http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-045561-A1

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_227dd812f56cc52ac96b934923e1e2bf
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-14
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-42
filingDate 2004-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2005-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-045561-A1
titleOfInvention PESTICIDED COMPOUNDS
abstract Derivatives and oxyalkylaminopyrazole substituted in position 5, processes for its preparation, compositions, its use for pest control (including arthropods and helminths) and its use for the preparation of a veterinary medicinal product. Claim 1: A compound of formula (1), wherein: R1 is CN, CSNH2 or C (= N-Z) -S (O) r-Q; Z is H, (C1-6) alkyl, halo (C1-6) alkyl, (C3-6) alkenyl, (C3-6) alkynyl, - (CH2) qR7, COR8, CO2-(C1-6) alkyl or S (O) pR8; Q is (C1-6) alkyl or CH2R7; W is C-halogen, C-CH3 or N; R2 is hydrogen, halogen or CH3; R3 is haloalkyl (C1-3), haloalkoxy (C1-3) or SF5; R4 is hydrogen, (C2-6) alkenyl, halo (C2-6) alkynyl, (C2-6) alkynyl; haloalkynyl (C2-6), cycloalkyl (C3-7), cycloalkyl (C3-7) -alkyl (C1-6), CO2-alkyl (C1-6), CO2-alkenyl (C3-6), CO2-alkynyl ( C3-6), CO2- (CH2) mR7 or SO2R8; or (C1-6) alkyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, (C1-6) alkoxy, halo (C1-6) alkoxy, (C3-6) alkenyloxy, (C3-6) haloalkenyloxy , (C3-6) alkynyloxy, (C3-6) haloalkyloxy, cycloalkyl, (C3-7), S (O) pR8, CN, NO2, OH, COR9, NR9R10, S (O) pR7, OR7 and CO2R9; A is (C1-6) alkylene or halo (C1-6) alkylene; X is C (= O), C (= S) or SO2; Y is O, NR11 or a covalent bond; R5 is (C3-6) alkenyl, (C3-6) haloalkenyl, (C3-6) alkynyl, (C3-6) haloalkynyl, C3-7) cycloalkyl (C3-7) cycloalkyl (C1-6) alkyl , - (CH2) qR7 or - (CH2) qR12; or is (C 1-6) alkyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, C 1-6 alkoxy, C 1-6 alkoxy, C 3-6 alkenyloxy, C 3-6 haloalkenyloxy ), (C3-6) alkynyloxy, (C3-6) haloalkyloxy, (C3-7) cycloalkyl, S (O) pR8, CN, NO2, OH, COR9, NR9R10, S (O) pR7, OR7 and CO2R9; R 6 is C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 haloalkenyl, C 2-6 alkynyl or C 2-6 haloalkynyl; R 7 is phenyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, (C 1-6) alkyl, halo (C 1-6) alkyl, C 1-6 alkoxy, C 1-6 haloalkoxy, CN, NO 2 , S (O) pR8, COR10, COR13, CONR9R10, SO2NR9R10, NR9R10 and OH; R8 is (C1-6) alkyl or halo (C1-6) alkyl; R9 and R10 are each independently of each other H, (C1-6) alkyl, halo (C1-6) alkyl, (C3-6) alkenyl, (C3-6) haloalkenyl, (C3-6) alkynyl, (C3-) cycloalkyl 6) or (C1-6) alkyl (C3-6) cycloalkyl; or R9 and R10 together with the attached N atom form a five or six membered saturated ring optionally containing an additional heteroatom in the ring that is selected from O, S and N, where the ring is not substituted or substituted with one or more radicals selected from the group consisting of halogen, (C 1-6) alkyl and halo (C 1-6) alkyl; R11 is H, (C1-6) alkyl, halo (C1-6) alkyl, (C3-6) alkenyl or (C3-6) alkynyl; R12 is heterocyclyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, (C1-4) alkyl, halo (C1-4) alkyl, (C1-4) alkoxy, (C1-4) haloalkoxy, NO2, CN , CO2-C1-6 alkyl, S (O) pR8, OH and oxo; R13 is phenyl unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, (C1-6) alkyl, haloalkyl (C1-6), alkoxy (C1-6), haloalkoxy (C1-6), CN, NO2 , S (O) pR8 and NR9R10; n, p and r are each independently zero, one or two; m and q are each independently zero or one; and each heterocyclyl in the above-mentioned radicals is independently a heterocyclic radical having 3 to 7 ring atoms and 1, 2 or 3 ring heteroatoms selected from the group consisting of N, O and S; or its salt acceptable for pesticide use.
priorityDate 2003-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457444288
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451

Total number of triples: 31.