http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1603395-A2

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filingDate 2004-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b673f1bc34b13b274d4839675eda6fb
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publicationDate 2005-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1603395-A2
titleOfInvention Amino substituted benzo(hetero)cyclic derivatives
abstract Use of compounds Formula (I), A = a 5- to 7-membered ring which may contain 1-3 heteroatoms and which may be saturated or partially or completely unsaturated; R1= OH, SH, NH2, CN, NO2, halogen, C1-C6-alkyl, C1-C6-haloalkyl; C1-C6- alkoxy, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C2-C6-alkenyl, C2-C6-alkenyloxy, C2-C6-alkenylthio, C2-C6-alkynyl, C2-C6­alkynyloxy, C2-C6-alkynylthio, C1-C6-alkylsulfonyl, C1-C6-alkylsulfoxyl, C2-C6-alkenylsulfonyl, C2-C6-alkynylsulfoxyl, C1-C6-alkylcarbonyl, C1-C6- alkoxycarbonyl, C1-C6-alkylcarbonyloxy; R2 = C1-C6-alkyl or a mono- or bicyclic 5- to 10-membered aromatic ringsystem which may contain 1 to 4 heteroatoms and which is either bonded directly or through an O, S, C1-C6-alkylene or C1-C6-alkyleneoxy linkage to A or fused to A and which may be substituted; R3, R4 = H, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkylamino, C1-C6-alkoxy, C3-C6-cycloalkyl, or R3 and R4 together with the nitrogen atom to which they are attached form a saturated or partially saturated mono- or bicyclic 5- to 10-membered ring system con-taining 1 to 3 heteroatoms or a 5-membered hetaryl containing 1 to 4 nitro-gen atoms, wherein the carbon and/or nitrogen atoms in the ring systems may be substituted or phenyl or benzyl which may be substituted; or R3 and R4 together form the chains -(CH2)2N+(O-)(CH2)2- or -(CH2)3N+(O-)(CH2)2-; m = 0 to 4; n is 0 to 4; and the enantiomers, diastereomers, cis/trans isomers or salts thereof for combatting insects, arachnids or nematodes, methods for the control of these pests and of protecting growing plants attack or infestation by these pests by applying a pesticidally effective amount of a compound of formula (I), processes for preparing them, and compositions comprising them.
priorityDate 2003-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226414121
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID105010
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226408344
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID254363
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6544
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID527636
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID7111
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419510486
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID527630
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457814462
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID13131
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID7108
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419572737
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231767710
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226415539
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID656900
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID82600
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231767701
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422032068
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID307658
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419572726
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231767558
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID131627
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226413893
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID157864
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID7394
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419572687
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231767549
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID977
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226423327

Total number of triples: 1224.