http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1016956-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_215dd152cd06928eff2d0047a1ac2c0b |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-68 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-68 |
filingDate | 1962-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_785a8d6b6e614816d4b0015447b1bf45 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_312ca73efc93a80253f2f2aa315a3067 |
publicationDate | 1966-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-1016956-A |
titleOfInvention | Chloramphenicol esters |
abstract | Chloramphenicol esters of the formula <FORM:1016956/C2/1> wherein R is an acyl radical selected from furoyl; 2,5-dichlorobenzoyl; 4-methoxybenzoyl; 3,4-dimethoxybenzoyl; 3,4,5-trimethoxybenzoyl; 4 - chlorophenylacetyl; 2 - chlorophenylacetyl; 2,4 - dichlorophenylacetyl; 4 - methoxyphenylacetyl; 3 - phenylpropionyl and 3 - (4 - chlorophenylacetyl, are stated to be new compounds. They may be prepared by reacting chloramphenicol with an appropriate acid chloride in solution in dioxan, preferably in the presence of an equivalent amount of pyridine at 0 DEG C. Pharmaceutical compositions of said esters together with a pharmaceutically acceptable carrier or diluent may further contain disintegrating agents, lubricating agents, sweetening or flavouring agents, suspending agents and wetting agents and may be formulated as solutions, suspensions, emulsions, linctus, lotions, creams, pastes, tablets, capsules or powders. |
priorityDate | 1962-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 21.