DK378781A - PROCEDURE FOR THE PREPARATION OF 4-AMINOBUTIC ACID AMIDES - Google Patents

PROCEDURE FOR THE PREPARATION OF 4-AMINOBUTIC ACID AMIDES

Info

Publication number
DK378781A
DK378781A DK378781A DK378781A DK378781A DK 378781 A DK378781 A DK 378781A DK 378781 A DK378781 A DK 378781A DK 378781 A DK378781 A DK 378781A DK 378781 A DK378781 A DK 378781A
Authority
DK
Denmark
Prior art keywords
group
alkyl group
carbon atoms
integer
linear
Prior art date
Application number
DK378781A
Other languages
Danish (da)
Inventor
J P Chambon
J C Molimard
Original Assignee
Sanofi Sa
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
Application filed by Sanofi Sa filed Critical Sanofi Sa
Publication of DK378781A publication Critical patent/DK378781A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/185Radicals derived from carboxylic acids from aliphatic carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/70Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

1. Claims for the Contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL, SE Amides of 4-aminobutyric acid corresponding to general formula : see diagramm : EP0046707,P19,F3 in which : R designates a linear or branched alkyl group having from 1 to 7 carbon atoms or a cycloalkyl group ; m represents an integer of from 0 to 3 ; n represents an integer of from 0 to 2, on condition that m + n is equal to or greater than 1 ; X represents hydrogen, a lower alkyl group (1 to 4 carbons), a phenylalkyl group in which the phenyl group is possibility substituted, R1 and R2 considered separately designate hydrogen, a linear or branched alkyl group having from 1 to 18 carbon atoms, an aralkyl group, a cycloalkyl group or a possibly substituted phenyl group, or R1 and R2 considered together with the nitrogen atom to which they are attached represent a heterocycle with 5 or 6 groupings possibly comprising a second heteroatom such as pyrrolidine, morpholine, piperazine or pyridine and its partially or totally hydrogenated derivatives. 1. Claims for the Contracting State : AT Process for preparing amides of 4-aminobutyric acid corresponding to general formula (I) : see diagramm : EP0046707,P20,F3 in which : R designates a linear or branched alkyl group having from 1 to 7 carbon atoms or a cycloalkyl group ; m represents an integer of from 0 to 3 ; n represents an integer from 0 to 2, condition that m + n is equal to or greater than 1 ; X represents hydrogen, a lower alkyl group (1 to 4 carbons), a phenylalkyl group in which the phenyl group is possibly substituted, R1 and R2 considered separately designate hydrogen, a linear or branched alkyl group having from 1 to 18 carbon atoms, an aralkyl group, a cycloalkyl group or a possibly substituted phenyl group, or R1 and R2 considered together with the nitrogen atom to which they are attached represent a theterocycle with 5 or 6 groupings possibly comprising a second heteroatom such as pyrrolidine, morpholine, piperazine or pyridine and its partially or totally hydrogenated derivatives, characterized in that the starting product is constituted by an aminoacid of formula : see diagramm : EP0046707,P20,F4 in which m, n and X are such as defined above and R' is a hydrogen atom or a lower alkyl group (1 to 4 carbon atoms), said product is reacted on an acid chloride of formula R-COCI so as to convert the amine of the starting product into an amide radical and the product obtained is subjected to an amidification with a product of formula see diagramm : EP0046707,P21,F1
DK378781A 1980-08-27 1981-08-26 PROCEDURE FOR THE PREPARATION OF 4-AMINOBUTIC ACID AMIDES DK378781A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8018609A FR2489319A1 (en) 1980-08-27 1980-08-27 DERIVATIVES OF AMINO-4 BUTYRIC ACID AND MEDICAMENTS, PARTICULARLY ACTIVE ON THE CENTRAL NERVOUS SYSTEM, CONTAINING

Publications (1)

Publication Number Publication Date
DK378781A true DK378781A (en) 1982-02-28

Family

ID=9245433

Family Applications (1)

Application Number Title Priority Date Filing Date
DK378781A DK378781A (en) 1980-08-27 1981-08-26 PROCEDURE FOR THE PREPARATION OF 4-AMINOBUTIC ACID AMIDES

Country Status (15)

