JP4982765B2 - 殺虫性5−置換−オキシアルキルアミノ−1−アリールピラゾール誘導体 - Google Patents
殺虫性5−置換−オキシアルキルアミノ−1−アリールピラゾール誘導体 Download PDFInfo
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- JP4982765B2 JP4982765B2 JP2006525067A JP2006525067A JP4982765B2 JP 4982765 B2 JP4982765 B2 JP 4982765B2 JP 2006525067 A JP2006525067 A JP 2006525067A JP 2006525067 A JP2006525067 A JP 2006525067A JP 4982765 B2 JP4982765 B2 JP 4982765B2
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- 230000000749 insecticidal effect Effects 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 161
- 239000000203 mixture Substances 0.000 claims description 93
- -1 2,6-difluorophenyl Chemical group 0.000 claims description 75
- 241000607479 Yersinia pestis Species 0.000 claims description 43
- 150000003839 salts Chemical class 0.000 claims description 41
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 40
- 239000004480 active ingredient Substances 0.000 claims description 35
- 229910052736 halogen Inorganic materials 0.000 claims description 35
- 150000002367 halogens Chemical class 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 32
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 26
- 241001465754 Metazoa Species 0.000 claims description 26
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims description 22
- 239000002917 insecticide Substances 0.000 claims description 19
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 12
- 125000006414 CCl Chemical group ClC* 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 239000003085 diluting agent Substances 0.000 claims description 6
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- 230000000694 effects Effects 0.000 claims description 6
- 125000001475 halogen functional group Chemical group 0.000 claims description 6
- 229910052727 yttrium Inorganic materials 0.000 claims description 6
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
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- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 3
- 229940079593 drug Drugs 0.000 claims description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- 125000004863 4-trifluoromethoxyphenyl group Chemical group [H]C1=C([H])C(OC(F)(F)F)=C([H])C([H])=C1* 0.000 claims 1
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
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- 235000002639 sodium chloride Nutrition 0.000 description 29
- 239000000843 powder Substances 0.000 description 24
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
- 239000000460 chlorine Substances 0.000 description 21
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
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- 239000002585 base Substances 0.000 description 19
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- 239000007787 solid Substances 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- 244000144972 livestock Species 0.000 description 16
- 239000004615 ingredient Substances 0.000 description 15
- 239000002904 solvent Substances 0.000 description 15
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 14
- 239000000543 intermediate Substances 0.000 description 14
- 241000255925 Diptera Species 0.000 description 13
- 229910052801 chlorine Inorganic materials 0.000 description 13
- 241000238876 Acari Species 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 12
- 239000002689 soil Substances 0.000 description 12
- 239000007921 spray Substances 0.000 description 12
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 11
- 241000238631 Hexapoda Species 0.000 description 10
- 125000000623 heterocyclic group Chemical group 0.000 description 10
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- 241000258924 Ctenocephalides felis Species 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 229910052794 bromium Inorganic materials 0.000 description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 8
