TW200838429A - Pesticidal mixtures based on azolopyrimidinylamines derivatives and insecticides - Google Patents
Pesticidal mixtures based on azolopyrimidinylamines derivatives and insecticides Download PDFInfo
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- TW200838429A TW200838429A TW097103586A TW97103586A TW200838429A TW 200838429 A TW200838429 A TW 200838429A TW 097103586 A TW097103586 A TW 097103586A TW 97103586 A TW97103586 A TW 97103586A TW 200838429 A TW200838429 A TW 200838429A
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- 239000000203 mixture Substances 0.000 title claims abstract description 144
- 230000000361 pesticidal effect Effects 0.000 title claims abstract description 4
- 239000002917 insecticide Substances 0.000 title claims description 7
- YRAWHADHBYNMDI-UHFFFAOYSA-N N1C(N)=NC=C2N=CC=C21 Chemical class N1C(N)=NC=C2N=CC=C21 YRAWHADHBYNMDI-UHFFFAOYSA-N 0.000 title abstract 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims abstract description 62
- 241000244206 Nematoda Species 0.000 claims abstract description 50
- 238000000034 method Methods 0.000 claims abstract description 22
- 241000238631 Hexapoda Species 0.000 claims abstract description 20
- 230000036541 health Effects 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims description 206
- -1 cyano, hydroxy, decyl Chemical group 0.000 claims description 95
- 241000196324 Embryophyta Species 0.000 claims description 93
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 69
- 125000000217 alkyl group Chemical group 0.000 claims description 32
- 239000000575 pesticide Substances 0.000 claims description 21
- 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 19
- 239000005899 Fipronil Substances 0.000 claims description 19
- 229940013764 fipronil Drugs 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 15
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 13
- 230000000855 fungicidal effect Effects 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000002367 halogens Chemical class 0.000 claims description 10
- 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 9
- 239000005939 Tefluthrin Substances 0.000 claims description 9
- 239000005941 Thiamethoxam Substances 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 9
- 230000012010 growth Effects 0.000 claims description 9
- 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 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 7
- 125000001188 haloalkyl group Chemical group 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 claims description 6
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products 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 6
- 239000007789 gas Substances 0.000 claims description 6
- 239000003112 inhibitor Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 241000894006 Bacteria Species 0.000 claims description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 claims description 4
- 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 4
- 229940123715 Chloride channel antagonist Drugs 0.000 claims description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 4
- 239000005930 Spinosad Substances 0.000 claims description 4
- 229960001901 bioallethrin Drugs 0.000 claims description 4
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 claims description 4
- 238000011049 filling Methods 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 230000020477 pH reduction Effects 0.000 claims description 4
- 229940014213 spinosad Drugs 0.000 claims description 4
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 claims description 4
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims description 3
- 239000005944 Chlorpyrifos Substances 0.000 claims description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 3
- 208000006558 Dental Calculus Diseases 0.000 claims description 3
- 239000005947 Dimethoate Substances 0.000 claims description 3
- 229940123925 Nicotinic receptor agonist Drugs 0.000 claims description 3
- 229940123859 Nicotinic receptor antagonist Drugs 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 claims description 3
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 229960005286 carbaryl Drugs 0.000 claims description 3
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims description 3
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims description 3
- 229960001591 cyfluthrin Drugs 0.000 claims description 3
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 claims description 3
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 claims description 3
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 claims description 3
- 235000013305 food Nutrition 0.000 claims description 3
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 claims description 3
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 239000000181 nicotinic agonist Substances 0.000 claims description 3
- 239000003367 nicotinic antagonist Substances 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 239000002728 pyrethroid Substances 0.000 claims description 3
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims description 3
- 150000003573 thiols Chemical class 0.000 claims description 3
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 claims description 2
- FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 claims description 2
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 claims description 2
- ZXQYGBMAQZUVMI-RDDWSQKMSA-N (1S)-cis-(alphaR)-cyhalothrin Chemical compound CC1(C)[C@H](\C=C(/Cl)C(F)(F)F)[C@@H]1C(=O)O[C@@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-RDDWSQKMSA-N 0.000 claims description 2
- XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- 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 2
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 claims description 2
- FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 claims description 2
- IQVNEKKDSLOHHK-FNCQTZNRSA-N (E,E)-hydramethylnon Chemical compound N1CC(C)(C)CNC1=NN=C(/C=C/C=1C=CC(=CC=1)C(F)(F)F)\C=C\C1=CC=C(C(F)(F)F)C=C1 IQVNEKKDSLOHHK-FNCQTZNRSA-N 0.000 claims description 2
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 claims description 2
- PCKNFPQPGUWFHO-SXBRIOAWSA-N (Z)-flucycloxuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC(C=C1)=CC=C1CO\N=C(C=1C=CC(Cl)=CC=1)\C1CC1 PCKNFPQPGUWFHO-SXBRIOAWSA-N 0.000 claims description 2
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 claims description 2
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 claims description 2
- BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 claims description 2
