http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-069197-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-50
filingDate 2008-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2010-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-069197-A1
titleOfInvention A METHOD TO COMBAT AND / OR CONTROL A PEST OF INSECTS OR ACAROS, COMPOUNDS DERIVED FROM IMIDAZOLINE, A METHOD FOR PREPARATION, AN INSECTICIATED COMPOSITION AND INTERMEDIATE COMPOUNDS
abstract This is related to phenoxy-imidazoline derivatives in which the phenoxy moiety is substituted with a nitro group. Claim 1: A method for combating and / or controlling a pest of insects or mites, comprising the application to said pest, or to the locus of said pest, or to a plant susceptible to attack by said pest, a compound of the formula (1 ) or a salt or N-oxide thereof, in which R1 is (i) an optionally substituted C1-6 alkyl, (ii) optionally substituted C2-6 alkenyl, (iii) optionally substituted C3-6 cycloalkyl, (iv) optionally substituted C3-6 cycloalkenyl or (v) optionally substituted C2-6 alkynyl; R2 is C1-5 alkyl, C1-5 haloalkyl, C2-5 alkenyl, C2-5 haloalkenyl, C2-5 alkynyl, C3-6 cycloalkyl, C1-5 alkoxy, C1-5 haloalkoxy, C1-3 alkoxy-C1- alkyl 3, C1-5 alkylthio, C1-5 haloalkylthio, C1-5 alkylsulfonyl, C1-5 alkylsulfinyl, C1-5 haloalkylsulfonyl, C1-5 haloalkylsulfinyl, cyano, nitro, halogen or formyl; R4 is H, methyl or halogen; R5 is H, methyl or halogen; R6 is H, methyl or halogen; Z is H, hydroxy, nitro, cyano, rhodan, formyl, G-, GS-, GSS-, GA-, GO-, GAO-, GXAO-, R7R8N-, R7R8N-S-, R7R8N-A-, GOA- , GSA-, (R10O) (R11O) P (X) -, (R10O) (R11S) P (X) -, (R10O) (R11) P (X) -, (R10S) (R11S) P (X) -, (R10O) (R14R15N) P (X) -, (R11) (R14R15N) P (X) -, (R14R15N) (R16R17N) P (X) -, GN = CH-, GON = CH-, N: :: CN = CH- or Z is a group of the formula (2) in which B is S-, SS-, S (O) -, C (O) - or (CH2) n-, n is an integer from 1 to 6; R1, R2, R4, R5 and R6 are as defined above, and G is optionally substituted C1-10 alkyl, optionally substituted C2-10 alkenyl, optionally substituted C2-10 alkynyl, C3-7 cycloalkyl optionally substituted, C3- cycloalkenyl 7 optionally substituted, optionally substituted aryl, optionally substituted heteroaryl or optionally substituted heterocyclyl; A is S (O), SO2, C (O) or C (S); each of R7 and R8 is independently H or G; or R7 and R8 together with the N atom to which they are attached, form a group N = CR12R13; or R7 and R8 together with the N atom to which they are attached, form a 5, 6 or 7 membered heterocyclic ring, which optionally contains 1 or 2 heteroatoms more selected from O, N and S, and is optionally substituted with 1 or 2 C1-6 alkyl groups; each of R10 and R11 is independently C1-6 alkyl, benzyl or phenyl, where the phenyl group is optionally substituted with halogen, nitro, cyano, C1-3 alkyl, C1-3 haloalkyl, C1-3 alkoxy, C1-3 haloalkoxy , each of R12, r13, R14, R15, R16 and R17 is independently H or C1-6 alkyl; X is O or S. Claim 5: A compound of the formula (1) or a salt or N-oxide thereof, wherein: R1 is (i) substituted C1-2 alkyl, provided said substitution is not a group hydroxy (ii) optionally substituted C3-6 alkyl, (iii) optionally substituted C2-6 alkenyl, (iv) optionally substituted C3-6 cycloalkyl, (v) optionally substituted C3-6 cycloalkenyl or (vi) optionally substituted C2-6 alkynyl and R2, R4, R5, R6 and Z are as defined in claim 1. Claim 8: A compound of the formula (3) in which R1, R2, R4, R5 and R6 are as defined in claim 1.
priorityDate 2007-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 26.