http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20200118025-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-04
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filingDate 2019-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f827026df92916d99d3d619dff536ade
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c71d9fee28f7efe52f73c1b6251e12a1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99ad3aee0523c1e98174d5acaf4513ae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bd8bbd3758e595cbb7b52ac0591c82d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98d58fe1ec0963e23a8d6386e403b4f3
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publicationDate 2020-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20200118025-A
titleOfInvention Pyrazole compound and preparation thereof
abstract The present invention provides a method for preparing a substituted pyrazole compound of formula II, which can be used as an intermediate for the preparation of a substituted piperidine urea compound useful in the treatment of dilated cardiomyopathy (DCM). R 2 is independently selected from F, C1-C4 alkyl, C1-C4 haloalkyl, R 3 is independently selected from H, F, C1-C4 alkyl, C1-C4 haloalkyl, and R 4 is C1-C4 Alkyl, R 6 is H or a protecting group, and R 7 is selected from H, Cl or trialkylsilyl.
priorityDate 2018-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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