- AWSZRJQNBMEZOI-UHFFFAOYSA-N 2-methoxyethyl 2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-[2-(trifluoromethyl)phenyl]propanoate Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(C#N)(C(=O)OCCOC)C(=O)C1=CC=CC=C1C(F)(F)F AWSZRJQNBMEZOI-UHFFFAOYSA-N 0.000 claims description 2
- AUQAUAIUNJIIEP-UHFFFAOYSA-N 3,4,5-trimethylphenyl methylcarbamate Chemical compound CNC(=O)OC1=CC(C)=C(C)C(C)=C1 AUQAUAIUNJIIEP-UHFFFAOYSA-N 0.000 claims description 2
- HDBQZGJWHMCXIL-UHFFFAOYSA-N 3,7-dihydropurine-2-thione Chemical compound SC1=NC=C2NC=NC2=N1 HDBQZGJWHMCXIL-UHFFFAOYSA-N 0.000 claims description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 claims description 2
- XJFIKRXIJXAJGH-UHFFFAOYSA-N 5-chloro-1,3-dihydroimidazo[4,5-b]pyridin-2-one Chemical group ClC1=CC=C2NC(=O)NC2=N1 XJFIKRXIJXAJGH-UHFFFAOYSA-N 0.000 claims description 2
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound 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 2
- VSVKOUBCDZYAQY-UHFFFAOYSA-N 7-chloro-1,2-benzothiazole Chemical compound ClC1=CC=CC2=C1SN=C2 VSVKOUBCDZYAQY-UHFFFAOYSA-N 0.000 claims description 2
- 239000005660 Abamectin Substances 0.000 claims description 2
- 239000005875 Acetamiprid Substances 0.000 claims description 2
- 239000005653 Bifenazate Substances 0.000 claims description 2
- 239000005874 Bifenthrin Substances 0.000 claims description 2
- 239000005885 Buprofezin Substances 0.000 claims description 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 claims description 2
- 229920002101 Chitin Polymers 0.000 claims description 2
- 239000005945 Chlorpyrifos-methyl Substances 0.000 claims description 2
- 239000005887 Chromafenozide Substances 0.000 claims description 2
- 239000005654 Clofentezine Substances 0.000 claims description 2
- 239000005888 Clothianidin Substances 0.000 claims description 2
- 239000005655 Cyflumetofen Substances 0.000 claims description 2
- 239000005946 Cypermethrin Substances 0.000 claims description 2
- 239000005891 Cyromazine Substances 0.000 claims description 2
- 239000005892 Deltamethrin Substances 0.000 claims description 2
- 239000005893 Diflubenzuron Substances 0.000 claims description 2
- AIGRXSNSLVJMEA-UHFFFAOYSA-N EPN Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 AIGRXSNSLVJMEA-UHFFFAOYSA-N 0.000 claims description 2
- YUGWDVYLFSETPE-JLHYYAGUSA-N Empenthrin Chemical compound CC\C=C(/C)C(C#C)OC(=O)C1C(C=C(C)C)C1(C)C YUGWDVYLFSETPE-JLHYYAGUSA-N 0.000 claims description 2
- 239000005895 Esfenvalerate Substances 0.000 claims description 2
- 239000005961 Ethoprophos Substances 0.000 claims description 2
- 239000005896 Etofenprox Substances 0.000 claims description 2
- 239000005897 Etoxazole Substances 0.000 claims description 2
- 239000005958 Fenamiphos (aka phenamiphos) Substances 0.000 claims description 2
- 239000005656 Fenazaquin Substances 0.000 claims description 2
- 239000005898 Fenoxycarb Substances 0.000 claims description 2
- 239000005657 Fenpyroximate Substances 0.000 claims description 2
- PNVJTZOFSHSLTO-UHFFFAOYSA-N Fenthion Chemical compound COP(=S)(OC)OC1=CC=C(SC)C(C)=C1 PNVJTZOFSHSLTO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005900 Flonicamid Substances 0.000 claims description 2
- 239000005901 Flubendiamide Substances 0.000 claims description 2
- 239000005948 Formetanate Substances 0.000 claims description 2
- 239000005959 Fosthiazate Substances 0.000 claims description 2
- 239000005903 Gamma-cyhalothrin Substances 0.000 claims description 2
- 239000005661 Hexythiazox Substances 0.000 claims description 2
- 239000005906 Imidacloprid Substances 0.000 claims description 2
- 239000005907 Indoxacarb Substances 0.000 claims description 2
- 239000005912 Lufenuron Substances 0.000 claims description 2
- 239000005949 Malathion Substances 0.000 claims description 2
- 239000005916 Methomyl Substances 0.000 claims description 2
- 239000005917 Methoxyfenozide Substances 0.000 claims description 2
- 239000005918 Milbemectin Substances 0.000 claims description 2
- 239000005950 Oxamyl Substances 0.000 claims description 2
- 239000005921 Phosmet Substances 0.000 claims description 2
- 239000005923 Pirimicarb Substances 0.000 claims description 2
- 239000005925 Pymetrozine Substances 0.000 claims description 2
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- 238000009827 uniform distribution Methods 0.000 description 1
- 238000002255 vaccination Methods 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000002861 ventricular Effects 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- AIFRHYZBTHREPW-UHFFFAOYSA-N β-carboline Chemical compound N1=CC=C2C3=CC=CC=C3NC2=C1 AIFRHYZBTHREPW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- A01N47/08—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
- A01N47/22—O-Aryl or S-Aryl esters thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Description
200838429 九、發明說明: 【發明所屬之技術領域】 本發明係關於農藥混合物,其包含: a)至少一種式I之唑并嘧啶胺:
其中各取代基係如下定義:
R1為c3-c12烧基、c2-c12稀基、c5_Cl2烧氧基烷基、 Cs-C6環烷基、苯基或苯基_Ci_c4烷基; R2為CrCu烷基、C2-Cl2烯基、Ci-C4鹵烷基或〇厂C4 烷氧基-CVC4烷基, 其中R1及/或R2中之脂族鏈可經1至4個相同或不同 之Ra基團取代:
Ra為鹵素、氰基、羥基、巯基、C1_C10烷基、C1_ C1〇i 烧基、C3-C0f 燒基、c2_Cig烯基、CrCl〇 块基、CVC6燒氧基、CW6烧基硫基、Ci_C6^ 氣基-C 1 - C 6烧基或nrArB · RA、RB為氫或CVC6燒基; 其中R】及/或^中之環狀基團可經1至4個1^基團 取代: R為鹵素、氰基、羥基、巯基、硝基、 NR R、CVCk燒基、Ci_C6_ 烧基、C2-c6 稀基、CVC6炔基或€1-(:6烷氧基; 128642.doc 200838429 R3為氫、鹵素、氰基、NRARB、羥基、酼基、CVC6 烷基、CVC6鹵烷基、C3-C8環烷基、CVC6烷氧 基、(VC6烷基硫基、C3-C8環烷氧基、C3-C8環烷 基硫基、羧基、曱醯基、CVCio烷基羰基、CVCw 烷氧基羰基、C2-C1G烯氧基羰基、(:2-(:10炔氧基羰 基、本基、苯氧基、苯硫基、节氧基、节硫基或 c「c6烷基-S(0)m-; m 為0、1或2 ; A 為CH或N ; 及 b)至少一種化合物II,其係選自以下族群: Α·1·有機(硫代)磷酸酯類:歐殺松(acephate)、甲基吡 噁填(azamethiphos)、益棉填(azinphos-ethyl)、穀速松 (azinphos_methyl)、氯氧填(chlorethoxyfos)、毒蟲畏 (chlorfenvinphos)、氯甲硫鱗(chlormephos)、毒死蜱 (chlorpyrifos)、甲基毒死蜱(chlorpyrifos-methyl)、繩 毒填(coumaphos)、殺填腈(cyanophos)、滅賜松 (demeton-S-methyl)、大利松(diazinon)、敵敵畏 (dichlorvos)/DDVP、雙特松(dicrotophos)、大滅松 (dimethoate)、甲基毒蟲畏(dimethylvinphos)、乙拌礙 (disulfoton)、EPN、乙硫填(ethion)、普伏松 (ethoprophos)、伐滅填(famphur)、苯線構(fenamiphos) 、殺填硫填(fenitrothion)、倍硫填(fenthion)、比氟硫 磷(flupyrazophos)、福賽絕(fosthiazate)、飛達松 128642.doc 200838429
(heptenophos)、異 °惡嗤石舞(isoxathion)、馬拉松 (malathion)、滅加松(mecarbam)、曱胺構 (methamidophos)、滅大松(methidathion)、速滅填 (mevinphos)、久效填(monocrotophos)、二澳磷 (naled)、氧樂果(omethoate)、滅多松(oxydemeton-methyl)、對硫_(031^1:]11〇11)、甲基對硫石粦(0&1^1111〇11-methyl)、賽達松(phenthoate)、甲拌填(phorate)、伏殺 填(phosalone)、亞胺硫磷(phosmet)、鱗胺 (phosphamidon)、巴賽松(phoxim)、亞特松(pirimiphos, methyl)、 丙 漠續:(profenofos)、撲達松 (propetamphos)、 丙石荒石粦(prothiofos)、白 克松 (pyraclofos)、必芬松(pyridaphenthion)、拜裕松 (quinalphos)、硫特普(sulfotep) 、 丁 17 密硫石舞 (tebupirimfos)、亞培松(temephos)、託福松 (terbufos)、殺蟲畏(tetrachlorvinphos)、硫滅松 (thiometon)、三 落松(triazophos) 、三 氣松 (trichlorfon)、繁米松(vamidothion); A.2·胺基甲酸醋類:得滅克(aldicarb)、阿蘭克 (alanycarb)、免敵克(bendiocarb)、免扶克 (benfuracarb)、丁酮威(butocarboxim)、丁酮石風威 (butoxycarboxim)、力口保利(carbaryl)、力口 保扶 (carbofuran)、丁基加保扶(carbosulfan)、乙硫苯威 (ethiofencarb)、丁基滅必乱(fenobucarb)、覆滅蜗 (formetanate)、夫硫克(furathiocarb)、滅必鼠 128642.doc 200838429 (isoprocarb)、滅賜克(methiocarb)、納乃得 (methomyl)、治滅風(metolcarb)、歐殺滅(oxamyl)、比 加普(pirimicarb)、安丹(propoxur)、硫地克 (thiodicarb)、久效威(thiofanox)、混殺威 (trimethacarb)、XMC、滅殺威(xylylcarb)、嗤财威 (triazamate);
