JPS5726690A - New preparation of cephamycin derivative - Google Patents
New preparation of cephamycin derivativeInfo
- Publication number
- JPS5726690A JPS5726690A JP10060380A JP10060380A JPS5726690A JP S5726690 A JPS5726690 A JP S5726690A JP 10060380 A JP10060380 A JP 10060380A JP 10060380 A JP10060380 A JP 10060380A JP S5726690 A JPS5726690 A JP S5726690A
- Authority
- JP
- Japan
- Prior art keywords
- protecting group
- give
- formula
- compound
- carboxyl
- 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
Landscapes
- Cephalosporin Compounds (AREA)
Abstract
PURPOSE: To obtain the titled compound useful as an antimicrobial agent, etc. in high yield, by treating a specific amide group-containing cephem carboxylic acid with a halogenating agent, followed by imino etherification with a lower alcohol, treatment with an acylating agent, and removal of protecting group.
CONSTITUTION: A compound shown by the formula I (R1 is amino-protecting group; R2 is H or amino-protecting group; R3 and R4 are carboxyl-protecting group) is treated with a halogenating agent in the presence of a base to give an imino halide derivative, which is reacted with a lower alcohol to give an imino ether derivative shown by the formula II (R5 is lower alkyl). This compound is reacted with an acylating agent to give a compound shown by the formula III [R6 is X2CH (X2 is halogen), etc.], the carboxyl-protecting group R4 is removed and the resulting compound is reacted with cysteine, etc., to give 7β-(2D-2-amino-2-carboxyl) eth ethyl-thioacetamido-7α-methoxy-3-( 1-methyl-1H-tetrazole-5-yl )thiomethyl-3-cephem-4-carboxylic acid shown by the formula IV or its salt.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10060380A JPS5726690A (en) | 1980-07-24 | 1980-07-24 | New preparation of cephamycin derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10060380A JPS5726690A (en) | 1980-07-24 | 1980-07-24 | New preparation of cephamycin derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5726690A true JPS5726690A (en) | 1982-02-12 |
Family
ID=14278432
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10060380A Pending JPS5726690A (en) | 1980-07-24 | 1980-07-24 | New preparation of cephamycin derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5726690A (en) |
-
1980
- 1980-07-24 JP JP10060380A patent/JPS5726690A/en active Pending
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