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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2009-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52d4f335f6dfda1a5d3e3cde6194e955
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0e6bcfd306c1991f202ca0f4113eb035
publicationDate 2013-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8557991-B2
titleOfInvention Process for preparing enantiomerically pure indolopyridines
abstract Disclosed is a novel process for the preparation of pharmacologically interesting indolopyridine derivatives containing tetracyclic tetrahydro-11-carboline-hydantoines linked to a basic side chain and the corresponding salts, which can be used as Eg5 inhibitors, with very high overall chemical yield and enantiomeric purity.
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priorityDate 2008-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 721.