JPS5690089A - Synthesis of 7-methoxycephem compound - Google Patents
Synthesis of 7-methoxycephem compoundInfo
- Publication number
- JPS5690089A JPS5690089A JP16767179A JP16767179A JPS5690089A JP S5690089 A JPS5690089 A JP S5690089A JP 16767179 A JP16767179 A JP 16767179A JP 16767179 A JP16767179 A JP 16767179A JP S5690089 A JPS5690089 A JP S5690089A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- compound shown
- lower alkyl
- 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 a synthetic intermediate for a compound having a strong resistance to β-lactamase extremely readily by one step, by reacting a cephem compound with methanol in the presence of a compound, e.g., chloramine T and boric acid.
CONSTITUTION: A cephem compound shown by the formula I (R1 is lower alkyl; R2 and R3 are carboxylic acid-protecting group; Y is halogen or lower alkyl; Z is organic or inorganic group residue) is reacted with methanol in the presence of a compound shown by the formula II (R4 is lower alkyl; n is 0-3; M is alkali metal; X is halogen) and boric acid, to give a compound shown by the formula III. The reaction is carried out in an inert solvent, e.g., dichloromethane, etc. at 0W40°C. The compound shown by the formula I as a starting material is obtained by reacting a compound shown by the formula IV and a compound shown by the formula V.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16767179A JPS5690089A (en) | 1979-12-25 | 1979-12-25 | Synthesis of 7-methoxycephem compound |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16767179A JPS5690089A (en) | 1979-12-25 | 1979-12-25 | Synthesis of 7-methoxycephem compound |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5690089A true JPS5690089A (en) | 1981-07-21 |
JPS6219432B2 JPS6219432B2 (en) | 1987-04-28 |
Family
ID=15854053
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16767179A Granted JPS5690089A (en) | 1979-12-25 | 1979-12-25 | Synthesis of 7-methoxycephem compound |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5690089A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0742219A1 (en) * | 1995-05-10 | 1996-11-13 | Bristol-Myers Squibb Company | Preparation and use of 7-((2-carbo-alkoxy-1-methylethenyl) amino)-3-hydroxymethyl-3-cephem-4-carboxylic acids |
-
1979
- 1979-12-25 JP JP16767179A patent/JPS5690089A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0742219A1 (en) * | 1995-05-10 | 1996-11-13 | Bristol-Myers Squibb Company | Preparation and use of 7-((2-carbo-alkoxy-1-methylethenyl) amino)-3-hydroxymethyl-3-cephem-4-carboxylic acids |
Also Published As
Publication number | Publication date |
---|---|
JPS6219432B2 (en) | 1987-04-28 |
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