http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2653205-T3

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14
filingDate 2012-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea04bb4a5e5b53a8a9fe4308d05d584f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15506762901639a58f0066cfb24d1a3f
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publicationDate 2018-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2653205-T3
titleOfInvention Process for the preparation of tetrazol-substituted anthranilic acid diamide derivatives by reacting pyrazole acids with anthranilic acid esters
abstract Procedure for the preparation of compounds of Formula (I), the ratio of compounds of Formula (I) being, in which Q represents Q-1 with respect to compounds of Formula (I) in which Q represents Q-2, of 90: 10 to 96: 4, and with the compounds of Formula (I) having a purity of> 90%, ** (See formula) ** in which R1, R3 independently of each other, represent (C1-C5) alkyl, R2 represents halogen or C1-C6 alkyl, R4 represents hydrogen, chlorine or cyano, Q represents a tetrazole ring that is monosubstituted with R5, selected from the group consisting of ** (See formula) ** R5 represents perfluoroalkyl (C1-C3), Z represents N, the compounds of general Formula (I) further include N-oxides and salts, characterized in that the tetrazole substituted pyrazole acids of Formula (II) ** (See formula) ** in which R2, Q and Z have the meanings indicated above are reacted with anthranilic acid esters of Formula (III) ** (See formula) ** ...
priorityDate 2011-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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