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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-82
filingDate 1999-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0623d6066e503ee5fe168d746cbc9ec4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5dd4fa092dfd0d7025cd34696ec8ecd8
publicationDate 2001-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2001039932-A
titleOfInvention Method for producing propargylaniline compound
abstract (57) [Problem] To provide an important intermediate of a phenylalkanoic acid amide compound having an excellent bactericidal effect. SOLUTION: The general formula: (Wherein, R 1 and R 2 each independently represent an alkyl group or a cycloalkyl group, R 3 and R 4 each represent a methoxy group or a hydrogen atom, and R 3 and R 4 simultaneously have the same substituent. ) And a lithium acetylide ethylenediamine complex represented by the general formula: (Wherein, R 1 , R 2 , R 3 and R 4 have the same meanings as described above), and the N-propargyl aniline compound is decomposed by reacting with an oxidizing agent. Having the general formula: (Wherein, R 1 and R 2 have the same meanings as described above).
priorityDate 1999-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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