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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-33
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-128
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filingDate 1987-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_396540969c8a5292dde196ce260e8961
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_375f821cf9d6087a9c93495d64a13c50
publicationDate 1989-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01106850-A
titleOfInvention Preparation of n-acyl-n-alkyl-2,6-dialkyl-3-chloroaniline
abstract PURPOSE: To easily obtain N-acyl-N-alkyl-2,6-dialkyl-3-chloroanilines including some having bactericidal activity in a good yield by acylating 2,6-dialkylanilines and allowing the resultant N-acyl-N-alkyl-2,6-dialkylanilines to react with chlorine atoms. n CONSTITUTION: 2,6-Dialkylanilines of formula I (where R 1 is methyl or ethyl) are allowed to react with a halide of formula II (where R 3 is alkoxymethyl, carboxyl, etc.; R 4 is H or methyl; R 3 and R 4 together may form a ring; and X is Cl or Br). The resultant N-alkyl-2,6-dialkylanilines of formula III are allowed to react with an acylating agent of formula IV [where X 1 is Cl, Br or O-CO-R 2 (R 2 is alkoxymethyl, chloromethyl, etc.)], and the resultant compds. of formula V are allowed to react with chlorine to obtain the objective compds. of formula VI, e.g. N-methoxyacetyl-N-(2-oxotetrahydro-3-furyl)-3-chloro-2,6- dimethylaniline. n COPYRIGHT: (C)1989,JPO
priorityDate 1986-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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