GB1350135A - Penicillin derivatives - Google Patents
Penicillin derivativesInfo
- Publication number
- GB1350135A GB1350135A GB1350135DA GB1350135A GB 1350135 A GB1350135 A GB 1350135A GB 1350135D A GB1350135D A GB 1350135DA GB 1350135 A GB1350135 A GB 1350135A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- aminopenicilleric
- penicillins
- carboxy
- aryl
- 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)
- Cephalosporin Compounds (AREA)
Abstract
1350135 Preparation of α-carboxy-penicillins CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT 16 Aug 1971 [18 Aug 1970] 38384/71 Heading C2A The invention comprises a process for the preparation of 6-aminopenicilleric acid derivatives of the general Formula I and salts thereof which comprises hydrolysing a 6-aminopenicilleric acid derivative of the general Formula II or a salt or an ester thereof, wherein R 1 represents hydrogen or an alkyl, aryl, arathyl, aryloxy or heterocyclic group, R<SP>2</SP> represents hydrogen or an alkyl, aryl, or aralkyl group, X represents a halogen atom, 7 represents a valeny bond or a (-CO-NH-CHR 3 -) n group wherein R<SP>3</SP> represents hydrogen or an alkyl, aryl, aralkyl, aryloxy or heterocyclic group, n represents an integral number and 6APA the 6-aminopenicilleric acid group. The process may be performed under weakly alkaline conditions, e.g. in the presence of an alkali metal hydrogen carbonate, an alkali metal borate or an alkali metal hydroxide. The reaction may be performed at a temperature between +5‹ C. and -10‹ C. The invention also comprises α-carboxyp - chlorobenzyl - penicillin, α - [(α<SP>1</SP> - carboxy)- α<SP>1</SP> - (p - chlorophenyl)] - acetamido - benzylpenicillin, α - [α<SP>1</SP> - carboxy) - α<SP>1</SP> - (o - ehlorophenyl)] - acetamido - benzylpenicillin and salts of these penicillins. The last-mentioned penicillins may be employed as antibiotically active ingredients in pharmaceutical preparations, veterinary products and animal feeds.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3838471 | 1971-08-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1350135A true GB1350135A (en) | 1974-04-18 |
Family
ID=10403132
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1350135D Expired GB1350135A (en) | 1971-08-16 | 1971-08-16 | Penicillin derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1350135A (en) |
-
1971
- 1971-08-16 GB GB1350135D patent/GB1350135A/en not_active Expired
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
435 | Patent endorsed 'licences of right' on the date specified (sect. 35/1949) | ||
PCNP | Patent ceased through non-payment of renewal fee |