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
- 244000000013 helminth Species 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 229910000104 sodium hydride Inorganic materials 0.000 description 8
- 239000012312 sodium hydride Substances 0.000 description 8
- 238000005507 spraying Methods 0.000 description 8
- 230000009261 transgenic effect Effects 0.000 description 8
- 239000004563 wettable powder Substances 0.000 description 8
- QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 7
- 241000254173 Coleoptera Species 0.000 description 7
- 239000012442 inert solvent Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 241000258937 Hemiptera Species 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 235000013339 cereals Nutrition 0.000 description 6
- 201000010099 disease Diseases 0.000 description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 239000000575 pesticide Substances 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000004293 19F NMR spectroscopy Methods 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- 241000254171 Curculionidae Species 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
- 241000238814 Orthoptera Species 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 241000209149 Zea Species 0.000 description 5
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 5
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
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- 229910000102 alkali metal hydride Inorganic materials 0.000 description 5
- 150000008046 alkali metal hydrides Chemical class 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 235000005822 corn Nutrition 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 5
- 125000001188 haloalkyl group Chemical group 0.000 description 5
- 238000003973 irrigation Methods 0.000 description 5
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- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
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- 238000013268 sustained release Methods 0.000 description 5
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- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 4
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- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
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- LABQLTFAPITERI-UHFFFAOYSA-N 4-(1-but-2-ynoxyethyl)-1,2-dimethoxybenzene Chemical compound COC1=CC=C(C(C)OCC#CC)C=C1OC LABQLTFAPITERI-UHFFFAOYSA-N 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
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- 235000013599 spices Nutrition 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- 229950004921 temefos Drugs 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- JWXZLCFGVKMEEK-UHFFFAOYSA-N triarathene Chemical compound C1=CC(Cl)=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)S1 JWXZLCFGVKMEEK-UHFFFAOYSA-N 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
- C07D231/42—Benzene-sulfonamido pyrazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Agronomy & Crop Science (AREA)
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- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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Description
本発明は、新規5−置換−オキシアルキルアミノピラゾール誘導体、この製造方法、この組成物、及びこの害虫(節足動物及び蠕虫を包含する)を防除するための使用に関する。
R1はCN、CSNH2又はC(=N−Z)−S(O)r−Qであり;
ZはH、(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C3−C6)−アルケニル、(C3−C6)−アルキニル、−(CH2)qR7、COR8、CO2−(C1−C6)−アルキル又はS(O)pR8であり;
Qは(C1−C6)−アルキル又はCH2R7であり;
WはC−ハロゲン、C−CH3又はNであり;
R2は水素、ハロゲン又はCH3であり;
R3は(C1−C3)−ハロアルキル、(C1−C3)−ハロアルコキシ又はSF5であり;
