http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2552087-C

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classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-30
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-04
filingDate 2005-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73e1bd8900e73fd85e01bb084a23c968
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac39359ceda6748ccc1bd89614bb4187
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb4aa1d482ae81bdb14931be72071b7c
publicationDate 2011-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2552087-C
titleOfInvention Methods for making 4-tetrazolyl-4-phenylpiperidine compounds
abstract Methods, composition, and intermediates are disclosed that are useful for making 4-Tetrazolyl-4-phenylpiperidine Compounds according to Formula (I), where Ar1 is -C3-C8 cycloalkyl, phenyl, naphthyl, anthryl, phenanthryl or -(5-7-membered) heteroaryl, each being unsubstituted or substituted with one or more R2 groups; Ar2 is phenyl, naphthyl, anthryl, phenanthryl or -(5-7-membered) heteroaryl, each being unsubstituted or substituted with one or more R2 groups; Z1 and Z2 are each independently a -(C1-C4 alkyl) group; R1 is -(CH2)nC(O)N(R3)(R4) where R3 and R4 are each independently H or -(C1-C4 alkyl); R2 is halogen, -C1-C3 alkyl, -O-(C1-C3 alkyl), -NH(C1-C3 alkyl) or -N(C1-C3 alkyl)2; n is an integer ranging from 1 to 4; m is an integer ranging from 0 to 4; and, in certain embodiments, the phenyl moiety attached to the 4-position of the piperidine ring of a compound according to Formula (I) can be optionally substituted with one or mor R2 groups.
priorityDate 2004-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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