GB952519A - Process for the production of penicillins - Google Patents
Process for the production of penicillinsInfo
- Publication number
- GB952519A GB952519A GB3684261A GB3684261A GB952519A GB 952519 A GB952519 A GB 952519A GB 3684261 A GB3684261 A GB 3684261A GB 3684261 A GB3684261 A GB 3684261A GB 952519 A GB952519 A GB 952519A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- group
- acid
- cyanomethyl
- para
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; 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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The 6-amino group of 6-aminopenicillanic acid, or a salt thereof, is acylated or thioacylated by reaction with a reactive ester of a carboxylic or thiocarboxylic acid of formula: <FORM:0952519/C2/1> where X and Y may be the same or different, and each is an oxygen atom or sulphur atom, <FORM:0952519/C2/2> is the acyl or thioacyl group it is desired to introduce into the 6-amino group of 6-amino-penicillanic acid, and R1 is a phenyl, cyanomethyl or para-nitro phenyl group when X is oxygen, and a methyl, ethyl, carboxymethyl, phenyl, cyanomethyl or a para-nitro-phenyl group when X is sulphur. Examples describe the reaction of 6-aminopenicillanic acid with carboxymethyl dithiobenzoate, phenyldithioacetate, ethoxydithioformate and 3-isonicotinoyldithiocarbazate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3684261A GB952519A (en) | 1961-10-13 | 1961-10-13 | Process for the production of penicillins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3684261A GB952519A (en) | 1961-10-13 | 1961-10-13 | Process for the production of penicillins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB952519A true GB952519A (en) | 1964-03-18 |
Family
ID=10391621
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3684261A Expired GB952519A (en) | 1961-10-13 | 1961-10-13 | Process for the production of penicillins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB952519A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3391141A (en) * | 1966-07-07 | 1968-07-02 | Bristol Myers Co | Synthetic cephalosporins |
FR2024556A1 (en) * | 1968-11-08 | 1970-08-28 | Istituto Biochimico Italiano |
-
1961
- 1961-10-13 GB GB3684261A patent/GB952519A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3391141A (en) * | 1966-07-07 | 1968-07-02 | Bristol Myers Co | Synthetic cephalosporins |
FR2024556A1 (en) * | 1968-11-08 | 1970-08-28 | Istituto Biochimico Italiano |
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