JPS57134487A - Preparation of 7alpha-methoxycephalosporin compound - Google Patents
Preparation of 7alpha-methoxycephalosporin compoundInfo
- Publication number
- JPS57134487A JPS57134487A JP56019615A JP1961581A JPS57134487A JP S57134487 A JPS57134487 A JP S57134487A JP 56019615 A JP56019615 A JP 56019615A JP 1961581 A JP1961581 A JP 1961581A JP S57134487 A JPS57134487 A JP S57134487A
- Authority
- JP
- Japan
- Prior art keywords
- compound shown
- formula
- methoxylation
- compound
- methanol
- 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
Landscapes
- Cephalosporin Compounds (AREA)
Abstract
PURPOSE: To obtain the titled compound useful as an antibacterial agent simply in high yield, by using 7β-side chain-Δ3-cephem-4-carboxylic acid having an amino-protecting group at 7-position to undergo easily 7α-methoxylation as a starting raw material.
CONSTITUTION: A compound shown by the formulaI(R1 is hydrocarbon group; A is H, halogen, alkyl, etc.; W is H, alkyl, aryl, etc.) is treated with a halogenating agent (e.g., chlorine, bromine) in the presence of an alkali metal salt (e.g., lithium methoxide) of methanol and methanol to give a compound shown by the formula II (W' is W), which is reacted with a compound shown by the formula III (R2 is H or carboxyl; R3 is H, carbamoyl, etc.) or its salt, to give a 7α-methoxycephalosporin compound shown by the formula IV. The compound shown by the formulaIis easily subjected to 7α-methoxylation, and after methoxylation, it can be introduced into the compound shown by the formula IV directly without removing the amino-protecting group.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56019615A JPS57134487A (en) | 1981-02-12 | 1981-02-12 | Preparation of 7alpha-methoxycephalosporin compound |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56019615A JPS57134487A (en) | 1981-02-12 | 1981-02-12 | Preparation of 7alpha-methoxycephalosporin compound |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57134487A true JPS57134487A (en) | 1982-08-19 |
JPH0132830B2 JPH0132830B2 (en) | 1989-07-10 |
Family
ID=12004084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56019615A Granted JPS57134487A (en) | 1981-02-12 | 1981-02-12 | Preparation of 7alpha-methoxycephalosporin compound |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57134487A (en) |
-
1981
- 1981-02-12 JP JP56019615A patent/JPS57134487A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH0132830B2 (en) | 1989-07-10 |
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