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filingDate 1977-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1981-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b67be76e12edaadee23e8148c3cf90b1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c067cd5009f5b8bd3f6532279f140be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c047c132110b0a833368f159b419cc8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3e33fb99eea60c4fdc4ba0c3f19b940
publicationDate 1981-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1097646-A
titleOfInvention Piperazine and piperidine derivatives
abstract ABSTRACT OF THE DISCLOSURE Novel compounds are disclosed of the formula: (I) and the pharmaceutically acceptable acid addition salts thereof, wherein: Ar1 and Ar2 are each independently selected from the group consisting of phenyl, substituted phenyl and pyridinyl, wherein said substituted phenyl is phenyl having from 1 to 2 substituents independently selected from the group consisting of halo, lower alkyl, lower alkyloxy trifluoromethyl and nitro; m is an integer zero or 1; A is a member selected from the group consisting of and , provided that when said A is then said m is zero and when said A is then said m is 1; n is an integer of from 2 to 6 inclusive, provided that when CnH2n represents a branched alkylene chain, then at least 2 carbon atoms are present in the linear portion of the chain linking B with the piperidine or piperazine nitrogen atom; and B is a member selected from the group consisting of: a) a radical having the formula wherein: R1 and R2 are each independently selected from the group consisting of hydrogen, halo, lower alkyl and trifluoromethyl; and Y is a member selected from the group consisting of oxygen, sulfur and a substituted nitrogen of the formula , wherein said L is a member selected from the group consisting of hydrogen, lower alkyl, lower alkylcarbonyl, lower alkyloxycarbonyl-lower alkyl, carboxy-lower alkyl, phenyl, phenylmethyl, lower alkylaminocarbonyl, hydroxy-methyl, and lower alkenyl; and b) a radical having the formula wherein: R1 and R2 are each independently selected from the group consisting of hydrogen, halo, lower alkyl and trifluoromethyl; and M is a member selected from the group consisting of hydrogen, lower alkyl, phenyl, phenylmethyl, mercapto, lower alkylthio, amino, lower alkylcarbonylamino, lower alkyloxycarbonylamino, and cycloalkyl having from 3 to 6 carbon atoms. Theses novel 1-substituted 4-(diarylmethyl)piperazine and 4-(diarylmethoxy) piperidine derivatives having anti-anaphylactic and antihistaminic properties.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007137417-A1
priorityDate 1976-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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