http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0554098-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ba045776bcd32d32e3100da8dfce4e28
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1993-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_878ae09636443153de6c9d15eb660fdd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02df4ca029a33647d67baa0d27eb5cff
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c523490e762aa18ee0e74228ae888d9a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_571b2b6f56071a5e94502acc4b697060
publicationDate 1993-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0554098-A2
titleOfInvention Process for the preparation of imidazo 4,5-b pyridine derivatives
abstract The invention provides a novel chemical process for the manufacture of certain imidazo[4,5-b]pyridine derivatives of the formula I wherein R 1 , R 2 , R 3 and R 4 have the various meanings defined herein, and their non-toxic salts, which are angiotensin II inhibitors. The process involves the removal of an electron-deficient phenyl group or a pyridyl or pyrimidyl group from a compound of the formula II as defined herein. Certain of the intermediates are novel and are provided as a further feature of the invention.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9556132-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102712606-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2014001363-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9534564-A1
priorityDate 1992-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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