R4は水素、(C2−C6)−アルケニル、(C2−C6)−ハロアルケニル、(C2−C6)−アルキニル、(C2−C6)−ハロアルキニル、(C3−C7)−シクロアルキル、(C3−C7)−シクロアルキル−(C1−C6)−アルキル、CO2−(C1−C6)−アルキル、CO2−(C3−C6)−アルケニル、CO2−(C3−C6)−アルキニル、CO2−(CH2)mR7又はSO2R8であるか、又は非置換であるかもしくはハロゲン、(C1−C6)−アルコキシ、(C1−C6)−ハロアルコキシ、(C3−C6)−アルケニルオキシ、(C3−C6)−ハロアルケニルオキシ、(C3−C6)−アルキニルオキシ、(C3−C6)−ハロアルキニルオキシ、(C3−C7)−シクロアルキル、S(O)pR8、CN、NO2、OH、COR9、NR9R10、S(O)pR7、OR7及びCO2R9からなる群の中から選択される1個又はそれ以上の基で置換された(C1−C6)−アルキルであり;
Aは(C1−C6)−アルキレン又は(C1−C6)−ハロアルキレンであり;
XはC(=O)、C(=S)又はSO2であり;
YはO、NR11又は共有結合であり;
R5は(C3−C6)−アルケニル、(C3−C6)−ハロアルケニル、(C3−C6)−アルキニル、(C3−C6)−ハロアルキニル、(C3−C7)−シクロアルキル、(C3−C7)−シクロアルキル−(C1−C6)−アルキル、−(CH2)qR7又は−(CH2)qR12であるか、又は非置換であるかもしくはハロゲン、(C1−C6)−アルコキシ、(C1−C6)−ハロアルコキシ、(C3−C6)−アルケニルオキシ、(C3−C6)−ハロアルケニルオキシ、(C3−C6)−アルキニルオキシ、(C3−C6)−ハロアルキニルオキシ、(C3−C7)−シクロアルキル、S(O)pR8、CN、NO2、OH、COR9、NR9R10、S(O)pR7、OR7及びCO2R9からなる群の中から選択される1個又はそれ以上の基で置換された(C1−C6)−アルキルであり;
R6は(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C2−C6)−アルケニル、(C2−C6)−ハロアルケニル、(C2−C6)−アルキニル又は(C2−C6)−ハロアルキニルであり;
R7は非置換であるか又はハロゲン、(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C1−C6)−アルコキシ、(C1−C6)−ハロアルコキシ、CN、NO2、S(O)pR8、COR10、COR13、CONR9R10、SO2NR9R10、NR9R10及びOHからなる群の中から選択される1個又はそれ以上の基で置換されたフェニルであり;
R8は(C1−C6)−アルキル又は(C1−C6)−ハロアルキルであり;
R9及びR10はそれぞれ独立してH、(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C3−C6)−アルケニル、(C3−C6)−ハロアルケニル、(C3−C6)−アルキニル、(C3−C6)−シクロアルキル又は−(C1−C6)−アルキル−(C3−C6)−シクロアルキルであるか;又は
R9及びR10は結合されたN原子と一緒になって環中にO、S及びN原子から選択される異種原子をさらに含有していてもよい5員又は6員飽和環を形成し〔但し、前記の環は非置換であるか又はハロゲン、(C1−C6)−アルキル及び(C1−C6)−ハロアルキルからなる群の中から選択される1個又はそれ以上の基で置換されている〕;
R11はH、(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C3−C6)−アルケニル又は(C3−C6)−アルキニルであり;
R12は非置換であるか又はハロゲン、(C1−C4)−アルキル、(C1−C4)−ハロアルキル、(C1−C4)−アルコキシ、(C1−C4)−ハロアルコキシ、NO2、CN、CO2(C1−C6)−アルキル、S(O)pR8、OH及びオキソからなる群の中から選択される1個又はそれ以上の基で置換されたヘテロシクリルであり;
R13は非置換であるか又はハロゲン、(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C1−C6)−アルコキシ、(C1−C6)−ハロアルコキシ、CN、NO2、S(O)pR8及びNR9R10からなる群の中から選択される1個又はそれ以上の基で置換されたフェニルであり;
n、p及びrはそれぞれ独立して0、1又は2であり;
m及びqはそれぞれ独立して独立して0又は1であり、及び
前記の基中のそれぞれのヘテロシクリルは、独立して、3から7個の環原子を有し、環中にN、O及びS原子からなる群の中から選択される1個、2個又は3個の異種原子を有する複素環式基である}
で示される5−置換−オキシアルキルアミノピラゾール誘導体又は殺虫剤に許容し得るこの塩である化合物を提供する。
ハロゲン原子とは、弗素、塩素、臭素又はヨウ素を意味する。
シクロアルキルで置換されたアルキルの例は、シクロプロピルメチルであり;
アルコキシで置換されたアルキルの例は、メトキシメチル(CH3OCH2−)であり;及び
アルキルチオで置換されたアルキルの例は、メチルチオメチル(CH3SCH2−)である。
−(CH2)qR7、(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり、式中のR7は非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、CN、NO2及びS(O)pR8からなる群の中から選択される1個又はそれ以上の基で置換されたフェニルであり、及びそれぞれのR8は(C1−C3)−アルキル又は(C1−C3)−ハロアルキルである。
R1がCN、CSNH2又はC(=N−Z)−S−Qであり(さらに好ましくは、R1がCN又はCSNH2であり);
ZがH、(C1−C3)−アルキル、−(CH2)qR7、COR8、CO2−(C1−C3)−アルキル又はS(O)pR8であり;
Qが(C1−C3)−アルキルであり;
WがC−Cl又はNであり;
R2がClであり;
R3がCF3又はOCF3であり(さらに好ましくは、R3がCF3であり);
R4が水素、(C2−C4)−アルケニル、(C2−C4)−ハロアルケニル、(C2−C4)−アルキニル、(C2−C4)−ハロアルキニル、(C3−C7)−シクロアルキル、CO2−(C1−C4)−アルキル、CO2−(C3−C4)−アルケニル、CO2−(C3−C4)−アルキニル、CO2−(CH2)mR7又はSO2R8であるか、又は非置換であるかもしくはハロゲン、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、(C3−C7)−シクロアルキル及びS(O)pR8からなる群の中から選択される1個又はそれ以上の基で置換された(C1−C4)−アルキルであり〔さらに好ましくは、R4がCO2−(C1−C3)−アルキル又はSO2R8であるか、又は非置換であるかもしくはハロゲン、(C1−C3)−アルコキシ、S(O)pR8及びCO2−(C1−C3)−アルキルからなる群の中から選択される1個又はそれ以上の基で置換された(C1−C3)−アルキルであり〕;
Aが(C1−C4)−アルキレンであり(さらに好ましくは、Aが−CH2CH2−又は−CH2CH2CH2−であり);
XがC(=O)、C(=S)又はSO2であり;
YがO、NH又は共有結合であり;
R5が(C3−C4)−アルケニル、(C3−C4)−アルキニル、(C3−C7)−シクロアルキル又は−(CH2)qR7であるか、又は非置換であるかもしくはハロゲン、(C1−C4)−アルコキシ、(C1−C4)−ハロアルコキシ、(C3−C4)−アルケニルオキシ、(C3−C4)−ハロアルケニルオキシ、(C3−C4)−アルキニルオキシ、(C3−C4)−ハロアルキニルオキシ、(C3−C7)−シクロアルキル、S(O)pR8、CN、NO2、OH、COR9及びCO2R9からなる群の中から選択される1個又はそれ以上の基で置換された(C1−C4)−アルキルであり〔さらに好ましくは、R5が(C3−C4)−アルケニル、(C3−C4)−アルキニル、−(CH2)qR7、(C1−C3)−アルコキシ、(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり〕;
R6が(C1−C3)−ハロアルキルであり(さらに好ましくはR6がCF3であり);
それぞれのR7が独立して非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、CN、NO2及びS(O)pR8からなる群の中から選択される1個又はそれ以上の基で置換されたフェニルであり;
それぞれのR8が独立して(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり、及び
