JPS6475488A - Production of beta-lactam compound - Google Patents
Production of beta-lactam compoundInfo
- Publication number
- JPS6475488A JPS6475488A JP62233260A JP23326087A JPS6475488A JP S6475488 A JPS6475488 A JP S6475488A JP 62233260 A JP62233260 A JP 62233260A JP 23326087 A JP23326087 A JP 23326087A JP S6475488 A JPS6475488 A JP S6475488A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- beta
- production
- alkyl
- 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
PURPOSE:To obtain the titled compound useful as an antimicrobial agent at low cost, by deprotecting a specific compound in an inert solvent in the presence of a nickel complex and a reaction auxiliary. CONSTITUTION:A compound shown by formula I [R1 is H or OH-protecting group; R2 is (substituted)2-alkenyl; X is S or group shown by formula II (R3 is H or alkyl); Y is H or group shown by formula III (R4 and R5 are H, alkyl or R4 and R5 are bonded to form ethylene or propylene chain; n is 0-4)] is deprotected in an inert solvent (e.g. diethyl ether or benzene) in the presence of a nickel complex and a reaction auxiliary preferably at 10-50 deg.C to give the aimed compound shown by formula IV (R1' is H or OH-protecting group).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62233260A JPS6475488A (en) | 1987-09-17 | 1987-09-17 | Production of beta-lactam compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62233260A JPS6475488A (en) | 1987-09-17 | 1987-09-17 | Production of beta-lactam compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6475488A true JPS6475488A (en) | 1989-03-22 |
Family
ID=16952290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62233260A Pending JPS6475488A (en) | 1987-09-17 | 1987-09-17 | Production of beta-lactam compound |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6475488A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7071330B2 (en) * | 2001-01-16 | 2006-07-04 | Williams John M | Process for carbapenem synthesis |
| CN101962383A (en) * | 2010-11-12 | 2011-02-02 | 上海巴迪生物医药科技有限公司 | Synthesis method of meropenem |
-
1987
- 1987-09-17 JP JP62233260A patent/JPS6475488A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7071330B2 (en) * | 2001-01-16 | 2006-07-04 | Williams John M | Process for carbapenem synthesis |
| CN101962383A (en) * | 2010-11-12 | 2011-02-02 | 上海巴迪生物医药科技有限公司 | Synthesis method of meropenem |
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