http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2009221091-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_19229fe7f5fcc0a484adc464fc5bdb8d
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-14
filingDate 2009-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0df8b51c33d01a1a278aad5c0b14578
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3f6a2bdc01b581a17426afc2c7a8ea5f
publicationDate 2013-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2009221091-B2
titleOfInvention Process for preparing enantiomerically pure indolopyridines
abstract The invention relates to a novel process for the preparation of pharmacologically interesting indolopyridine derivatives containing tetracyclic tetrahydro-β-carboline-hydantoines linked to a basic side chain and the corresponding salts, which can be used as Eg5 inhibitor, with very high overall chemical yield and enantiomeric purity.
priorityDate 2008-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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