R9がH又は(C1−C3)−アルキルである
化合物である。
R1がCN、CSNH2又はC(=N−Z)−S−Qであり;
ZがH、(C1−C3)−アルキル、−(CH2)qR7、COR8、CO2−(C1−C3)−アルキル又はS(O)pR8であり;
Qが(C1−C3)−アルキルであり;
WがC−Clであり;
R2がClであり;
R3がCF3であり;
R4が水素、(C2−C4)−アルケニル、(C2−C4)−アルキニル、(C3−C7)−シクロアルキル、CO2−(C1−C4)−アルキル、CO2−(C3−C4)−アルケニル、CO2−(C3−C4)−アルキニル、CO2−(CH2)mR7又はSO2R8であるか、又は非置換であるかもしくはハロゲン、(C1−C3)−アルコキシ、S(O)pR8及びCO2−(C1−C3)−アルキルからなる群の中から選択される1個又はそれ以上の基で置換された(C1−C3)−アルキルであり;
Aが−CH2CH2−又は−CH2CH2CH2−であり;
XがC(=O)又はSO2であり;
YがO、NH又は共有結合であり;
R5が(C3−C4)−アルケニル、(C3−C4)−アルキニル、−(CH2)qR7、(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり;
R6がCF3であり;
それぞれのR7が独立して非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、CN、NO2及びS(O)pR8からなる群の中から選択される1個又はそれ以上の基で置換されたフェニルであり、及び
それぞれのR8が独立して(C1−C3)−アルキル又は(C1−C3)−ハロアルキルである
化合物である。
R1がCN又はCSNH2であり;
WがC−Clであり;
R2がClであり;
R3がCF3であり;
R4が(C1−C3)−アルキルであり;
Aが−CH2CH2−又は−CH2CH2CH2−であり;
XがC(=O)であり;
YがO、NH又は共有結合であり;
R5が(C3−C4)−アルケニル、(C3−C4)−アルキニル、−(CH2)qR7、(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり;
R6がCF3であり;
R7が非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、CN、NO2及びS(O)pR8からなる群の中から選択される1個又はそれ以上の基で置換されたフェニルであり、及び
R8が独立して(C1−C3)−アルキル又は(C1−C3)−ハロアルキルである
化合物である。
R1がCNであり;
WがC−Clであり;
R2がClであり;
R3がCF3であり;
R4がメチルであり;
Aが−CH2CH2−であり;
XがC(=O)又はSO2であり;
YがO、NH又は共有結合であり;
R5が(C3−C4)−アルケニル、(C3−C6)−シクロアルキル又は−(CH2)qR7であるか、又はハロゲン及び(C1−C6)−アルコキシからなる群の中から選択される1個又はそれ以上の基で置換された(C1−C3)−アルキルであり;
R6がCF3であり、及び
R7が非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ及びNO2からなる群の中から選択される1個又はそれ以上の基で置換されたフェニルである
化合物である。
で示される化合物を用いてアシル化するか又はスルホニル化することによって製造し得る。アシル化については、XがCO又はCSであり、YがO又は共有結合である場合には、化合物(III)は、酸ハロゲン化物であることが好ましく、Lは好ましくは塩素又は臭素(さらに好ましくは塩素)である。塩基は、場合によって反応に存在させてもよく、反応は一般に不活性溶媒、例えばテトラヒドロフラン、ジオキサン、アセトニトリル、トルエン、ジエチルエーテル、ジクロロメタン、ジメチルスルホキシド又はN,N−ジメチルホルムアミド中で、0から150℃、好ましくは20℃から100℃の温度で行なわれる。前記の塩基は、一般にアルカリ金属水酸化物、例えば水酸化カリウム、アルカリ金属水素化物、例えば水素化ナトリウム、アルカリ金属炭酸塩、例えば炭酸カリウム又は炭酸ナトリウム、アルカリ金属アルコキシド、例えばナトリウムメトキシド、アルカリ土類金属炭酸塩、例えば炭酸カルシウムであるか、又は有機塩基、例えば三級アミン例えば、トリエチルアミン又はエチルジイソプロピルアミン、又はピリジン、又は1,8−ジアザビシクロ[5.4.0]ウンデカ−7−エン(DBU)である。
R5−N=C=O (IV) R5−N=C=S (V)
(式中、R5は前記で定義した通りである)
で示されるイソシアネート又はイソチオシアネート化合物と反応させることによって製造し得る。この反応は、場合により、塩基、例えばアルカリ金属水素化物、例えば水素化ナトリウムの存在下で、溶媒、例えばアセトニトリル又はテトラヒドロフラン中で、0℃から100℃の温度で行なわれる。
Q−L1 (VI) Q3O+BF4 − (VII)
(式中、Qは前記で定義した通りであり、L1は脱離基、一般的にはハロゲン、好ましくは塩素、臭素又はヨウ素である)
で示されるアルキル化剤と反応させることによって製造し得る。この反応は、一般に、塩基、例えばアルカリ金属水素化物、例えば水素化ナトリウム、又はアルカリ金属アルコキシド、例えばカリウムtert−ブトキシドの存在下で、不活性溶媒、例えばテトラヒドロフラン中で、0から60℃の温度で行なわれる。別法として、アルカリ金属炭酸塩、例えば炭酸カリウム、又は有機塩基、例えばトリアルキルアミン、例えばトリエチルアミン又はN,N−ジイソプロピルエチルアミンを、不活性溶媒、例えばアセトン中で0℃から溶媒の還流温度までの温度で使用してもよい。式(VII)で示される化合物、例えばトリメチルオキソニウムテトラフルオロボレートをアルキル化剤として使用する場合には、塩基はアルカリ金属炭酸水素塩、例えば炭酸水素ナトリウムであることが好ましく、溶媒は例えばジクロロメタンであり、温度は0℃から溶媒の還流温度までの温度である。
Z−L2 (VIII)
(式中、ZはHを除いて前記で定義した通りであり、L2は脱離基である)
で示される化合物を用いてアルキル化、アシル化又はスルホニル化することによって製造し得る。アルキル化については、Zが(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C3−C6)−アルケニル、(C3−C6)−アルキニル又は−(CH2)qR7である場合には、L2は好ましくはハロゲン、アルキルスルホニルオキシ又はアリールスルホニルオキシ(さらに好ましくは塩素、臭素、ヨウ素、メチルスルホニルオキシ又はp−トルエンスルホニルオキシ)である。塩基は、場合により反応に存在させてもよく、反応は一般に不活性溶媒、例えばテトラヒドロフラン、ジオキサン、アセトニトリル、トルエン、ジエチルエーテル、ジクロロメタン、ジメチルスルホキシド又はN,N−ジメチルホルムアミド中で、−30℃から200℃、好ましくは20℃から100℃の温度で行なわれる。塩基は、一般にアルカリ金属水酸化物、例えば水酸化カリウム、アルカリ金属水素化物、例えば水素化ナトリウム、アルカリ金属炭酸塩、例えば炭酸カリウム又は炭酸ナトリウム、アルカリ金属アルコキシド、例えばナトリウムメトキシド、アルカリ土類金属炭酸塩、例えば炭酸カルシウム、又は有機塩基、例えば三級アミン、例えばトリエチルアミン又はエチルジイソプロピルアミン、又はピリジン、又は1,8−ジアザビシクロ[5.4.0]ウンデカ−7−エン(DBU)である。
で示される化合物と反応させることによって製造し得る。この反応は、塩基の存在下で、不活性溶媒、例えばテトラヒドロフラン、ジオキサン、アセトニトリル、トルエン、ジエチルエーテル、ジクロロメタン、ジメチルスルホキシド又はN,N−ジメチルホルムアミド中で、0℃から100℃の温度で行なわれる。塩基は、一般的にアルカリ金属水素化物、例えば水素化ナトリウム、アルカリ金属炭酸塩、例えば炭酸カリウム又は炭酸ナトリウム、アルカリ金属アルコキシド、例えばナトリウムメトキシド、又はアルカリ土類金属炭酸塩、例えば炭酸カルシウムである。
NMRスペクトルは、特に断らない限りはジューテロクロロホルム中で測定した。
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−{N−メチル−N−[2−(4−トルエンスルホニルオキシ)エチル]アミノ}−4−トリフルオロメチルスルホニルピラゾール