A.3·擬除蟲菊醋類(Pyrethroid):阿納寧(acdnathrin)、 亞列寧(allethrin)、d-川貝反式亞列寧、d-反式亞列寧、 畢芬寧(bifenthrin)、百亞列寧(bioallethrin)、S-環戊稀 基百亞列寧(bioallethrin S-cylclopentenyl)、百列滅寧 (bioresmethrin)、乙氰菊酉旨(cycloprothrin)、赛扶寧 (cyfluthrin)、β-賽扶寧(betacyfluthrin)、賽洛寧 (cyhalothrin)、λ-賽洛寧(lambda-cyhalothrin)、γ-賽洛 寧(gamma-cyhalothrin)、赛滅寧(cypermethrin)、α-賽 滅寧、β-賽滅寧、θ-賽滅寧、ζ-賽滅寧、賽酚寧 (cyphenothrin)、第滅寧(deltamethrin)、益避寧 (empenthrin)、益化利(esfenvalerate)、依芬寧 (etofenprox)、芬普寧(fenpropathrin)、芬化利 (fenvalerate)、護賽寧(flucythrinate)、氟氯苯菊酯 (flumethrin)、τ-福化利(tau-fluvalinate)、合芬寧 (halfenprox)、依普寧(imiprothrin)、百滅寧 (permethrin)、紛 丁滅乱(phenothrin)、普亞歹>J 寧 (prallethrin)、異列滅寧(resmethrin)、RU 15525、西拉 福芬(silafluofen)、七氟菊酉旨(tefluthrin)、胺菊酯 128642.doc 200838429 (tetramethdn)、泰滅寧(tralomethrin)、四氟苯菊酯 (transfluthrin)、ZXI 8901 ; A.4.保幼激素擬似物:烯蟲乙酯(hydroprene)、烯蟲炔 酯(kinoprene)、美賜年(methoprene)、芬諾克(fenoxycarb) 、百利普芬(pyriproxyfen);
A.5.菸鹼受體促效劑/拮抗劑化合物:亞滅培 (acetamiprid)、免速達(561131^&口)、培丹鹽酸鹽(〇&1^叩 hydrochloride)、可尼丁(clothianidin)、呋蟲胺 (dinote fur an)、盈達胺(imidacloprid)、嗟蟲口秦 (thiamethoxam)、稀啶蟲胺(nitenpyram)、菸驗、賜諾 殺(spinosad)(別位促效劑)、ϋ塞蟲琳(thiacl〇Prid)、殺蟲 環(thiocyclam)、殺蟲雙(thiosultaP-sodium)、式(Γ1)之 σ塞嗤化合物:
A.6. GABA門控氯離子通道拮抗劑化合物:可氣丹 (chlordane)、安殺番(endosulfan)、Y-HCH(靈丹(lindane)) 、乙駄蟲脂(acetoPr〇le)、乙蟲清(ethipr〇le)、氟蟲腈 (fipronil)、17比氟普羅(pyrafluprole)、吼普羅(pyriprole) 、凡利普羅(vaniliPr〇le)、5_胺基-丨-(2,6-二氯-4_三氟 甲基-苯基)-4-三氯曱烷亞磺醯基-1H-吡唑-3-硫代碳酸 醯胺; A.7·氯離子通道活化劑:阿巴汀(abamectin)、因滅汀 128642.doc -10- 200838429 苯甲酸鹽(emamectin benzoate)、密滅汀(milbemectin)、 樂匹滅汀(lepimectin); Α·8· METI I化合物:喧蜗醚(fenazaquin)、芬普蜗 (fenpyroximate)、續蜗醚(pyrimidifen)、比達本 (pyridaben)、11比蜗胺(tebufenpyrad)、嗤蟲酿胺 (tolfenpyrad)、啼轰胺(flufenerim)、魚藤精 (rotenone);
Α_9· METI II 及 III化合物:亞酿i 蜗(acequinocyl)、氟阿 西普(fluacyprim)、伏蟻腙(hydramethylnon); A. 10.氧化構酸化解偶聯劑:蟲蜗腈(chlorfenapyr)、 DNOC ; A_ 11 _ 氧化填酸化抑制劑:亞環錫(azocyclotin)、鍚瞒 丹(cyhexatin)、汰芬隆(diafenthiuron)、苯丁錫 (fenbutatin oxide)、克蜗特(propargite)、得脫蜗 (tetradifon); Α·12·蜆皮破壞劑:賽滅淨(cyromazine)、環蟲醯肼 (chromafenozide)、氯蟲醯肼(halofenozide)、曱氧蟲醯 肼(methoxyfenozide)、蟲醯肼(tebufenozide); A.13. 增效劑:增效醚(piperonyl butoxide)、脫葉填 (tribufos); A.14.納離子通道阻斷劑化合物:因得克(indoxacarb) 、氰氟蟲胺(metafiumiz〇ne); A. 15.燻蒸劑:曱基溴、氯化苦(chloropicrin)硫醯 氟; 128642.doc -11 - 200838429 Α·16·選擇性攝食阻斷劑:可羅替(crylotie)、吼財酮 (pymetrozine)、氟咬蟲醯胺(flonicamid); A. 17.蜗生長抑制劑:克芬瞒(clofentezine)、合賽多 (hexythiazox)、依殺蜗(etoxazole);
Α· 1 8.甲殼素合成抑制劑:布芬淨(buprofezin)、雙三 氟蟲脲(bistrifluron)、克福隆(chlorfluazuron)、二福隆 (diflubenzuron)、氟環脲(flucycloxuron)、氟芬隆 (flufenoxuron)、六伏隆(hexaflumuron)、祿芬隆 (lufenuron)、諾華隆(novaluron)、多氟脲(noviflumuroii) 、得福隆(teflubenzuron)、殺蟲隆(trinumuron); A. 19.脂質生物合成抑制劑:螺蜗酯(spirodiclofen)、 螺曱虫茜酉旨(spiromesifen)、螺蟲乙酉旨(spirotetramat); A.20.章魚胺促效劑(octapaminergic agonsit):三亞蠕 (amitraz); Α·21·蘭尼定(ryanodine)受體調節劑··氟蟲醢胺 (flubendiamide); Α·22· 各種殺蟲劑··鱗化銘、醯胺氟美(amidoflumet)、 苯克咯嚷(benclothiaz)、西脫蜗(benzoximate)、聯苯肼 酯(bifenazate)、硼砂、新殺蜗(bromopropylate)、氰化 物、賽諾 11 比芬(cyenopyrafen)、丁 I 蜗酯(cyflumetofen) 、滅蜗猛(chinomethionate)、大克蜗(dicofol)、氟乙酸 鹽、膦、咬蟲丙醚(pyridalyl)、比氟奎宗(pyrifluquinazon) 、硫、吐酒石(tartar emetic); Α·23· N-R’-2,2-二鹵基-1-R”環-丙烷甲醯胺-2-(2,6·二 128642.doc -12- 200838429 氯-α,α,α-三氟·對甲苯基)腙或N-R,-2,2-二(R"’)丙醯胺-2-(2,6-二氯-α,α,α-三氟-對曱苯基)·腙,其中R’為甲基 或乙基,鹵基為氣基或溴基,R"為氫或甲基,且R",為 甲基或乙基; Α·24·丙二腈化合物:CF3(CH2)2C(CN)2CH2(CF2)3CF2H、 CF3(CH2)2C(CN)2CH2(CF2)5CF2H、 cf3(ch2)2c(cn)2(ch2)2c(cf3)2f、 CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3、 CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H、 CF3(CH2)2C(CN)2CH2(CF2)3CF3、 cf3(cf2)2ch2c(cn)2ch2(cf2)3cf2h 及 CF3CF2CH2C(CN)2CH2(CF2)3CF2H ; A.25.微生物破壞劑:蘇力菌以色列亞種 subsp. 、球形芽孢桿菌 (Bacillus 、蘇力菌餘澤亞種 subsp. J/zawaz·)、蘇力菌庫斯塔克亞種 似 i/zwrkg/e似以 subsp. 蘇力菌擬步 行甲亞種(万subsp· Γβπβ办rzom\y)。 本發明亦係關於植物保護混合物且係關於一種藉由將該 等混合物施用於植物或其位點來改良該等植物之健康狀況 的方法。 此外,本發明係關於一種控制真菌及/或改良植物健康 狀況之方法,其包含用本發明混合物中所存在之農藥依任 何所要次序或同時(亦即聯合或分開)對受真菌侵染或易受 128642.doc -13- 200838429 真菌侵染之位點(例如植物或植物繁殖材料)進行處理。 此外,本發明係關於一種控制有害昆蟲或線蟲之方法, 其包含用本發明混合物中所存在之農藥依任何所要次序或 同時(亦即聯合或分開)對受該等害蟲侵染或易受該等害蟲 侵染之位點(例如植物或植物繁殖材料)進行處理。 【先前技術】
在害蟲控制領域中出現的一個典型問題在於需要降低活 性成份之劑量率,以便減少或避免不利的環境效應或毒物 學效應,同時仍允許有效地控制害蟲及病原體。 所遭遇之另一問題係關於需要取得對廣譜害蟲與病原體 有效之害蟲控制劑。 本發明潛在的另一問題為需要一種可改良植物之組合 物,此方法在下文中通稱為"植物健康"。舉例而言,可提 及之有利特性為改良之作物特徵,包括:出芽、作物產 量、蛋白質含量、油含量、澱粉含量、更為發達之根系 (良之根生長)、改良之逆境抗性(例如針對乾旱、執、 鹽、紫外線、水、寒冷)、減少乙稀(減少產生及/或抑制 收)、分藥增加、植物高度增加、較大葉片、較少死的其 生葉、較強壯之分蘖枝、較綠之葉顏色、色素含量、光二 活性、所需投入量(諸如肥料或水)較少、所需種子較少: 較多有效分蘖、較早關y ^ ^ 早期祓物成熟度、植物倒伏 ging)較少、苗條生長增加、植物活力增強、掷 加之植物群叢及提早與較佳萌芽;或為増 熟知之任何其他優點。 項技術者所 128642.doc • 14 - 200838429 與使用農藥有關之另一困難為重複且專門施用個別農藥 化合物時’在多種情況下會導致害蟲或病原體對所施用活 性化合物快速顯現天然或適應抗性的選擇性。 【發明内容】 口此,本發明之一目標為提供解決上述問題之農藥混合 物0
抗擊有害植物病原性真菌並非農民不得不面對之唯一問 題。有害昆蟲及其他害蟲亦可能對作物及其他植物造成很 大損害。殺真g活性與殺蟲活性之有效組合有利於克服此 問題。因&,本發明之另一目標為提供一種一方面具有良 好殺真菌活性且另一方面具有良好殺蟲活性之混合物,以 擴大殺蟲作用範圍。 【實施方式】 吾人已發現,藉由本文初所定義之活性化合物的組合可 部分或完全實現此目標。 尤其已發現’與可能由個別化合物達成之控制率相比, 如本文初所定義之至少一種幻化合物與至少一種化合物η 之混合物顯示針對植物病原體之作用顯著增強,且/或备 經施用於植物、植物部分、種子或其生長位點時,適用: 改良植物之健康狀況。 ' 已發現,本發明混合物(例如如開始所定義之式!化合物 與化合物η之混合物)之作用遠遠超過單獨存在於混合 之活性化合物的殺真菌及殺蟲作用。 U展不,在本發明之 框架内該等混合物展現植物健康效應。術語植物健康包括 128642.doc •15- 200838429 各種與害蟲控制無關的對於植物之改良。 上文稱作組份a之式I之唑并嘧啶-7-基胺,其製備及其針 對有害真菌之作用係自如下文獻得知(EP-A 71 792 ; EP-A 141 317 ; WO 03/009687 ; WO 05/087771 ; WO 05/087772 ; WO 05/087773 ; PCT/EP/05/002426 ; PCT/EP 2006/050922 ; • PCT/EP 2006/060399)。 . 族群Α·1至A.25之市售化合物II可見於The Pesticide
Manual,第 13版,British Crop Protection Council (2003) ^ 連同其他公開物,諸如 http://www.hclrss.demon.co.uk/ index.html 〇 5-胺基-l-(2,6-二氯-4-三氟甲基-苯基)-4-三氣曱烷亞磺 醯基-1H-吡唑-3-硫代碳酸醯胺及其製備已描述於WO 98/28279 中。樂匹滅汀係自 Agro Project,PJB Publications Ltd,2004年11月得知。苯克咯噻及其製備已描述於EP-A1 454621中。滅大松與對氧磷及其製備已描述於Farm • Chemicals Handbook,第 88卷,Meister Publishing Company, 2001中。乙酞蟲脂及其製備已描述於WO 98/28277中。氰 氟蟲胺及其製備已描述於EP-A1 462 456中。吡氟硫磷 (Flupyrazofos)已描述於 Pesticide Science 54,1988,第 237-
