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filingDate 1988-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96a70b21dbb136d1abd8fa377174f09f
publicationDate 1991-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1634136-A3
titleOfInvention Method of prepation arylpiperazinylalkylenphenylheterocyclic compund or their acid=additive salts suitable for pharmacy
abstract An arylpiperazinyl-alkylenephenyl-p-heterocyclic compound, useful in the treatment of psychotic disorders, of the formula- <CHEM> or a pharmaceutically-acceptable acid-addition salt thereof, wherein:- Ar is phenyl, 3-trifluoromethylphenyl, 3-cyanopyridyl, naphthyl, or a five- or six-membered aromatic heterocyclic ring, said ring being attached to the N atom of the adjacent piperazinyl group by a carbon atom and having one nitrogen, oxygen or sulfur, or two nitrogens one of which may be replaced by oxygen or sulfur, or said heterocyclic ring is condensed with benzo, said naphthyl, heterocyclic and benzoheterocyclic rings being optionally substituted by one fluoro, chloro or trifluoromethyl substituent, said substitution in the case of said naphthyl and benzoheterocyclic rings being in the ring not attached to the piperazinyl group; n is 2, 3 or 4; and "Het" is a group of the formula:- <CHEM> in which R is H or C1-C3 alkyl, and Y is -H, -OH, -SH, -NH2, C1-C3 alkyl or C1-C3 alkylamino.
priorityDate 1987-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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