Country Link
EP (1) EP0046707B1 (en)
JP (1) JPS5772949A (en)
AT (1) ATE21099T1 (en)
AU (1) AU547392B2 (en)
CA (1) CA1208230A (en)
DE (1) DE3175030D1 (en)
DK (1) DK378781A (en)
ES (1) ES505004A0 (en)
FR (1) FR2489319A1 (en)
GR (1) GR75299B (en)
IE (1) IE52415B1 (en)
NO (1) NO156608C (en)
NZ (1) NZ198110A (en)
PT (1) PT73558B (en)
ZA (1) ZA815662B (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5654301A (en) * 1985-02-15 1997-08-05 Research Corporation Technologies, Inc. Amino acid derivative anticonvulsant
US5378729A (en) * 1985-02-15 1995-01-03 Research Corporation Technologies, Inc. Amino acid derivative anticonvulsant
EP0194464B1 (en) * 1985-02-15 1991-04-03 Research Corporation Technologies, Inc. (a Delaware corp.) Amino acid derivatives and use thereof for the preparation of an anticonvulsant
CA1320734C (en) * 1986-02-04 1993-07-27 Suntory Limited Pyrrolidineamide derivative of acylamino acid and pharmaceutical composition containing the same
US5198458A (en) * 1986-02-04 1993-03-30 Suntory Limited Pyrrolidineamide derivatives of acylamino acid and pharmaceutical composition containing the same
NZ222045A (en) * 1986-08-21 1989-10-27 Res Corp Technologies Inc From diamides up to tetrapeptides for use as anticanvulsants
US4992472A (en) * 1987-06-16 1991-02-12 The United States Of America As Represented By The Department Of Health And Human Services Chemical differentiating agents
US5770625A (en) * 1988-02-08 1998-06-23 The Trustees Of Columbia University In The City Of New York Butyryl-tyrosinyl spermine, analogs thereof and methods of preparing and using same
DE3915756A1 (en) * 1989-05-13 1990-11-29 Bayer Ag CYCLOPROPANOYLAMINOSAEUREAMID DERIVATIVES
DE3915755A1 (en) * 1989-05-13 1990-11-29 Bayer Ag FUNGICIDAL AGENTS AND SUBSTITUTED AMINO ACID DERIVATIVES AND THE PRODUCTION THEREOF
NZ233728A (en) * 1989-05-19 1993-04-28 Res Corp Technologies Inc Amino acid compounds and pharmaceutical compositions thereof
DE4102042A1 (en) * 1991-01-24 1992-07-30 Bayer Ag SUBSTITUTED AMINO ACID DERIVATIVES THEIR PRODUCTION AND USE AS FUNGICIDES
US5585358A (en) * 1993-07-06 1996-12-17 Yissum Research Development Corporation Of The Hebrew University Of Jerusalem Derivatives of valproic acid amides and 2-valproenoic acid amides, method of making and use thereof as anticonvulsant agents
US6037472A (en) * 1993-11-04 2000-03-14 Syntex (U.S.A.) Inc. Matrix metalloprotease inhibitors
IL114483A0 (en) * 1994-07-12 1995-11-27 Yissum Res Dev Co Glycinamide derivatives pharmaceutical compositions containing the same and methods utilizing the same
AU771115B2 (en) * 1999-08-10 2004-03-11 Uab Research Foundation Use of GABA agonists for treatment of spastic disorders, convulsions, and epilepsy
WO2002007677A2 (en) * 2000-07-21 2002-01-31 Teva Pharmaceutical Industries, Ltd. Use of derivatives of valproic acid and 2-valproenic acid amides for the treatment of mania in bipolar disorder
EP1604656A1 (en) 2004-06-09 2005-12-14 Schwarz Pharma Ag Novel use of peptide compounds for treating amyotrophic lateral sclerosis (ALS)
AU2007325686A1 (en) * 2006-11-30 2008-06-05 Cenerx Biopharma, Inc. Dialkylamino alkyl esters of pivagabine as medicaments for the treatment of central nervous system disorders

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB732415A (en) * 1952-07-12 1955-06-22 Ruhrchemie Ag Process for the production of aroylated aminocarboxylic acids
US3022314A (en) * 1955-06-20 1962-02-20 Upjohn Co Alpha-phenyl-omega-amino-alkanamides
IE33790B1 (en) * 1968-06-04 1974-10-30 Beecham Group Ltd Derivatives of n-acylaminoacid amides

Also Published As

Publication number Publication date
IE52415B1 (en) 1987-10-28
IE811835L (en) 1982-02-27
EP0046707A1 (en) 1982-03-03
FR2489319B1 (en) 1984-04-06
EP0046707B1 (en) 1986-07-30
ATE21099T1 (en) 1986-08-15
NZ198110A (en) 1984-12-14
DE3175030D1 (en) 1986-09-04
NO812890L (en) 1982-03-01
CA1208230A (en) 1986-07-22
NO156608B (en) 1987-07-13
ES8206445A1 (en) 1982-08-16
AU7425981A (en) 1982-03-04
AU547392B2 (en) 1985-10-17
JPS5772949A (en) 1982-05-07
ES505004A0 (en) 1982-08-16
GR75299B (en) 1984-07-13
PT73558B (en) 1982-11-03
ZA815662B (en) 1982-08-25
FR2489319A1 (en) 1982-03-05
PT73558A (en) 1981-09-01
NO156608C (en) 1987-10-21

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Legal Events

Date Code Title Description
AHB Application shelved due to non-payment