ES8606845A1 - Un procedimiento para preparar un compuesto hidrolizable para formar un -aminoacido - Google Patents
Un procedimiento para preparar un compuesto hidrolizable para formar un -aminoacidoInfo
- Publication number
- ES8606845A1 ES8606845A1 ES537664A ES537664A ES8606845A1 ES 8606845 A1 ES8606845 A1 ES 8606845A1 ES 537664 A ES537664 A ES 537664A ES 537664 A ES537664 A ES 537664A ES 8606845 A1 ES8606845 A1 ES 8606845A1
- Authority
- ES
- Spain
- Prior art keywords
- amino acids
- enamides
- alpha
- catalytic reaction
- hydroxyl compound
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
- Indole Compounds (AREA)
Abstract
PROCEDIMIENTO PARA LA OBTENCION DE ESTERES DE N-ACIL-A-AMINOACIDOS, DE FORMULA (I), EN LA QUE R1, R2, R3, R4, R5 Y R6 PUEDEN SER VARIOS TIPOS DE RADICALES. CONSISTE EN LA REACCION DE UNA ENAMIDA DE FORMULA (II) CON UN MONOXIDO DE CARBONO Y AGUA O UN COMPUESTO HIDROXILICO ORGANICO, DE FORMULA R6OH, EN LAS QUE TODOS LOS SIMBOLOS TIENEN EL MISMO SIGNIFICADO QUE EN LA FORMULA (I). LA REACCION SE LLEVA A CABO EN UN DISOLVENTE ORGANICO INERTE, EN PRESENCIA DE UN CATALIZADOR, COMPUESTO DE PALADIO, A UNA TEMPERATURA COMPRENDIDA ENTRE 0JC Y 250JC. ESTOS COMPUESTOS TIENEN APLICACIONES PARA LA OBTENCION DE A-AMINOACIDOS EMPLEADOS EN LA PRODUCCION DE PEPTIDOS Y PROTEINAS PARA ALIMENTACION ANIMAL.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/552,561 US4710574A (en) | 1983-11-16 | 1983-11-16 | α-amino acids through catalytic reaction of CO and a hydroxyl compound with enamides |
Publications (2)
Publication Number | Publication Date |
---|---|
ES8606845A1 true ES8606845A1 (es) | 1986-05-01 |
ES537664A0 ES537664A0 (es) | 1986-05-01 |
Family
ID=24205868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES537664A Expired ES8606845A1 (es) | 1983-11-16 | 1984-11-15 | Un procedimiento para preparar un compuesto hidrolizable para formar un -aminoacido |
Country Status (8)
Country | Link |
---|---|
US (1) | US4710574A (es) |
EP (1) | EP0145265B1 (es) |
JP (1) | JPS60185753A (es) |
KR (1) | KR850004100A (es) |
BR (1) | BR8405713A (es) |
CA (1) | CA1228858A (es) |
DE (1) | DE3479797D1 (es) |
ES (1) | ES8606845A1 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4929755A (en) * | 1985-10-07 | 1990-05-29 | The Standard Oil Company | Process for making an optically active mixture of an N-acyl-amino acid or ester containing at least two chiral centers |
US4749811A (en) * | 1985-10-29 | 1988-06-07 | The Standard Oil Company | Method of making a diastereomeric mixture containing two diastereomeric α-acyloxy acid esters |
US4721803A (en) * | 1985-10-29 | 1988-01-26 | The Standard Oil Company | Method of making a diastereomeric mixture containing two diastereomeric N-acyl-amino acid esters |
US4891442A (en) * | 1987-03-09 | 1990-01-02 | Texaco Inc. | Process for synthesis of β-phenylalanine |
WO1998035930A1 (en) * | 1997-02-13 | 1998-08-20 | Monsanto Company | Method of preparing amino carboxylic acids |
AU754281B2 (en) * | 1998-08-12 | 2002-11-14 | Monsanto Company | Continuous process for the preparation of N-(phosphonomethyl) iminodiacetic acid |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5521737B2 (es) * | 1972-12-23 | 1980-06-12 | ||
FR2395252A1 (fr) * | 1977-06-21 | 1979-01-19 | Inst Francais Du Petrole | Procede de fabrication de derive n-acyle d'acide amine |
-
1983
- 1983-11-16 US US06/552,561 patent/US4710574A/en not_active Expired - Fee Related
-
1984
- 1984-10-05 CA CA000464805A patent/CA1228858A/en not_active Expired
- 1984-10-26 JP JP59225652A patent/JPS60185753A/ja active Pending
- 1984-11-07 DE DE8484307683T patent/DE3479797D1/de not_active Expired
- 1984-11-07 EP EP84307683A patent/EP0145265B1/en not_active Expired
- 1984-11-08 BR BR8405713A patent/BR8405713A/pt unknown
- 1984-11-15 ES ES537664A patent/ES8606845A1/es not_active Expired
- 1984-11-15 KR KR1019840007161A patent/KR850004100A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0145265A2 (en) | 1985-06-19 |
JPS60185753A (ja) | 1985-09-21 |
US4710574A (en) | 1987-12-01 |
EP0145265B1 (en) | 1989-09-20 |
DE3479797D1 (en) | 1989-10-26 |
ES537664A0 (es) | 1986-05-01 |
KR850004100A (ko) | 1985-07-01 |
BR8405713A (pt) | 1985-09-10 |
CA1228858A (en) | 1987-11-03 |
EP0145265A3 (en) | 1985-07-10 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD1A | Patent lapsed |
Effective date: 19970519 |