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−[N−(2−ヒドロキシエチル)−N−メチルアミノ]−4−トリフルオロメチルスルホニルピラゾール(0.100g、0.2ミリモル)と水素化ナトリウム(0.016g、0.4ミリモル)とを乾燥テトラヒドロフランに溶解した溶液を、窒素雰囲気下に20℃で1時間激しく攪拌した。次いで、4−トルエンスルホニルクロリド(0.056g、0.3ミリモル)を加え、攪拌を20℃で1時間続けた。次いで、得られた混合物を飽和塩化アンモニウム溶液と酢酸エチルに加え;有機層を水及び食塩水で洗浄し、乾燥し(硫酸ナトリウム)、及び蒸発させた。残留物を、フラッシュカラムクロマトグラフィーで、ヘプタン/酢酸エチル(4:1)を用いて溶出することにより精製して、表題化合物を微細白色粉末として得た(0.074g、化合物93、収率55%)。19F−NMR:−64.2、−79.2。
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−{N−メチル−N−[2−(4−トリフルオロメチル−ベンゾイルオキシ)エチル]アミノ}−4−トリフルオロメチルスルホニルピラゾール
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−[N−(2−ヒドロキシエチル)−N−メチルアミノ]−4−トリフルオロメチルスルホニルピラゾール(0.100g、0.2ミリモル)を乾燥テトラヒドロフランに溶解した溶液に、水素化ナトリウム(0.012g、0.3ミリモル)を加え、混合物を窒素雰囲気下に20℃で1時間激しく攪拌した。4−トリフルオロメチルベンゾイルクロリド(0.053g、0.3ミリモル)を加え、混合物を20℃で2時間攪拌した。得られた混合物を飽和塩化アンモニウム溶液及び酢酸エチルに注ぎ、有機層を水及び食塩水で洗浄し、乾燥し(硫酸ナトリウム)、及び蒸発させた。残留物を、フラッシュカラムクロマトグラフィーで、ヘプタン/酢酸エチル(4:1)を用いて溶出することにより精製して、表題化合物を淡い色の油状物として得た(0.085g、化合物54、収率61%)。19F−NMR:−63.7、−63.8、−78.6。
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−{N−メチル−N−[2−(4−エトキシフェニルアミノカルボニルオキシ)エチル]アミノ}−4−トリフルオロメチルスルホニルピラゾール
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−[N−(2−ヒドロキシエチル)−N−メチルアミノ]−4−トリフルオロメチルスルホニルピラゾール(0.100g、0.2ミリモル)を乾燥テトラヒドロフランに溶解した溶液に水素化ナトリウム(0.012g、0.3ミリモル)を加え、窒素雰囲気下で20℃で1時間激しく攪拌した。4−エトキシフェニルイソシアネート(0.041g、0.3ミリモル)を加え、攪拌を20℃で2時間続けた。得られた混合物を飽和塩化アンモニウム溶液と酢酸エチルに注ぎ、有機層を水及び食塩水で洗浄し、乾燥し(硫酸ナトリウム)、及び蒸発させた。残留物をフラッシュカラムクロマトグラフィーによりヘプタン/酢酸エチル(4:1から2:1)を用いて溶出することにより精製して、表題化合物を白色粉末として得た(0.041g、化合物69、収率30%)、19F−NMR:−63.7、−78.5。
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−{N−メチル−N−[2−(エトキシカルボニルオキシ)エチル]アミノ}−4−トリフルオロメチルスルホニルピラゾール
1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−[N−(2−ヒドロキシエチル)−N−メチルアミノ]−4−トリフルオロメチルスルホニルピラゾール(0.100g、0.2ミリモル)を乾燥テトラヒドロフランに溶解した溶液に、水素化ナトリウム(0.012g、0.3ミリモル)を加え、窒素雰囲気下で20℃で2時間攪拌した。クロロギ酸エチル(0.029g、0.3ミリモル)を加え、攪拌を20℃で1時間続けた。次いで、得られた混合物を飽和塩化アンモニウム溶液と酢酸エチルに加え、有機層を水及び食塩水で洗浄し、乾燥し(硫酸ナトリウム)、及び蒸発させた。残留物をフラッシュカラムクロマトグラフィーでヘプタン/酢酸エチル(4:1)を用いて溶出することにより精製して、表題化合物を白色粉末として得た(0.098g、化合物6、収率:81%)、19F−NMR:−63.8、−78.6。
5−ブロモ−1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−4−トリフルオロメチルスルホニルピラゾール(10.00g、19.3ミリモル)を乾燥N,N−ジメチルホルムアミド(85ml)に溶解した溶液に、微粉砕炭酸カリウム(7.29g、52.2ミリモル)を加え、20℃で1時間攪拌した。次いで、2−(メチルアミノ)エタノール(3.11ml、38.7ミリモル)を加え、攪拌を20℃で2時間続けた。得られた混合物を飽和塩化アンモニウム溶液に注ぎ、酢酸エチルで抽出し、有機層を水及び食塩水で洗浄し、乾燥し(硫酸ナトリウム)、蒸発させ、カラムクロマトグラフィーでヘキサン及び酢酸エチル(2:1)を用いて溶出することにより精製して、1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−5−[N−(2−ヒドロキシエチル)−N−メチルアミノ]−4−トリフルオロメチルスルホニルピラゾールを微細白色粉末として得た(5.65g、収率57%)。19F−NMR:−63.7、−78.4。
5−アミノ−1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−4−トリフルオロメチルスルホニルピラゾール(100g、0.221モル)をブロモホルム(320ml)に懸濁した懸濁物に、t−ブチルニトリル(84ml、0.662モル)を加えた。得られた混合物を60から70℃に3時間加熱した。別量のt−ブチルニトリル(84ml、0.662モル)を加え、混合物を60から70℃でさらに2.5時間攪拌した。次いで、この混合物を冷却し、ヘキサン、ヘキサン−トルエンで洗浄し、次いで濾過した。固体をペンタンで洗浄し、真空乾燥して、5−ブロモ−1−(2,6−ジクロロ−4−トリフルオロメチルフェニル)−3−シアノ−4−トリフルオロメチルスルホニルピラゾールを黄色固体として得た(96.69g、収率79%)。mp142℃。
土壌昆虫、例えば根切り虫(corn rootworm)、シロアリ(特に建造物の保護のため)、根食い虫、コメツキムシ、ルート・ウィービル(root weevils)、ストークボーラー(stalkborer)、ヤガ類、根アブラムシ又は地虫の防除のため。本発明の化合物はまた、植物病原性線虫、例えばネコブセンチュウ、シストセンチュウ、オオハリセンチュウ、ネグサレセンチュウ又はナミキクセンチュウに対して、又はダニに対して活性を提供するために使用し得る。土壌害虫、例えばコーン・ルートワームの防除のために、本発明の化合物は、作物を植えてあるか又は植えるべき土壌に、又は種子もしくは栽培中の植物の根に、有効量で都合よく施用又は混合される。
栽培中の作物に対しては、茎葉散布剤(例えば、畝間内散布剤として)、粉剤、粒剤、煙霧剤又は発泡剤として、又はまた液体潅注液、粉剤、粒剤、くん煙剤又は発泡剤による土壌又は根の処理として微細化又はカプセル化組成物の懸濁剤として;作物の種子に対しては液体スラリー又は粉剤による種子粉衣剤として;
節足動物又は蠕虫が寄生した動物又はこれらの寄生に暴露された動物に対しては、有効成分が節足動物又は蠕虫に対して即時作用及び/又は一定の期間にわたる持続作用を示す組成物を、非経口、経口又は局所施用することにより、例えば飼料中への配合、又は適切な経口摂取可能な医薬製剤、食用ベイト、家畜用岩塩、栄養補助側品、ポアオン製剤、噴霧剤、浴剤、ディップ、シャワー、ジェット、粉剤、グリース、シャンプー、クリーム、ワックス・スミア又は家畜自己処理システムにより;
一般環境に対して又は害虫が潜伏し得る特定の場所、例えば貯蔵品、材木、家庭用品、又は家屋もしくは工業施設に対しては、噴霧剤、煙霧剤、粉剤、くん煙剤、ワックス・スミア、ラッカー、粒剤又はベイトとして、又は水路、井戸、貯水池又はこの他の流水もしくは貯留水への細流供給において。
1.リン化合物の群から
