http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2253927-A1

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filingDate 1997-05-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c2009e34d4f57dcac464356104b40aa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c823df3118a01c24bc5ea6e657dede75
publicationDate 1997-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2253927-A1
titleOfInvention Tetrahydroisoquinoline derivatives as modulators of dopamine d3 receptors
abstract Compounds of formula (I), wherein: R1 represents a substituant selected from: a hydrogen or halogen atom; a hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, trifluoromethanesulfonyloxy, C1-4alkyl, C1-4alkoxy, arylC14alkoxy, C1-4alkylthio, C1-4alkoxyC1-4alkyl, C3-6cycloalkylC1-4alkoxy, C14alkanoyl, C1-4alkoxycarbonyl, C1-4alkylsulfonyl, C1-4alkylsulfonyloxy, C14alkylsulfonylC1-4alkyl, arylsulfonyl, arylsulfonyloxy, arysulfonylC1-4alkyl, C1-4alkylsulfonamido, C1-4alkylamido, C1-4alkylsulfonamidoC1-4alkyl, C14alkylamidoC1-4alkyl, arylsulfonamido, arylcarboxamido, arylsulfonamidoC14alkyl, arylcarboxamidoC1-4alkyl, aroyl, aroylC1-4alkyl, or arylC1-4alkanoyl group; a group R3OCO(CH2)p, R3CON(R4)(CH2)p, R3R4NCO(CH2)p or R3R4NSO2(CH2)p where each of R3 and R4 independently represents a hydrogen atom or a C14alkyl group or R3R4 forms part of a C3-6azacycloalkane or C3-6(2-oxo)azacycloalkane ring and p represents zero or an integer from 1 to 4; or a group Ar2-Z, wherein Ar2 represents an optionally substituted phenyl ring or an optionally substituted 5- or 6- membered aromatic heterocyclic ring and Z represents a bond, O, S, or CH2; R2 represents a hydrogen atom or a C1-4alkyl group; q is 1 or 2; Ar and Ar1 each independently represent an optionally substituted phenyl ring or an optionally substituted 5- or 6- membered aromatic heterocyclic ring; and Y represents a bond, -NHCO-, -CONH-, -CH2-, or -(CH2)mY1(CH2)n-, wherein Y1 represents O, S, SO2, or CO and m and n each represent zero or 1 such that the sum of m+n is zero or 1; and salts thereof, have activity at dopamine receptors and are useful in the treatment of psychoses such as schizophrenia.
priorityDate 1996-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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