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]adenineInfo
- 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
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 Table
- 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
-
- 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 Table
- 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
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)
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)
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)
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 |
-
2014
- 2014-06-06 WO PCT/GB2014/051752 patent/WO2014195724A1/en active Application Filing
- 2014-06-06 CA CA2914381A patent/CA2914381A1/en not_active Abandoned
- 2014-06-06 EP EP14732301.8A patent/EP3004121A1/en not_active Withdrawn
- 2014-06-06 US US14/896,313 patent/US9676803B2/en not_active Expired - Fee Related
- 2014-06-06 ZA ZA2014/04147A patent/ZA201404147B/en unknown
- 2014-06-06 IN IN1967MU2013 patent/IN2013MU01967A/en unknown
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 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Discontinued |
Effective date: 20190606 |