NO812890L - PROCEDURE FOR THE PREPARATION OF AMIDES OF 4-AMINO ACID ACID - Google Patents

PROCEDURE FOR THE PREPARATION OF AMIDES OF 4-AMINO ACID ACID

Info

Publication number
NO812890L
NO812890L NO812890A NO812890A NO812890L NO 812890 L NO812890 L NO 812890L NO 812890 A NO812890 A NO 812890A NO 812890 A NO812890 A NO 812890A NO 812890 L NO812890 L NO 812890L
Authority
NO
Norway
Prior art keywords
group
alkyl group
carbon atoms
integer
linear
Prior art date
Application number
NO812890A
Other languages
Norwegian (no)
Other versions
NO156608C (en
NO156608B (en
Inventor
Jean-Pierre Chambon
Jean-Charles 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 NO812890L publication Critical patent/NO812890L/en
Publication of NO156608B publication Critical patent/NO156608B/en
Publication of NO156608C publication Critical patent/NO156608C/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
NO812890A 1980-08-27 1981-08-26 ANALOGUE PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE AMIDES OF 4-AMINO ACID ACID. NO156608C (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 (3)

Publication Number Publication Date
NO812890L true NO812890L (en) 1982-03-01
NO156608B NO156608B (en) 1987-07-13
NO156608C NO156608C (en) 1987-10-21

Family

ID=9245433

Family Applications (1)

Application Number Title Priority Date Filing Date
NO812890A NO156608C (en) 1980-08-27 1981-08-26 ANALOGUE PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE AMIDES OF 4-AMINO ACID ACID.

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) ES8206445A1 (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
US5378729A (en) * 1985-02-15 1995-01-03 Research Corporation Technologies, Inc. Amino acid derivative anticonvulsant
ATE62222T1 (en) * 1985-02-15 1991-04-15 Res Corp Technologies Inc AMINO ACID DERIVATIVES AND THEIR APPLICATION FOR THE PREPARATION OF AN ANTI-SEMPK AGENT.
US5654301A (en) * 1985-02-15 1997-08-05 Research Corporation Technologies, Inc. Amino acid derivative 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
JPH03506045A (en) * 1989-05-19 1991-12-26 リサーチ・コーポレイション・テクノロジーズ・インコーポレイテッド Amino acid derivative anticonvulsant
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
CA2378955A1 (en) * 1999-08-10 2001-02-15 Uab Research Foundation Use of gaba agonists for treatment of spastic disorders, convulsions, and epilepsy
IL153942A0 (en) * 2000-07-21 2003-07-31 Teva Pharma 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
NO156608C (en) 1987-10-21
NZ198110A (en) 1984-12-14
PT73558B (en) 1982-11-03
DE3175030D1 (en) 1986-09-04
ZA815662B (en) 1982-08-25
NO156608B (en) 1987-07-13
PT73558A (en) 1981-09-01
IE52415B1 (en) 1987-10-28
GR75299B (en) 1984-07-13
CA1208230A (en) 1986-07-22
ATE21099T1 (en) 1986-08-15
EP0046707B1 (en) 1986-07-30
ES505004A0 (en) 1982-08-16
ES8206445A1 (en) 1982-08-16
IE811835L (en) 1982-02-27
AU547392B2 (en) 1985-10-17
DK378781A (en) 1982-02-28
AU7425981A (en) 1982-03-04
FR2489319A1 (en) 1982-03-05
FR2489319B1 (en) 1984-04-06
EP0046707A1 (en) 1982-03-03
JPS5772949A (en) 1982-05-07

Similar Documents

Publication Publication Date Title
NO812890L (en) PROCEDURE FOR THE PREPARATION OF AMIDES OF 4-AMINO ACID ACID
ES450643A1 (en) Pyrrolidine derivatives
ES467288A1 (en) N-(substituted-aminoalkyl)-2-oxo-1-pyrrolidineacetamides
ES403503A1 (en) Procedure for the preparation of piperidine derivatives and their use as stabilizers (Machine-translation by Google Translate, not legally binding)
ES8604543A1 (en) Piperazine derivatives with anticholinergic and/or antihistaminic activity
ATE162517T1 (en) PRODUCTION OF THIOAMIDS
ES456991A1 (en) 1,2,3-Thiadiazole-5-yl-urea derivatives, process for making the same and plant retardation and defoliation composition containing same
FR2459793B1 (en)
GB1304786A (en)
ES446444A1 (en) Process for the preparation of carbonyl alpha-perfluoro derivatives
FR2494272B1 (en)
ES394484A1 (en) 1,4-benzodiazepine derivatives
ES440438A1 (en) Procedure for the preparation of new derivatives of fenilbutazona. (Machine-translation by Google Translate, not legally binding)
ES427592A1 (en) Dihydroapovincaminic acid amines
ES441029A1 (en) Acetylsalicylic acid derivatives their preparation and compo sitions containing them
ES379188A3 (en) A procedure for the preparation of adamantan derivatives. (Machine-translation by Google Translate, not legally binding)
ES414821A3 (en) A procedure for the preparation of 4-substituted syringic acid thyoamides. (Machine-translation by Google Translate, not legally binding)
IE811611L (en) Thiazolyl oxamic acid derivatives
ES472090A2 (en) Derivatives of amidoximes
IL71929A0 (en) Alpha-alkoxylated n-(trimethylcyclohexen-1-yl)-n-alkyl-(or-n-allyl-)acetamides,their manufacture and phytotoxic compositions containing them
ES277617A2 (en) Procedure to prepare acid amidas 0,0-di (fluoro-alkil) -ditiofosforilacºticos (Machine-translation by Google Translate, not legally binding)
ES391146A3 (en) A procedure for preparing an aminopropionil-orto-totoludine. (Machine-translation by Google Translate, not legally binding)
ES269194A3 (en) Procedure for obtaining phosphoric esters (Machine-translation by Google Translate, not legally binding)
ES437134A1 (en) Process for the manufacture of 2-aminobenzenesulphonamides
ES469894A1 (en) Procedure for the production of new polypedotype derivatives. (Machine-translation by Google Translate, not legally binding)