http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IE-921059-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0d269c8e41f178194d858c230c9f85e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00
filingDate 1992-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d031cc9eaca082d9a1c2cd3fbc421836
publicationDate 1992-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IE-921059-A1
titleOfInvention Triazole antifungal agents
abstract The invention provides antifungal compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein R is phenyl optionally substituted by 1 to 3 substituents each independently selected from halo and CF3; R<1> is C1-C4 alkyl; R<2> is H or C1-C4 alkyl; and "Het" is oxazol-2-yl, thiazol-2-yl, 1,2,4-oxadiazol-3 or 5-yl, 1,2,4-thiadiazol-5-yl, 1,3,4-oxadiazol-2-yl or 1,3,4-thiadiazol-2-yl, all of which may be optionally substituted by C1-C4 alkyl or CF3, together with pharmaceutical compositions containing, and processes and intermediates used for the preparation of said compounds.
priorityDate 1991-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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