http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-045561-A1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_227dd812f56cc52ac96b934923e1e2bf |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-10 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 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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