http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105934431-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-08
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C269-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-64
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-44
filingDate 2015-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105934431-B
titleOfInvention Preparation method of substituted urea compounds
abstract The present invention relates to a compound having the structure of formula A, a preparation method of a pharmaceutically acceptable salt or derivative thereof, or a preparation method of a substituted urea compound of formula IIa, a pharmaceutically acceptable salt or ester thereof, ( The method of formula IIa) comprises the reaction of an imidazole intermediate of formula IIa' with a carbamoyl halide of formula R1R2NC(=O)Hal, wherein Hal represents Cl, F, I or Br, wherein the intermediate of formula IIa' is passed through Oxidation of derivatives of R5 and R6, R6-C(=O)CH 2 R5 forms glyoxal intermediate R6-C(=O)(C=O)R5, which is then prepared by treating with ammonium hydroxide and aldehyde R8CHO, wherein the compound substituents are as defined herein.
priorityDate 2014-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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