BR112017001516A2 - método de ressolubilização quiral, estereoisômero, método para preparar um composto, composto, composição, e kit de ressolubilização quiral - Google Patents
método de ressolubilização quiral, estereoisômero, método para preparar um composto, composto, composição, e kit de ressolubilização quiralInfo
- Publication number
- BR112017001516A2 BR112017001516A2 BR112017001516-1A BR112017001516A BR112017001516A2 BR 112017001516 A2 BR112017001516 A2 BR 112017001516A2 BR 112017001516 A BR112017001516 A BR 112017001516A BR 112017001516 A2 BR112017001516 A2 BR 112017001516A2
- Authority
- BR
- Brazil
- Prior art keywords
- chiral
- resolubilization
- compound
- acid
- preparing
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B57/00—Separation of optically-active compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/42—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/42—Separation; Purification; Stabilisation; Use of additives
- C07C303/44—Separation; Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/04—Monocyclic monocarboxylic acids
- C07C63/06—Benzoic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/56—Amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
o presente relatório descritivo refere-se a um método de ressolubilização quiral de uma mistura de estereoisômeros, compreendendo uma etapa de mistura estereoisomérica de compostos na qual um grupo amina é ligado a um átomo de carbono assimétrico, com um auxiliar quiral e um composto auxiliar formador de sal, em que o auxiliar quiral é um derivado de ácido o,o?-diaciltartárico, mais especificamente, de um ácido 2,3-dibenzoil-tartárico ou ácido o,o?di-p-toluoil tartárico, e o composto auxiliar formador de sal é ácido mandélico ou ácido canforsulfônico, e um isômero óptico contendo um alto nível de pureza óptica que pode ser obtido usando o método. portanto, de acordo com um aspecto da presente invenção, o método pode ser útil no campo farmacêutico ou cosmético quando se prepara um isômero óptico contendo uma pureza óptica alta.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2015-0024334 | 2015-02-17 | ||
KR1020150024334A KR20160101554A (ko) | 2015-02-17 | 2015-02-17 | N-[4-(1-아미노에틸)-페닐]-메탄술폰아미드 유도체의 카이랄 분할 방법 |
EP15174617.9 | 2015-06-30 | ||
EP15174617 | 2015-06-30 | ||
PCT/KR2016/001474 WO2016133317A1 (ko) | 2015-02-17 | 2016-02-15 | N-[4-(1-아미노에틸)-페닐]-술폰아미드 유도체의 카이랄 분할 방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
BR112017001516A2 true BR112017001516A2 (pt) | 2018-01-30 |
BR112017001516B1 BR112017001516B1 (pt) | 2023-10-31 |
Family
ID=56692658
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112017001516-1A BR112017001516B1 (pt) | 2015-02-17 | 2016-02-15 | Método de ressolubilização quiral, estereoisômero, método para preparar um composto, composto, composição, e kit de ressolubilização quiral |
Country Status (8)
Country | Link |
---|---|
US (1) | US10479763B2 (pt) |
EP (1) | EP3162793B1 (pt) |
JP (1) | JP6687596B2 (pt) |
KR (1) | KR101791119B1 (pt) |
CN (1) | CN106660949B (pt) |
BR (1) | BR112017001516B1 (pt) |
TW (1) | TWI687396B (pt) |
WO (1) | WO2016133317A1 (pt) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102565407B1 (ko) * | 2016-01-04 | 2023-08-10 | (주)아모레퍼시픽 | 극성 비양자성 용매를 이용한 n-[4-(1-아미노에틸)-페닐]-술폰아미드 유도체의 카이랄 분할 방법 |
KR102599958B1 (ko) | 2016-09-28 | 2023-11-09 | (주)아모레퍼시픽 | (r)-n-[4-(1-아미노-에틸)-2,6-다이플루오로-페닐]-메테인설폰아마이드의 제조방법 |
KR102587339B1 (ko) * | 2016-12-22 | 2023-10-12 | (주)아모레퍼시픽 | N-[4-(1-아미노-에틸)-2,6-다이플루오로-페닐]-메테인설폰아마이드의 거울상 이성질체들의 라세미화 방법 |
CN109608368B (zh) * | 2018-10-24 | 2021-03-09 | 常州市阳光药业有限公司 | N-[4-(1-氨基乙基)-2,6-二氟苯基]甲磺酰胺的合成及拆分方法 |
KR20200053746A (ko) * | 2018-11-09 | 2020-05-19 | (주)아모레퍼시픽 | 졸-겔 조성물 |
MX2022010079A (es) * | 2020-02-16 | 2022-09-02 | Ayala Pharmaceuticals Inc | Metodos para preparar derivados quirales de benzodiazepinona. |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60152425A (ja) | 1984-01-20 | 1985-08-10 | Oyo Seikagaku Kenkyusho:Kk | ラセミ体の新規な光学分割法 |
