IN2013MU01967A - - Google Patents
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- Publication number
- IN2013MU01967A IN2013MU01967A IN1967MU2013A IN2013MU01967A IN 2013MU01967 A IN2013MU01967 A IN 2013MU01967A IN 1967MU2013 A IN1967MU2013 A IN 1967MU2013A IN 2013MU01967 A IN2013MU01967 A IN 2013MU01967A
- Authority
- IN
- India
- Prior art keywords
- phenoxyphosphinyl
- isopropoxycarbonyl
- adenine
- methoxy
- propyl
- Prior art date
Links
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 abstract 1
- 229930024421 Adenine Natural products 0.000 abstract 1
- 229960000643 adenine Drugs 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- LDEKQSIMHVQZJK-GNGHXOLXSA-N propan-2-yl (2s)-2-[[[(2r)-1-(6-aminopurin-9-yl)propan-2-yl]oxymethyl-phenoxyphosphoryl]amino]propanoate Chemical compound O([P@](=O)(CO[C@H](C)CN1C2=NC=NC(N)=C2N=C1)N[C@@H](C)C(=O)OC(C)C)C1=CC=CC=C1 LDEKQSIMHVQZJK-GNGHXOLXSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- LDEKQSIMHVQZJK-CAQYMETFSA-N tenofovir alafenamide Chemical compound O([P@@](=O)(CO[C@H](C)CN1C2=NC=NC(N)=C2N=C1)N[C@@H](C)C(=O)OC(C)C)C1=CC=CC=C1 LDEKQSIMHVQZJK-CAQYMETFSA-N 0.000 abstract 1
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)
Abstract
Abstract The present invention relates to an efficient process for the separation of diastereomers of 9-[(R)-2-[[(R,S)-[[(S)-1-(Isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine and to a process for preparing 9-[(R)-2-[[(R)-[[(S)-1-(Isopropoxycarbonyl)ethyl]amino]phenoxyphosphinyl]methoxy]propyl]adenine and 9-[(R)-2-[[(S)-[[(S)-1-(Isopropoxycarbonyl)ethyl]amino]phenoxyphosphinyl]methoxy]propyl] adenine.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2914381A 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 |
US14/896,313 US9676803B2 (en) | 2013-06-07 | 2014-06-06 | Efficient process for separation of diastereomers of 9-[(R)-2-[[(R,S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine |
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 |
EP14732301.8A EP3004121A1 (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 |
ZA2014/04147A ZA201404147B (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 (en) | 2013-06-07 | 2014-06-06 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1967MU2013 IN2013MU01967A (en) | 2013-06-07 | 2014-06-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
IN2013MU01967A true IN2013MU01967A (en) | 2015-06-12 |
Family
ID=50981561
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IN1967MU2013 IN2013MU01967A (en) | 2013-06-07 | 2014-06-06 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9676803B2 (en) |
EP (1) | EP3004121A1 (en) |
CA (1) | CA2914381A1 (en) |
IN (1) | IN2013MU01967A (en) |
WO (1) | WO2014195724A1 (en) |
ZA (1) | ZA201404147B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9676803B2 (en) | 2013-06-07 | 2017-06-13 | Cipla Limited | Efficient process for separation of diastereomers of 9-[(R)-2-[[(R,S)-[[(S)-1-(isopropoxycarbonyl)ethyl]amino]-phenoxyphosphinyl]methoxy]propyl]adenine |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015107451A2 (en) * | 2014-01-14 | 2015-07-23 | Mylan Laboratories Ltd. | Purification of tenofovir alafenamide and its intermediates |
CN105085571A (en) * | 2014-05-20 | 2015-11-25 | 四川海思科制药有限公司 | Tenofovir alafenamide compound, preparation method and purpose thereof |
CZ2015384A3 (en) * | 2015-06-05 | 2016-12-14 | Zentiva, K.S. | Tenofovir alafenamide solid forms |
JP2018524308A (en) * | 2015-06-17 | 2018-08-30 | ギリアード サイエンシーズ, インコーポレイテッド | Co-crystals, salts and crystalline forms of tenofovir arafenamide |
WO2017118928A1 (en) | 2016-01-06 | 2017-07-13 | Lupin Limited | Process for the separation of diastereomers of tenofovir alafenamide |
CZ2016156A3 (en) | 2016-03-17 | 2017-09-27 | Zentiva, K.S. | The method of preparation of diastereomerically pure Tenofovir Alafenamide or its salts |
WO2017203395A1 (en) * | 2016-05-21 | 2017-11-30 | Shilpa Medicare Limited | Crystalline forms of tenofovir alafenamide hemi fumarate |
TW202402300A (en) | 2017-01-31 | 2024-01-16 | 美商基利科學股份有限公司 | Crystalline forms of tenofovir alafenamide |
CN108484672A (en) * | 2018-05-23 | 2018-09-04 | 中国药科大学制药有限公司 | The chiral separation method of the third tenofovir of phosphorus |
CN110283208B (en) * | 2018-06-22 | 2022-07-08 | 南京济群医药科技股份有限公司 | Chiral resolution method of tenofovir alafenamide |
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 |
---|---|---|---|---|
PL213214B1 (en) | 2000-07-21 | 2013-01-31 | Gilead Sciences | Prodrugs of phosphonate nucleotide analogues and methods for selecting and making same |
WO2013052094A2 (en) * | 2011-10-07 | 2013-04-11 | Gilead Sciences, Inc. | Methods for preparing anti-viral nucleotide analogs |
US9676803B2 (en) | 2013-06-07 | 2017-06-13 | Cipla Limited | 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 US US14/896,313 patent/US9676803B2/en not_active Expired - Fee Related
- 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 IN IN1967MU2013 patent/IN2013MU01967A/en unknown
- 2014-06-06 WO PCT/GB2014/051752 patent/WO2014195724A1/en active Application Filing
- 2014-06-06 ZA ZA2014/04147A patent/ZA201404147B/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9676803B2 (en) | 2013-06-07 | 2017-06-13 | Cipla Limited | 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 |
---|---|
US20160122373A1 (en) | 2016-05-05 |
CA2914381A1 (en) | 2014-12-11 |
WO2014195724A1 (en) | 2014-12-11 |
ZA201404147B (en) | 2016-01-27 |
EP3004121A1 (en) | 2016-04-13 |
US9676803B2 (en) | 2017-06-13 |
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