、 243頁及US 4822779中。吡氟普羅及其製備已描述於JP 2002193709及WO 01/00614中。吡普羅及其製備已描述於 WO 98/45274及US 6335357中。醯胺氟美及其製備已描述 於US 6221890及JP 21010907中。啼蟲胺及其製備已描述 於 WO 03/007717 及 WO 03/007718 中。類似於 AKD-1022 之 128642.doc -16- 200838429 新菸鹼類的製備方法已由Zhang,A.等人描述於 J.Neurochemistry,75(3),2000中。丁氟蟎酯及其製備已描 述於 WO 04/080180 中。丙二腈化合物 CF3(CH2)2C(CN)2CH2(CF2)3CF2H、CF3(CH2)2C(CN)2CH2(CF2)5CF2H、 CF3(CH2)2C(CN)2(CH2)2C(CF3)2F、CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3、 CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H、CF3(CH2)2C(CN)2CH2(CF2)3CF3、 cf3(cf2)2ch2c(cn)2ch2(cf2)3cf2h 及 cf3cf2ch2c(cn)2ch2(cf2)3cf2h 已描述於WO 05/63694中。 在針對上文各式給出之符號定義中,使用通常表示以下 取代基之集體術語: 鹵素:氟、氯、溴及碘; 烷基:具有1至4、6、8或10個碳原子之飽和直鏈或支鏈 烴基,例如Ci-Cs烷基,諸如甲基、乙基、丙基、1-曱基乙 基、丁基、1-甲基丙基、2-甲基丙基、1,1-二曱基乙基、 戊基、1-甲基丁基、2-甲基丁基、3-甲基丁基、2,2-二曱 基丙基、1-乙基丙基、己基、1,1-二甲基丙基、1,2-二甲基 丙基、1-曱基戊基、2-曱基戊基、3-甲基戊基、4-甲基戊 基、1,1-二甲基丁基、1,2·二甲基丁基、1,3-二甲基丁基、 2,2-二曱基丁基、2,3-二甲基丁基、3,3-二甲基丁基、1-乙 基丁基、2-乙基丁基、1,1,2-三甲基丙基、1,2,2-三甲基丙 基、1-乙基-1-甲基丙基及1-乙基-2-甲基丙基; 鹵烷基:具有1至2、4或6個碳原子之直鏈或支鏈烷基 (如上文所提及),其中該等基團中之一些或所有氫原子可 經如上提及之鹵素原子置換:詳言之為鹵烷基,諸 128642.doc -17- 200838429 如氯甲基、溴甲基、二氯甲基、三氯甲基、氟甲基、二氟 甲基、二氟甲基、氯氟甲基、二氯氟甲基、氯二氟甲基、 1-氯乙基、1_溴乙基、1_氟乙基、2_氟乙基、2,2_二氟乙 基、2,2,2-三氟乙基、2-氯_2_氟乙基、2_氯_2,2_二氟乙 基2,2· 一氣·2_氟乙基、2,2,2-三氯乙基、五氟乙基戈 1,1,1 _三氟丙-2-基。 - 鑒於本發明中式1之唑并嘧啶胺的意欲用途,特別較佳 _ 為忒等取代基在各種情況下獨立或組合地具有以下含義。 根據本發明特別適用者為如下式I之化合物,其中Rl為 可經1至3個鹵素或匚^。烷基取代之直鏈或支鏈^^^烷基 或苯基。 & 在式I化合物之一個實施例中,Ra基團不存在。 較佳實施例係關於如下式!之化合物,其中Rl為直鏈或 支鏈C5_C1()烷基,尤其為乙基、3,5,5-三曱基己基、正庚 基、正辛基、正壬基及正癸基。 • 另一實施例係關於如下式I之化合物,其中R1為未經取 代或經1至4個i素、氰基、羥基、酼基、硝基、nrArB、 CVC1()烧基、CrC』烧基、c2_c6烯基、c2_c6快基及Ci_c6 ' 烷氧基取代之苯基。 較佳之式I化合物為如下之彼 團之經取代苯基 L3 等者,其中R1為對應於G基
其中 128642.doc -18 200838429
Ll 為氰基、自素、經基、M基、硝'基、nrArb、Ci- c10烧基、Cl-c6鹵烧基、C2_C6稀基、C2_e6快基及 Ci-C6烧氧基;且 L2、L3彼此獨立地為氫或在Li下所提及之基團之一,且 #表示連接至。坐并喷咬骨架之鍵。 在式I化合物之另一實施例中,Ll為氰基、鹵素、羥 基、巯基、硝基、NRH Cl_C0烷基、齒甲基或C〗_C2烷 氧基,較佳為氰基、函素、Cl_c0烷基、鹵甲基或〇:1<2烷 氧基。 在式I化合物之另一實施例中,L2為氫或上述基團之 〇 在式I化合物之另一實施例中,L3為氫、氰基、鹵素、 羥基、巯基、硝基、NRarb、Ci_C6烷基 '画甲基或Ci_C2 烷氧基,較佳為氫。 較佳為如下式〗之化合物,其中R2為直鏈或支鏈烷 基、Ci-CU烷氧基-CVC4烷基或(VC4鹵烷基。 在式I化合物之特別較佳實施例中,R2為甲基、乙基、 正丙基、正辛基、三氟甲基或甲氧基甲基,尤其為甲基、 乙基、三氟曱基或曱氧基甲基。 此外,較佳為如下式I之化合物,其中R3為氫。 在式I化合物之另一實施例中,R3為胺基。 式Ϊ化合物之一個實施例係關於A為N之彼等者。該等化 合物對應於式IA,其中變數係如關於式I所定義: 128642.doc -19- 200838429
式1化合物之另一實施例係關於A為CH之彼等者。該等 化合物對應於式IB,其中變數係如關於式〗所定義:
在軚佳化合物I之另一實施例中,…與反2之碳鏈一起不 具有12個以上之碳原子。 蓉於化合物之用途’尤其較佳為㈣於下表巾之化合物 I。此外’纟中關於取代基所提及之基團本身(與其中提及 其之組合無關)為所討論取代基之特別較佳實施例。 表1 式IA之化合物(其中化合物之反1、 2 八次R的組合在各種 情況下對應於表I之一列) 表2 式IB之化合物(其中化合物之Ri、 2 八及R的組合在各種 情況下對應於表I之一列)
表I
128642.doc -20- 200838429
編號 R1 R2 R3 1-7 4-F-C6H4 ch3 H 1-8 2,4-ClrC6H3 ch3 H 1-9 3,4-Cl2-C6H3 ch3 H 1-10 2,4-F2-C6H3 ch3 H 1-11 3,4-F2-C6H3 ch3 H 1-12 4-CH3-C6H4 ch3 H 1-13 4-CH2CH3-C6H4 ch3 H 1-14 4-CH2CH2CH3-C6H4 ch3 H 1-15 4-CH(CH3)2-C6H4 ch3 H 1-16 4-CH2CH2CH2CH3-C6H4 ch3 H 1-17 4-C(CH3)CH2CH3-C6H4 ch3 H 1-18 4_C(CH3)3-C6H4 ch3 H 1-19 CH2CH2CH2CH3 ch3 H 1-20 CH2CH2CH2CH2CH3 ch3 H 1-21 CH2CH2CH2CH2CH2CH3 ch3 H 1-22 ch2ch(ch3)ch2ch2ch3 ch3 H 1-23 ch2ch(ch2ch3)2 ch3 H 1-24 CH2CH2CH2CH2CH2CH2CH3 ch3 H 1-25 ch2ch2ch2ch2ch2ch2ch2ch3 ch3 H 1-26 CH2CH2CH2CH2CH2CH2CH2CH2CH3 ch3 H 1-27 CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 ch3 H 1-28 ch2ch2ch(ch3)ch2ch(ch3)3 ch3 H 1-29 CH2CH2CH2CH3 ch3 nh2 1-30 CH2CH2CH2CH2CH3 ch3 nh2 1-31 CH2CH2CH2CH2CH2CH3 ch3 nh2 1-32 ch2ch(ch3)ch2ch2ch3 ch3 nh2 1-33 CH2CH(CH2CH3)2 ch3 nh2 1-34 CH2CH2CH2CH2CH2CH2CH3 ch3 nh2 1-35 CH2CH2CH2CH2CH2CH2CH2CH3 ch3 nh2 1-36 CH2CH2CH2CH2CH2CH2CH2CH2CH3 ch3 nh2 1-37 ch2ch2ch2ch2ch2ch2ch2ch2ch2ch3 ch3 nh2 1-38 CH2CH2CH(CH3)CH2CH(CH3)3 ch3 nh2 1-39 CH2CH2CH2CH3 ch3 ch3 1-40 CH2CH2CH2CH2CH3 ch3 ch3 1-41 CH2CH2CH2CH2CH2CH3 ch3 ch3 1-42 ch2ch(ch3)ch2ch2ch3 ch3 ch3 1-43 ch2ch(ch2ch3)2 ch3 ch3 128642.doc 21 - 200838429
編號 R1 R2 R3 1-44 CH2CH2CH2CH2CH2CH2CH3 ch3 ch3 1-45 CH2CH2CH2CH2CH2CH2CH2CH3 ch3 ch3 1-46 CH2CH2CH2CH2CH2CH2CH2CH2CH3 ch3 ch3 1-47 CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 ch3 ch3 Μ8 ch2ch2ch(ch3)ch2ch(ch3)3 ch3 ch3 1-49 (ch2)3-o-ch3 ch3 H 1-50 (ch2)3-o-ch2ch3 ch3 H 1-51 (ch2)3-o-ch2ch2ch3 ch3 H 1-52 (ch2)3-o-ch2ch2ch2ch3 ch3 H 1-53 (ch2)3-o-ch2ch2ch2ch2ch3 ch3 H 1-54 (ch2)3-o-ch2ch2ch2ch2ch2ch3 ch3 H 1-55 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch3 ch3 H 1-56 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch3 ch3 H 1-57 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 ch3 H 1-58 (ch2)3-o-ch(ch3)2 ch3 H 1-59 (ch2)3-o-c(ch3)3 ch3 H 1-60 (ch2)3-o-ch2c(ch3)3 ch3 H 1-61 (ch2)3-o-ch(ch3)ch2c(ch3)3 ch3 H 1-62 (ch2)3-o-ch(ch2ch3)ch2c(ch3)3 ch3 H 1-63 (ch2)3_o-ch2ch(ch3)ch2ch(ch3)2 1 ch3 H 1-64 (ch2)3-o-ch2ch(ch2ch3)ch2ch2ch3 ch3 H 1-65 (ch2)3-o-ch2ch2ch(ch3)ch2ch(ch3)2 ch3 H 1-66 (ch2)3-o-ch2ch2ch(ch3)ch2c(ch3)3 ch3 H 1-67 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 ch3 H 1-68 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 ch3 H 1-69 (ch2)3-o-ch3 ch3 ch3 1-70 (ch2)3-o-ch2ch3 ch3 ch3 1-71 (CH2)3-〇-CH2CH2CH3 ch3 ch3 1-72 (ch2)3-o-ch2ch2ch2ch3 ch3 ch3 1-73 (ch2)3-o-ch2ch2ch2ch2ch3 ch3 ch3 1-74 (ch2)3-o-ch2ch2ch2ch2ch2ch3 ch3 ch3 1-75 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch3 ch3 ch3 1-76 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch3 ch3 ch3 1-77 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 ch3 ch3 1-78 (ch2)3-o-ch(ch3)2 ch3 ch3 1-79 (ch2)3-o-c(ch3)3 ch3 ch3 1-80 (CH2)3-0-CH2C(CH3)3 ch3 ch3 128642.doc -22- 200838429
編號 R1 R2 R3 1-81 (ch2)3-o-ch(ch3)ch2c(ch3)3 ch3 ch3 1-82 (ch2)3-o-ch(ch2ch3)ch2c(ch3)3 ch3 ch3 1-83 (ch2)3-o-ch2ch(ch3)ch2ch(ch3)2 ch3 ch3 1-84 (ch2)3-o-ch2ch(ch2ch3)ch2ch2ch3 ch3 ch3 1-85 (ch2)3-o-ch2ch2ch(ch3)ch2ch(ch3)2 ch3 ch3 1-86 (ch2)3-o-ch2ch2ch(ch3)ch2c(ch3)3 ch3 ch3 1-87 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 ch3 ch3 1-88 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 ch3 ch3 1-89 ch2-c6h5 cf3 H 1-90 CH2-(4-Cl-C6H4) cf3 H 1-91 ch2ch2ch3 cf3 H 1-92 CH2CH2CH2CH3 cf3 H 1-93 CH2CH2CH2CH2CH3 CFs H 1-94 CH2CH2CH2CH2CH2CH3 cf3 H 1-95 ch2ch(ch3)ch2ch2ch3 cf3 H 1-96 CH2CH(CH2CH3)2 cf3 H 1-97 CH2CH2CH2CH2CH2CH2CH3 cf3 H 1-98 CH2CH2CH2CH2CH2CH2CH2CH3 cf3 H 1-99 CH2CH2CH2CH2CH2CH2CH2CH2CH3 cf3 H MOO CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 cf3 H 1-101 ch2ch2ch(ch3)ch2ch(ch3)3 cf3 H 1-102 環-c5h9 cf3 H M03 環-C6Hn cf3 H 1-104 CH2CH2CH2CH3 CH2CH3 H 1-105 CH2CH2CH2CH2CH3 CH2CH3 H 1-106 CH2CH2CH2CH2CH2CH3 CH2CH3 H 1-107 ch2ch(ch3)ch2ch2ch3 CH2CH3 H 1-108 ch2ch(ch2ch3)2 CH2CH3 H 1-109 CH2CH2CH2CH2CH2CH2CH3 CH2CH3 H 1-110 CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 H 1-111 CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 H 1-112 CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 H 1-113 CH2CH2CH(CH3)CH2CH(CH3)3 CH2CH3 H 1-114 CH2CH2CH2CH3 CH2CH3 nh2 1-115 CH2CH2CH2CH2CH3 CH2CH3 nh2 1-116 CH2CH2CH2CH2CH2CH3 CH2CH3 nh2 1-117 ch2ch(ch3)ch2ch2ch3 CH2CH3 nh2 128642.doc -23- 200838429