US4968837A (en) * | 1989-07-28 | 1990-11-06 | Ethyl Corporation | Resolution of racemic mixtures |
DK0418770T3 (da) | 1989-09-19 | 1995-10-30 | Hoechst Roussel Pharma | Fremgangsmåde til kemisk spaltning af 5-alkoxysubstituerede (+-)-1,3-dimethyloxindolylethylaminer |
US6265615B1 (en) | 1998-07-01 | 2001-07-24 | The Regents Of The University Of California | Chiral recognition polymer and its use to separate enantiomers |
DE19956786A1 (de) | 1999-11-25 | 2001-05-31 | Basf Ag | Verfahren zur Herstellung optisch aktiver Amine |
US7301023B2 (en) | 2001-05-31 | 2007-11-27 | Pfizer Inc. | Chiral salt resolution |
KR100927915B1 (ko) * | 2005-03-17 | 2009-11-19 | 화이자 인코포레이티드 | 통증 치료에 유용한 n-(n-설폰일아미노메틸)사이클로프로판카복사마이드 유도체 |
US20120041225A1 (en) * | 2006-02-03 | 2012-02-16 | Vaidya Niteen A | Kit for automated resolving agent selection and method thereof |
US20120088746A1 (en) | 2006-05-10 | 2012-04-12 | Pfizer Inc. | Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same |
WO2007129188A1 (en) | 2006-05-10 | 2007-11-15 | Pfizer Japan Inc. | Cyclopropanecarboxamide compound |
EP1862454A1 (en) * | 2006-06-02 | 2007-12-05 | Amorepacific Corporation | Novel compounds, isomer thereof or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and a pharmaceutical composition containing the same |
EP1882687A1 (en) * | 2006-07-27 | 2008-01-30 | Amorepacific Corporation | Heterocyclic compounds useful as vanilloid receptor antagonists and pharmaceutical compositions containing the same |
AR063211A1 (es) * | 2006-07-27 | 2009-01-14 | Amorepacific Corp | Derivados de 3-(piridin-3-il)acrilamida y 3-(piridin-3-il)propionamida, un metodo para su preparacion, una composicion farmaceutica que los comprende y su uso en la fabricacion de medicamentos para el tratamiento de enfermedades asociadas con el receptor vaniloide. |
JP2011201778A (ja) | 2008-07-23 | 2011-10-13 | Mochida Pharmaceut Co Ltd | p−置換アリールアセトアミドを有するヘテロシクリデン誘導体 |
US8461334B2 (en) | 2008-11-07 | 2013-06-11 | Cipla Limited | Process for resolving zopiclone |
KR20160101554A (ko) | 2015-02-17 | 2016-08-25 | (주)아모레퍼시픽 | N-[4-(1-아미노에틸)-페닐]-메탄술폰아미드 유도체의 카이랄 분할 방법 |
-
2016
- 2016-02-15 BR BR112017001516-1A patent/BR112017001516B1/pt active IP Right Grant
- 2016-02-15 KR KR1020177000413A patent/KR101791119B1/ko active IP Right Grant
- 2016-02-15 EP EP16752647.4A patent/EP3162793B1/en active Active
- 2016-02-15 US US15/325,349 patent/US10479763B2/en active Active
- 2016-02-15 WO PCT/KR2016/001474 patent/WO2016133317A1/ko active Application Filing
- 2016-02-15 CN CN201680002149.0A patent/CN106660949B/zh active Active
- 2016-02-15 JP JP2017502582A patent/JP6687596B2/ja active Active
- 2016-02-16 TW TW105104399A patent/TWI687396B/zh active
Also Published As
Publication number | Publication date |
---|---|
EP3162793A1 (en) | 2017-05-03 |
WO2016133317A1 (ko) | 2016-08-25 |
EP3162793B1 (en) | 2019-04-10 |
CN106660949A (zh) | 2017-05-10 |
TWI687396B (zh) | 2020-03-11 |
EP3162793A4 (en) | 2018-01-03 |
US20170342027A1 (en) | 2017-11-30 |
KR20170042548A (ko) | 2017-04-19 |
US10479763B2 (en) | 2019-11-19 |
BR112017001516B1 (pt) | 2023-10-31 |
JP2018506503A (ja) | 2018-03-08 |
TW201636319A (zh) | 2016-10-16 |
KR101791119B1 (ko) | 2017-11-20 |
CN106660949B (zh) | 2020-11-13 |
JP6687596B2 (ja) | 2020-04-22 |
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B07D | Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette] |
Free format text: DE ACORDO COM O ARTIGO 229-C DA LEI NO 10196/2001, QUE MODIFICOU A LEI NO 9279/96, A CONCESSAO DA PATENTE ESTA CONDICIONADA A ANUENCIA PREVIA DA ANVISA. CONSIDERANDO A APROVACAO DOS TERMOS DO PARECER NO 337/PGF/EA/2010, BEM COMO A PORTARIA INTERMINISTERIAL NO 1065 DE 24/05/2012, ENCAMINHA-SE O PRESENTE PEDIDO PARA AS PROVIDENCIAS CABIVEIS. |
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B09A | Decision: intention to grant [chapter 9.1 patent gazette] | ||
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Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 15/02/2016, OBSERVADAS AS CONDICOES LEGAIS |