BR112013016546A2 - processo para aperfeiçoamento de rilpivirina - Google Patents
processo para aperfeiçoamento de rilpivirinaInfo
- Publication number
- BR112013016546A2 BR112013016546A2 BR112013016546A BR112013016546A BR112013016546A2 BR 112013016546 A2 BR112013016546 A2 BR 112013016546A2 BR 112013016546 A BR112013016546 A BR 112013016546A BR 112013016546 A BR112013016546 A BR 112013016546A BR 112013016546 A2 BR112013016546 A2 BR 112013016546A2
- Authority
- BR
- Brazil
- Prior art keywords
- rilpivirine
- hydrochloride
- isomer
- less
- improvement
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/04—Preparation of carboxylic acid nitriles by reaction of cyanogen halides, e.g. ClCN, with organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/34—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring with cyano groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by unsaturated carbon chains
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C269/06—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups by reactions not involving the formation of carbamate groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/04—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Virology (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- AIDS & HIV (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
processo para aperfeiçoamento da rilpivirina. a presente invenção refere-se à preparação de um intermediário chave de rilpivirina, a saber, o cloridrato de (e)-4-(2-cianoetenil)-2,6-dimetilfenilamina (ll), por um processo que compreende a reação do sal de diazônio tetrafluoroborato do composto 2,6-dimetil-4-amino-1-carboxibenzil fenilamina (vi) com acrilonitrila na presença de acetato de paládio, seguido pelo tratamento com um ácido e a sua subsequente conversão no sal cloridrato (ll), caracterizado por o isômero z indesejado ser inferior a 0,5%, e proporcionar o cloridrato de rilpivirina com isômero z inferior a 0,1%.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1223MU2011 | 2011-04-15 | ||
PCT/IN2012/000246 WO2012143937A2 (en) | 2011-04-15 | 2012-04-09 | An improved rilpivirine process |
Publications (1)
Publication Number | Publication Date |
---|---|
BR112013016546A2 true BR112013016546A2 (pt) | 2016-09-27 |
Family
ID=47041983
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112013016546A BR112013016546A2 (pt) | 2011-04-15 | 2012-04-09 | processo para aperfeiçoamento de rilpivirina |
Country Status (10)
Country | Link |
---|---|
US (1) | US8952155B2 (pt) |
EP (1) | EP2643294B1 (pt) |
JP (1) | JP5870183B2 (pt) |
KR (1) | KR101879468B1 (pt) |
AP (1) | AP2013006779A0 (pt) |
BR (1) | BR112013016546A2 (pt) |
EA (1) | EA024409B1 (pt) |
ES (1) | ES2604405T3 (pt) |
WO (1) | WO2012143937A2 (pt) |
ZA (1) | ZA201302020B (pt) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2848631C (en) * | 2011-09-16 | 2019-10-01 | Hetero Research Foundation | Rilpivirine hydrochloride |
WO2013153162A1 (en) * | 2012-04-11 | 2013-10-17 | Sandoz Ag | Polymorph of rilpivirine hydrochloride |
WO2013153161A2 (en) * | 2012-04-11 | 2013-10-17 | Sandoz Ag | Novel polymorph of rilpivirine hydrochloride |
CZ201532A3 (cs) * | 2015-01-21 | 2015-02-25 | Zentiva, K.S. | Způsob výroby vysoce čistého Rilpivirinu a jeho solí |
CN107162987A (zh) * | 2016-03-07 | 2017-09-15 | 宜昌人福药业有限责任公司 | 一种利匹韦林的工业化合成方法及中间体化合物 |
WO2020084142A1 (en) | 2018-10-25 | 2020-04-30 | Minakem | Process for the preparation of rilpivirine |
CN112778214A (zh) * | 2021-01-13 | 2021-05-11 | 安徽贝克联合制药有限公司 | 用于合成利匹韦林的中间体、其合成方法和利匹韦林的合成方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2757543B1 (fr) * | 1996-12-23 | 1999-04-02 | Sanofi Sa | Procede pour la cristallisation d'un derive de tetrahydropyridine et formes cristallines ainsi obtenues |
ES2422196T3 (es) * | 2002-08-09 | 2013-09-09 | Janssen Pharmaceutica Nv | Procesos para la preparación de 4-4-4-(2-cianoetenil)-2,6-dimetilfenil)amino)-2-pirimidinil)aminobenzonitrilo |
EP1632232B3 (en) * | 2004-09-02 | 2022-03-30 | Janssen Pharmaceutica NV | Salt of 4[[4-[[4-(2-Cyanoethenyl)-2,6-dimethylphenyl]amino]-2-Pyrimidinyl]amino]benzonitrile |
-
2012
- 2012-04-09 EP EP12774414.2A patent/EP2643294B1/en not_active Not-in-force
- 2012-04-09 AP AP2013006779A patent/AP2013006779A0/xx unknown
- 2012-04-09 JP JP2014504449A patent/JP5870183B2/ja not_active Expired - Fee Related
- 2012-04-09 KR KR1020137011114A patent/KR101879468B1/ko active IP Right Grant
- 2012-04-09 US US13/880,843 patent/US8952155B2/en not_active Expired - Fee Related
- 2012-04-09 EA EA201301170A patent/EA024409B1/ru not_active IP Right Cessation
- 2012-04-09 BR BR112013016546A patent/BR112013016546A2/pt not_active Application Discontinuation
- 2012-04-09 WO PCT/IN2012/000246 patent/WO2012143937A2/en active Application Filing
- 2012-04-09 ES ES12774414.2T patent/ES2604405T3/es active Active
-
2013
- 2013-03-18 ZA ZA2013/02020A patent/ZA201302020B/en unknown
Also Published As
Publication number | Publication date |
---|---|
KR20130143046A (ko) | 2013-12-30 |
ES2604405T3 (es) | 2017-03-06 |
JP2014522385A (ja) | 2014-09-04 |
US8952155B2 (en) | 2015-02-10 |
WO2012143937A3 (en) | 2013-03-21 |
ZA201302020B (en) | 2014-05-28 |
WO2012143937A2 (en) | 2012-10-26 |
EA024409B1 (ru) | 2016-09-30 |
AP2013006779A0 (en) | 2013-03-31 |
KR101879468B1 (ko) | 2018-07-17 |
EP2643294A4 (en) | 2014-12-24 |
US20140275538A1 (en) | 2014-09-18 |
JP5870183B2 (ja) | 2016-02-24 |
EP2643294A2 (en) | 2013-10-02 |
EA201301170A1 (ru) | 2014-02-28 |
EP2643294B1 (en) | 2016-08-24 |
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Legal Events
Date | Code | Title | Description |
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B06T | Formal requirements before examination [chapter 6.20 patent gazette] | ||
B11E | Dismissal acc. art. 34 of ipl - requirements for examination incomplete | ||
B11T | Dismissal of application maintained [chapter 11.20 patent gazette] |