JPS54106490A - Propargylglycine derivative and its preparation - Google Patents
Propargylglycine derivative and its preparationInfo
- Publication number
- JPS54106490A JPS54106490A JP1341378A JP1341378A JPS54106490A JP S54106490 A JPS54106490 A JP S54106490A JP 1341378 A JP1341378 A JP 1341378A JP 1341378 A JP1341378 A JP 1341378A JP S54106490 A JPS54106490 A JP S54106490A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- amino
- compound
- group
- propargylglycine
- 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)
- Cephalosporin Compounds (AREA)
Abstract
NEW MATERIAL:A propargylglycine derivative of formula I: [X is (CH3)2, formula IV (R3 is H, or acetoxy group); R1 is H, lower alkylcarbonyl, 4-lower alkyl-2,3-dioxo-1-piperazynocarbonyl group, etc,; R2 is H or alkyl group], and its non-toxic salt.
EXAMPLE: 6-(α-amino-α-propargylacetamido) penicillanic acid.
USE: Antibacterials.
PROCESS: A compound of formula II: (R4 is R1, amino-protecting group) or its reactive derivation is reacted with a compound of formula III: (R5 is H or ester residue) or its salt in a solvent, e.g. THF or acetone, preferably at -20°C to room temperature, and, if necessary, the amino-protecting group is removed to give the compound of formula I. When an acid is formed by the reaction, a base, e.g. alkali carbonate or picoline is added.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1341378A JPS54106490A (en) | 1978-02-10 | 1978-02-10 | Propargylglycine derivative and its preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1341378A JPS54106490A (en) | 1978-02-10 | 1978-02-10 | Propargylglycine derivative and its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS54106490A true JPS54106490A (en) | 1979-08-21 |
Family
ID=11832442
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1341378A Pending JPS54106490A (en) | 1978-02-10 | 1978-02-10 | Propargylglycine derivative and its preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS54106490A (en) |
-
1978
- 1978-02-10 JP JP1341378A patent/JPS54106490A/en active Pending
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