AR115475A2 - Método para la síntesis de (1s,2r)-milnaciprán - Google Patents
Método para la síntesis de (1s,2r)-milnacipránInfo
- Publication number
- AR115475A2 AR115475A2 ARP190101513A ARP190101513A AR115475A2 AR 115475 A2 AR115475 A2 AR 115475A2 AR P190101513 A ARP190101513 A AR P190101513A AR P190101513 A ARP190101513 A AR P190101513A AR 115475 A2 AR115475 A2 AR 115475A2
- Authority
- AR
- Argentina
- Prior art keywords
- formula
- previous step
- reaction
- amide
- milnacipran
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/16—Preparation of optical isomers
- C07C231/18—Preparation of optical isomers by stereospecific synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/57—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
- C07C233/58—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Steroid Compounds (AREA)
Abstract
Reivindicación 1: Un método para sintetizar una sal de adición de ácido farmacéutica aceptable de (1S,2R)-milnaciprán de la fórmula (1), que comprende los siguientes pasos sucesivos: (a) reacción de fenilacetonitrilo y de (R)-epiclorhidrina en presencia de una base que contiene un metal alcalino, seguida por un tratamiento básico, y luego por un tratamiento ácido para obtener la lactona de la fórmula (2); (b) reacción de la lactona de fórmula (2) obtenida en el paso (a) previo con MNEt₂, en donde M representa un metal alcalino, o con NHEt₂ en presencia de un complejo de ácido de Lewis-amina en donde la amina es seleccionada entre dietilamina, trietilamina, diisopropiletilamina, N,N-dietilanilina, N,N-dimetilbencilamina, N-metilpiperidina, N-metilmorfolina, N,N-dimetilpiperazina y hexametilentetramina, para obtener el amida-alcohol de la fórmula (3); (c) reacción del amida-alcohol de fórmula (3) obtenido en el paso (b) previo con cloruro de tionilo para obtener la amida clorada de la fórmula (4); (d) reacción de la amida clorada de fórmula (4) obtenida en el paso (c) previo con una sal de ftalimida, tal como la sal de potasio, para obtener el derivado de ftalimida de la fórmula (5); (e) hidrólisis del grupo ftalimida del derivado de ftalimida de fórmula (5) obtenido en el paso (d) previo, para obtener (1S,2R)-milnaciprán; y (f) salificación del (1S,2R)-milnaciprán obtenido en el paso (e) previo en un sistema adecuado de solventes, en presencia de un ácido farmacéuticamente aceptable, caracterizado porque los pasos (a) a (e) son llevados a cabo en un medio de reacción que comprende un mismo y único solvente que es tolueno.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0950552A FR2941454B1 (fr) | 2009-01-29 | 2009-01-29 | Proced de synthese du (1s,2r)-milnacipran |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR115475A2 true AR115475A2 (es) | 2021-01-20 |
Family
ID=40920574
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100100245A AR077526A1 (es) | 2009-01-29 | 2010-01-29 | Metodo para la sintesis de (1s,2r)- milnacipran |
| ARP190101513A AR115475A2 (es) | 2009-01-29 | 2019-06-04 | Método para la síntesis de (1s,2r)-milnaciprán |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100100245A AR077526A1 (es) | 2009-01-29 | 2010-01-29 | Metodo para la sintesis de (1s,2r)- milnacipran |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US8604241B2 (es) |
| EP (1) | EP2391599B1 (es) |
| JP (1) | JP5646509B2 (es) |
| KR (1) | KR101719011B1 (es) |
| CN (2) | CN110204455A (es) |
| AR (2) | AR077526A1 (es) |
| AU (1) | AU2010209686B2 (es) |
| BR (1) | BRPI1007404B8 (es) |
| CA (1) | CA2750488C (es) |
| ES (1) | ES2472695T3 (es) |
| FR (1) | FR2941454B1 (es) |
| GE (1) | GEP20135903B (es) |
| IL (1) | IL214241A (es) |
| MA (1) | MA33025B1 (es) |
| MX (1) | MX2011007846A (es) |
| NZ (1) | NZ594291A (es) |
| PL (1) | PL2391599T3 (es) |
| RU (1) | RU2521342C2 (es) |
| TN (1) | TN2011000363A1 (es) |
| TW (1) | TWI455911B (es) |
