JPS5569591A - Azetidinone derivative and its preparation - Google Patents
Azetidinone derivative and its preparationInfo
- Publication number
- JPS5569591A JPS5569591A JP14269278A JP14269278A JPS5569591A JP S5569591 A JPS5569591 A JP S5569591A JP 14269278 A JP14269278 A JP 14269278A JP 14269278 A JP14269278 A JP 14269278A JP S5569591 A JPS5569591 A JP S5569591A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- group
- protecting group
- eliminated
- 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
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
NEW MATERIAL:An azetidinone derivative of formula I: (R1 is H or acyl group; R2 is H, alkyl, halogenoalkyl group, etc.; n is an integer 2-5), and a 2-ketopenicillin ester derivative of formula II: (R3 is R2 except H).
EXAMPLE: 5R-3-(2'-Hydroxy)ethoxy-7-oxo-4-thia-1-azabicyclo[3,2,0]hept-2-ene-2- carboxylic acid.
USE: Antibacterials, β-lactamase inhibitors, and intermediates for their synthesis, effective against β-lactam antibiotic-resistant bacteria.
PROCESS: The compound of formula II, obtained from a compound of formula III: (X is halogen), is reacted with a compound of formula IV (R4 is OH-protecting group), and the protecting group is eliminated to give a compound of formula V. The group R1 is changed into an acyl group, or the carboxyl-protecting group is eliminated to form the compound of formula I.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14269278A JPS5569591A (en) | 1978-11-17 | 1978-11-17 | Azetidinone derivative and its preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14269278A JPS5569591A (en) | 1978-11-17 | 1978-11-17 | Azetidinone derivative and its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5569591A true JPS5569591A (en) | 1980-05-26 |
Family
ID=15321302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14269278A Pending JPS5569591A (en) | 1978-11-17 | 1978-11-17 | Azetidinone derivative and its preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5569591A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5625110A (en) * | 1978-12-18 | 1981-03-10 | Bristol Myers Co | Antibacterial |
-
1978
- 1978-11-17 JP JP14269278A patent/JPS5569591A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5625110A (en) * | 1978-12-18 | 1981-03-10 | Bristol Myers Co | Antibacterial |
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