR (1) CR20140204A (es)
EA (1) EA027086B1 (es)
EC (1) ECSP14000074A (es)
ES (2) ES2746859T3 (es)
HK (3) HK1200834A1 (es)
IL (1) IL231879B (es)
MX (1) MX353064B (es)
PE (1) PE20141160A1 (es)
PL (1) PL3333173T3 (es)
PT (2) PT2764002T (es)
SI (1) SI3333173T1 (es)
TW (4) TWI557133B (es)
UY (1) UY34361A (es)
WO (1) WO2013052094A2 (es)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3070088A1 (en) 2011-08-16 2016-09-21 Gilead Sciences, Inc. Tenofovir alafenamide hemifumarate
KR102033802B1 (ko) * 2011-10-07 2019-10-17 길리애드 사이언시즈, 인코포레이티드 항-바이러스 뉴클레오티드 유사체의 제조 방법
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
WO2014195724A1 (en) * 2013-06-07 2014-12-11 Cipla Limited An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine
CN104628773B (zh) * 2013-11-06 2018-10-23 杭州和泽医药科技有限公司 (r)-9-[2-(磷酰苯酚基甲氧基)丙基]腺嘌呤的制备方法
WO2015079455A2 (en) * 2013-11-27 2015-06-04 Laurus Labs Private Limited A recycling process for preparing tenofovir alafenamide diastereomers
WO2015107451A2 (en) * 2014-01-14 2015-07-23 Mylan Laboratories Ltd. Purification of tenofovir alafenamide and its intermediates
TWI660965B (zh) 2014-01-15 2019-06-01 美商基利科學股份有限公司 泰諾福韋之固體形式
WO2015161781A1 (zh) * 2014-04-21 2015-10-29 四川海思科制药有限公司 一种核苷类似物及其中间体的制备方法
WO2015197006A1 (zh) * 2014-06-25 2015-12-30 四川海思科制药有限公司 一种取代的氨基酸硫酯类化合物、其组合物及应用
CN105399771B (zh) * 2014-07-21 2020-11-24 江苏豪森药业集团有限公司 替诺福韦前药晶型及其制备方法和用途
CN108191913A (zh) * 2014-11-12 2018-06-22 四川海思科制药有限公司 一种替诺福韦艾拉酚胺晶型a及其制备方法
CN104817593B (zh) * 2015-04-27 2016-11-16 广州同隽医药科技有限公司 半富马酸替诺福韦艾拉酚胺关键中间体的合成工艺
LT3331891T (lt) 2015-08-05 2022-02-25 Eisai R&D Management Co., Ltd. Iš esmės diastereomeriškai gryno fosforodiamidato oligomero gamybos būdas, tokiu būdu pagamintas fosforodiamidato oligomeras, ir farmacinė kompozicija, apimanti tokį fosforodiamidato oligomerą
TWI616452B (zh) * 2015-08-26 2018-03-01 Preparation method of nucleoside analog and intermediate thereof
CN105330700A (zh) * 2015-12-17 2016-02-17 中国药科大学 富马酸替诺福韦艾拉酚胺杂质的制备方法
WO2017118928A1 (en) 2016-01-06 2017-07-13 Lupin Limited Process for the separation of diastereomers of tenofovir alafenamide
CZ2016156A3 (cs) * 2016-03-17 2017-09-27 Zentiva, K.S. Způsob přípravy diastereomerně čistého Tenofoviru Alafenamidu nebo jeho solí
CN107286190A (zh) * 2016-04-13 2017-10-24 刘沛 核苷之烃氧基苄基氨基磷酸/膦酸酯衍生物的制备及其医药用途
CN109562107A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的杂环降解决定子体
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
CN106565785B (zh) * 2016-11-09 2019-11-12 周雨恬 一种具有抗hbv/hiv活性的核苷氨基磷酸酯类化合物及其盐和用途
CN106946935B (zh) * 2017-04-28 2020-01-07 福建广生堂药业股份有限公司 一种非对映异构体核苷衍生物的制备方法
EP3692041A1 (en) * 2017-10-04 2020-08-12 Celgene Corporation Processes for the preparation of cis-4 [2-{(3s.4r)-3-fluorooxan-4-yl]amino)-8-(2,4,6-trichloroanilino)-9h-purin-9-yl]-1-methylcyclohexane-1-carboxamide
CN109942633B (zh) * 2017-12-20 2021-08-31 上海新礼泰药业有限公司 替诺福韦艾拉酚胺中间体的制备方法
CN109942632B (zh) * 2017-12-20 2021-08-31 上海博志研新药物研究有限公司 替诺福韦艾拉酚胺中间体的制备方法
CN110092803A (zh) * 2018-01-31 2019-08-06 北京睿创康泰医药研究院有限公司 替诺福韦艾拉酚胺富马酸盐工艺杂质的制备及其应用
CN108409788B (zh) * 2018-03-12 2020-05-08 科兴生物制药股份有限公司 一种富马酸替诺福韦艾拉酚胺的制备方法
CN110305163A (zh) * 2018-03-27 2019-10-08 北京济美堂医药研究有限公司 替诺福韦艾拉酚胺半富马酸盐的制备方法
CN108467410B (zh) * 2018-04-09 2021-04-09 重庆三圣实业股份有限公司 一种taf中间体的制备方法及产品和应用
CN108484672A (zh) * 2018-05-23 2018-09-04 中国药科大学制药有限公司 磷丙替诺福韦的手性拆分方法
CN108822149B (zh) * 2018-06-01 2020-08-11 成都苑东生物制药股份有限公司 一种富马酸替诺福韦艾拉酚胺关键中间体的制备方法
CN110283208B (zh) * 2018-06-22 2022-07-08 南京济群医药科技股份有限公司 一种替诺福韦艾拉酚胺的手性拆分方法
CN109081853A (zh) * 2018-09-03 2018-12-25 南京正大天晴制药有限公司 一种磷丙替诺福韦有关物质的制备方法
CN111484527A (zh) * 2019-01-25 2020-08-04 上海清松制药有限公司 一种替诺福韦艾拉酚胺中间体的制备方法
CN111943981A (zh) * 2019-05-14 2020-11-17 博瑞生物医药泰兴市有限公司 一种磷丙替诺福韦的制备方法
CN112175003B (zh) * 2019-07-01 2022-02-15 上海医药工业研究院 一种苯基氢膦酸酯及其中间体的制备方法
US20220257619A1 (en) 2019-07-18 2022-08-18 Gilead Sciences, Inc. Long-acting formulations of tenofovir alafenamide
CN112390824B (zh) * 2019-08-19 2022-07-05 鲁南制药集团股份有限公司 一种替诺福韦艾拉酚胺中间体的制备方法
CN110981911A (zh) * 2019-10-08 2020-04-10 浙江车头制药股份有限公司 一种替诺福韦艾拉酚胺的制备方法
CN111171076A (zh) * 2019-12-26 2020-05-19 合肥启旸生物科技有限公司 一种替诺福韦二聚体的制备方法
WO2021188959A1 (en) 2020-03-20 2021-09-23 Gilead Sciences, Inc. Prodrugs of 4'-c-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same
KR20210125298A (ko) 2020-04-08 2021-10-18 주식회사 파마코스텍 테노포비어 알라펜아미드 헤미타르트레이트의 신규한 제조방법
US20220144923A1 (en) 2020-11-11 2022-05-12 Gilead Sciences, Inc. METHODS OF IDENTIFYING HIV PATIENTS SENSITIVE TO THERAPY WITH gp120 CD4 BINDING SITE-DIRECTED ANTIBODIES
KR20220141457A (ko) 2021-04-13 2022-10-20 경동제약 주식회사 신규 결정형의 테노포비어 알라펜아미드 말레산염 및 이를 포함하는 약제학적 조성물
TWI843506B (zh) 2022-04-06 2024-05-21 美商基利科學股份有限公司 橋聯三環胺甲醯基吡啶酮化合物及其用途
TW202402280A (zh) 2022-07-01 2024-01-16 美商基利科學股份有限公司 可用於hiv病毒感染之疾病預防性或治療性治療的治療性化合物
US20240083984A1 (en) 2022-08-26 2024-03-14 Gilead Sciences, Inc. Dosing and scheduling regimen for broadly neutralizing antibodies
US20240226130A1 (en) 2022-10-04 2024-07-11 Gilead Sciences, Inc. 4'-thionucleoside analogues and their pharmaceutical use