| UA (1) | UA104884C2 (es) |
| WO (1) | WO2010086394A1 (es) |
| ZA (1) | ZA201105414B (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2944011B1 (fr) * | 2009-04-03 | 2011-05-20 | Pf Medicament | Derives d'aminocyclobutane ou d'aminocyclobutene, leur procede de preparation et leur utilisation a titre de medicaments. |
| WO2011158249A1 (en) * | 2010-06-16 | 2011-12-22 | Glenmark Generics Limited | Process for preparation of milnacipran intermediate and its use in preparation of pure milnacipran |
| WO2012046247A2 (en) * | 2010-10-06 | 2012-04-12 | Msn Laboratories Limited | Process for the preparation of (±m1r(s), 2srr)l-2-(aminomethyl)-n,n-diethyl-l-phenylcyclopropane carboxamide hydrochloride |
| MX2013008595A (es) * | 2011-01-24 | 2013-08-14 | Bayer Ip Gmbh | Procedimiento mejorado para la preparacion de 2,2-difluoroetilamina. |
| ES2733750T3 (es) * | 2012-02-17 | 2019-12-02 | Eisai R&D Man Co Ltd | Métodos y compuestos útiles en la síntesis de antagonistas del receptor de orexina-2 |
| WO2014009767A1 (en) | 2012-07-07 | 2014-01-16 | Micro Labs Limited | An improved process for the preparation of 1-aryl 2-aminomethyl cyclopropane carboxyamide (z) derivatives, their isomers and salts |
| EP2805936A1 (en) | 2013-05-20 | 2014-11-26 | Cosma S.p.A. | Process for preparing levomilnacipran HCL |
| WO2014203277A2 (en) * | 2013-06-19 | 2014-12-24 | Msn Laboratories Private Limited | Process for the preparation of (1s,2r)-2-(aminomethyl)-n,n-diethyl-1-phenylcyclopropanearboxamide hydrochloride |
| CN103694162B (zh) * | 2014-01-03 | 2015-09-02 | 上海现代制药股份有限公司 | (1s,2r)-1-苯基2-(酞酰亚胺)甲基-n,n-二乙基-环丙甲酰胺的制备方法 |
| CN104058992A (zh) * | 2014-06-13 | 2014-09-24 | 上海现代制药股份有限公司 | 左旋米那普仑盐酸盐的晶型 |
| WO2016050894A1 (en) | 2014-10-03 | 2016-04-07 | Purac Biochem Bv | Method for the manufacture of n, n-diallkyllactamide |
| US10131624B2 (en) | 2014-11-04 | 2018-11-20 | Quimica Sintetica, S.A. | Process for the preparation of (1S,2R)-Milnacipran |
| CN106083638A (zh) * | 2016-07-07 | 2016-11-09 | 佛山市隆信医药科技有限公司 | 一种盐酸左旋米那普仑的制备方法 |
| CN111175387B (zh) * | 2018-11-13 | 2022-06-07 | 成都康弘药业集团股份有限公司 | 一种米那普仑异构体的检测方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2508035A1 (fr) | 1981-06-23 | 1982-12-24 | Fabre Sa Pierre | Derives d'aryl-1-aminomethyl-2 cyclopropanes carboxamides (z), leur preparation et leur application en tant que medicaments utiles dans le traitement des troubles du systeme nerveux central |
| FR2581059B1 (fr) | 1985-04-25 | 1988-04-22 | Pf Medicament | Procede de preparation du chlorhydrate de phenyl-1 diethyl amino carbonyl-1 aminomethyl-2 cyclopropane (z) |
| FR2640972B1 (es) | 1988-12-28 | 1991-04-19 | Pf Medicament | |
| JPH0834765A (ja) * | 1994-02-22 | 1996-02-06 | Asahi Chem Ind Co Ltd | アミノアルキルシクロプロパン誘導体 |
| EP0747348A4 (en) | 1994-02-22 | 1999-07-07 | Asahi Chemical Ind | AMINOALKYLCYCLOPROPAN DERIVATIVES |
| US7309799B2 (en) | 2004-06-01 | 2007-12-18 | Collegium Pharmaceutical, Inc. | Methods for the synthesis of milnacipran and congeners thereof |
| JP4712320B2 (ja) * | 2004-06-16 | 2011-06-29 | 住友化学株式会社 | 2−オキソ−1−フェニル−3−オキサビシクロ[3.1.0]ヘキサンの製造方法 |
| JP4418717B2 (ja) * | 2004-06-24 | 2010-02-24 | 住友化学株式会社 | (z)−1−フェニル−1−ジエチルアミノカルボニル−2−アミノメチルシクロプロパン塩酸塩の製造方法 |
| KR101070721B1 (ko) | 2004-06-25 | 2011-10-07 | 스미또모 가가꾸 가부시키가이샤 | (z)-1-페닐-1-디에틸아미노카르보닐-2-히드록시메틸시클로프로판의 제조 방법 |
| JP4828863B2 (ja) | 2005-01-28 | 2011-11-30 | 住友化学株式会社 | (z)−1−フェニル−1−(n,n−ジエチルアミノカルボニル)−2−フタルイミドメチルシクロプロパンの製造方法 |
| KR100772244B1 (ko) * | 2005-07-20 | 2007-11-01 | 안국약품 주식회사 | 밀나시프란염산염의 제조방법 |
| CN102986288B (zh) | 2009-12-04 | 2016-12-07 | 交互数字专利控股公司 | 用于混合网络中的汇聚网关的扩展本地ip接入 |
-
2009
- 2009-01-29 FR FR0950552A patent/FR2941454B1/fr active Active
-
2010
- 2010-01-25 TW TW099101933A patent/TWI455911B/zh active
- 2010-01-29 KR KR1020117019602A patent/KR101719011B1/ko active Active