編號 R1 R2 R3 1-118 ch2ch(ch2ch3)2 CH2CH3 nh2 1-119 CH2CH2CH2CH2CH2CH2CH3 ch2ch3 nh2 1-120 CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 nh2 1-121 CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 nh2 1-122 CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 nh2 H23 ch2ch2ch(ch3)ch2ch(ch3)3 CH2CH3 nh2 1-124 CH2CH2CH2CH3 CH2CH3 ch3 1-125 CH2CH2CH2CH2CH3 CH2CH3 ch3 1-126 CH2CH2CH2CH2CH2CH3 CH2CH3 ch3 1-127 ch2ch(ch3)ch2ch2ch3 CH2CH3 ch3 1-128 ch2ch(ch2ch3)2 CH2CH3 ch3 1-129 CH2CH2CH2CH2CH2CH2CH3 CH2CH3 ch3 1-130 CH2CH2CH2CH2CH2CH2CH2CH3 ch2ch3 ch3 1-131 CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 ch3 1-132 CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH3 ch3 1-133 ch2ch2ch(ch3)ch2ch(ch3)3 CH2CH3 ch3 1-134 (ch2)3-o-ch3 CH2CH3 H 1-135 (ch2)3-o-ch2ch3 CH2CH3 H 1-136 (ch2)3-o-ch2ch2ch3 CH2CH3 H 1-137 (ch2)3-o-ch2ch2ch2ch3 CH2CH3 H 1-138 (ch2)3-o-ch2ch2ch2ch2ch3 CH2CH3 H 1-139 (ch2)3-o-ch2ch2ch2ch2ch2ch3 CH2CH3 H 1-140 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch3 CH2CH3 H 1-141 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH3 H 1-142 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH3 H 1-143 (ch2)3-o-ch(ch3)2 CH2CH3 H 1-144 (ch2)3-o-c(ch3)3 CH2CH3 H 1-145 (ch2)3-o-ch2c(ch3)3 CH2CH3 H 1-146 (ch2)3-o-ch(ch3)ch2c(ch3)3 CH2CH3 H 1-147 (ch2)3-o-ch(ch2ch3)ch2c(ch3)3 CH2CH3 H 1-148 (ch2)3-o-ch2ch(ch3)ch2ch(ch3)2 CH2CH3 H 1-149 (ch2)3-o-ch2ch(ch2ch3)ch2ch2ch3 CH2CH3 H 1-150 (ch2)3-o-ch2ch2ch(ch3)ch2ch(ch3)2 CH2CH3 H 1-151 (ch2)3-o-ch2ch2ch(ch3)ch2c(ch3)3 CH2CH3 H 1-152 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 CH2CH3 H 1-153 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 CH2CH3 H 1-154 (ch2)3-o-ch3 CH2CH3 ch3 128642.doc -24- 200838429
編號 R1 R2 R3 1-155 (ch2)3-o-ch2ch3 CH2CH3 ch3 1-156 (ch2)3-o-ch2ch2ch3 CH2CH3 ch3 1-157 (ch2)3-o-ch2ch2ch2ch3 CH2CH3 ch3 1-158 (ch2)3-o-ch2ch2ch2ch2ch3 CH2CH3 ch3 1-159 (ch2)3-o-ch2ch2ch2ch2ch2ch3 CH2CH3 ch3 1-160 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch3 CH2CH3 ch3 1-161 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH3 ch3 1-162 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH3 ch3 1-163 (ch2)3-o-ch(ch3)2 CH2CH3 ch3 1-164 (CH2)3-0-C(CH3)3 CH2CH3 ch3 1-165 (ch2)3-o-ch2c(ch3)3 CH2CH3 ch3 1-166 (ch2)3-o-ch(ch3)ch2c(ch3)3 CH2CH3 ch3 1-167 (ch2)3-o-ch(ch2ch3)ch2c(ch3)3 CH2CH3 ch3 1-168 (ch2)3-o-ch2ch(ch3)ch2ch(ch3)2 CH2CH3 ch3 1-169 (ch2)3-o-ch2ch(ch2ch3)ch2ch2ch3 CH2CH3 ch3 1-170 (ch2)3-o-ch2ch2ch(ch3)ch2ch(ch3)2 CH2CH3 ch3 1-171 (ch2)3-o-ch2ch2ch(ch3)ch2c(ch3)3 CH2CH3 ch3 1-172 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 CH2CH3 ch3 Μ 73 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 CH2CH3 ch3 1-174 CH2CH2CH2CH3 CH2CH2CH3 H 1-175 CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-176 CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-177 ch2ch(ch3)ch2ch2ch3 CH2CH2CH3 H 1-178 ch2ch(ch2ch3)2 CH2CH2CH3 H 1-179 CH2CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-180 CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-181 ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-182 CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-183 ch2ch2ch(ch3)ch2ch(ch3)3 CH2CH2CH3 H 1-184 CH2-0-CH2CH2CH2CH3 CH2CH2CH3 H 1-185 CH2-0-CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-186 CH2-0-CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-187 CH2-0-CH2CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-188 CH2-0-CH2CH2CH2CH2CH2CH2CH2CH3 CH2CH2CH3 H 1-189 ch2-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-190 ch2-o-c(ch3)3 CH2CH2CH3 H 1-191 ch2-o-ch2c(ch3)3 CH2CH2CH3 H 128642.doc -25- 200838429
編號 R1 R2 R3 1-192 ch2-o-ch(ch3)ch2c(ch3)3 ch2ch2ch3 H 1-193 ch2-o-ch(ch2ch3)ch2c(ch3)3 CH2CH2CH3 H Μ 94 ch2-o-ch2ch(ch3)ch2ch(ch3)2 CH2CH2CH3 H 1-195 ch2-o-ch2ch(ch2ch3)ch2ch2ch3 CH2CH2CH3 H 1-196 ch2-o-ch2ch2ch(ch3)ch2ch(ch3)2 CH2CH2CH3 H 1-197 ch2-o-ch2ch2ch(ch3)ch2c(ch3)3 CH2CH2CH3 H 1-198 ch2-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 CH2CH2CH3 H Μ 99 ch2-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 CH2CH2CH3 H 1-200 (ch2)2-o-ch2ch2ch3 CH2CH2CH3 H 1-201 (ch2)2-o-ch2ch2ch2ch3 CH2CH2CH3 H 1-202 (ch2)2-o-ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-203 (ch2)2-o-ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-204 (ch2)2-o-ch2ch2ch2ch2ch2ch2ch3 ch2ch2ch3 H 1-205 (ch2)2-o-ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-206 (ch2)2-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-207 (ch2)2-o-ch(ch3)2 CH2CH2CH3 H 1-208 (CH2)2-〇-C(CH3)3 CH2CH2CH3 H 1-209 (ch2)2-o-ch2c(ch3)3 CH2CH2CH3 H 1-210 (ch2)2-o-ch(ch3)ch2c(ch3)3 CH2CH2CH3 H 1-211 (ch2)2-o-ch(ch2ch3)ch2c(ch3)3 CH2CH2CH3 H 1-212 (ch2)2-o-ch2ch(ch3)ch2ch(ch3)2 CH2CH2CH3 H 1-213 (ch2)2-o-ch2ch(ch2ch3)ch2ch2ch3 ch2ch2ch3 H 1-214 (ch2)2-o-ch2ch2ch(ch3)ch2ch(ch3)2 ch2ch2ch3 H 1-215 (ch2)2-o-ch2ch2ch(ch3)ch2c(ch3)3 CH2CH2CH3 H 1-216 (ch2)2-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 CH2CH2CH3 H 1-217 (ch2)2-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 CH2CH2CH3 H 1-218 (ch2)3-o-ch3 CH2CH2CH3 H 1-219 (ch2)3-o-ch2ch3 CH2CH2CH3 H 1-220 (ch2)3-o-ch2ch2ch3 CH2CH2CH3 H 1-221 (ch2)3-o-ch2ch2ch2ch3 CH2CH2CH3 H 1-222 (ch2)3-o-ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-223 (ch2)3-〇-ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-224 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-225 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-226 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH2CH2CH3 H 1-227 (ch2)3-o-ch(ch3)2 CH2CH2CH3 H 1-228 (ch2)3-o-c(ch3)3 ch2ch2ch3 H 128642.doc -26- 200838429
編號 R1 R2 R3 1-229 (ch2)3-o-ch2c(ch3)3 CH2CH2CH3 H 1-230 (ch2)3-o-ch(ch3)ch2c(ch3)3 CH2CH2CH3 H 1-231 (ch2)3-o-ch(ch2ch3)ch2c(ch3)3 CH2CH2CH3 H 1-232 (ch2)3-o-ch2ch(ch3)ch2ch(ch3)2 CH2CH2CH3 H 1-233 (ch2)3-o-ch2ch(ch2ch3)ch2ch2ch3 CH2CH2CH3 H 1-234 (ch2)3-o-ch2ch2ch(ch3)ch2ch(ch3)2 CH2CH2CH3 H 1-235 (ch2)3-o-ch2ch2ch(ch3)ch2c(ch3)3 CH2CH2CH3 H 1-236 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 CH2CH2CH3 H 1-237 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 CH2CH2CH3 H 1-238 CH2CH2CH3 CH20CH3 H 1-239 CH2CH2CH2CH3 CH20CH3 H 1-240 CH2CH2CH2CH2CH3 CH20CH3 H 1-241 CH2CH2CH2CH2CH2CH3 CH20CH3 H 1-242 CH2CH(CH3)CH2CH2CH3 CH20CH3 H 1-243 ch2ch(ch2ch3)2 CH20CH3 H 1-244 CH2CH2CH2CH2CH2CH2CH3 CH20CH3 H 1-245 CH2CH2CH2CH2CH2CH2CH2CH3 CH20CH3 H 1-246 CH2CH2CH2CH2CH2CH2CH2CH2CH3 CH20CH3 H 1-247 ch2ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH20CH3 H 1-248 ch2ch2ch(ch3)ch2ch(ch3)3 CH20CH3 H 1-249 (ch2)3-o-ch3 CH20CH3 H 1-250 (CH2)3-〇-CH2CH3 CH20CH3 H 1-251 (ch2)3-o-ch2ch2ch3 CH20CH3 H 1-252 (ch2)3-o-ch2ch2ch2ch3 CH20CH3 H 1-253 (CH2)r〇-CH2CH2CH2CH2CH3 CH20CH3 H 1-254 (ch2)3-o-ch2ch2ch2ch2ch2ch3 CH20CH3 H 1-255 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch3 CH20CH3 H 1-256 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch3 CH20CH3 H 1-257 (ch2)3-o-ch2ch2ch2ch2ch2ch2ch2ch2ch3 CH20CH3 H 1-258 (ch2)3-o-ch(ch3)2 CH20CH3 H 1-259 (ch2)3_o-c(ch3)3 CH2OCH3 H 1-260 (ch2)3-o-ch2c(ch3)3 CH20CH3 H 1-261 (ch2)3-o-ch(ch3)ch2c(ch3)3 CH20CH3 H 1-262 (ch2)3-o-ch(ch2ch3)ch2c(ch3)3 CH20CH3 H 1-263 (ch2)3-o-ch2ch(ch3)ch2ch(ch3)2 CH20CH3 H 1-264 (ch2)3-o-ch2ch(ch2ch3)ch2ch2ch3 CH20CH3 H 1-265 (ch2)3-o-ch2ch2ch(ch3)ch2ch(ch3)2 CH20CH3 H 128642.doc -27- 200838429
