http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1164877-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97a285d8ecd0184a7e5d89a1e4e07997 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-61 |
filingDate | 1983-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1984-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ddd9693f84085706a4876a37768133f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85cdcf415ae4ea84fd6e20d922e61ab1 |
publicationDate | 1984-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CA-1164877-A |
titleOfInvention | 1-(2-acyl-aminophenyl)imidazoles |
abstract | ABSTRACT Novel 1-(2-acylaminophenyl) imidazole compounds of the formula: in which -X2 is -R5 or -NHR2, wherein: (1) R5 is an aliphatic, cycloaliphatic, phenyl, substituted phenyl, fused bicyclic aryl or monocyclic aryl substituted aliphatic group bonded to the carbonyl carbon through a carbon-to-carbon linkage; and (2) R2 is a radical bonded to the nitrogen by a carbon to nitrogen linkage and selected from the group consisting of aliphatic, cycloaliphatic, phenyl, substituted phenyl and fused bicyclic aryl; and methods of making same from 1-(2-aminophenyl)imidazole are disclosed. These compounds are useful as intermediates in the preparation of certain 4-substituted imidazo [1,2-a] quinoxalines, which exhibit one or more of the following activities: immunosuppressant, anti-inflammatory and antifungal activity. |
priorityDate | 1977-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 58.