- 2010-01-29 EP EP10701538.0A patent/EP2391599B1/en active Active
- 2010-01-29 BR BRPI1007404A patent/BRPI1007404B8/pt active IP Right Grant
- 2010-01-29 UA UAA201110404A patent/UA104884C2/uk unknown
- 2010-01-29 MA MA34052A patent/MA33025B1/fr unknown
- 2010-01-29 AU AU2010209686A patent/AU2010209686B2/en active Active
- 2010-01-29 JP JP2011546850A patent/JP5646509B2/ja active Active
- 2010-01-29 US US13/146,361 patent/US8604241B2/en active Active
- 2010-01-29 WO PCT/EP2010/051045 patent/WO2010086394A1/en not_active Ceased
- 2010-01-29 NZ NZ594291A patent/NZ594291A/xx unknown
- 2010-01-29 CN CN201910530393.XA patent/CN110204455A/zh active Pending
- 2010-01-29 AR ARP100100245A patent/AR077526A1/es not_active Application Discontinuation
- 2010-01-29 RU RU2011135326/04A patent/RU2521342C2/ru active
- 2010-01-29 ES ES10701538.0T patent/ES2472695T3/es active Active
- 2010-01-29 PL PL10701538T patent/PL2391599T3/pl unknown
- 2010-01-29 MX MX2011007846A patent/MX2011007846A/es active IP Right Grant
- 2010-01-29 GE GEAP201012350A patent/GEP20135903B/en unknown
- 2010-01-29 CN CN2010800057211A patent/CN102300840A/zh active Pending
- 2010-01-29 CA CA2750488A patent/CA2750488C/en active Active
-
2011
- 2011-07-21 IL IL214241A patent/IL214241A/en active IP Right Grant
- 2011-07-22 ZA ZA2011/05414A patent/ZA201105414B/en unknown
- 2011-07-22 TN TN2011000363A patent/TN2011000363A1/fr unknown
-
2019
- 2019-06-04 AR ARP190101513A patent/AR115475A2/es active IP Right Grant
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR115475A2 (es) | Método para la síntesis de (1s,2r)-milnaciprán | |
| JP5186722B2 (ja) | スルフリルフルオリドを用いるフッ素化反応 | |
| RU2015142826A (ru) | Способ получения натриевой соли (2s, 5r)-2-карбоксамидо-7-оксо-6-сульфоокси-1, 6-диаза-бицикло[3.2.1]октана | |
| EA201290872A1 (ru) | Способ получения бензоксаборолов | |
| RU2018132264A (ru) | Промежуточные продукты в синтезе эрибулина и соответствующие способы синтеза | |
| CO6290754A2 (es) | Método para producir bicarbonato de arginina | |
| PE20090956A1 (es) | PROCESO PARA LA OBTENCION DE DERIVADOS DE PIRIDO [2,1-a] - ISOQUINOLINA | |
| Neelarapu et al. | A one-pot selective synthesis of N-Boc protected secondary amines: tandem direct reductive amination/N-Boc protection | |
| JP5681985B2 (ja) | 二酸化炭素固定化による尿素化合物の製造法 | |
| CN1331849C (zh) | 甲砜霉素和氟苯尼考的新合成方法及其关键中间体 | |
| NO20082271L (no) | Framgangsmate for framstilling av ioheksol | |
| CN103709194B (zh) | 光学活性的羟基保护的脂肪族磷酸酯的制备方法 | |
| JP6377676B2 (ja) | 新規なヒドロキサム酸誘導体の製造方法 | |
| AR047686A1 (es) | Un procedimiento de sintesis de compuestos de 1,3-dihidro-2h-3-benzazepin-2-ona, y su aplicacion a la sintesis de la ivabradina y sus sales de adicion con un acido farmaceuticamente aceptable | |
| Mao et al. | A practical, chemoselective approach to O-methylation of carboxylic acids with dimethyl malonate | |
| US11708341B2 (en) | Synthesis of (S)-2-amino-4-methyl-((R)-2-methyloxirane-2-yl)-pentan-1-one and pharmaceutically acceptable salts thereof | |
| Lee et al. | Ring-opening of cis-3-Substituted-2-vinylaziridines with Heteroatom Nucleophiles | |
| Bouillon et al. | Efficient synthesis of esters containing tertiary amine functionalities via active cyanomethyl ester intermediates | |
| Leiris et al. | Synthesis and biological evaluation of cyclic nitrogen mustards based on carnitine framework | |
| CA3032963C (en) | Synthesis of (s)-2-amino-4-methyl-1-((r)-2-methyloxirane-2-yl)-pentan-1-one and pharmaceutically acceptable salts thereof | |
| Jacobo et al. | An efficient preparation of stereospecific β-hydroxy nitriles | |
| CN104031060B (zh) | 青蒿素简化类似物及其制备方法和用途 | |
| JP6426015B2 (ja) | 光学活性含フッ素アミン化合物及びその製造方法 | |
| ITMI20040582A1 (it) | Processo per la semisintesi di deserpidina | |
| JP5645537B2 (ja) | ヒドロキシエステル誘導体の製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |