JP2021531334A - インダゾールを含む殺虫混合物 - Google Patents
インダゾールを含む殺虫混合物 Download PDFInfo
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- JP2021531334A JP2021531334A JP2021523575A JP2021523575A JP2021531334A JP 2021531334 A JP2021531334 A JP 2021531334A JP 2021523575 A JP2021523575 A JP 2021523575A JP 2021523575 A JP2021523575 A JP 2021523575A JP 2021531334 A JP2021531334 A JP 2021531334A
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- JP
- Japan
- Prior art keywords
- compound
- cypermethrin
- compounds
- composition
- pests
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 174
- 230000000749 insecticidal effect Effects 0.000 title claims description 7
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 190
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 116
- 238000000034 method Methods 0.000 claims abstract description 70
- 229940125904 compound 1 Drugs 0.000 claims abstract description 44
- -1 amidoflumeth Chemical compound 0.000 claims description 131
- 239000003085 diluting agent Substances 0.000 claims description 39
- 239000007788 liquid Substances 0.000 claims description 37
- 239000003795 chemical substances by application Substances 0.000 claims description 35
- 239000004094 surface-active agent Substances 0.000 claims description 29
- 239000005946 Cypermethrin Substances 0.000 claims description 28
- 229960005424 cypermethrin Drugs 0.000 claims description 28
- 239000007787 solid Substances 0.000 claims description 26
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims description 25
- 241000700605 Viruses Species 0.000 claims description 17
- 241000894006 Bacteria Species 0.000 claims description 15
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims description 12
- 241000233866 Fungi Species 0.000 claims description 11
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 claims description 10
- 239000005660 Abamectin Substances 0.000 claims description 10
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical group O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 claims description 9
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 claims description 9
- 239000005930 Spinosad Substances 0.000 claims description 9
- 229950008167 abamectin Drugs 0.000 claims description 9
- 201000010099 disease Diseases 0.000 claims description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 claims description 9
- 229940014213 spinosad Drugs 0.000 claims description 9
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims description 8
- 241000193388 Bacillus thuringiensis Species 0.000 claims description 8
- 239000005892 Deltamethrin Substances 0.000 claims description 8
- 239000005906 Imidacloprid Substances 0.000 claims description 8
- 239000005907 Indoxacarb Substances 0.000 claims description 8
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 claims description 8
- 239000005663 Pyridaben Substances 0.000 claims description 8
- 239000005934 Sulfoxaflor Substances 0.000 claims description 8
- 239000005940 Thiacloprid Substances 0.000 claims description 8
- 239000005941 Thiamethoxam Substances 0.000 claims description 8
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 claims description 8
- 229960002587 amitraz Drugs 0.000 claims description 8
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 claims description 8
- 229940097012 bacillus thuringiensis Drugs 0.000 claims description 8
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims description 8
- 229960002483 decamethrin Drugs 0.000 claims description 8
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 8
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 claims description 8
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 claims description 8
- 229940056881 imidacloprid Drugs 0.000 claims description 8
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims description 8
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 claims description 8
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims description 8
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 claims description 8
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 claims description 8
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 claims description 8
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 claims description 7
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 claims description 7
- 239000005652 Acrinathrin Substances 0.000 claims description 7
- 239000005877 Alpha-Cypermethrin Substances 0.000 claims description 7
- 239000005885 Buprofezin Substances 0.000 claims description 7
- 239000005899 Fipronil Substances 0.000 claims description 7
- 239000005926 Pyridalyl Substances 0.000 claims description 7
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 claims description 7
- YLFSVIMMRPNPFK-WEQBUNFVSA-N acrinathrin Chemical compound CC1(C)[C@@H](\C=C/C(=O)OC(C(F)(F)F)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YLFSVIMMRPNPFK-WEQBUNFVSA-N 0.000 claims description 7
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 claims description 7
- IRUJZVNXZWPBMU-UHFFFAOYSA-N cartap Chemical compound NC(=O)SCC(N(C)C)CSC(N)=O IRUJZVNXZWPBMU-UHFFFAOYSA-N 0.000 claims description 7
- 229940013764 fipronil Drugs 0.000 claims description 7
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 claims description 7
- 229960005199 tetramethrin Drugs 0.000 claims description 7
- 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 claims description 7
- 239000005943 zeta-Cypermethrin Substances 0.000 claims description 7
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 claims description 6
- 239000005875 Acetamiprid Substances 0.000 claims description 6
- 239000005894 Emamectin Substances 0.000 claims description 6
- 239000005897 Etoxazole Substances 0.000 claims description 6
- HMIBKHHNXANVHR-UHFFFAOYSA-N Fenothiocarb Chemical compound CN(C)C(=O)SCCCCOC1=CC=CC=C1 HMIBKHHNXANVHR-UHFFFAOYSA-N 0.000 claims description 6
- 239000005927 Pyriproxyfen Substances 0.000 claims description 6
- 239000005664 Spirodiclofen Substances 0.000 claims description 6
- MWFQAAWRPDRKDG-KOLCDFICSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1C=C(Cl)Cl MWFQAAWRPDRKDG-KOLCDFICSA-N 0.000 claims description 6
- APEPLROGLDYWBS-UHFFFAOYSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl 2,2,3,3-tetramethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)C1C(C)(C)C1(C)C APEPLROGLDYWBS-UHFFFAOYSA-N 0.000 claims description 6
- LRZWFURXIMFONG-HRSIRGMGSA-N afidopyropen Chemical compound C([C@@]1(C)[C@H]2[C@]([C@H]3[C@@H](O)C=4C(=O)OC(=CC=4O[C@]3(C)[C@@H](O)C2)C=2C=NC=CC=2)(C)CC[C@@H]1OC(=O)C1CC1)OC(=O)C1CC1 LRZWFURXIMFONG-HRSIRGMGSA-N 0.000 claims description 6
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 claims description 6
- LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 claims description 6
- CXEGAUYXQAKHKJ-NSBHKLITSA-N emamectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](NC)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 CXEGAUYXQAKHKJ-NSBHKLITSA-N 0.000 claims description 6
- IXSZQYVWNJNRAL-UHFFFAOYSA-N etoxazole Chemical compound CCOC1=CC(C(C)(C)C)=CC=C1C1N=C(C=2C(=CC=CC=2F)F)OC1 IXSZQYVWNJNRAL-UHFFFAOYSA-N 0.000 claims description 6
- BKACAEJQMLLGAV-PLNGDYQASA-N heptafluthrin Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)C1C(C)(C)C1\C=C/C(F)(F)F BKACAEJQMLLGAV-PLNGDYQASA-N 0.000 claims description 6
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- 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 claims description 6
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 claims description 6
- 239000005896 Etofenprox Substances 0.000 claims description 5
- INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 claims description 5
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 claims description 5
- 229950005085 etofenprox Drugs 0.000 claims description 5
- AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 claims description 4
- 239000005874 Bifenthrin Substances 0.000 claims description 4
- KAATUXNTWXVJKI-HBFSDRIKSA-N [(r)-cyano-(3-phenoxyphenyl)methyl] (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-HBFSDRIKSA-N 0.000 claims description 4
- OOWCJRMYMAMSOH-UHFFFAOYSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)C1C(C)(C)C1C=C(C)C OOWCJRMYMAMSOH-UHFFFAOYSA-N 0.000 claims description 4
- MIOBBYRMXGNORL-UHFFFAOYSA-N pyrifluquinazon Chemical compound C1C2=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C2N(C(=O)C)C(=O)N1NCC1=CC=CN=C1 MIOBBYRMXGNORL-UHFFFAOYSA-N 0.000 claims description 4
- YYXSCUSVVALMNW-FOWTUZBSSA-N pyriminostrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C(F)(F)F)=NC(NC=2C(=CC(Cl)=CC=2)Cl)=N1 YYXSCUSVVALMNW-FOWTUZBSSA-N 0.000 claims description 4
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 claims description 3
- ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 claims description 3
- HEMGBDXIEAZWNH-UHFFFAOYSA-N 7-fluoro-N-(2-methyl-1-methylsulfanylpropan-2-yl)-2-pyridin-3-ylindazole-4-carboxamide Chemical compound CC(CSC)(C)NC(=O)C=1C2=CN(N=C2C(=CC=1)F)C=1C=NC=CC=1 HEMGBDXIEAZWNH-UHFFFAOYSA-N 0.000 claims description 3
- BMLSHSXWJUIAKK-UHFFFAOYSA-N 7-fluoro-N-(2-methyl-1-methylsulfinylpropan-2-yl)-2-pyridin-3-ylindazole-4-carboxamide Chemical compound C1=C(C=2C(C(=C1)C(=O)NC(C)(C)CS(=O)C)=CN(N=2)C1=CN=CC=C1)F BMLSHSXWJUIAKK-UHFFFAOYSA-N 0.000 claims description 3
- AFUFRARZANPTGC-UHFFFAOYSA-N 7-fluoro-N-(2-methyl-1-methylsulfonylpropan-2-yl)-2-pyridin-3-ylindazole-4-carboxamide Chemical compound CC(CS(=O)(=O)C)(C)NC(=O)C=1C2=CN(N=C2C(=CC=1)F)C=1C=NC=CC=1 AFUFRARZANPTGC-UHFFFAOYSA-N 0.000 claims description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000005944 Chlorpyrifos Substances 0.000 claims description 3
- 239000005888 Clothianidin Substances 0.000 claims description 3
- 239000005949 Malathion Substances 0.000 claims description 3
- FAMPWUDOHZGUFU-UHFFFAOYSA-N N-[1-(difluoromethyl)cyclopropyl]-2-pyridin-3-ylindazole-4-carboxamide Chemical compound C=1C=C(C(=O)NC2(CC2)C(F)F)C2=CN(N=C2C=1)C1=CC=CN=C1 FAMPWUDOHZGUFU-UHFFFAOYSA-N 0.000 claims description 3
- 229930001406 Ryanodine Natural products 0.000 claims description 3
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Classifications
-
- 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
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-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
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
本出願は、2018年7月14日に出願された米国特許仮出願第62/698,035号および2018年12月13日に出願された米国特許仮出願第62/778,992号の利益を主張する。
実施形態1.化合物1。
実施形態2.nは0、1または2である、式2の化合物。
実施形態3.nは0である、式2の化合物。
実施形態4.nは1である、式2の化合物。
実施形態5.nは2である、式2の化合物。
N−[1−(ジフルオロメチル)シクロプロピル]−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド(化合物1)の製造
ステップA:N−[1−(ジフルオロメチル)シクロプロピル]−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミドの製造
DMF(2mL)中の2−(3−ピリジニル)−2H−インダゾール−4−カルボン酸(100mg、0.42mmol、CAS登録番号2001277−98−9)、HATU(190mg、0.5mmol)、1−(ジフルオロメチル)シクロプロパンアミン塩酸塩(71mg、0.5mmol)の溶液を、トリエチルアミン(174μL、1.25mmol)で処理した。反応混合物を室温で終夜撹拌した。次いで、逆相カラムクロマトグラフィー[C18カラム、水に対して10%〜100% MeCN/MeOH(1:1)で溶離]によって直接反応混合物を精製して標記化合物の本発明の化合物(105mg、収率76%)を生成した。1H NMR (500 MHz, DMSO-d6) δ ppm 9.35-9.39 (m, 2H) 9.14 (s, 1H) 8.67-8.68 (m, 1H) 8.55-8.58 (m, 1H) 7.94-7.97 (m, 1H), 7.73-7.75 (m, 1H), 7.63-7.67 (m, 1H), 7.41-7.45 (m, 1H), 6.21 (t, 1H), 1.13-1.17 (m, 2H), 1.02-1.06 (m, 2H).
N−[1,1−ジメチル−2−(メチルチオ)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド(化合物2a)の製造
ステップA:N−[1,1−ジメチル−2−(メチルチオ)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド(化合物2a)の製造
DMF(100mL)中の7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボン酸(10g、39mmol)、HATU(17.7g、47mmol)、2−メチル−1−メチルスルファニル−プロパン−2−アミン(7g、58mmol)の溶液を、トリエチルアミン(16mL、117mmol)で処理した。反応混合物を室温で4時間撹拌した。EtOAc(300mL)を用いて反応混合物を希釈し、水(6×100mL)で洗浄した。真空内で有機層を分離し濃縮した。結果として得られた粗製の固体を順相クロマトグラフィー(シリカゲル、ヘキサン中70〜100%のEtOAcを用いて溶離)によって精製して標記化合物の本発明の化合物(9.9g、収率71%)を生成した。1H NMR (500 MHz,DMSO-d6) δ ppm 9.37-9.43 (m, 2H), 8.69-8.72 (m, 1H), 8.56-8.60 (m, 1H), 8.00 (s, 1H), 7.64-7.70 (m, 2 H), 7.22-7.27 (m, 1H), 3.11 (s, 2H), 2.09 (s, 3H), 1.47 (s, 6H).
化合物2b(N−[1,1−ジメチル−2−(メチルスルフィニル)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド、および化合物2c(N−[1,1−ジメチル−2−(メチルスルホニル)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミドはそれぞれ、化合物2aの酸化によって製造することができる。
試験A〜Dに対する、配合物および噴霧方法論
試験化合物を、10%のアセトン、90%の水、ならびにアルキルアリールポリオキシエチレン、遊離脂肪酸、グリコールおよびイソプロパノールを含む300ppm X−77(登録商標)Spreader Lo−Foam Formula非イオン性界面活性剤(Loveland Industries,Inc.Greeley,Colorado,USA)を含有する溶液を用いて配合した。配合した化合物を、1mLの液体中に、各試験ユニットの最上部から1.27cm(0.5インチ)上方に位置する1/8 JJカスタムボディを備えるSUJ2噴霧器ノズル(Spraying Systems Co.、Wheaton、Illinois、USA)を通して適用した。試験化合物を示した率で噴霧し、各試験を3回繰り返した。
接触および/または浸透手段を介したモモアカアブラムシ(ミュズス・ペルシカエ(Myzus persicae)(Sulzer))の防除を評価するために、試験ユニットを、12〜15日齢のダイコン植物を中に有する小型の開放型容器で構成した。培養植物から切除した一枚の葉の上の30〜40匹のアブラムシをテスト植物の葉の上に置くことによりこれを予め外寄生させた(カットリーフ法)。葉片が乾燥するにつれて、アブラムシは試験植物上に移動した。予め外寄生させた後、試験ユニットの土壌を砂層で覆った。
接触および/または浸透手段を介したワタアブラムシ(アピス・ゴッシュピイ(Aphis gossypii)(Glover))の防除を評価するために、試験ユニットを、6〜7日齢の綿植物を中に有する小型の開放型容器で構成した。これを、カットリーフ法に従い、一片の葉の上に30〜40匹の昆虫で予め外寄生させ、試験ユニットの土壌を砂層で覆った。
接触および/または浸透手段を介したワタコナジラミ(ベミシア・タバキ(Bemisia tabaci)(Gennadius))の防除を評価するために、試験ユニットを、12〜14日齢の綿植物を中に有する小型の開放型容器で構成した。噴霧を適用する前に、植物から子葉を両方とも除去し、アッセイのために1枚の本葉を残した。成虫コナジラミに卵を植物に置かせ、次いでコナジラミを試験ユニットから取り出した。少なくとも15個の卵が寄生した綿植物を、噴霧についての試験にかけた。
接触および/または浸透手段を介したミカンキイロアザミウマ(フランクリニエラ・オシデンタリス(Frankliniellla occidentalis)(Pergande))の防除を評価するために、試験ユニットを5〜7日齢ソレイユビーン植物を中に有する小型の開放容器で構成した。
Claims (11)
- 請求項1に記載の化合物。
- nが0である、請求項1に記載の式2の化合物。
- nが1である、請求項1に記載の式2の化合物。
- nが2である、請求項1に記載の式2の化合物。
- N−[1−(ジフルオロメチル)シクロプロピル]−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド、N−[1,1−ジメチル−2−(メチルチオ)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド、N−[1,1−ジメチル−2−(メチルスルフィニル)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド、およびN−[1,1−ジメチル−2−(メチルスルホニル)エチル]−7−フルオロ−2−(3−ピリジニル)−2H−インダゾール−4−カルボキサミド;または前述の化合物のうちのいずれかの組合せから選択される、請求項1に記載の化合物。
- 請求項1に記載の化合物、ならびに界面活性剤、固体希釈剤および液体希釈剤からなる群から選択される少なくとも1種の追加の成分を含む組成物であって、場合により、少なくとも1種の追加の生物学的に活性な化合物または薬剤をさらに含む前記組成物。
- 前記少なくとも1種の追加の生物学的に活性な化合物または薬剤は、アバメクチン、アセフェート、アセキノシル、アセタミプリド、アクリナトリン、アフィドピロペン、アミドフルメト、アミトラズ、アベルメクチン、アザジラクチン、アジンホス−メチル、ベンフラカルブ、ベンサルタップ、ビフェントリン、ビフェナゼート、ビストリフルロン、ホウ酸塩、ブプロフェジン、カルバリル、カルボフラン、カルタップ、カルゾール、クロラントラニリプロール、クロルフェナピル、クロルフルアズロン、クロルピリホス、クロルピリホス−メチル、クロマフェノジド、クロフェンテジン、クロチアニジン、シアントラニリプロール、シクラニリプロール、シクロプロトリン、シクロキサプリド、シフルメトフェン、シフルトリン、ベータ−シフルトリン、シハロトリン、ガンマ−シハロトリン、ラムダ−シハロトリン、シペルメトリン、アルファ−シペルメトリン、ゼータ−シペルメトリン、シロマジン、デルタメトリン、ジアフェンチウロン、ダイアジノン、ディルドリン、ジフルベンズロン、ジメフルトリン、ジメヒポ、ジメトエート、ジノテフラン、ジオフェノラン、エマメクチン、エンドスルファン、エスフェンバレレート、エチプロール、エトフェンプロックス、エトキサゾール、酸化フェンブタスズ、フェニトロチオン、フェノチオカルブ、フェノキシカルブ、フェンプロパトリン、フェンバレレート、フィプロニル、フロメトキン、フロニカミド、フルベンジアミド、フルシトリネート、フルフェネリム、フルフェノクスロン、フルフェノキシストロビン、フルフェンスルホン、フルオルピラム、フルピプロール、フルピラジフロン、フルバリネート、タウ−フルバリネート、ホノホス、ホルメタネート、ホスチアゼート、ハロフェノジド、ヘプタフルトリン、ヘキサフルムロン、ヘキシチアゾクス、ヒドラメチルノン、イミダクロプリド、インドキサカルブ、殺虫性石鹸、イソフェンホス、ルフェヌロン、マラチオン、メペルフルトリン、メタフルミゾン、メタアルデヒド、メタミドホス、メチダチオン、メチオジカルブ、メソミル、メトプレン、メトキシクロル、メトフルトリン、モノクロトホス、モノフルトリン、メトキシフェノジド、ニテンピラム、ニチアジン、ノバルロン、ノビフルムロン、オキサミル、パラチオン、パラチオン−メチル、ペルメトリン、ホレート、ホサロン、ホスメット、ホスファミドン、ピリミカルブ、プロフェノホス、プロフルトリン、プロパルギット、プロトリフェンブト、ピフロブミド、ピメトロジン、ピラフルプロール、ピレトリン、ピリダベン、ピリダリル、ピリフルキナゾン、ピリミノストロビン、ピリプロール、ピリプロキシフェン、ロテノン、リアノジン、シラフルオフェン、スピネトラム、スピノサド、スピロジクロフェン、スピロメシフェン、スピロテトラマト、スルプロホス、スルホキサフロル、テブフェノジド、テブフェンピラド、テフルベンズロン、テフルトリン、テルブホス、テトラクロルビンホス、テトラメトリン、テトラメチルフルトリン、チアクロプリド、チアメトキサム、チオジカルブ、チオスルタップ−ナトリウム、トルフェンピラド、トラロメトリン、トリアザメート、トリクロルホン、トリフルムロン、バチルス・チューリンゲンシス、昆虫病原性バクテリア、昆虫病原性ウイルスおよび昆虫病原性菌類からなる群から選択される、請求項7に記載の組成物。
- 前記少なくとも1種の追加の生物学的に活性な化合物または薬剤は、アバメクチン、アセタミプリド、アクリナトリン、アフィドピロペン、アミトラズ、アベルメクチン、アザジラクチン、ベンフラカルブ、ベンスルタップ、ビフェントリン、3−ブロモ−1−(3−クロロ−2−ピリジニル)−N−[4−シアノ−2−メチル−6−[(メチルアミノ)カルボニル]フェニル]−1H−ピラゾール−5−カルボキサミド、ブプロフェジン、カルバリル、カルタップ、クロラントラニリプロール、クロルフェナピル、クロルピリホス、クロチアニジン、シアントラニリプロール、シクラニリプロール、シクロプロトリン、シフルトリン、ベータシフルトリン、シハロトリン、ラムダシハロトリン、ガンマシハロトリン、シペルメトリン、アルファシペルメトリン、ゼータシペルメトリン、シロマジン、デルタメトリン、ジエルドリン、ジノテフラン、ジオフェノラン、エマメクチン、エンドスルファン、エスファンバレレート、エチプロール、エトフェンプロックス、エトキサゾール、フェニトロチオン、フェノチオカルブ、フェノキシカルブ、フェンバレレート、フィプロニル、フロメトキン、フロニカミド、フルベンジアミド、フルフェノクスロン、フルフェノキシストロビン、フルフェンスルホン、フルピプロール、フルピラジフロン、フルバリネート、ホルメタネート、ホスチアゼート、ヘプタフルトリン、ヘキサフルムロン、ヒドラメチルノン、イミダクロプリド、インドキサカルブ、ルフェヌロン、メペルフルトリン、メタフルミゾン、メチオジカルブ、メソミル、メトプレン、メトキシフェノジド、メトフルトリン、モノフルトリン、ニテンピラム、ニチアジン、ノバルロン、オキサミル、ピフロブミド、ピメトロジン、ピレトリン、ピリダベン、ピリダリル、ピリミノストロビン、ピリプロキシフェン、リアノジン、スピネトラム、スピノサド、スピロジクロフェン、スピロメシフェン、スピロテトラマト、スルホキサフロル、テブフェノジド、テトラメトリン、チアクロプリド、チアメトキサム、チオジカルブ、チオスルタップナトリウム、トラロメトリン、テトラメチルフルトリン、トリアザマート、トリフルムロン、バチルス・チューリンゲンシスのすべての株および核多角体病ウイルスのすべての株からなる群から選択される、請求項7に記載の組成物。
- 無脊椎有害生物を防除する方法であって、無脊椎有害生物またはその環境を、生物学的有効量の請求項1に記載の化合物と接触させる工程を含む前記方法。
- 処理前の種子の約0.0001〜1重量%の量で請求項1に記載の化合物を含む、処理された種子。
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016144351A1 (en) * | 2015-03-11 | 2016-09-15 | E. I. Du Pont De Nemours And Company | Heterocycle-substituted bicyclic azole pesticides |
JP2016530310A (ja) * | 2013-09-13 | 2016-09-29 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | 複素環置換二環式アゾール有害生物防除剤 |
JP2022540441A (ja) * | 2019-07-11 | 2022-09-15 | エフ エム シー コーポレーション | インダゾール殺生物剤を含む混合物 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2891855A (en) | 1954-08-16 | 1959-06-23 | Geigy Ag J R | Compositions and methods for influencing the growth of plants |
US3235361A (en) | 1962-10-29 | 1966-02-15 | Du Pont | Method for the control of undesirable vegetation |
US3060084A (en) | 1961-06-09 | 1962-10-23 | Du Pont | Improved homogeneous, readily dispersed, pesticidal concentrate |
US3299566A (en) | 1964-06-01 | 1967-01-24 | Olin Mathieson | Water soluble film containing agricultural chemicals |
US3309192A (en) | 1964-12-02 | 1967-03-14 | Du Pont | Method of controlling seedling weed grasses |
US4144050A (en) | 1969-02-05 | 1979-03-13 | Hoechst Aktiengesellschaft | Micro granules for pesticides and process for their manufacture |
US3920442A (en) | 1972-09-18 | 1975-11-18 | Du Pont | Water-dispersible pesticide aggregates |
US4172714A (en) | 1976-12-20 | 1979-10-30 | E. I. Du Pont De Nemours And Company | Dry compactible, swellable herbicidal compositions and pellets produced therefrom |
GB2095558B (en) | 1981-03-30 | 1984-10-24 | Avon Packers Ltd | Formulation of agricultural chemicals |
DE3246493A1 (de) | 1982-12-16 | 1984-06-20 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von wasserdispergierbaren granulaten |
US5180587A (en) | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
EP0415688B1 (en) | 1989-08-30 | 1998-12-23 | Aeci Ltd | Dosage device and use thereof |
BR9106147A (pt) | 1990-03-12 | 1993-03-09 | Du Pont | Granulos de pesticidas dispersaveis em agua ou soluveis em agua feitos a partir de ligantes termo-ativados |
ES2091878T3 (es) | 1990-10-11 | 1996-11-16 | Sumitomo Chemical Co | Composicion plaguicida. |
US6406690B1 (en) | 1995-04-17 | 2002-06-18 | Minrav Industries Ltd. | Bacillus firmus CNCM I-1582 or Bacillus cereus CNCM I-1562 for controlling nematodes |
TW200724033A (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
WO2006101828A1 (en) * | 2005-03-15 | 2006-09-28 | Bayer Cropscience Ag | Insecticidal alkylamino phenyl sulfonamide derivatives |
US8106066B2 (en) * | 2005-09-23 | 2012-01-31 | Memory Pharmaceuticals Corporation | Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof |
US20140005245A1 (en) * | 2011-02-09 | 2014-01-02 | Syngenta Participations Ag | Insecticidal compounds |
TWI568721B (zh) * | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
CN103497156A (zh) * | 2013-09-18 | 2014-01-08 | 苏州岚云医药科技有限公司 | 稠环吡唑类化合物1-n-取代方法 |
BR112017021529B1 (pt) * | 2015-04-09 | 2020-05-26 | Fmc Corporation | Composto, composição e método para controlar uma praga |
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016530310A (ja) * | 2013-09-13 | 2016-09-29 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | 複素環置換二環式アゾール有害生物防除剤 |
WO2016144351A1 (en) * | 2015-03-11 | 2016-09-15 | E. I. Du Pont De Nemours And Company | Heterocycle-substituted bicyclic azole pesticides |
JP2022540441A (ja) * | 2019-07-11 | 2022-09-15 | エフ エム シー コーポレーション | インダゾール殺生物剤を含む混合物 |
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AU2019308165A2 (en) | 2021-07-01 |
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CL2023001879A1 (es) | 2023-12-11 |
KR20210032418A (ko) | 2021-03-24 |
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AU2019308165A1 (en) | 2021-01-28 |
ZA202100486B (en) | 2023-10-25 |
ECSP21002441A (es) | 2021-02-26 |
BR112021000430A2 (pt) | 2021-04-06 |
WO2020018362A1 (en) | 2020-01-23 |
IL280090B1 (en) | 2024-07-01 |
CO2021000131A2 (es) | 2021-01-18 |
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