NO812890L - PROCEDURE FOR THE PREPARATION OF AMIDES OF 4-AMINO ACID ACID - Google Patents
PROCEDURE FOR THE PREPARATION OF AMIDES OF 4-AMINO ACID ACIDInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic 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
- C07D295/16—Heterocyclic 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
- C07D295/18—Heterocyclic 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
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic 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
- C07D211/70—Heterocyclic 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
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)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5378729A (en) * | 1985-02-15 | 1995-01-03 | Research Corporation Technologies, Inc. | Amino acid derivative anticonvulsant |
| CA1340902C (en) * | 1985-02-15 | 2000-02-22 | Harold L. Kohn | Amino acid derivative anticonvulsant |
| US5654301A (en) * | 1985-02-15 | 1997-08-05 | Research Corporation Technologies, Inc. | Amino acid derivative anticonvulsant |
| US5198458A (en) * | 1986-02-04 | 1993-03-30 | Suntory Limited | Pyrrolidineamide derivatives of acylamino acid and pharmaceutical composition containing the same |
| CA1320734C (en) * | 1986-02-04 | 1993-07-27 | Suntory Limited | Pyrrolidineamide derivative 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 |
| CA2017217C (en) * | 1989-05-19 | 2002-02-19 | Harold L. Kohn | 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 |
| IL148052A0 (en) * | 1999-08-10 | 2002-09-12 | Uab Research Foundation | Use of gaba antagonists for treatment of spastic disorders, convulsions, and epilepsy |
| KR100843703B1 (en) * | 2000-07-21 | 2008-07-04 | 이섬 리서치 디벨러프먼트 컴파니 오브 더 히브루 유니버시티 오브 예루살렘 | 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) |
| KR20090100360A (en) * | 2006-11-30 | 2009-09-23 | 세넉스 바이오파마, 인크. | Dialkylamino alkyl esters of pivagabine as medicaments for the treatment of central nervous system disorders |
Family Cites Families (3)
| 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 |
-
1980
- 1980-08-27 FR FR8018609A patent/FR2489319A1/en active Granted
-
1981
- 1981-08-11 GR GR65767A patent/GR75299B/el unknown
- 1981-08-11 IE IE1835/81A patent/IE52415B1/en unknown
- 1981-08-13 DE DE8181401299T patent/DE3175030D1/en not_active Expired
- 1981-08-13 AT AT81401299T patent/ATE21099T1/en not_active IP Right Cessation
- 1981-08-13 EP EP81401299A patent/EP0046707B1/en not_active Expired
- 1981-08-17 ZA ZA815662A patent/ZA815662B/en unknown
- 1981-08-18 AU AU74259/81A patent/AU547392B2/en not_active Ceased
- 1981-08-20 NZ NZ198110A patent/NZ198110A/en unknown
- 1981-08-21 CA CA000384370A patent/CA1208230A/en not_active Expired
- 1981-08-24 PT PT73558A patent/PT73558B/en unknown
- 1981-08-26 NO NO812890A patent/NO156608C/en unknown
- 1981-08-26 DK DK378781A patent/DK378781A/en not_active Application Discontinuation
- 1981-08-26 JP JP56132669A patent/JPS5772949A/en active Pending
- 1981-08-26 ES ES505004A patent/ES8206445A1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EP0046707A1 (en) | 1982-03-03 |
| GR75299B (en) | 1984-07-13 |
| AU547392B2 (en) | 1985-10-17 |
| ZA815662B (en) | 1982-08-25 |
| DK378781A (en) | 1982-02-28 |
| EP0046707B1 (en) | 1986-07-30 |
| NO156608C (en) | 1987-10-21 |
| FR2489319A1 (en) | 1982-03-05 |
| ES505004A0 (en) | 1982-08-16 |
| NZ198110A (en) | 1984-12-14 |
| PT73558A (en) | 1981-09-01 |
| FR2489319B1 (en) | 1984-04-06 |
| DE3175030D1 (en) | 1986-09-04 |
| IE52415B1 (en) | 1987-10-28 |
| PT73558B (en) | 1982-11-03 |
| ATE21099T1 (en) | 1986-08-15 |
| JPS5772949A (en) | 1982-05-07 |
| ES8206445A1 (en) | 1982-08-16 |
| NO156608B (en) | 1987-07-13 |
| CA1208230A (en) | 1986-07-22 |
| IE811835L (en) | 1982-02-27 |
| AU7425981A (en) | 1982-03-04 |
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