GB874416A - Antibacterial agents - Google Patents
Antibacterial agentsInfo
- Publication number
- GB874416A GB874416A GB16651/60A GB1665160A GB874416A GB 874416 A GB874416 A GB 874416A GB 16651/60 A GB16651/60 A GB 16651/60A GB 1665160 A GB1665160 A GB 1665160A GB 874416 A GB874416 A GB 874416A
- Authority
- GB
- United Kingdom
- Prior art keywords
- propionamido
- acid
- amino
- penicillins
- formula
- 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
Relates to penicillins of the formula <FORM:0874416/IV (b)/1> wherein R1, R2 and R3 are the same or different and each is a hydrogen atom or a nitro, amino, lower alkylamino, lower dialkylamino, lower alkanoylamino, lower alkyl, chloro, bromo, iodo, lower alkoxy, hydroxy or sulphamyl group, "lower" referring to radicals containing up to 10 carbon atoms, such as 6-[3-phenylpropionamido], 6-[3-(p-chlorophenyl)propionamido], 6-[3-(p-sulphamylphenyl) propionamido], 6-[3-m,p-dimethoxyphenyl) propionamido] and 6-[3-p-methoxyphenyl propionamido] penicillanic acid and to non-toxic salts thereof. The Specification contains a list of other penicillins of the above formula. The compounds may be prepared by reacting 6-amino-penicillanic acid or a neutral salt thereof with an acid chloride having the general formula <FORM:0874416/IV (b)/2> or its functional equivalent as an acylating agent for a primary amino group, such as the corresponding acid bromides, acid anhydrides and mixed anhydrides with other carboxylic acids, including monoesters of carbonic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US874416XA | 1959-05-25 | 1959-05-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB874416A true GB874416A (en) | 1961-08-10 |
Family
ID=22205217
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16651/60A Expired GB874416A (en) | 1959-05-25 | 1960-05-11 | Antibacterial agents |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB874416A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2100730A1 (en) * | 1970-06-06 | 1972-03-24 | Istituto Biochimico Italiano | Semisynthetic penicillin prodn - from 6-apa |
FR2282269A1 (en) * | 1974-08-22 | 1976-03-19 | Bayer Ag | NEW ANTIBIOTICS OF THE B-LACTAM CLASS, THEIR PREPARATION PROCESS AND THE MEDICINAL PRODUCT CONTAINING THEM |
-
1960
- 1960-05-11 GB GB16651/60A patent/GB874416A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2100730A1 (en) * | 1970-06-06 | 1972-03-24 | Istituto Biochimico Italiano | Semisynthetic penicillin prodn - from 6-apa |
FR2282269A1 (en) * | 1974-08-22 | 1976-03-19 | Bayer Ag | NEW ANTIBIOTICS OF THE B-LACTAM CLASS, THEIR PREPARATION PROCESS AND THE MEDICINAL PRODUCT CONTAINING THEM |
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