JPS5522606A - Preparation of 3-amino-2-hydroxy-4-p-hydroxyphenyl- butanoylleucine and its derivative - Google Patents
Preparation of 3-amino-2-hydroxy-4-p-hydroxyphenyl- butanoylleucine and its derivativeInfo
- Publication number
- JPS5522606A JPS5522606A JP8518578A JP8518578A JPS5522606A JP S5522606 A JPS5522606 A JP S5522606A JP 8518578 A JP8518578 A JP 8518578A JP 8518578 A JP8518578 A JP 8518578A JP S5522606 A JPS5522606 A JP S5522606A
- Authority
- JP
- Japan
- Prior art keywords
- amino
- hydroxy
- derivative
- protecting group
- butanoylleucine
- 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.)
- Granted
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 title compound which is an anticarcinogenic immunizing agent, etc., in high yield, by the diazotization of 3-amino-2-hydroxy-4-p- aminophenylbutanoylleucine derivative obtained from easily available bestatin, followed by the decomposition.
CONSTITUTION: 3-Amino-2-hydroxy-4-p-aminophenylbutanoylleucine derivative of formula I(R1 is H; R2 is amino-protecting group; R1 and R2 may form a phthalyl group; R3 is H or protecting group of COOH) is converted into diazonium salt by acting diazotizing agent on it. The title compound of formula II(R4 is H or amino- protecting group; R1 and R4 may form a phthalyl group; R5 is H or protecting group of COOH) is obtained by the decomposition of the diazonium salt. The compound I is produced from bestatin obtained by synthesis or fermentation.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53085185A JPS6039264B2 (en) | 1978-07-14 | 1978-07-14 | Method for producing 3-amino-2-hydroxy-4-p-hydroxyphenylbutanoylleucine and its derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53085185A JPS6039264B2 (en) | 1978-07-14 | 1978-07-14 | Method for producing 3-amino-2-hydroxy-4-p-hydroxyphenylbutanoylleucine and its derivatives |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5522606A true JPS5522606A (en) | 1980-02-18 |
JPS6039264B2 JPS6039264B2 (en) | 1985-09-05 |
Family
ID=13851594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP53085185A Expired JPS6039264B2 (en) | 1978-07-14 | 1978-07-14 | Method for producing 3-amino-2-hydroxy-4-p-hydroxyphenylbutanoylleucine and its derivatives |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6039264B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5793253U (en) * | 1980-11-29 | 1982-06-08 | ||
JPS63268910A (en) * | 1987-04-24 | 1988-11-07 | Mazda Motor Corp | Exhaust purifier for engine |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0216779A (en) * | 1988-07-04 | 1990-01-19 | Matsushita Electric Ind Co Ltd | Light emitting diode type indicator |
-
1978
- 1978-07-14 JP JP53085185A patent/JPS6039264B2/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5793253U (en) * | 1980-11-29 | 1982-06-08 | ||
JPS5938933Y2 (en) * | 1980-11-29 | 1984-10-30 | フランスベッド株式会社 | spring structure |
JPS63268910A (en) * | 1987-04-24 | 1988-11-07 | Mazda Motor Corp | Exhaust purifier for engine |
Also Published As
Publication number | Publication date |
---|---|
JPS6039264B2 (en) | 1985-09-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS5522606A (en) | Preparation of 3-amino-2-hydroxy-4-p-hydroxyphenyl- butanoylleucine and its derivative | |
JPS5414932A (en) | Purification of phenylhydrazine | |
JPS57192340A (en) | Isoprenylamine derivative | |
JPS5318510A (en) | Preparation of geranyl farnesylacetate | |
JPS6446A (en) | Production of 4-hydroxy-2-cyclopentenone derivative | |
JPS5289603A (en) | Preparation of perfluorovinyl compounds | |
JPS51122043A (en) | Process for preparation of 3-hydroxy-5- cycloxycyclopento-1-ene deriva tives | |
JPS5625166A (en) | 5-fluorouracil derivative | |
JPS5344548A (en) | Preparation of 1,3-indandion | |
JPS5242807A (en) | Process for preparation of alkyleneglycol | |
JPS5231059A (en) | Preparation of oxybenzoylbenzoic acids | |
JPS5369883A (en) | Preparation of l-serine by fermentation | |
JPS539786A (en) | Preparation of 6-aminopenicillanic acid acylates | |
JPS5368777A (en) | Preparation of phenyathridine | |
JPS5346926A (en) | Preparation of 6-methyl-2,3,4-trimethoxyphenol | |
JPS5439073A (en) | Preparation of 2,3,3-trimethylindolenine | |
JPS5387358A (en) | Gamma-pyrone compound, its preparation and agricultural medicine therefrom | |
JPS5283706A (en) | Novel propargyl alcohol derivatives and preparation thereof | |
JPS5432438A (en) | Preparation of tyrosinol derivatives | |
JPS5422353A (en) | 2-chloro-2-cyano-7-alkylidene-bicyclo(2,2,1)-5-heptene and its preparation | |
JPS51133249A (en) | A process for preparing alkyl-2,4- dichloro-nitrophenylcarbonates | |
JPS5579366A (en) | Preparation of 2-aminoindolenine | |
JPS52111513A (en) | Preparation of 3,3-dimethyl-4-penthnoic acid methyl ester | |
JPS52105153A (en) | Preparation of 5-cyanomethyl-2-oxo-cyclopentanecarboxylic acid ester | |
JPS51143645A (en) | Process for preparation of 3,3-dimethyl- 2-(2,2-dihalo)cyclopropanecar boxylic acid ester |