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filingDate 1997-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33738a6701212f7c12a7d6f3ed220beb
publicationDate 1998-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2268195-A1
titleOfInvention Azaheterocyclylmethyl derivatives of 2,3,8,9-tetrahydro-7h-1,4-dioxino[2,3-e]indol-8-one
abstract The compounds of formula (I) wherein X is H2 or O; R1 is hydrogen, hydroxy, halo, trifluoromethyl, trifluoromethoxy, alkyl, alkoxy, aralkoxy, alkanoyloxy, amino, mono- or di-alkylamino, alkanamido or alkanesulfonamido; Z is defined by formula (II), (III) or (IV) wherein R2 is hydrogen, alkyl, cycloalkyl, phenyl optionally substituted with R1 as defined above, .omega.-phenylalkyl or .omega.-diphenylalkyl, in which the phenyl ring is optionally substituted with R1 as defined above, or R2 is naphthyl, indolyl, indazolyl, thienyl, pyridinyl, pyrimidinyl, quinolinyl, benzoisothiazolyl or benzisoxazolyl, each optionally substituted with R1 as defined above; R3 is hydrogen and R4 is hydrogen, I-benzimidazolyl-2-one, indolyl, benzoisothiazolyl or benzisoxazolyl, each optionally substituted with R1 as defined above, or R4 is -Y-Ar, in which Y is C=O, CHOH, or (CH2)m, wherein m is 0 to 4, and Ar is phenyl, optionally substituted with R1 as defined above; or R3 and R4, taken together with the carbon atom to which they are attached form (V) or (VI) in which R5 is hydrogen and R6 is phenyl, naphthyl, thienyl, indolyl, benzoisothiazolyl or benzisoxazolyl, each optionally substituted with R1 as defined above; or R5 and R6, taken together with the carbon atoms to which they are attached complete a benzene ring optionally substituted with R1; or a pharmaceutically acceptable salt thereof; are useful for the treatment of brain dopamine dysregulation.
priorityDate 1996-10-15-04:00^^<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: 42.