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ES2495815T3 - Proceso para la síntesis de lacosamida - Google Patents

Proceso para la síntesis de lacosamida Download PDF

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Publication number
ES2495815T3
ES2495815T3 ES10814670.5T ES10814670T ES2495815T3 ES 2495815 T3 ES2495815 T3 ES 2495815T3 ES 10814670 T ES10814670 T ES 10814670T ES 2495815 T3 ES2495815 T3 ES 2495815T3
Authority
ES
Spain
Prior art keywords
compound
formula
lacosamide
synthesis
salt
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.)
Active
Application number
ES10814670.5T
Other languages
English (en)
Inventor
Alberto Bologna
Patrizia Castoldi
Domenico Vergani
Giorgio Bertolini
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Archimica SpA
Original Assignee
Euticals SpA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42174220&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2495815(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Euticals SpA filed Critical Euticals SpA
Application granted granted Critical
Publication of ES2495815T3 publication Critical patent/ES2495815T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/12Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/16Preparation of optical isomers
    • C07C231/20Preparation of optical isomers by separation of optical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/04Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C237/06Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/22Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Saccharide Compounds (AREA)

Abstract

Proceso para la síntesis de lacosamida que comprende los siguientes pasos: (a) hidroximetilación del compuesto de fórmula V para obtener el compuesto de fórmula VI (b) hidrólisis del compuesto de fórmula VI para obtener el compuesto de fórmula VII (c) salificación del compuesto de fórmula VII con un ácido quiral (HX*) en un disolvente orgánico, para obtener la mezcla diastereoisomérica VIII; (d) resolución de la mezcla diastereoisomérica VIII para obtener la sal IX; (e) conversión de la sal IX en lacosamida

Description

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Claims (1)

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ES10814670.5T 2010-01-29 2010-12-22 Proceso para la síntesis de lacosamida Active ES2495815T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
ITMI2010A000127A IT1398044B1 (it) 2010-01-29 2010-01-29 Processo per la preparazione della lacosamide
ITMI20100127 2010-01-29
PCT/IB2010/056014 WO2011092559A1 (en) 2010-01-29 2010-12-22 Process for the synthesis of lacosamide

Publications (1)

Publication Number Publication Date
ES2495815T3 true ES2495815T3 (es) 2014-09-17

Family

ID=42174220

Family Applications (1)

Application Number Title Priority Date Filing Date
ES10814670.5T Active ES2495815T3 (es) 2010-01-29 2010-12-22 Proceso para la síntesis de lacosamida

Country Status (12)

Country Link
US (1) US8796488B2 (es)
EP (1) EP2528892B1 (es)
JP (1) JP5779592B2 (es)
KR (1) KR101766506B1 (es)
CN (1) CN102822140B (es)
BR (1) BR112012018625A2 (es)
CL (1) CL2012002082A1 (es)
ES (1) ES2495815T3 (es)
IL (1) IL220936A (es)
IT (1) IT1398044B1 (es)
RU (1) RU2585762C2 (es)
WO (1) WO2011092559A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013030654A1 (en) 2011-08-29 2013-03-07 Signa S.A. De C.V. Processes for the preparation of (r)-2-acetamido-n-benzyl-3-methoxypropionamide and intermediates thereof
CN102424655B (zh) * 2011-10-28 2014-04-16 杭州迪克化工技术有限公司 一种r-(-)-2-乙酰胺基-3-甲氧基-n-苄基丙酰胺的制备方法
CN102516114B (zh) * 2011-10-28 2014-04-16 杭州迪克化工技术有限公司 一种r-(-)-2-氨基-3-甲氧基-n-苄基丙酰胺-d-酒石酸盐及其制备方法
GB201219627D0 (en) 2012-11-01 2012-12-12 Cambrex Karlskoga Ab New process
WO2016021711A1 (ja) * 2014-08-07 2016-02-11 株式会社エーピーアイ コーポレーション アミノ酸誘導体の製造方法
WO2016039393A1 (ja) * 2014-09-10 2016-03-17 株式会社エーピーアイ コーポレーション アミノ酸誘導体の製造方法
CN106699595B (zh) * 2015-07-21 2019-04-12 上海医药集团股份有限公司 一种拉科酰胺制备方法
CN106699605B (zh) * 2015-07-21 2019-08-20 上海医药集团股份有限公司 一种拉科酰胺中间体的甲基化方法
IN2015CH05001A (es) * 2015-09-18 2015-10-16 Divis Lab Ltd
WO2017082396A1 (ja) 2015-11-13 2017-05-18 株式会社エーピーアイ コーポレーション ラコサミド及びその中間体の製造方法
CN107641087A (zh) * 2017-06-01 2018-01-30 合肥远志医药科技开发有限公司 一种工业化拉科酰胺的制备方法
JP2022072636A (ja) * 2020-10-30 2022-05-17 住友化学株式会社 アミド化合物の製造方法
CN112574058B (zh) * 2020-12-31 2023-04-28 珠海润都制药股份有限公司 一种拉考沙胺的合成路线

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5773475A (en) 1997-03-17 1998-06-30 Research Corporation Technologies, Inc. Anticonvulsant enantiomeric amino acid derivatives
ATE268169T1 (de) * 1996-03-15 2004-06-15 Res Corp Technologies Inc Antikonvulsive enantiomerische aminosäurederivate
EP1642889A1 (en) * 2004-10-02 2006-04-05 Schwarz Pharma Ag Improved synthesis scheme for lacosamide
CN100584821C (zh) * 2007-07-31 2010-01-27 浙江九洲药业股份有限公司 一种制备光学纯度叔亮氨酸的方法
US8093426B2 (en) 2007-12-04 2012-01-10 Ranbaxy Laboratories Limited Intermediate compounds and their use in preparation of lacosamide
CN101333175A (zh) * 2008-07-29 2008-12-31 东南大学 制备d-天冬酰胺及d-高丝氨酸的方法
WO2010052011A1 (en) * 2008-11-07 2010-05-14 Ucb Pharma, S.A. Novel process for the preparation of amino acid derivatives

Also Published As

Publication number Publication date
CL2012002082A1 (es) 2013-07-26
IL220936A (en) 2014-11-30
RU2012131215A (ru) 2014-03-10
IT1398044B1 (it) 2013-02-07
JP2013518092A (ja) 2013-05-20
KR20130006438A (ko) 2013-01-16
JP5779592B2 (ja) 2015-09-16
EP2528892A1 (en) 2012-12-05
ITMI20100127A1 (it) 2011-07-30
US8796488B2 (en) 2014-08-05
EP2528892B1 (en) 2014-06-04
KR101766506B1 (ko) 2017-08-08
RU2585762C2 (ru) 2016-06-10
WO2011092559A1 (en) 2011-08-04
IL220936A0 (en) 2012-09-24
US20130030216A1 (en) 2013-01-31
BR112012018625A2 (pt) 2016-04-05
CN102822140A (zh) 2012-12-12
CN102822140B (zh) 2014-10-22

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