http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2345357-A1

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filingDate 1999-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_332a55a832eee4cdd2451ee4880a360c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6909d3c6003cd397015916e17d6e9ffa
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publicationDate 2000-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2345357-A1
titleOfInvention Benzimidazolinyl piperidines as cgrp ligands
abstract A compound of formula I, wherein: R1 is naphthyl or benzothienyl which is unsubstituted or substituted at up to three substitutable positions independently by C1-6 alkyl, halogen, C1-6 alkoxy, CF3, OCF3, NO2, CN, methylenedioxy or ethylenedioxy; R2 is hydrogen, C1-8 alkyl, -(CH2)t-aryl wherein aryl is selected from phenyl, biphenyl and naphthyl, -(CH2)t-heteroaryl wherin heteroaryl is selected from tetrazolyl, oxadiazolyl, thiadiazolyl, triazolyl and pyrazinyl, -(CH2)qC(O)OR6, -(CH2)qOR6, -(CH2)qOC(O)R6, -(CH2)qC(O)R6, -(CH2)qC(O)(CH2)taryl, -(CH2)qN(R6)C(O)R6, -(CH2)qC(O)N(R6)2, -(CH2)qN(R6)SO2R6, -(CH2)qN(R6)C(O)N(R6)2, -(CH2)qOC(O)N(R6)2, -(CH2)qN(R6)C(O)OR6, -(CH2)qN(R6)SO2N(R6)2 and -(CH2)qS(O)mR6; R3 is NH2; R4 is hydrogen, C1-6 alkyl, C1-6 alkoxy, halogen, OCF3 or CF3; R5 is hydrogen, C1-6 alkyl, C1-6 alkoxy, halogen, OCF3 or CF3; R6 is hydrogen, C1-8 alkyl or C3-7 cycloalkyl, and when two R6 groups are present and both represent C1-8 alkyl they may optionally together with the atom to which they are both attached form a C3-8 ring; Q is -(CH2)x-C(R7)(R7a)-(CH2)y-or -(CH2)x-V-(CH2)y-; R7 and R7a are independently chosen from hydrogen, CF3, halogen, C1-6 alkyl and C1-6 alkoxy; V is a C3-8 non-aromatic cyclic or bicyclic ring or an aromatic ring which is benzene or naphthalene, said ring being unsubstituted or substituted at up to three substitutable positions independently by C1-6 alkyl, C1-6 alkoxy, halogen, OCF3, CF3, CN, NO2, methylenedioxy or ethylenedioxy; m is 0, 1 or 2; q is 0, 1, 2, 3 or 4; t is 0, 1, 2 or 3; x and y are independently 0, 1, 2, 3 or 4; or a pharmaceutically acceptable salt thereof; useful as CGRP (calcitonin gene-related peptide) receptor ligands, processes for their preparation, their use in therapy, pharmaceutical compositions comprising them and methods of treatment using them.
priorityDate 1998-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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