JPS5756487A - Novel 7alpha-methoxycephalosporin and its preparation - Google Patents
Novel 7alpha-methoxycephalosporin and its preparationInfo
- Publication number
- JPS5756487A JPS5756487A JP56116188A JP11618881A JPS5756487A JP S5756487 A JPS5756487 A JP S5756487A JP 56116188 A JP56116188 A JP 56116188A JP 11618881 A JP11618881 A JP 11618881A JP S5756487 A JPS5756487 A JP S5756487A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- preparation
- formulai
- reaction
- methoxycephalosporin
- 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
NEW MATERIAL:A compound of formulaI(R1 is H, carboxyl-protecting group, salt-forming cation; R2 is acyloxy, carbamoyloxy; A is alkyl; X is H, hydroxyl).
EXAMPLE: 7β-[D(-)-α-(4-ethyl-2,3-dioxo-1-piperazinylcarbonylamino) phenylacetamide]-7α-methoxy-3-acetoxymethyl-Δ3-cephem-4-carboxylic acid.
USE: Antibiotic: it shows activity against gram-positive and -negative bacteria and has a wide range of antibacterial spectrum. Further, it is stable to cephalosporinase.
PREPARATION: The reaction of a compound of formula II (R8 is organic silyl, organic phosphorus) with a reactive derivative of a compound of formula III at the carboxyl groups is carried out in an inert solvent at -40W50°C to give the compound of formulaI. The reaction may be effected in the presence of a base such as alkali hydroxide or trimethylamine, too.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56116188A JPS6019915B2 (en) | 1981-07-24 | 1981-07-24 | Novel 7α-methoxycephalosporins and their production method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56116188A JPS6019915B2 (en) | 1981-07-24 | 1981-07-24 | Novel 7α-methoxycephalosporins and their production method |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51006117A Division JPS6026800B2 (en) | 1976-01-22 | 1976-01-22 | Novel 7α-methoxycephalosporins and their production method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5756487A true JPS5756487A (en) | 1982-04-05 |
JPS6019915B2 JPS6019915B2 (en) | 1985-05-18 |
Family
ID=14680998
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56116188A Expired JPS6019915B2 (en) | 1981-07-24 | 1981-07-24 | Novel 7α-methoxycephalosporins and their production method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6019915B2 (en) |
-
1981
- 1981-07-24 JP JP56116188A patent/JPS6019915B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS6019915B2 (en) | 1985-05-18 |
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