編號 R1 R2 R3 1-266 (ch2)3-o-ch2ch2ch(ch3)ch2c(ch3)3 CH20CH3 H 1-267 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch(ch3)2 CH20CH3 H 1-268 (ch2)3-o-ch2ch2ch(ch3)ch2ch2ch2ch(ch3)2 CH2OCH3 H 1-269 ch3 (CH2)3CH3 H 1-270 CH2CH3 (ch2)3ch3 H 1-271 CH2CH2CH3 (ch2)3ch3 H 1-272 CH2CH2CH2CH3 (ch2)3ch3 H 1-273 CH2CH2CH2CH2CH3 (ch2)3ch3 H 1-274 ch3 (ch2)4ch3 H 1-275 CH2CH3 (ch2)4ch3 H 1-276 CH2CH2CH3 (ch2)4ch3 H 1-277 CH2CH2CH2CH3 (CH2)4CH3 H 1-278 CH2CH2CH2CH2CH3 (CH2)4CH3 H 1-279 ch3 (CH2)5CH3 H 1-280 CH2CH3 (CH2)5CH3 H 1-281 CH2CH2CH3 (ch2)5ch3 H 1-282 CH2CH2CH2CH3 (ch2)5ch3 H 1-283 ch2ch2ch2ch2ch3 (CH2)5CH3 H 1-284 ch3 (CH2)6CH3 H 1-285 CH2CH3 (CH2)6CH3 H 1-286 CH2CH2CH3 (CH2)6CH3 H 1-287 CH2CH2CH2CH3 (ch2)6ch3 H 1-288 CH2CH2CH2CH2CH3 (ch2)6ch3 H 1-289 ch3 (CH2)7CH3 H 1-290 CH2CH3 (ch2)7ch3 H 1-291 CH2CH2CH3 (CH2)7CH3 H 1-292 CH2CH2CH2CH3 (CH2)7CH3 H 1-293 CH2CH2CH2CH2CH3 (CH2)7CH3 H 1-294 ch3 (CH2)8CH3 H 1-295 CH2CH3 (ch2)8ch3 H 1-296 CH2CH2CH3 (CH2)8CH3 H 1-297 CH2CH2CH2CH3 (CH2)8CH3 H 1-298 CH2CH2CH2CH2CH3 (ch2)8ch3 H 本發明之混合物的較佳實施例包含作為式i之活性化合 物的化合物,其係選自以下列表: 128642.doc -28 - 200838429 6-(3,4-二氯苯基)_5_甲基·[ 胺; “开[!,5,〜基 6-(4-第三丁基苯基)·5_甲基_π,2,4] 胺; 坐开[Ha]鳴咬_7_基 5·甲基-6·(3,5,5_三甲基己基)_π,2,4]^ 基胺; 开[,54]嘧啶 5- 甲基-6·辛基.[山]三咬并[仏㈣⑸·基胺;
5_ 乙基 _6·辛基·[1,2,4]三 4 并 7.二胺. 6- 乙基-5-辛基·π,2,4]三嗤并[丨叫嘧林基胺;, 5-乙基冬辛基_Π,2,4]三嗤并n’5a]鳴咬基胺; 5-乙基-6·(3,5,5·三甲基己基)·⑴ ’ 基胺; J—坐开[l,5-a]喷啶 6-辛基-5-丙基-[山]三唾并嘯唆_7_基胺; 5- 甲氧基甲基·6·辛師,2,4]三㈣㈣_7·基胺; 6- 辛基-5-三氟甲基七训三唾并[…]喷咬·7·基胺;及 5:三I甲基·6·(3,5,5.三甲基己基Wl,2,4]三唾并鳴 °定-7 -基胺。 本發明之車乂佳實施例係關於至少一種式工化合物、尤 2上述較佳化合物列表中之—者與至少_種來自如開_ 疋義之胺基甲酉夂酯類族群之化合物η的混合物。胺基甲酸 酉曰類較佳係選自加保扶、丁基加保扶及硫地克。 、本么明之另一較佳實施例係關於至少一種式合物、 尤其上述列表中之_者與至少_種來自如開始所定義之擬 除蟲菊酯類族群之化合物π的混合物。擬除蟲菊酯類較佳 128642.doc -29- 200838429 係選自畢芬寧、賽扶寧、#滅寧、α_賽滅寧及七氟菊醋。 本發明之另-較佳實施例係關於至少一種式他合物、 尤其上述列表中之-者與至少—種來自如開始所定義之於 驗受體促效劑/拮抗劑化合物族群之化合物η的混合物。於 鹼受體促效劑/拮抗劑化合物較佳係選自亞滅培、可尼 丁、吱蟲胺、盈達胺、賜諾殺、嗟蟲嗪及嘆蟲啉。
本發明之另一較佳實施例係關於至少一種式以匕合物、 尤其上述列表中之-者與至少—種來自如開始所定義之 GAB Α門控氯離子通道拮抗劑化合物族群之化合物η的混 a物。較佳之GAB Α門控氯離子通道拮抗劑化合物為氟蟲 腈0 較佳實施例為表A中所列之組合,其中在各種情況下表 A之一列對應於包含所提及之式j之特定化合物(組份a)及所 提及族群中之一種活性化合物11(組份b)的農藥組合,此活 性化合物Π較佳係選自上文定義之較佳實施例。
表A
編號 組份a 組份b A-1 表1,1-9 來自族群A.2之活性化合物II A-2 表卜1_9 來自族群A.3之活性化合物II A-3 表1,1-9 來自族群A.5之活性化合物II A-4 卜 表1,1-9 來自族群A.6之活性化合物II A-5 表1,1-18 來自族群A.2之活性化合物II A-6 表1,1-18 來自族群A.3之活性化合物II A-7 表1,1-18 來自族群A.5之活性化合物II Α·8 ^ 表1,1-18 來自族群A.6之活性化合物II Α-9 表1,1-25 來自族群A.2之活性化合物II Α-10 表1,1-25 來自族群A.3之活性化合物II A-11 表1,Ι·25 來自族群A.5之活性化合物II 128642.doc -30- 200838429
A-12 表1,1-25 來自族群Α.6之活性化合物II A-13 表1,1-28 來自族群Α.2之活性化合物II A-14 表 1,1-28 來自族群Α.3之活性化合物II A-15 表1,1-28 來自族群Α.5之活性化合物II A-16 表 1,1-28 來自族群Α.6之活性化合物II ΑΛΊ 表1,1-98 來自族群Α.2之活性化合物II A-18 表1,1-98 來自族群Α.3之活性化合物II A-19 表1,1-98 來自族群Α.5之活性化合物II A-20 表1,1-98 來自族群Α.6之活性化合物II A-21 表卜1-101 來自族群Α.2之活性化合物II A-22 表1,Ι·101 來自族群Α·3之活性化合物II A-23 表卜1-101 來自族群Α.5之活性化合物II A-24 表卜1-101 來自族群Α.6之活性化合物II A-25 表卜1_110 來自族群Α.2之活性化合物II A-26 表1,1-110 來自族群Α.3之活性化合物II A-27 表卜1-110 來自族群Α.5之活性化合物II A-28 表1,1-110 來自族群Α.6之活性化合物II A-29 表1,1-113 來自族群Α.2之活性化合物II A-30 表1,1-113 來自族群Α.3之活性化合物II A-31 表卜1-113 來自族群Α.5之活性化合物II A-32 表1,1-113 來自族群Α.6之活性化合物II A-33 表卜1-120 來自族群Α.2之活性化合物II A-34 表卜1-120 來自族群Α.3之活性化合物II A-35 表1,1-120 來自族群Α.5之活性化合物II A-36 表1,1-120 來自族群Α.6之活性化合物II A-37 表卜1-180 來自族群Α.2之活性化合物II A-38 表卜1-180 來自族群Α.3之活性化合物II A-39 表1,1-180 來自族群Α·5之活性化合物II A-40 表1,1-180 來自族群Α.6之活性化合物II A-41 表卜1-245 來自族群Α.2之活性化合物II A-42 表卜1-245 來自族群Α.3之活性化合物II A-43 表 1,1-245 來自族群Α.5之活性化合物II A-44 表1,1-245 來自族群Α.6之活性化合物II A-45 表 1,1-290 來自族群Α.2之活性化合物II A-46 表1,1-290 來自族群Α.3之活性化合物II A-47 表 1,Ι·290 來自族群Α.5之活性化合物II A-48 表1,1-290 來自族群Α.6之活性化合物II 128642.doc -31 - 200838429 式I化合物及化合物II能夠與無機酸或有機酸或與金屬離 子形成鹽或加合物。 無機酸之實例為氫_酸,諸如氟化氫、氣化氫、溴化氫 及埃化氫;硫酸、磷酸及確酸。 合適之有機酸為(例如)甲酸、碳酸及諸如乙酸、三氟乙 酸、二氯乙酸及丙酸之烷酸,以及乙醇酸、乳酸、丁二 酸、檸檬酸、苯曱酸、肉桂酸、草酸、對曱苯磺酸、水揚 酸、對胺基水楊酸、2-苯氧基苯甲酸或乙醯氧基苯甲 酸。 合適之金屬離子詳言之為以下元素之離子:第一至第八 過渡族元素’尤其為鉻、錳、鐵、鈷、鎳、銅、鋅;以及 (另外)第二主族元素,尤其為鈣及鎂;及第三及第四主族 π素,詳言之為鋁、錫及鉛。若適當,金屬可以其可呈現 之不同化合價存在。 上述活性化合物亦可以其農業相容性鹽之形式來採用。 該等鹽通常為鹼金屬或鹼土金屬鹽,諸如鈉鹽、鉀鹽或鈣 鹽° 式I化合物可以各種晶體變體形式存在,其生物活性可 能不同。其亦構成本發明標的之部分。 在本發明之一較佳實施例中,使用式唑并嘧啶胺與 活性化合物II的混合物。在某些條件下,將唑并嘧啶胺與 兩種或兩種以上活性化合物合可為有利的。另外,兩 種或兩種以上化合物j與一或多種活性化合物π之混合物亦 可為合適的。 128642.doc -32- 200838429 當製備混合物時,較佳使用純活性化合物,若需要,可 將該等純活性化合物與其他針對有害真菌或其他害蟲(諸 如昆蟲類、蜘蛛類或線蟲類)的活性化合物或者作為另外 活性組份之具除草活性或生長調節活性之化合物或肥料混 合0 較佳之其他殺蟲劑為在開始作為組份b所提及之彼等 者,更佳為如上提及之較佳化合物II。 較佳之其他殺真菌劑為選自由以下各者組成之群的彼等 殺真菌劑: •嗜毯果傘素類(strobilurins),諸如亞托敏 (azoxystrobin)、醚菌胺(dimoxystrobin)、烯肟菌酯 (enestroburin)、氟氧菌胺(nuoxastrobin)、克收欣 (kresoxim-methyl)' 苯氧菌胺(methominostrobin)、奥瑞 菌胺(orysastrobin)、唆氧菌醋(口1〇0:^:^]:〇13111)、百克敏 (pyraclostrobin)、比本卡(pyribencarb)、三氟敏 (trifloxystrobin)、2_(鄰-((2,5-二甲基苯基-氧基亞甲基) 苯基)-3-甲氧基-丙烯酸甲酯; •碳酸醯胺類,諸如苯胺類(anilides):苯霜靈 (benalaxyl)、苯霜靈_M、麥鏽靈(benodanil)、畢紗芬 (bixafen)、白克列(boscalid)、萎鏽靈(carboxin)、加普 胺(carpropamid)、雙氣氰菌胺(diclocymet)、甲吱醯胺 (fenfuram)、環隨菌胺(fenhexamid)、福多寧(flutolanil) 、福拉比(furametpyr)、異嗔菌胺(isotianil)、開拉樂 (kiralaxyl)、雙炔醢菌胺(mandipropamid)、滅鏽胺 128642.doc -33· 200838429 (mepronil)、滅達樂(metalaxyl)、呋醯胺(ofurace)、歐 殺斯(oxadixyl)、氧化萎鏽靈(oxycarb〇xin)、吡噻菌胺 (penthiopyrad)、矽硫芬(siithiofam)、赛氟滅 (thifluzamide)、汰敵寧(tiadinil)、N-(3,,4f-二氣-5-氟-聯 苯-2-基)·3-二氟甲基-1-甲基_ih_°比峻-4-甲酸酸胺、 • (2-(1,3-二甲基-丁基)-苯基)-1,3_二甲基-5-氟-111-吼唑- 4-甲酸醯胺、Ν_(4,-氯-3,,5_二氟-聯苯-2-基)-3-二氟曱 基-1-甲基-1H-吡唑-4-甲酸醯胺、N-(4,-氯-3,,5-二氟-聯 •苯-2-基)-3-三氟甲基-;[_曱基-1H_吡唑-4_甲酸醯胺、N_ (3’,4’_二氯-5-氟-聯苯基)·3_三氟甲基·ι_甲基巧札吡 唑-4-甲酸醯胺、Ν_(3,,5_二氟_4,_甲基-聯苯基)_3_二 氟甲基·1·曱基-1Η-吡唑冰甲酸醯胺、Ν-(3,,5-二氟-4,· 甲基·聯苯-2-基)-3-三氟甲基_丨_甲基_1Η·吡唑_4_甲酸醯 胺、Ν-(2·雙環两基_2-基·苯基)_3_二氟甲基甲基]η_ 吼峻-4-甲酸酿胺、Ν_(順_2_雙環丙基_2_基_苯基)_3_二 φ 氟甲基小甲基比唑_4_甲酸醯胺、Ν-(反_2_雙環丙 基-2-基-苯基)-3-二氟甲基小曱基·他吼唑_4_甲酸醯 胺; ' 碳酸嗎啉類·· i拿:成-w 卜 每職分(dimethomorph)、亂嗎琳 ' (flumorph); 苯甲酸釀胺類:氟美醯胺(flumetover)、氟吡菌胺 (P丨1^)伏普蘭(fluopyram)、氣苯醯胺 (zoxamide); • °坐類,諸如三嗅_ · κτ此+ 只·阿紮康°坐(azaconazole)、比多農 128642.doc -34- 200838429
(bitertanol)、糠菌嗤(bromuconazole)、環克嗤 (cyproconazole)、苯 _ 甲環峻(difenoconazole)、稀峻醇 (diniconazole)、It 環峻(epoxiconazole)、芬克嗤 (fenbuconazole)、氟啥吐(fluquinconazole)、護石夕得 (flusilazole)、護汰芬(flntriafol)、己0坐醇(hexaconazol) 、易胺嗤(imibenconazole)、種菌0坐(ipconazole)、葉菌 口坐(metconazole)、邁克尼(myclobutanil)、σ惡味嗤 (oxpoconazol)、巴克素(paclobutrazol)、平克口坐 (penconazole)、普克利(propiconazole)、丙硫醇克口垒 (prothioconazole)、石夕氟口坐(simeconazole)、得克利 (tebuconazole)、四克利(tetraconazole)、三泰芬 (triadimefon)、三泰隆(triadimenol)、滅菌吐 (triticonazole); 口米峻類:賽嗤滅(cyazofamid)、依滅列(imazalil)、稻痕 酯(pefurazoate)、撲克拉(prochloraz)、賽福嗤 (triflumizole); 苯并咪σ坐類:免賴得(benomyl)、貝芬替(carbendazim)、 麥穗寧(fuberidazole)、σ塞苯喷。坐(thiabendazole); 其他··乙嚷博胺(ethaboxam)、依得利(etridiazole)、°惡 黴靈(hymexazole)、1-(4-氯-苯基)-1-(丙炔-2-基氧基)-3· (4-(3,4·二曱氧基-苯基^異11惡哇-5-基丙-2 -嗣; • 含氮雜環類,諸如σ比唆類:扶吉胺(fluazinam)、比芬諾 (pyrifenox)、3-[5-(4•氯-苯基)-2,3-二曱基-異噁嗤唆-3-基]比啶; 128642.doc -35 - 200838429 喊唆類:布瑞莫(bupirimate)、賽普洛(cyprodinil)、氣 嘴菌胺(diflumetorim)、芬瑞莫(fenarimol)、嘴菌月宗 (ferimzone)、滅派林(mepanipyrim)、三氯曱基吼咬 (nitrapyrin)、尼瑞莫(nuarimol)、派美尼(pyrimethanil); 口比口各類:拌種洛(fenpiclonil)、護汰寧(fludioxonil); 嗎琳類:阿迪嗎琳(aldimorph)、嗎菌靈(dodemorph)、 芬普福(fenpropimorph)、三得芬(tridemorph); 二魏酸亞胺類:峻吱草(fluoroimid)、依普同(iprodione) 、撲滅寧(procymidone)、免克寧(vinclozolin); 非芳族五員環類:°惡峻菌酮(famoxadone)、咪唾菌酮 (fenamidone)、辛嗟酮(octhilinone) 、 σ塞菌靈 (probenazole); 其他:酸化苯并σ塞二唆-S-甲醋(acibenzolar-S-methyl)、 吲嗤石黃菌胺(amisulbrom)、敵菌靈(anilazin)、保米黴素 (blasticidin-S)、四氯丹(captafol)、蓋普丹(captan)、滅 蟎猛(chinomethionat)、邁隆(dazomet)、咪菌威 (debacarb)、嚏菌清(diclomezine)、禾草靈(fenoxanil)、 苯鏽啶(fenpropidin)、福爾培(folpet)、粉病靈(piperalin) 、丙氧喧琳(proquinazid)、百快隆(pyroquilon)、快諾芬 (quinoxyfen)、唑菌嗓(triazoxid)、三賽唑(tricyclazole)、 賽福寧(triforine)、5-氯-7-(4-甲基-旅啶-1-基)-6-(2,4,6-三氟-苯基Hl,2,4]三唑并[l,5-a]嘧啶、2-丁氧基-6-碘_ 3 -丙基-咬稀-4 -綱; • 胺基甲酸酯類及二硫代胺基甲酸酯類,諸如:二硫代 128642.doc -36- 200838429 胺基甲酸ί旨類:福美鐵(ferbam)、鋅锰乃浦(mancozeb)、 锰乃浦(maneb)、威百故(metam)、免得爛(metiram)、甲 基辞乃浦(propineb)、得恩地(thiram)、辞乃浦(zineb)、 益穗(ziram); 胺基甲酸酯類:乙黴威(diethofencarb)、氟苯售瓦利 (flubenthiavalicarb)、顯黴威(iprovalicarb)、霜黴威 (propamocarb)、伐利非那(valiphenal)、N-( 1-(1-(4-氰基 苯基)乙烷磺醯基)-丁-2-基)胺基曱酸-(4-氟苯基)酯; • 脈類,諸如:多寧(dodine)、克熱淨(guazatine)、雙脈 辛胺(iminoctadine); • 抗生素類··春曰黴素(kasugamycin)、多氧菌素 (polyoxine)、鏈黴素(streptomycin)、維利黴素八 (validamycin A); • 有機金屬化合物:三苯基錫鹽(例如三苯基乙酸錫、三 苯基氯化錫、三苯基氫氧化錫); •含硫雜環類,諸如:腈硫S昆(dithianon)、稻瘦靈 (isoprothiolane); • 有機填化合物,諸如:護粒松(edifenphos)、三乙膦酸 (fosetyl)、三乙膦酸銘(fosetyl-aluminium)、丙基喜樂松 (iprobenfos)、白粉松(pyrazophos)、脫克松(tolcl〇fos_ methyl); • 有機氯化合物,諸如:四氯異苯腈(chlorothalonil)、益 發靈(dichlofluanid)、雙氯酴(dichlorophen)、石黃菌胺 (flusulfamide)、六氯苯、賓克隆(pencycuron)、笨歐 128642.doc •37- 200838429 (phthalide)、奎脫辛(quintozene)、曱基多保淨 (thiophanate-methyl)、益洛寧(tolylfluanid); • 無機化合物,諸如:硫、亞磷酸(h3po3)及其鹽、銅 鹽,例如波爾多混合物(bordeaux mixture)、乙酸銅、 氫氧化銅、驗性氯氧化銅(copper oxychloride)、驗性硫 酸銅; • 硝基苯基衍生物,諸如:百蟎克(binapacryl)、大克爛 (dicloran)、大脫蜗(dinobuton)、白粉克(dinocap)、四 氯硝基笨(tecnazen); • 生長延緩劑:調環酸(prohexadione)及其鹽、抗倒酯 (trinexapac-ethyl)、克美素(chlormequat)、縮節胺 (mepiquat-chloride)及二氟 °比l(difliifenzopyr); •其他:漠硝丙二醇(bronopol)、嗟芬胺(cyflufenamid)、 霜腺氰(cymoxanil)、二苯胺、美曲芬諾(metrafenone)、 滅粉黴素(mildiomycin)、螺環菌胺(spiroxamine)、益洛 寧(tolylfluanid)、N-(環丙基甲氧基亞胺基-(6-二氟甲氧 基-2,3-二氣-苯基)-甲基)-2 -苯基乙酿胺。 更佳之其他殺真菌劑為選自由以下各者組成之群的彼等 殺真菌劑 • 唑類:免賴得、苯醚曱環唑、氟環唑、氟喹唑、護汰 芬、噁黴靈、依滅列、葉菌唑、丙硫醇克唑、得克 利;噻苯咪唑、三泰隆、撲克拉、滅菌唑、貝芬替; •嗜毯果傘素類:亞托敏、克收欣、奥瑞菌胺、百克 敏、三氟敏; 128642.doc -38- 200838429 • 缓酸胺類,边,,+… ^ _ 歐殺斯、 派美尼; 免得爛、得 、 诸如白克列、萎鏽靈、滅達樂 達滅^ ’石夕硫芬、雙快醯菌胺; •雜%、化合物,諸如護汰寧;蓋普丹、邁隆 依普同; •胺基甲酸_類,諸如鋅錳乃浦、錳乃浦 恩地;
•其他活性化合物,其係選自無機活性化合物:硫、波 爾多混合物、乙酸銅、氫氧化銅、鹼性氯氧化二鹼 性硫酸銅;其他:克熱淨、鏈黴素。 另較佳實施例為表B中所列之組合,其中在各種情況 下表:之一列對應於包含所提及之式Z之特定化合物(組份約 及特定化合物Π(組份b)的農藥組合。該等二元組合中之每 者可另外含有-或多種、尤其_種如上提及之其他殺蟲 劑或殺真菌劑。
表B
編號 組份b B-1 表1,1-9 加保扶 B-2 表1,1-9 丁基加保扶 B-3 表I , 1-9 硫地克 B-4 表1,1-9 畢 B-5 表1,1-9 赛扶寧 B-6 表1,1-9 赛麥寧 B-7 表1,1-9 α-賽滅寧 B-8 表1,1-9 七氟菊酯 B-9 表1,1-9 亞滅培 B-10 表1,1-9 可尼丁 B-11 表1,1-9 σ夫蟲胺 B-12 表1,1-9 益達胺 B-13 表1,1-9 ----- -_____ 賜諾殺 128642.doc 編號 組份a 組份b B-14 表1,1-9 。塞蟲嘻 B-15 表卜1-9 α塞蟲琳 B-16 表卜1-9 氟蟲猜 B-17 表 1 ’ I-18 加保扶 B-18 表 1 ’ I-18 丁基加保技 B-19 表1,1-18 硫地— B-20 表1,1-18 畢芬寧 B-21 表1,1-18 赛扶寧 B-22 表1,1-18 賽滅寧 B-23 表1,1_18 α-赛滅寧 B-24 B-25 表1,1-18 七氟菊酉旨 表1,1-18 亞滅培 B-26 表1,1-18 可尼丁 -39· 200838429
編號 組份a 組份b B-27 表1,1-18 σ夫蟲胺 B-28 表1,1-18 益達胺 B-29 表卜1-18 賜諸殺 B-30 表卜1-18 噻蟲嗪 B-31 表1,1-18 嗟蟲琳 B-32 表1,1-18 氟蟲腈 B-33 表1,1-25 加保扶 B-34 表卜1-25 丁基加保扶 B-35 表 1,1-25 硫地克 B-36 表1,1-25 畢芬寧 B-37 表1,1-25 賽扶寧 B-38 表1,1-25 賽滅寧 B-39 表 1,1-25 α-賽滅寧 B-40 表 1,1-25 七氟*菊酯 B-41 表1,1-25 亞滅培 B-42 表1,1-25 可尼丁 B-43 表1,1-25 呋蟲胺 B-44 表 1,1-25 益達胺 B-45 表1,1-25 賜諾殺 B-46 表1,1-25 售蟲°秦 B-47 表1,1-25 售蟲琳 B-48 表1,1-25 氟蟲腈 B-49 表1,1-28 加保扶 B-50 表卜1-28 丁基加保扶 B-51 表1,1-28 硫地克 B-52 表1,1-28 畢芬寧 B-53 表1,1-28 賽扶寧 B-54 表卜1-28 賽滅寧 B-55 表1,1-28 α-賽滅寧 B-56 表1,Ι·28 七氟菊酯 B-57 表1,1-28 亞滅培 B-58 表 1,1-28 可尼丁 B-59 表卜1-28 呋蟲胺 B-60 表1,1-28 益達胺 B-61 表1,1-28 賜諾殺 B-62 表1,1-28 噻蟲嗪 B-63 表1,1-28 嗟蟲琳 編號 組份a 組份b Β·64 表卜1-28 氟蟲猜 Β-65 表1,1-98 加保扶 Β-66 表1,1-98 丁基加保扶 Β-67 表1,1-98 硫地克 Β-68 表 1,1-98 畢芬寧 Β-69 表1,1-98 賽扶寧 Β-70 表 1,1-98 賽滅寧 Β-71 表 1,1-98 α-賽滅寧 Β-72 表1,1-98 七氟菊酯 Β-73 表1,1-98 亞滅培 Β-74 表1,1-98 可尼丁 Β-75 表1,1-98 呋蟲胺 Β-76 表1,1-98 益達胺 Β-77 表1,1-98 賜諾殺 Β-78 表1,1-98 噻蟲嗓 Β-79 表1,1-98 α塞蟲琳 Β-80 表1,1-98 氟蟲腈 Β-81 表1,1-101 加保扶 Β-82 表1,1-101 丁基加保扶 Β_83 表1,1-101 硫地克 Β-84 表1,1-101 畢芬寧 Β-85 表1,1-101 賽扶寧 Β-86 表卜1-101 賽滅寧 Β-87 表1,1-101 α-賽滅寧 Β-88 表1,1-101 七氟菊酯 Β-89 表卜1-101 亞滅培 Β-90 表卜1-101 可尼丁 Β-91 表1,1-101 呋蟲胺 Β-92 表1,1-101 益達胺 Β-93 表1,1-101 賜諾殺 Β-94 表卜1-101 噻蟲嗪 Β-95 表1,1-101 嚷蟲琳 Β-96 表1,1-101 氟蟲腈 Β-97 表卜1-110 加保扶 Β-98 表卜1-110 丁基加保扶 Β-99 表1,1-110 硫地克 Β-100 表1,1-110 畢芬寧 128642.doc -40 200838429
編號 組份a 組份b Β-101 表1,1-110 賽扶寧 Β-102 表1,1-110 賽滅寧 Β-103 表1,1-110 α-賽滅寧 Β-104 表1,1-110 七氟菊酯 Β-105 表1,1-110 亞滅培 Β-106 表1,1-110 可尼丁 Β-107 表1,1-110 呋蟲胺 Β-108 表卜1-110 益達胺 Β-109 表卜1-110 賜諾殺 Β-110 表1,Ι·110 噻蟲嗪 Β-111 表1,1-110 售蟲淋 Β-112 表卜1-110 氟蟲腈 Β-113 表1,1-113 加保扶 Β-114 表1,1-113 丁基加保扶 Β-115 表1,Μ13 硫地克 Β-116 表卜1-113 畢芬寧 Β-117 表卜1-113 賽扶寧 Β-118 表卜1-113 賽滅寧 Β-119 表1,1-113 α-赛滅寧 Β-120 表卜1-113 七氣菊醋 Β-121 表1,1-113 亞滅培 Β-122 表卜1-113 可尼丁 Β-123 表卜1-113 吱蟲胺 Β-124 表卜1-113 益達胺 Β-125 表卜1-113 賜諸殺 Β-126 表卜1-113 噻蟲嗪 Β-127 表卜1-113 σ塞蟲琳 Β-128 表卜1-113 氟蟲腈 Β-129 表1,1-120 加保扶 Β-130 表1,1-120 丁基加保扶 Β-131 表卜1-120 硫地克 Β-132 表卜1-120 畢芬寧 Β-133 表卜1-120 賽扶寧 Β-134 表1,1-120 賽滅寧 Β-135 表1,1-120 α-賽滅寧 Β-136 表卜1-120 七氟菊酯 Β-137 表卜1-120 亞滅培 編號 組份a 組份b B-138 表1,M20 可尼丁 B-139 表1,1-120 11夫蟲胺 B-140 表1,1-120 益達胺 B-141 表卜1-120 賜諾殺 B-142 表1,1-120 噻蟲唤 B-143 表1,1-120 嗟蟲琳 B-144 表1,1-120 氣蟲猜 B-145 表卜1-180 加保扶 B-146 表1,1-180 丁基加保扶 B-147 表1,1-180 硫地克 B-148 表1,1-180 畢芬寧 B-149 表1,1-180 赛扶寧 B-150 表1,1-180 賽滅寧 B-151 表1,1-180 α-賽滅寧 B-152 表卜1-180 七氟菊酯 B-153 表1,1-180 亞滅培 B-154 表卜1_180 可尼丁 B-155 表1,1-180 呋蟲胺 B-156 表1,1-180 益達胺 B-157 表1,1-180 賜諾殺 B-158 表卜1-180 噻蟲嗪 B-159 表1,1-180 σ塞蟲琳 B-160 表1,1-180 氟蟲腈 B-161 表卜1-245 加保扶 B-162 表卜1-245 丁基加保扶 B-163 表1,1-245 疏地克 B-164 表卜1-245 畢芬寧 B-165 表卜1-245 賽扶寧 B-166 表卜1-245 賽滅寧 B-167 表1,1-245 α-賽滅寧 B-168 表1,1-245 七11菊酯 B-169 表卜1-245 亞滅培 B-170 表1,1-245 可尼丁 B-171 表1,1-245 咬蟲胺 B-172 表1,1-245 益達胺 B-173 表1,1-245 賜諾殺 B-174 表卜1-245 噻蟲嗪 128642.doc •41 200838429 編號 組份a 組份b B-175 表卜1-245 噻蟲琳 B-176 表1,1-245 氟蟲睛 B-177 表 1,1-290 加保扶 B-178 表1,1-290 丁基加保扶 B-179 表1,1-290 硫地克 B-180 表1,1-290 畢芬寧 B-181 表 1,Ι-29Ό 赛扶寧 B-182 表卜1-290 賽滅寧 B-183 表1,1-290 ct-赛滅寧 B-184 表1,1-290 七氟菊酯 編號 組份a 組份b B-185 表1,1-290 亞滅培 B-186 表1,1-290 可尼丁 B-187 表1,1-290 呋蟲胺 B-188 表1,1-290 益達胺 B-189 表卜1-290 賜諾殺 B-190 表1,1-290 噻蟲嗪 B-191 表1,1-290 σ塞蟲琳 B-192 表1,1-290 氟蟲腈
