http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-112019019589-A2

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_374bd30b140c412aedda14571cbbc4a7
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-02
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C211-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-04
filingDate 2018-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b01a06835c3d74f194eae8596a5d688
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5fc7e89b2baefa40d473739f4a79ad29
publicationDate 2020-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112019019589-A2
titleOfInvention process for the preparation of a sulfonamide structured kinase inhibitor
abstract the present invention relates to an improved process for the preparation of a sulfonamide structured kinase inhibitor, namely n- (2 ', 4'-diflĂșor-5- (5- (1-methyl-1h-pyrazol-4-yl ) -1h-benzo [d] imidazol-1-yl) - [1,1'-biphenyl] -3-yl) cyclopropanesulfonamide (1a) and pharmaceutically acceptable salts thereof. compound of formula (1a) is a selective inhibitor of the fgrf / vegfr kinase families and is useful in the treatment of cancer.
priorityDate 2017-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414269447
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID117777927
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432178119
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID146457734

Total number of triples: 20.