CA2914381A1 - An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine - Google Patents

An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine

Info

Publication number
CA2914381A1
CA2914381A1 CA2914381A CA2914381A CA2914381A1 CA 2914381 A1 CA2914381 A1 CA 2914381A1 CA 2914381 A CA2914381 A CA 2914381A CA 2914381 A CA2914381 A CA 2914381A CA 2914381 A1 CA2914381 A1 CA 2914381A1
Authority
CA
Canada
Prior art keywords
amino
propyl
adenine
methoxy
phenoxyphosphinyl
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.)
Abandoned
Application number
CA2914381A
Other languages
English (en)
French (fr)
Inventor
Dharmaraj Ramachandra Rao
Ashwini Amol Sawant
Nayan SHIVALKAR
Nitin THAKUR
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.)
Cipla Ltd
Original Assignee
Cipla Ltd
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 Cipla Ltd filed Critical Cipla Ltd
Publication of CA2914381A1 publication Critical patent/CA2914381A1/en
Abandoned legal-status Critical Current

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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
CA2914381A 2013-06-07 2014-06-06 An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine Abandoned CA2914381A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN1967/MUM/2013 2013-06-07
PCT/GB2014/051752 WO2014195724A1 (en) 2013-06-07 2014-06-06 An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine
IN1967MU2013 IN2013MU01967A (enEXAMPLES) 2013-06-07 2014-06-06

Publications (1)

Publication Number Publication Date
CA2914381A1 true CA2914381A1 (en) 2014-12-11

Family

ID=50981561

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2914381A Abandoned CA2914381A1 (en) 2013-06-07 2014-06-06 An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine

Country Status (6)

Country Link
US (1) US9676803B2 (enEXAMPLES)
EP (1) EP3004121A1 (enEXAMPLES)
CA (1) CA2914381A1 (enEXAMPLES)
IN (1) IN2013MU01967A (enEXAMPLES)
WO (1) WO2014195724A1 (enEXAMPLES)
ZA (1) ZA201404147B (enEXAMPLES)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
WO2015107451A2 (en) * 2014-01-14 2015-07-23 Mylan Laboratories Ltd. Purification of tenofovir alafenamide and its intermediates
CN105085571A (zh) * 2014-05-20 2015-11-25 四川海思科制药有限公司 替诺福韦艾拉酚胺复合物及其制备方法和用途
CZ2015384A3 (cs) * 2015-06-05 2016-12-14 Zentiva, K.S. Pevné formy Tenofovir alafenamidu
CA2987085A1 (en) 2015-06-17 2016-12-22 Gilead Sciences, Inc. Co-crystals, salts and solid forms of tenofovir alafenamide
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
WO2017203395A1 (en) * 2016-05-21 2017-11-30 Shilpa Medicare Limited Crystalline forms of tenofovir alafenamide hemi fumarate
TWI820984B (zh) 2017-01-31 2023-11-01 美商基利科學股份有限公司 替諾福韋埃拉酚胺(tenofovir alafenamide)之晶型
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
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
US11667656B2 (en) 2021-01-27 2023-06-06 Apotex Inc. Crystalline forms of Tenofovir alafenamide

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020119443A1 (en) 2000-07-21 2002-08-29 Gilead Sciences, Inc. Prodrugs of phosphonate nucleotide analogues and methods for selecting and making same
TWI689513B (zh) 2011-10-07 2020-04-01 美商基利科學股份有限公司 抗病毒核苷酸類似物的製備方法
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

Also Published As

Publication number Publication date
WO2014195724A1 (en) 2014-12-11
US20160122373A1 (en) 2016-05-05
EP3004121A1 (en) 2016-04-13
ZA201404147B (en) 2016-01-27
IN2013MU01967A (enEXAMPLES) 2015-06-12
US9676803B2 (en) 2017-06-13

Similar Documents

Publication Publication Date Title
CA2914381A1 (en) An efficient process for separation of diastereomers of 9-[(r)-2-[[(r,s)-[[(s)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl] methoxy]propyl]adenine
EP3077404B1 (en) Purification of tenofovir alafenamide and its intermediates
JP5780657B2 (ja) 光学活性ジアミン誘導体の塩の製造方法
JP6618569B2 (ja) キラルキヌレニン化合物の合成方法
MX2011007445A (es) Proceso para la elaboracion y resolucion del acido 2-acil-amino-3-difenil-propionico.
WO2014157612A1 (ja) (1s,4s,5s)-4-ブロモ-6-オキサビシクロ[3.2.1]オクタン-7-オンの製造方法
EP3078665A1 (en) Efficient method for the preparation of tofacitinib citrate
US8497374B2 (en) Process for preparing and purifying bortezomib
TW201831500A (zh) 使用麻黃素製備l-草銨膦或其鹽的方法
WO2017118928A9 (en) Process for the separation of diastereomers of tenofovir alafenamide
JP5534460B2 (ja) 光学活性なα−アミノアセタール類の製造方法
JP5927126B2 (ja) 2−(シクロヘキシルメチル)−n−{2−[(2s)−1−メチルピロリジン−2−イル]エチル}−1,2,3,4−テトラヒドロイソキノリン−7−スルホンアミドの製造方法
TW201837047A (zh) 使用麻黃素製備草銨膦或其鹽之方法
EP3230258B1 (en) Process for the preparation of (1s,2r)-milnacipran
CN113121549B (zh) 立体选择性合成手性内酯的方法和手性化合物及其应用
KR101304640B1 (ko) 신규의 로수바스타틴 엔-메틸벤질아민 염 및 그의 제조방법
US9981965B2 (en) Process for preparing idelalisib
JP2007332050A (ja) 光学活性N−tert−ブチルカルバモイル−L−tert−ロイシンの製造方法
RU2741389C1 (ru) Способ получения промежуточного соединения для синтеза лекарственного средства
US20190010141A1 (en) Process for the synthesis of efinaconazol
CN113773297A (zh) 屈昔多巴关键中间体的拆分方法
EP3242879A1 (en) Novel process for the preparation of dipeptidyl peptidase-4 (dpp-4) enzyme inhibitor
WO2019098551A1 (ko) 의약품 합성용 중간체 화합물의 제조 방법
JP2018525366A (ja) イブルチニブの製法及び新規な合成中間体
JP2003246754A (ja) 光学活性スルフォスチン及びその類縁体の製造における光学活性中間体の製造方法

Legal Events

Date Code Title Description
FZDE Discontinued

Effective date: 20190606