http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105051010-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-40
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-46
filingDate 2014-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfbb1fe6f6aab165af3963af4b521b2a
publicationDate 2015-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105051010-A
titleOfInvention A novel process for the preparation of n-(4-nitro-2-sulfamoyl-phenyl)-malonamic acid methyl ester and n-(4-amino-2-sulfamoyl-phenyl)-malonamic acid methyl ester
abstract The present invention provides a novel method for preparing compounds N-(4-nitro-2- sulfamoyl-phenyl)-malonamic acid methyl ester and N-(4-amino-2-sulfamoyl-phenyl)- malonamic acid methyl ester, which are novel intermediates for preparing a key intermediate N- (4-methanesulfonylamino-2-sulfamoyl-phenyl)-malonamic acid methyl ester, for the preparation of N-(3 - {( 1 R,2S,7R,8S)-3 -[(4-fluorophenyl)methyl] -6-hydroxy-4-oxo-3 -azatricyclo [6.2.1.02'7]undec-5-en-5-yl}-l,l-dioxo-l,4-dihydro-lX6,2,4-benzothiadiazin-7- yl)methanesulfonamide, also known commercially as Setrobuvir, a compound useful in treating hepatitis C.
priorityDate 2013-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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