http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2280417-T3

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filingDate 2001-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cca876413af4e3b23e39558b395db7b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62c1e5ca071e48c45cc532dc4414d5fd
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publicationDate 2007-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2280417-T3
titleOfInvention DERIVATIVES OF BENZOXAZINONA, ITS PREPARATION AND USE.
abstract A compound of ** formula * or a pharmaceutically acceptable salt thereof, wherein Ar is phenyl, naphthyl, a monocyclic heteroaromatic group or a bicyclic heteroaromatic group, said Ar group being optionally substituted with 1-4 substituents, which may be the same or different, and which are selected from the group consisting of: halogen, hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, C1-6 alkyl, trifluoromethanesulfonyloxy, pentafluoroethyl, C1-6 alkoxy, aryl-alkoxy (C1-6), alkyl ( C1-6) -thio, (C1-6) alkoxy- (C1-6) alkyl, (C3-7) cycloalkyl (C1-6) alkoxy, C1-6 alkanoyl, (C1-6) alkoxycarbonyl, (C1-6) alkyl-sulfonyl, (C1-6) -sulfinyl alkyl, (C1-6) -sulfonyloxy, (C1-6) -sulfonyl-(C1-6) alkyl, arylsulfonyl, arylsulfonyloxy, arylsulfonyl-alkyl (C1-6), alkyl (C1-6) -sulfonamido, alkyl (C1-6) -amido, alkyl (C1-6) -sulfonamido-alkyl (C1-6), alkyl (C1-6) -amido-alkyl (C1-6), arylsulfonamido, arylcarboxamido, arylsulfonamido-alkyl (C1-6), arylcarboxamido-alkyl yl (C1-6), aroyl, aroyl-C1-6 alkyl, aryl-alkanoyl (C1-6), a group R3OCO (CH2) s, R3CON (R4) (CH2) s, R3R4NCO (CH2) or R3R4NSO2 (CH2) s, where each of R3 and R4 independently represent a hydrogen atom or C1-4 alkyl, or R3 and R4 form part of a C3-6 azacycloalkane or (2-oxo) C3-6 azacycloalkane ring and represents zero or an integer from 1 to 4.
priorityDate 2000-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 403.