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2627903T3 (es) * 2000-07-21 2017-08-01 Gilead Sciences, Inc. Profármacos de análogos de nucleótidos de fosfonato y métodos para seleccionar y preparar los mismos
US20050239054A1 (en) 2002-04-26 2005-10-27 Arimilli Murty N Method and compositions for identifying anti-HIV therapeutic compounds
ES2363160T3 (es) 2004-07-27 2011-07-22 Gilead Sciences, Inc. Conjugados de fosfonato nucelosidico como agentes anti-vih.
WO2007126812A2 (en) * 2006-03-29 2007-11-08 Gilead Sciences, Inc. Process for preparation of hiv protease inhibitors
PT2038290E (pt) * 2006-07-07 2013-12-10 Gilead Sciences Inc Moduladores de receptor do tipo toll 7
EP2049547A2 (en) * 2006-07-21 2009-04-22 Gilead Sciences, Inc. Aza-peptide protease inhibitors
CA2658479A1 (en) * 2006-07-24 2008-02-07 Gilead Sciences, Inc. Novel hiv reverse transcriptase inhibitors
WO2009005693A1 (en) * 2007-06-29 2009-01-08 Gilead Sciences, Inc. Novel hiv reverse transcriptase inhibitors
EP3070088A1 (en) 2011-08-16 2016-09-21 Gilead Sciences, Inc. Tenofovir alafenamide hemifumarate
KR102033802B1 (ko) 2011-10-07 2019-10-17 길리애드 사이언시즈, 인코포레이티드 항-바이러스 뉴클레오티드 유사체의 제조 방법