アセフェート、アザメチホス、アジンホス・エチル、アジンホス・メチル、ブロモホス、ブロモホス・エチル、カズサホス(F−67825)、クロルエトキシホス、クロルフェンビンホス、クロルメホス、クロルピリホス、クロルピリホス・メチル、ジメトン、ジメトン−S−メチル、ジメトン−S−メチルスルホン、ジアリホス、ダイアジノン、ジクロルボス、ジクロトホス、ジメトエート、ジスルホトン、EPN、エチオン、エトプロホス、エトリムホス、ファムフル、フェナミホス、フェニトリオチオン、フェンスルホチオン、フェンチオン、フルピラゾホス、ホノホス、ホルモチオン、ホスチアゼート、ヘプテノホス、イサゾホス、イソチオエート、イソキサチオン、マラチオン、メタクリホス、メタミドホス、メチダチオン、サリチオン、メビンホス、モノクロトホス、ナレッド、オメトエート、オキシジメトン・メチル、パラチオン、パラチオン・メチル、フェントエート、ホレート、ホサロン、ホスホラン、ホスホカルブ(BAS−301)、ホスメット、ホスファミドン、ホキシム、ピリミホス、ピリミホス・エチル、ピリミホス・メチル、プロフェノホス、プロパホス、プロエタムホス(proetamphos)、プロチオホス、ピラクロホス、ピリダフェンチオン、キナルホス、スルプロホス、テメホス、テルブホス、テブピリムホス、テトラクロルビンホス、チオメトン、トリアゾホス、トリクロルホン、バミドチオン;
アラニカルブ(OK−135)、アルジカルブ、メチルカルバミン酸2−sec−ブチルフェニル(BPMC)、カルバリル、カルボフラン、カルボスルファン、クロエトカルブ、ベンフラカルブ、エチオフェンカルブ、フラチオカルブ、HCN−801、イソプロカルブ、メソミル、5−メチル−m−クメニルブチリル(メチル)カルバメート、オキサミル、ピリミカーブ、プロポキスル、チオジカルブ、チオファノックス、1−メチルチオ(エチリデンアミノ)−N−メチル−N−(モルホリノチオ)カルバメート(UC 51717)、トリアザメート;
アクリナトリン、アレスリン、アルファメトリン、(E)−(1R)−シス−2,2−ジメチル−3−(2−オキソチオラン−3−イリデンメチル)シクロプロパンカルボン酸5−ベンジル−3−フリルメチル、β−シフルトリン、α−シペルメトリン、β−シペルメトリン、ビオアレスリン、ビオアレスリン〔(S)−シクロペンチル異性体〕、ビオレスメトリン、ビフェントリン、(1RS)−トランス−3−(4−tert−ブチルフェニル)−2,2−ジメチルシクロプロパンカルボン酸(RS)−1−シアノ−1−(6−フェノキシ−2−ピリジル)メチル(NCI85193)、シクロプロトリン、シフルトリン、シハロトリン、シチトリン(cythithrin)、シペルメトリン、シフェノトリン、デルタメトリン、エンペントリン、エスフェンバレレート、フェンフルトリン、フェンプロパトリン、フェンバレレート、フルシトリネート、フルメトリン、フルバリネート(D異性体)、イミプロトリン(S−41311)、λ−シハロトリン、ペルメトリン、フェノトリン(R異性体)、プラレスリン、ピレトリン(天然生成物)、レスメトリン、テフルトリン、テトラメトリン、θ−シペルメトリン、トラロメトリン、トランスフルトリン、ζ−シペルメトリン(F−56701);
アミトラズ、クロルジメホルム;
シヘキサチン、酸化フェンブタスズ;
アバメクチン、ABG−9008、アセタミプリド、アセキノシル、アナグラファ・ファルシテラ(Anagrapha falcitera)、AKD−1022、AKD−3059、ANS−118、アザジラクチン、バシラス・スリンジエンシス(Bacillus thuringiensis)、ボーベリア・バシアーナ(Beauveria bassiana)、ベンスルタップ、ビフェナゼート、ビナパクリル、BJL−932、ブロモプロピレート、BTG−504、BTG−505、ブプロフェジン、カンフェクロル、カルタップ、クロルベンジレート、クロルフェナピル、クロルフルアズロン、2−(4−クロロフェニル)−4,5−ジフェニルチオフェン(UBI−T930)、クロルフェンテジン、クロルプロキシフェン(chlorproxyfen)、クロマフェノジド、クロチアニジン、シクロプロパンカルボン酸2−ナフチルメチル(Ro12−0470)、シロマジン、ジアクロデン(チアメトキサム)、ジアフェンチウロン、DBI−3204、エチル=2−クロロ−N−(3,5−ジクロロ−4−(1,1,2,3,3,3−ヘキサフルオロ−1−プロピルオキシ)フェニル)カルバモイル)−2−カルボキシイミデート、DDT、ジコホル、ジフルベンズロン、N−(2,3−ジヒドロ−3−メチル−1,3−チアゾール−2−イリデン)−2,4−キシリデン、ジヒドロキシメチルジヒドロキシピロリジン、ジノブトン、ジノカップ、ジオフェノラン、エマメクチン安息香酸塩、エンドスルファン、エチプロール(スルフェチプロール)、エトフェンプロックス、エトキサゾール、フェナザキン、フェノキシカルブ、フィプロニル、フロニカミド (IKI−220)、フルアズロン、flumite〔フルフェンジン(flufenzine)、SZI−121〕、2−フルオロ−5−(4−(4−エトキシフェニル)−4−メチル−1−ペンチル)ジフェニルエーテル(MTI800)、顆粒病ウィルス及び核多核体病ウィルス、フェンピロキシメート、フェンチオカルブ、フルアクリプリム、フルベンジミン、フルブロシトリネート、フルシクロクスロン(flucycloxuron)、フルフェノクスロン、フルフェンジン(flufenzine)、フルフェンプロックス、フルプロキシフェン、γ−HCH、ハロフェノジド、ハロフェンプロックス、ヘキサフルムロン(DE 473)、ヘキシチアゾックス、HOI−9004、ヒドラメチルノン(AC217300)、インドキサカルブ、イベルメクチン、L−14165、イミダクロプリド、インドキサカルブ(DPXMP062)、カネマイト(AKD−2023)、ルフェヌロン、M−020、M−020、メトキシフェノジド、ミルベメクチン、NC−196、ニームガード(neemgard)、ニジノテルフラン(nidinoterfuran)、ニテンピラム、2−ニトロメチル−4,5−ジヒドロ−6H−チアジン(DS52618)、2−ニトロメチル−3,4−ジヒドロチアゾール(SD35651)、2−ニトロメチレン−1,2−チアジナン−3−イルカルバムアルデヒド(WL108477)、ノバルロン、ピリダリル(pirydaryl)、プロパルギット、プロトリフェンブテ(protrifenbute)、ピメトロジン、ピリダベン、ピリミジフェン、ピリプロキシフェン、NC−196、NC−1111、NNI−9768、ノバルロン(MCW−275)、OK−9701、OK−9601、OK−9602、OK−9802、R−195、RH−0345、RH−2485、RYI−210、S−1283、S−1833、SI−8601、シラフルオフェン、シロマジン(CG−177)、スピノサド、スピロジクロフェン、SU−9118、テブフェノジド、テブフェンピラド、テフルベンズロン、テトラジホン、テトラサル、チアクロプリド、チオシクラム、チアメトキサム、トルフェンピラド、トリアザメート、トリエトキシスピノシンA、トリフルムロン、ベルブチン(verbutin)、バータレック(mykotal)、YI−5301
である。
商品名 化学的説明
Ethylan BCP ノニルフェノールエチレンオキシド縮合物
Soprophor BSU トリスチリルフェノールエチレンオキシド縮合物
Arylan CA ドデシルベンゼンスルホネン酸カルシウムの70%w/v溶液
Solvesso 150 軽質C10芳香族系溶媒
Arylan S ドデシルベンゼンスルホン酸ナトリウム
Darvan NO2 リグノスルホン酸ナトリウム
Celite PF 合成ケイ酸マグネシウム担体
Sopropon T36 ポリカルボン酸のナトリウム塩
Rhodigel 23 多糖キサンタンガム
Bentone 38 マグネシウムモンモリロナイトの有機誘導体
Aerosil 超微粒二酸化ケイ素
下記の組成を有する水溶性濃厚物を製造した:
有効成分 7%
Ethylan BCP 10%
N−メチルピロリドン 83%
Ethylan BCPをN−メチルピロリドンの一部に溶解した溶液に、有効成分を加熱し撹拌しながら溶解するまで加えた。得られた溶液に、残りの溶媒を加えて容量を調整した。
下記の組成を有する乳剤(EC)を製造した:
有効成分 25%(最大)
Soprophor BSU 10%
Arylan CA 5%
N−メチルピロリドン 50%
Solvesso 150 10%
最初の3つの成分をN−メチルピロリドンに溶解し、次いでこれにSolvesso 150を加えて最終容量を得た。
下記の組成を有する水和剤(WP)を製造した:
有効成分 40%
Arylan S 2%
Darvan NO2 5%
Celite PF 53%
前記の成分を混合し、ハンマーミルで粒径50ミクロン未満の粒度をもつ粉末に粉砕した。
