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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5712b4838bdb16ebbc41121239e165b9
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-22
filingDate 1978-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1979-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8e2704bb394b0c37262c838df50b51e
publicationDate 1979-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4153718-A
titleOfInvention Anti-inflammatory compounds
abstract 4-(Thien-2-oyl- and thien-3-olyphenyl)pentan-2-ones and 4-(thien-2-oyl- and thien-3-oylphenyl)butan-2-ones, the corresponding pentan-2-ols and butan-2-ols, and esters of the latter alkanols are anti-inflammatory agents. The compounds, of which 4-[4-(2-thienoyl)phenyl]pentan-2-one is a representative embodiment, can be prepared by acylation of the corresponding 4-phenyl-pentan-2-one, 4-phenylbutan-2-one, or an ester of the corresponding pentan-2-ol or butan-2-ol, with a thienylcarboxylic acid, or by acylation of a 4-(4-carboxyphenyl)pentan-2-one, 4-(4-carboxyphenyl)butan-2-one or an ester of the corresponding pentan-2-ol or butan-2-ol with thiophene, optionally in either case with subsequent reduction of the resultant alkanone and with optional esterification of the resultant alkanol.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4352935-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4223039-A
priorityDate 1976-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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