Also Published As

Publication number Publication date
ECSP14000074A (es) 2016-01-29
JP6190372B2 (ja) 2017-08-30
KR102139440B1 (ko) 2020-07-29
KR102033802B1 (ko) 2019-10-17
BR112014011340A2 (pt) 2017-06-13
US9346841B2 (en) 2016-05-24
CN103842366A (zh) 2014-06-04
TW201716418A (zh) 2017-05-16
NZ624513A (en) 2016-06-24
EP2764002A2 (en) 2014-08-13
EP3333173A1 (en) 2018-06-13
KR20140090170A (ko) 2014-07-16
CN103842366B (zh) 2017-06-16
US20140128602A1 (en) 2014-05-08
JP2017160228A (ja) 2017-09-14
TW202003531A (zh) 2020-01-16
WO2013052094A2 (en) 2013-04-11
EA201490753A1 (ru) 2014-09-30
SI3333173T1 (sl) 2019-08-30
US20150291638A1 (en) 2015-10-15
KR20190086576A (ko) 2019-07-22
CA2850466A1 (en) 2013-04-11
TW201331218A (zh) 2013-08-01
MX2014003952A (es) 2014-08-01
TWI613211B (zh) 2018-02-01
WO2013052094A3 (en) 2013-06-20
CN107266498B (zh) 2023-10-03
CO6940431A2 (es) 2014-05-09
US9676804B2 (en) 2017-06-13
US20130090473A1 (en) 2013-04-11
CA2850466C (en) 2020-07-28
KR20200090975A (ko) 2020-07-29
US20160311840A1 (en) 2016-10-27
PT3333173T (pt) 2019-09-10
AU2012319172B2 (en) 2014-06-12
TW201811808A (zh) 2018-04-01
CN107266498A (zh) 2017-10-20
AR088109A1 (es) 2014-05-07
IL231879B (en) 2019-11-28
PL3333173T3 (pl) 2019-12-31
CA3042169C (en) 2021-09-07
PT2764002T (pt) 2018-05-16
EP2764002B1 (en) 2018-02-28
ES2746859T3 (es) 2020-03-09
UY34361A (es) 2013-05-31
EA027086B1 (ru) 2017-06-30
ES2661705T3 (es) 2018-04-03
JP2014530809A (ja) 2014-11-20
CL2014000827A1 (es) 2014-09-05
AU2012319172A1 (en) 2013-05-16
PE20141160A1 (es) 2014-09-22
US8664386B2 (en) 2014-03-04
CN117343101A (zh) 2024-01-05
HK1200834A1 (en) 2015-08-14
CA3042169A1 (en) 2013-04-11
TWI557133B (zh) 2016-11-11
US9029534B2 (en) 2015-05-12
HK1255222B (zh) 2020-07-17
HK1245798A1 (zh) 2018-08-31
CN113264959A (zh) 2021-08-17
TWI689513B (zh) 2020-04-01
MX353064B (es) 2017-12-19
TWI709567B (zh) 2020-11-11
EP3333173B1 (en) 2019-06-26

Similar Documents

Publication Publication Date Title
CR20140204A (es) Métodos para preparar análogos nucleotídicos antivirales
IN2014MU00118A (es)
CR20140132A (es) Derivados de pirrolopirimidina y purina
UY34092A (es) Nuevos compuestos como inhibidores de jak
CL2016001732A1 (es) Métodos sintéticos para compuestos espiro-oxoindol (div. sol. 3633-13).
EA202190619A1 (ru) Противовирусные соединения
ECSP13012451A (es) Métodos para la preparación de profármacos de fosforamidato diastereoméricamente puros
UY33337A (es) DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS
UY34352A (es) 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de la idh mutante
UY33958A (es) Inhibidores de la glucosilceramida sintasa
CR20130470A (es) INHIBIDORES DE QUINASA RELACIONADOS CON PIRROLO [2,3-d]PIRIMIDINA TROMPOMIOSINA
UY34051A (es) Derivados de pirrolotriazinona como inhibidores de pi3k
ECSP12011805A (es) Compuestos
ZA201404147B (en) An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine
EA201490596A1 (ru) Новые производные дигидрохинолин-2-она
UY34365A (es) Compuestos heterociclicos
AU2012213775A8 (en) 7-azaindole derivatives
UY33929A (es) Compuestos de ciclohexilo tetrasustituido como inhibidores de quinasas
UY33930A (es) Inhibidores novedosos de quinasas
EA201490567A1 (ru) Новые бициклические производные дигидрохинолин-2-она
EA201391274A1 (ru) Аминохинолины в качестве ингибиторов киназ
ME01665B (me) Analozi buprenorfina
CR20130539A (es) Triazolopiridinas
UY33888A (es) Derivados de (1,2,4) triazolo [4,3-a) quinoxalina como inhibidores de fosfodiesterasas
EA201201645A1 (ru) СПОСОБ ПОЛУЧЕНИЯ F-18 МЕЧЕННЫХ Аβ-ЛИГАНДОВ