下記の組成を有する水性フロアブル剤を製造した:
有効成分 40.00%
Ethylan BCP 1.00%
Sopropon T360 0.20%
エチレングリコール 5.00%
Rhodigel 230 0.15%
水 53.65%
前記の成分を均質に混合し、ビーズミルで3ミクロン未満の平均粒径が得られるまで粉砕した。
下記の組成を有する乳化性SC剤を製造した:
有効成分 30.0%
Ethylan BCP 10.0%
Bentone 38 0.5%
Solvesso 150 59.5%
下記の組成を有する水和性顆粒剤を製造した:
有効成分 30%
Darvan No2 15%
Arylan S 8%
Celite PF 47%
前記の成分を混合し、流体エネルギーミルで微粉砕し、次いで水(最大10%)を噴霧することにより回転ペレタイザー中で造粒した。得られた顆粒を流動床式乾燥機中で乾燥して過剰の水分を除去した。
下記の組成を有する粉剤を製造した:
有効成分 1から10%
超微細タルク粉末 99から90%
下記の組成を有する食用ベイトを製造した:
有効成分 0.1から1.0%
小麦粉 80%
糖蜜 19.9から19%
下記の組成を有する液剤を製造した:
有効成分 15%
ジメチルスルホキシド 85%
下記の組成を有する水和剤を製造した:
有効成分 50%
Ethylan BCP 5%
Aerosil 5%
Celite PF 40%
徐放性ボーラス組成物を、下記の成分を必要性に応じて(前記組成について記載した%と同様の)種々の%で含有する粒剤から形成した:
有効成分
密度調整剤
徐放剤
結合剤
下記の組成を有する粒剤、錠剤、ブリケットなどの形の徐放性組成物を製造した:
有効成分 0.5から25%
塩化ポリビニル 75から99.5%
フタル酸ジオクチル(可塑剤)
下記の組成を有する水和性顆粒剤を製造した:
有効成分 85%(最大)
ポリビニルピロリドン 5%
アタパルジャイトクレー 6%
ラウリル硫酸ナトリウム 2%
グリセリン 2%
本発明の化合物を使用して下記の代表的な試験操作を行って、本発明の化合物の殺寄生虫活性を測定した。
試験容器にネコノミ(Ctenocephalides felis)の成虫10匹を入れた。ガラスシリンダーの一端をパラフィルムで密閉し、試験容器の上部に置いた。次に、試験化合物溶液をピペットでウシの血液に入れ、これをガラスシリンダーに加えた。処理したネコノミをこの擬似イヌ試験(血液37℃、相対湿度40から60%;ネコノミ20から22℃、相対湿度40から60%)に付し、施用して24および48時間後に評価を行なった。
Claims (14)
- 式(I):
R1はCNであり;
WはC−ハロゲンであり;
R2はハロゲンであり;
R3は(C1−C3)−ハロアルキルであり;
R4 は非置換(C1−C6)−アルキルであり;
Aは(C1−C6)−アルキレンであり;
XはC(=O)、C(=S)又はSO2であり;
YはO、NR11又は共有結合であり;
R5は(C3−C6)−アルケニル又は−(CH2)qR7であるか、又は非置換であるかもしくはハロゲン、(C1−C6)−アルコキシ、(C1−C6)−ハロアルコキシ、OH及びNR9R10からなる群から選択される1個又はそれ以上の基で置換された(C1−C6)−アルキルであり;
R6は(C1−C6)−アルキル又は(C1−C6)−ハロアルキルであり;
R7は非置換であるか又はハロゲン、(C1−C6)−アルキル、(C1−C6)−ハロアルキル、(C1−C6)−アルコキシ、(C1−C6)−ハロアルコキシ、CN、NO2、NR9R10及びOHからなる群から選択される1個又はそれ以上の基で置換されたフェニルであり;
R9及びR10はそれぞれ独立してH又は(C1−C6)−アルキルであり;
R11はH又は(C1−C6)−アルキルであり;
nは0、1又は2であり;及び
qは0又は1である}
で示される化合物又は殺虫剤に許容し得るその塩。 - R6がCF3である、請求項1に記載の化合物又はその塩。
- WがC−Clであり;
R2がClであり;
R3がCF3であり;
R4 が非置換(C1−C3)−アルキルであり;
Aが−CH2CH2−又は−CH2CH2CH2−であり;
XがC(=O)又はSO2であり;
YがO、NH又は共有結合であり;
R5が(C3−C4)−アルケニル、−(CH2)qR7、(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり;
R6がCF3であり;及び
R 7 が非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、CN及びNO2からなる群から選択される1個又はそれ以上の基で置換されたフェニルである、請求項1に記載の化合物又はその塩。 - WがC−Clであり;
R2がClであり;
R3がCF3であり;
R4が(C1−C3)−アルキルであり;
Aが−CH2CH2−又は−CH2CH2CH2−であり;
XがC(=O)であり;
YがO、NH又は共有結合であり;
R5が(C3−C4)−アルケニル、−(CH2)qR7、(C1−C3)−アルキル又は(C1−C3)−ハロアルキルであり;
R6がCF3であり;及び
R7が非置換であるか又はハロゲン、(C1−C3)−アルキル、(C1−C3)−ハロアルキル、(C1−C3)−アルコキシ、(C1−C3)−ハロアルコキシ、CN及びNO2からなる群から選択される1個又はそれ以上の基で置換されたフェニルである、請求項1から3のいずれか1項に記載の化合物又はその塩。 - a)R2、R3、R4、R5、R6、W、A及びnが請求項1で定義した通りであり、R1がCNであり、Y及びXが、−Y−X−が−NH−CO−又は−NH−CS−である化合物を除いて、請求項1で定義した通りである場合には、式(II):
で示される化合物を、式(III):
で示される化合物を用いてアシル化又はスルホニル化し、及び
(h)必要に応じて、得られた式(I)で示される化合物をその殺虫剤に許容し得る塩に転化させる
ことからなる請求項1に記載の式(I)で示される化合物又はその塩の製造方法。 - b)R1がCNであり、R2、R3、R4、R5、R6、W、A及びnが請求項1で定義した通りである場合には、式(II)〔式中、R1、R2、R3、R6、W、A及びnは請求項1で定義した通りであり、−Y−X−は−NH−CO−又は−NH−CS−である〕で示される化合物を、式(IV)又は(V):
R5−N=C=O (IV)
R5−N=C=S (V)
〔式中、R5は式(I)で定義した通りである〕
で示されるイソシアネート又はイソチオシアネート化合物と反応させ、及び
(h)必要に応じて、得られた式(I)で示される化合物をその殺虫剤に許容し得る塩に転化させる
ことからなる請求項1に記載の式(I)で示される化合物又はその塩の製造方法。 - c)R1がCNであり、nが1又は2であり、R2、R3、R4、R5、R6、W、A、X及びYが請求項1で定義した通りである場合には、nが0又は1である対応化合物を酸化し、及び
(h)必要に応じて、得られた式(I)で示される化合物をその殺虫剤に許容し得る塩に転化させる
ことからなる請求項1に記載の式(I)で示される化合物又はその塩の製造方法。 - 殺虫剤として有効な量の請求項1から4のいずれか1項に記載の式(I)で示される化合物又はその殺虫剤に許容し得る塩を、殺虫剤に許容し得る希釈剤又は担体及び/又は界面活性剤と共に含有してなる殺虫剤組成物。
- 動物薬を製造するための請求項1から4のいずれか1項に記載の式(I)で示される化合物若しくはその塩又は請求項8に記載の組成物の使用。
- ヒトを除く動物の寄生虫を防除するための請求項1から4のいずれか1項に記載の式(I)で示される化合物もしくはその塩又は請求項8に記載の組成物の使用。
- 有効量の請求項1から4のいずれか1項に記載の式(I)で示される化合物もしくはその塩又は請求項8に記載の組成物をヒトを除く害虫の活動場所に施用することからなる害虫の防除方法。
- 人を除く動物内又は上の害虫を防除する方法であって、前記動物に活性成分として請求項1から4のいずれか1項に記載の式(I)で示される化合物もしくはその塩を含有する動物薬を害虫防除に有効な量投与することを含む害虫防除方法。
- R1がCNであり;R4がメチルであり;R6がCF3であり、Aが−CH2−CH2−であり、WがC−Clであり;R2がClであり;及びR3がCF3である請求項1に記載の化合物又はその塩。
- 式(I):
(a)XがC(=O)であり、YがOであり、R5がエチルであり、及びnが2であるか;
(b)XがC(=O)であり、YがOであり、R5が4−ニトロフェニルであり、及びnが2であるか;
