JPS6445350A - Production of n-substituted-l-amino acid derivative - Google Patents
Production of n-substituted-l-amino acid derivativeInfo
- Publication number
- JPS6445350A JPS6445350A JP62200865A JP20086587A JPS6445350A JP S6445350 A JPS6445350 A JP S6445350A JP 62200865 A JP62200865 A JP 62200865A JP 20086587 A JP20086587 A JP 20086587A JP S6445350 A JPS6445350 A JP S6445350A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- acid derivative
- compound
- amino acid
- base
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Abstract
PURPOSE:To obtain the titled compound useful as a synthetic intermediate for angiotensinase inhibitor, in high yield, by reacting an L-amino acid derivative with a 2-(R)-halogeno-4-phenylbutyric acid derivative in the presence of a base. CONSTITUTION:The objective compound of formula III is produced by reacting an L-amino acid derivative of formula I (R is lower alkyl; R<1> is H or carboxyl- protecting group) with a 2-(R)-halogeno-4-phenylbutyric acid derivative of formula II (R<2> is H or carboxyl-protecting group; X is Br or Cl) in the presence of a base (e.g. ammonium carbonate) in a solvent (e.g. nitromethane-water) at room temperature - 100 deg.C. The amount of the base is >=1mol. per 1mol. of the compound of formula I. The starting compound of formula I is easily available or producible. The compound of formula II can be easily induced from an optically inactive hydantoin derivative as a starting raw material via an optically active N-carbamoyl-2-amino-4-phenylbutyric acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62200865A JPS6445350A (en) | 1987-08-13 | 1987-08-13 | Production of n-substituted-l-amino acid derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62200865A JPS6445350A (en) | 1987-08-13 | 1987-08-13 | Production of n-substituted-l-amino acid derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6445350A true JPS6445350A (en) | 1989-02-17 |
Family
ID=16431508
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62200865A Pending JPS6445350A (en) | 1987-08-13 | 1987-08-13 | Production of n-substituted-l-amino acid derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6445350A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002074728A1 (en) * | 2001-03-19 | 2002-09-26 | Kaneka Corporation | Purification method of n-(1(s)-ethoxycarbonyl-3-phenylpropyl)-l-alanine |
US6518434B2 (en) | 2000-02-07 | 2003-02-11 | Astrazeneca Ab | Coupling process |
-
1987
- 1987-08-13 JP JP62200865A patent/JPS6445350A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6518434B2 (en) | 2000-02-07 | 2003-02-11 | Astrazeneca Ab | Coupling process |
WO2002074728A1 (en) * | 2001-03-19 | 2002-09-26 | Kaneka Corporation | Purification method of n-(1(s)-ethoxycarbonyl-3-phenylpropyl)-l-alanine |
US7071349B2 (en) | 2001-03-19 | 2006-07-04 | Kanaka Corporation | Purification method of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanine |
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