JPS57125808A - Preparation of cephapyrine - Google Patents
Preparation of cephapyrineInfo
- Publication number
- JPS57125808A JPS57125808A JP1260981A JP1260981A JPS57125808A JP S57125808 A JPS57125808 A JP S57125808A JP 1260981 A JP1260981 A JP 1260981A JP 1260981 A JP1260981 A JP 1260981A JP S57125808 A JPS57125808 A JP S57125808A
- Authority
- JP
- Japan
- Prior art keywords
- radical
- substituted
- tertiary amine
- salt
- acid
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cephalosporin Compounds (AREA)
Abstract
PURPOSE:To prepare high purity cephapyrine with high yield, by adding tertiary amine to a mixture of 7-aminocephalosporanic acid ester and alkali metallic salt of 4-pyridylthioacetic acid and allowing these components to react. CONSTITUTION:Tertiary amine is added to a mixture of 7-aminocephalosporane protected carboxyl radial in a form of ester, alkali metallic salt of 4-pridyl- thioacetic acid and 1-substituted-2-halopyridinium salt to allow to react, thereafter, a protective radical of carboxyl radical is eliminated. A compound shown by the general formula[in the formula, R1 is a lower alkyl radical, benzyl radical or phenacyl radical, X is a halogen atom, Y is a halogen atom, R2-SO4 (R2 is lower alkyl radical) or a R3-SO4(R3 is a phenyl radical which may be substituted by a methyl radical)]is used for said 1-substituted-2-halopyridinium salt and adding quantity of tertiary amine is suitable to be nearly an equivalent mol to 7-aminocephalosporanic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1260981A JPS57125808A (en) | 1981-01-30 | 1981-01-30 | Preparation of cephapyrine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1260981A JPS57125808A (en) | 1981-01-30 | 1981-01-30 | Preparation of cephapyrine |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57125808A true JPS57125808A (en) | 1982-08-05 |
JPS6126998B2 JPS6126998B2 (en) | 1986-06-23 |
Family
ID=11810098
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1260981A Granted JPS57125808A (en) | 1981-01-30 | 1981-01-30 | Preparation of cephapyrine |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57125808A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52144688A (en) * | 1976-05-27 | 1977-12-02 | Ono Pharmaceut Co Ltd | Preparation of penicillin and cephalosporin derivatives |
-
1981
- 1981-01-30 JP JP1260981A patent/JPS57125808A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52144688A (en) * | 1976-05-27 | 1977-12-02 | Ono Pharmaceut Co Ltd | Preparation of penicillin and cephalosporin derivatives |
Also Published As
Publication number | Publication date |
---|---|
JPS6126998B2 (en) | 1986-06-23 |
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