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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-10
filingDate 1998-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c601ca4f6a16be2360ac2794b341956
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1278d7e5a797006a286dbe717b4818b
publicationDate 2000-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000119252-A
titleOfInvention Method for producing 3-substituted phenylpyridinone compounds
abstract (57) [Summary] [Problem] To provide a new manufacturing method. Kind Code: A1 Formula (I): [Wherein, Rf represents a C 1 -C 4 haloalkyl group, X represents a halogen atom, R represents a C 1 -C 4 alkyl group, and R 1 , R 2, R 3, R 4 and R 5 are each independently , Hydrogen atom, halogen atom, nitro group, cyano group, Represents a thiocarbamoyl group or the like. 6-haloalkyl-4-halogeno-3-substituted phenyl-2 (1 In the preparation of H) -pyridinone compounds, the compound of formula (II) And a β-keto acid ester compound represented by the formula (III): Formula (V) produced by reacting a phenylacetonitrile compound represented by the following formula in the presence of a base: 6-haloalkyl-4-hydroxy-2 represented by Formula (VII) produced by reacting a (1H) -pyridinone compound with a halogenating agent followed by hydrolysis. 6-haloalkyl-4-halogeno-2 (1 H)-A method for producing, characterized by reacting a pyridinone compound with an alkylating agent.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004000812-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7189855-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103896827-A
priorityDate 1998-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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