(c)XがC(=O)であり、Yが共有結合であり、R5がCH3であり、及びnが2であるか;
(d)XがC(=O)であり、Yが共有結合であり、R5がCH2OCH3であり、及びnが2であるか;
(e)XがC(=O)であり、Yが共有結合であり、R5が4−トリフルオロメチルフェニルであり、及びnが2であるか;
(f)XがC(=O)であり、Yが共有結合であり、R5が2,6−ジフルオロフェニルであり、及びnが2であるか;
(g)XがC(=O)であり、Yが共有結合であり、R5が2−フルオロフェニルであり、及びnが2であるか;
(h)XがC(=O)であり、YがNHであり、R5が4−エトキシフェニルであり、及びnが2であるか;
(i)XがC(=O)であり、YがNHであり、R5が4-トリフルオロメトキシフェニルであり、及びnが2であるか;
(j)XがSO2であり、Yが共有結合であり、R5がプロピルであり、及びnが2であるか;
(k)XがSO2であり、Yが共有結合であり、R5が4-クロロフェニルであり、及びnが2であるか;又は
(l)XがSO2であり、Yが共有結合であり、R5が4-メチルフェニルであり、及びnが2である}
化合物又はその塩。
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Application Number | Priority Date | Filing Date | Title |
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EP03019618 | 2003-09-04 | ||
EP03019618.2 | 2003-09-04 | ||
PCT/EP2004/009378 WO2005023776A1 (en) | 2003-09-04 | 2004-08-21 | Pesticidal 5-substituted-oxyalkylamino-1-arylpyrazole derivatives |
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JP4982765B2 true JP4982765B2 (ja) | 2012-07-25 |
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US (1) | US7879897B2 (ja) |
EP (1) | EP1663986B1 (ja) |
JP (1) | JP4982765B2 (ja) |
KR (1) | KR101139269B1 (ja) |
CN (1) | CN1845902B (ja) |
AR (1) | AR045561A1 (ja) |
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BR (1) | BRPI0413333B8 (ja) |
CA (1) | CA2536642C (ja) |
ES (1) | ES2409681T3 (ja) |
HK (1) | HK1099649A1 (ja) |
MX (1) | MXPA06002381A (ja) |
NZ (1) | NZ545658A (ja) |
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NZ540463A (en) * | 2002-12-03 | 2008-03-28 | Merial Ltd | Pesticidal 1-aryl-3-amidoxime-pyrazole derivatives for controlling arthropods and helminths |
KR20110044900A (ko) | 2008-08-14 | 2011-05-02 | 바이엘 크롭사이언스 아게 | 살충성 4-페닐-1h-피라졸 |
CN104582696B (zh) | 2012-08-30 | 2018-07-03 | 国立大学法人东京大学 | 体内寄生虫防治剂及其使用方法 |
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GB8531485D0 (en) | 1985-12-20 | 1986-02-05 | May & Baker Ltd | Compositions of matter |
GB8713768D0 (en) | 1987-06-12 | 1987-07-15 | May & Baker Ltd | Compositions of matter |
DE3606476A1 (de) | 1986-02-28 | 1987-09-03 | Bayer Ag | 1-arylpyrazole |
DE3911556A1 (de) * | 1989-04-08 | 1990-10-11 | Bayer Ag | Substituierte 1-arylpyrazole |
NO179282C (no) * | 1991-01-18 | 1996-09-11 | Rhone Poulenc Agrochimie | Nye 1-(2-pyridyl)pyrazolforbindelser til kontroll av skadeinsekter |
US5556873A (en) | 1993-02-24 | 1996-09-17 | Rhone-Poulenc Inc. | Pesticidal 1-aryl-5-(substituted alkyl (thio) amido)pyrazoles |
US5629335A (en) * | 1995-04-07 | 1997-05-13 | Rhone-Poulenc Inc. | Pesticidal 1-arylpyrazole-3-carboximidothioic acid esters |
TW362952B (en) | 1996-01-30 | 1999-07-01 | Takeda Chemical Industries Ltd | Arylpyrazole insecticides |
EP0948487A1 (en) | 1996-12-24 | 1999-10-13 | Rhone-Poulenc Agrochimie | Pesticidal 1-aryl and pyridylpyrazole derivatives |
WO2002066423A1 (fr) | 2001-02-22 | 2002-08-29 | Nihon Nohyaku Co., Ltd. | Procede de preparation de composes de polyfluoroalkylsulfenyle |
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WO2005023776A1 (en) | 2005-03-17 |
EP1663986B1 (en) | 2013-03-27 |
ZA200601794B (en) | 2007-04-25 |
AU2004270342B2 (en) | 2011-10-13 |
KR101139269B1 (ko) | 2012-05-21 |
MXPA06002381A (es) | 2006-06-20 |
BRPI0413333B1 (pt) | 2014-09-09 |
CA2536642A1 (en) | 2005-03-17 |
CN1845902A (zh) | 2006-10-11 |
US7879897B2 (en) | 2011-02-01 |
AU2004270342A1 (en) | 2005-03-17 |
BRPI0413333B8 (pt) | 2022-06-28 |
US20070066596A1 (en) | 2007-03-22 |
NZ545658A (en) | 2009-03-31 |
KR20060096992A (ko) | 2006-09-13 |
ES2409681T3 (es) | 2013-06-27 |
BRPI0413333A (pt) | 2006-10-10 |
CA2536642C (en) | 2011-12-06 |
AR045561A1 (es) | 2005-11-02 |
JP2007504185A (ja) | 2007-03-01 |
HK1099649A1 (en) | 2007-08-17 |
EP1663986A1 (en) | 2006-06-07 |
CN1845902B (zh) | 2011-04-20 |
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