JPS56150094A - Preparation of cephamycin antibiotic - Google Patents
Preparation of cephamycin antibioticInfo
- Publication number
- JPS56150094A JPS56150094A JP5305880A JP5305880A JPS56150094A JP S56150094 A JPS56150094 A JP S56150094A JP 5305880 A JP5305880 A JP 5305880A JP 5305880 A JP5305880 A JP 5305880A JP S56150094 A JPS56150094 A JP S56150094A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- group
- cephem
- protecting group
- 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 an antimicrobial agent Cefmetazole, etc. readily without using an unstable raw material, by cyanomethylating a novel cephem compound.
CONSTITUTION: A 7β-mercaptoacetamido-7α-methoxy-3-cephem compound of formula I (R1 is a group which will not participate in the reaction; R2 is carboxyl or protected carboxyl) is reacted with a novel compound of the formula NCCH2X (X is halogen, etc.) in the presence of a base, and the protecting group is removed when R2 is an esterified carboxyl group to give a 7β-cyanomethylthioacetamido- 7α-methoxy-3-substituted-3-cephem-4-carboxylic acid of formula II. An unstable raw material such as cyanomethylthioacetyl halide need not be used. The novel compound of formula I is obtained by removing the protecting group R3 from a compound of formula III (R3 is a protecting group of the mercapto group) by the conventional method.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5305880A JPS56150094A (en) | 1980-04-22 | 1980-04-22 | Preparation of cephamycin antibiotic |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5305880A JPS56150094A (en) | 1980-04-22 | 1980-04-22 | Preparation of cephamycin antibiotic |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56150094A true JPS56150094A (en) | 1981-11-20 |
JPH0128037B2 JPH0128037B2 (en) | 1989-05-31 |
Family
ID=12932242
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5305880A Granted JPS56150094A (en) | 1980-04-22 | 1980-04-22 | Preparation of cephamycin antibiotic |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56150094A (en) |
-
1980
- 1980-04-22 JP JP5305880A patent/JPS56150094A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0128037B2 (en) | 1989-05-31 |
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