http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5750699-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1996-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_818c623cae85e31ebfd80bcefeb72f15
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57d73493af9efca191899aa1df0b4730
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5cc7a008640c28ba4095827d9e67b690
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2fe3f8749981beed98e6ea544198934a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ec2cf780573ebfcfd1128f05f900f72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_660c3ad376d9a1ca3969b01230201efb
publicationDate 1998-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5750699-A
titleOfInvention Method of preparing certain 3-halo-imidazopyridines
abstract The invention relates to bradykinin antagonists of the formula: <IMAGE> wherein R1 is halogen, R2 and R3 are each hydrogen, lower alkyl, halo(lower)alkyl or acyl, R4 is aryl having suitable substituent(s), or a heterocyclic group optionally having suitable substituent(s), Q is O or N-R11, in which R11 is hydrogen or acyl, and A is lower alkylene, and pharmaceutically acceptable salts thereof.
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priorityDate 1992-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 4460.