http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2653205-T3
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_96ec3985e3ce9b24614fb87bf51a4f12 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-713 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 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b15b769cffcce400fcf46cbaaa6204a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_35c21bb3d74c52edb4902e93ced53f40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_337f43e8c9fc705f49986aa28d58caca |
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 |
Incoming Links
Total number of triples: 102.