JPS5649381A - Preparation of cephalosporin analogue - Google Patents
Preparation of cephalosporin analogueInfo
- Publication number
- JPS5649381A JPS5649381A JP12488879A JP12488879A JPS5649381A JP S5649381 A JPS5649381 A JP S5649381A JP 12488879 A JP12488879 A JP 12488879A JP 12488879 A JP12488879 A JP 12488879A JP S5649381 A JPS5649381 A JP S5649381A
- Authority
- JP
- Japan
- Prior art keywords
- salt
- cephalosporin
- analogue
- thiourea
- reacting
- 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
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
PURPOSE: To prepare the titled compound useful as a medicine having extremely excellent antibacterial activity, economically, in an industrial scale, by reacting a cephalosporin analogue or its salt with thiourea.
CONSTITUTION: The compound of formula II (R1 is H, etc.; R2 is H, lower alkyl, etc.; R3 is carboxy) is obtained by reacting the cephalosporin analogue of formula I (X is halogen) or its salt with thiourea in a reaction solvent (e.g. water, alcohol, etc.), and if necessary, eliminating the protecting group of R3 by conventional method, and further converting to a proper pharmacologically acceptable salt. The reaction is carried out at room temperature or with heat for 1hr to several days.
EFFECT: The protection and deprotection of the 2-position amino group of the thiazolyl group are not necessary.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12488879A JPS5649381A (en) | 1979-09-28 | 1979-09-28 | Preparation of cephalosporin analogue |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12488879A JPS5649381A (en) | 1979-09-28 | 1979-09-28 | Preparation of cephalosporin analogue |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5649381A true JPS5649381A (en) | 1981-05-02 |
Family
ID=14896571
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12488879A Pending JPS5649381A (en) | 1979-09-28 | 1979-09-28 | Preparation of cephalosporin analogue |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5649381A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0082501A1 (en) * | 1981-12-18 | 1983-06-29 | Kyowa Hakko Kogyo Co., Ltd | Beta-lactam compound and a pharmaceutical composition containing the same |
-
1979
- 1979-09-28 JP JP12488879A patent/JPS5649381A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0082501A1 (en) * | 1981-12-18 | 1983-06-29 | Kyowa Hakko Kogyo Co., Ltd | Beta-lactam compound and a pharmaceutical composition containing the same |
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