在另一較佳實施例中,混合物僅包含兩種活性成份。各 較佳實施例係與上述實施例一致。 在另一較佳實施例中,混合物僅包含三種活性成份。更 佳為可另外含有另一種活性化合物、尤其為另一種殺真菌 劑的組合B-1至B_ 192中之任一者。相應之較佳實施例係與 上述實施例一致。 在一實施例中,將本發明之混合物用於對抗有害真菌及 有害昆蟲或線蟲。 在另一實施例中,將本發明之混合物用於對抗有害真 菌。 式I化合物與化合物II之混合物尤其適用於控制以下類別 之有害真菌:印菌綱(Per⑽(同義詞: ,諸如霜黴菌種、疫黴菌 種、葡萄生單軸徽及 假霜黴屬(h⑽而;種,尤其為對應於下述彼等 者之真菌。 在另一實施例中,將本發明之混合物用於對抗有害昆蟲 128642.doc •42- 200838429 或線蟲。 在另一實施例中,本發明之混合物包含增效有效量 I化合物與化合物η。 ^ 在另一實施财,本發明之混合物包 1化合物與化合㈣且係用於對抗有害昆蟲或線L式
=-實施例中’將本發明之混合物用於控制真菌及/ 或改良植物健康狀況之枝,該方以含用至少一種式J 化合物及至少一種化合物_任何所要次序或同時(亦即聯 合或分開)處理受真菌侵染或易受真菌侵染之位點(例如植 物或植物繁殖材料)。 f %例中’將本發明之混合物用於控制有害昆蟲 或線蟲之方法,該方法包含用至少一種式!化合物及至少 種化合物II依任何所要次序或同時(亦即聯合或分開)處 理受真菌侵染或易受真菌侵染之位點(例如植物或植物繁 殖材料)。 在另一實施例中,將本發明之混合物用於一種改良植物 健康狀況之方法,該方法包含用至少一種式J化合物及至 少一種化合物II依任何所要次序或同時(亦即聯合或分開) 處理文真菌侵染或易受:真菌侵染之位點(例如植物或植物 繁殖材料)。 在該方法之另一實施例中,至少一種式J化合物及至少 一種化合物II之施用可在無害蟲壓力之情況下進行。 在另一實施例中,本發明之混合物包含增效有效量之式 I化合物與化合物II且係經用於改良植物之健康狀況。該方 128642.doc -43· 200838429 法可在害蟲壓力下或在無害蟲壓力之情況下應用。 在另一較佳實施例中,將本發明之混合物用於活的植物 作物之葉面施用、用於播種或種植前之土壌施用(包括整 個土壤處理及溝畦施用法)以及尤其用於針對植物繁殖材 料之追肥施用。後者術語涵蓋所有種類之種子(果實、塊 莖、穀粒)、插枝、伐條及其類似物。一種特殊應用領域 為所有種類種子之處理。
本發明之混合物對於控制各種作物植物及該等植物之種 子或牧草及牧草種子上之大量真菌及昆蟲或線蟲而言尤其 重要’其中該等作物植物諸如小麥、玉米、黑麥、大麥、 燕麥、高粱、水稻、玉蜀黍、草、香蕉、棉花、大豆、咖 非树、甘蔗、葡萄藤、水果種類、觀賞植物及蔬菜,諸如 頁瓜、豆、乾豆、番茄、馬鈴薯、萵苣、葫蘆、甘藍菜、 胡蘿蔔、十字花科、向日葵及葫蘆。在一特殊實施例中, 將本發明之混合物施用於大豆上。在另一較佳實施例中, 將本發明之混合物施用於種子上。在一特定實施例中,將 本發明之混合物施用於大豆種子上。 化合物I可用作大量不同活性化合物π之增效劑。同時 (亦即聯合地或分別地)施用至少一種式][化合物與活性化合 物Π係以超加性方式增強殺真菌活性及/或增進植物健康之 活性。 具體而言,式I化合物及混合物適用於控制以下有害真 菌中之各者: •蔬菜、油菜、甜菜、榖物、水果及水稻上之鏈格孢菌 128642.doc -44- 200838429 (J/ier/taria)種,諸如馬鈴薯及番茄上之底腐病菌(A 或赤星病菌(A α/ier⑽ία); • 甜菜及蔬菜上之根腐病菌«pk⑽myces)種; •穀物及蔬菜上之婉豆斑莢病菌(種,例如小麥 上之小麥殼二孢菌irz7zW); • 玉米、穀物、水稻及草坪上之平臍蠕孢及内 臍罐孢(Drec/^/era)種,諸如玉米上之玉米小斑病菌(£)· maydis);
• 榖物(例如小麥或大麥)上之禾本科布氏白粉菌(万/wmer/a gra心>b)(白粉病); •草莓、蔬菜、花、小麥及葡萄上之灰黴孢菌沿 灰黴病); •萵苣上之萵苣霜黴病菌(万remk /aciwcae); • 玉米、大豆、水稻及甜菜上之葉斑病(Cercc^pora)種, 例如大豆上之大豆灰斑病菌(Cercwpora soyζ·πα)或大豆 繁斑病菌(Cercospora kikuchii) ·, • 4、麥 Jl 之草冬枝抱(Cladosporium herbarum) ·, • 玉米、穀物、水稻上之旋孢腔菌(Coc/z/ZMo/i^)種,諸 如榖物上之禾旋孢腔菌χαί/νΜβ)、水稻上 之水稻旋抱腔菌(Cochliobolus miyabeanus) ·, • 大豆及棉花上之炭疽菌(CW/eioiric/zwm)種,例如大豆 Jl 之大 1 良痕病遠(Colletotrichum truncatum) ·, • 大豆上之多主棒抱菌; • 大豆上之白紋羽束絲菌; 128642.doc -45- 200838429 •欠瓦 Jl 之大立 1 潰瘍病窗(Diaporthe phaseolorum) ·, • 玉米、穀物、水稻及草坪上之内臍蠕孢種、核腔菌 種,諸如大麥上之大麥網斑病菌(D. 仏厂以)或小麥上之小麥德氏黴菌(/).以///〇/-厂^^/7"5); •葡萄藤上之埃斯卡病(£%α),其係由厚孢輪枝菌 {Phaeoacremonium chlamydosporium) ^ (葡萄木腐菌(Ph· A le op hilum))反斑孔太層孔菌(For mi tip or a punctata)(同 義言可·· Phellinus punctatus)所弓\ 起·,
• 小麥上之疮囊腔菌(Elsinoe ampelina) ·, • 水稻上之稻葉黑粉菌(五oryzM); • 小麥上之黑附球菌屬(五p/coccwm spp.); • 玉米上之突臍罐孢(jExsero/nVwm)種; •黃瓜上之煙草白粉病//7/ze cichoracearum)3^ ^ ^ 絲、數菌(Sphaerotheca fuligirtea) ·, •各種植物上之鐮孢菌(Fwsar/wm)種及輪枝孢菌 (Verticillium)楂,諸如穀物上之禾穀鐮孢菌(F. graminearum)氣大7]嫌抱菌(F· cw/morwm)或大量植物 (諸如番茄)上之炎孢鐮抱菌(jp. ,及大豆上 之腐皮鐮孢菌(Fwsar/wm π/απζ·); • 榖物(例如小麥或大麥)上之禾頂囊殼菌 (Gaeumannomyces graminis) ·, • 葡萄及其他作物上之圍小叢殼真菌(G7omere//a cingulata) \ • 穀物及水稻上之赤黴菌(G/6^re//a)種(例如水稻上之藤 128642.doc • 46· 200838429 食赤数儀(Gibberella fujikuroi)) ·, • 水稻上之複雜穀染菌comp/ex); •葡萄上之葡萄球座菌6 wdwe//z·); • 玉米及水稻上之長螺孢菌種; • 葡萄上之葡萄褐斑病菌(/•yariop/s c/av/spora); • 大旦上之莱豆殼球抱菌(Macrop/zomMa ρ/ζαπο/Μα); • 穀物上之雪徽葉枯病菌(MzYrc^ocWww m’va/e); • 大豆上之擴散叉絲殼菌(Micro^p/^era ;
• 穀物、香焦及花生上之球腔菌(Mj;⑶w/mere/Za)種,諸 如小麥上之禾穀根結線蟲(M. gram/m’^/a)或香蕙上之 斐濟球腔菌(M. /(/化似以); •甘藍菜及球根植物上之霜黴菌(i^rc^ovora)種,諸如 甘藍菜上之芸苔根腫菌(Ρ· hrasdcae)、洋蔥上之蔥霜黴 菌(P· (iesirwcior)或大豆上之東北霜徽菌(/>· 似/zwr/ca); •大豆上之豆箸層鏽菌(Phakopsara pachyrhizi)及邁博姆 層鏽菌(Phakopsara meibomiae) ’, • 大豆上之大豆莖褐腐病菌(P/z/a/c^/zora gregaia); • 向曰葵、大豆(例如菜豆擬莖點黴菌(Ρ. ρ/ζααο/ζ·))及葡 萄(例如葡萄生單軸黴(凡Wiico/α))上之擬莖點黴菌 (Phomopsis)楂·, • 各種植物上之晚疫病菌(P/73;i〇p/7i/26>ra)種,諸如甜椒上 之辣椒疫黴(P· capWcz·」、大豆上之大雄疫黴(P. meg似perma)及馬鈴薯與番茄上之致病疫黴(ρ· infestans) ·, 128642.doc -47- 200838429 •葡萄藤上之葡萄生單軸徽Wi/co/α); •雜、果上之白又絲單囊殼菌; •毅物(小麥或大麥)上之卷毛狀假小尾孢 {Pseudocercosporella herpotrichoides); •各種植物上之假霜黴菌(PwW〇per〇n〇iSp〇ra),諸如黃瓜 * 上之古巴假霜黴(凡cMewb)或啤酒花上之葎草假霜黴 . (P. humili); •葡萄上之葡萄角斑葉焦病菌心/β 馨 tracheiphilai); •各種植物上之柄鏽菌(Pwccz’Wa)種,諸如穀物(小麥或大 麥)上之小麥葉鏽菌(八ir/i/c/πα)、小麥條鏽菌(户 Wr(/brmz·似)、大麥柄鏽菌(ρ· 或向曰葵柄鏽菌(p gramkb)或蘆筍上之天冬柄鏽菌(ρ· aiyparag/); •水稻上之稻梨孢菌(Pyr/cw/arz’a oryzae)、水稻紋枯病菌 [Corticium sasakif)、ψ 便技抱〔Sarocladium oryzae)、 f枝撤屬真囷($· 、稻葉黑粉菌(五π❶;所“ oryzae); •小麥上之偃麥草核腔菌或 大麥上之大麥網斑病菌QPyrenophora teres) ·, 一 ·草坪及穀物上之稻痕病菌(/^yWcw/arz。gr/πα); •草坪、水稻、玉米、小麥、棉花、油菜、向日葵、甜 采、滅米及其他植物上之腐撤囷屬(户少,諸 如各種植物上之棉腐病(P. w/i/wmi/w)、草坪上之瓜果腐 敬{P· aphanidermatum) ’, 128642.doc -48- 200838429 • 大麥上之RCC菌coHo-cygni,枉隔抱屬 (生理葉斑病); •棉花、水稻、馬鈴薯、草坪、玉米、油菜、馬鈴薯、 甜菜、蔬菜及各種植物上之絲核菌(i?/2/Z(7Ci(977/(2)種,諸 如甜菜及各種植物上之立枯絲核菌(及.so/am·),以及小 麥或大麥上之禾穀絲核菌(及cerea/b); • 尺麥、黑麥反票、4、麥上之黑麥兔抱菌(Rhynehosporium secalis) \ • 油菜及向曰葵上之核盤菌(Sc/eroi/Wa)種,以及(例如) 大豆上之菌核病菌(& sc/eroibrwm)或齊整小核菌(&· rolfsii) \ • 大豆上之褐紋病菌g/ye/Hes); • 小麥上之小麥殼針抱菌(iSepiw/a iWizW)及穎枯殼針孢 儀{Stagonospora nodorum) ’, • 葡萄藤上之葡萄白粉病菌weeWor)(同義詞: 葡萄鉤絲殼菌(ί/㈣//iw/a ziecaior)); • 玉米及草坪上之毛球腔菌(&ί6^/7ΜΓΖ·(3)種; • 玉米上之玉米絲黑穗病菌(Sp/mce/oi/zeca ; • 小麥上之穎枯殼針孢菌; • 大豆及棉花上之根串珠黴(77π·βνα//<9ρ/$)種; • 穀物上之腥黑粉菌(Π//βίζ·α)種; • 小麥或大麥上之肉孢核瑚菌(7yp7^/a ; • 穀物、玉米及甘蔗上之黑粉菌(C/Wi/ago)種,諸如玉米 上之玉米黑粉菌([/· mb); 128642.doc -49- 200838429 • 蘋果及梨上之黑星菌(FeWwrk)種(瘡痂病),諸如蘋果 上之蘋果黑星菌(F· /似叫⑽仏)。 其亦適用於控制以下目之有害昆蟲:
•鱗翅目似,,例如小地老虎 (』groi以>7?以7仍)、黃地老虎wgeiwm)、棉葉波 紋葉蛾、黎豆夜蛾 gemmaia/b)、蘋實巢蛾、丫紋 夜蛾(Autographa gamma)、松樹尺蠖(Bupalus piniarius) ^ {Cacoecia murinana) > ^ ^ 蛾[Capua reticulana)、冬 & 複蛾(Cheimatobia brumata)、 雲杉卷葉蛾(C/zor/Wo加ι/ra 、西方雲杉卷葉 織{Choristoneura occidentalism 、美?、州霉占蟲(C7/77/^5 unipuncta) - M ^ S {Cydia pomonella) ^ ^ ^ (Dendrolimuspini)、)^ff^{Diaphanianitidalis)'^]^ 玉米填(Diairaea 、棉斑實蛾(五 insulana)、小玉米模(£/似"g7?c^e//Miy)、葡萄 填蛾(五z/poeci/k 、夏梢小卷蛾(五vwr/a bouliana)、粒膚地老虎(Fe/ha subterranea)、大樣煩 (Galleria mellonella)、李 4、食心氣(Grapholitha funebrana)、梨小食心蟲、棉鈴蟲 (Heliothis armigera)、美洲煙葉蛾(Heliothis virescens)、 矣洲梅龄美(Heliothis zea)、菜镇(Hellula undalis)、反 裙超冬緩(Hibernia defoliaria)、美厲白蛾(jfyphantria cz^ea)、蘋果巢峨⑽)、番茄蠹蛾 128642.doc -50- 200838429 {Keiferia lycopersicella)、鐵衫 J^i^{LambcUna fiscellaria)、 甜菜夜蛾、咖啡潛葉蛾 、旋紋潛葉蛾、斑幕細蛾 (Lithocolletis blancardelia)、葡萄策篆卷蛾(Lobesia botrana)、黃綠條填、舞毒蛾 (Lymantria dispar)、僧見秦織(Lymantria monacha)、窄 翅潛葉蛾(Ayc^ei/α c/er々e//a)、天幕毛蟲(Ma/acasoma neustria) ^ ^ ^ ^ ^(Mamestra brassicae) ^ ^ Μ
(Orgyz.a 、歐洲玉米填、 冬夜蛾(戶⑽flammea) ^參工铃备(Pectinophora 客〇*^>7?化//<2)、雜色地老虎(PerzWroma sawc/a)、圓掌舟 織{Phalera bucephala)、馬铃薯塊莖蛾(P/zi/zor/maea operculella)、橋細潛蛾(Phyllocnistis citrella)、大菜粉 碟(Pieris brassicae)、苢辕綠夜蛾(Plathypena scabra)、 ,\、I 蛾(Plutella xylostella)、大 I 夜蛾(Pseudoplusia /加/“(^似)、松梢卷葉蛾(及/2};(2(^(9以(^/>41^以(37?(2)、馬铃薯 成 Ά 織(Scrobipalpula absoluta)、麥峨[Sitotroga cerealella)、葡萄長 Μ 卷葉蛾(Sparganothis pilleriana)、 草地黏蟲(iSpodoj^era/rwgberda)、灰翅夜蛾 //Hora/b)、斜紋夜蛾/fiwra)、松異帶蛾 (Thaumatopoea pityocampa)、楝綠卷葉蛾 vz>/d⑽α)、粉紋夜蛾(JWc/zo/7/i/ha πζ·)及雲杉小卷葉蛾 {Zeiraphera canadensis); •曱蟲類(鞘翅目(Co/eopiera)),例如梨長吉丁(dgrz7w 128642.doc •51· 200838429
似)、具條叩甲、黯金針蟲 {Agriotes obscurus、、馬街集無金 I [Amphimallus M/si/i/aZ/s)、橫帶王者渐、棉铃象 "f (Anthonomus grawiZ/s)、蘋果花象甲(dw/zo⑽m似 pomorum)、條隱食甲(Jiomaria /inearb)、大松小蠹 (Blastophagus piniperdcT)、天幕枯葉蛾(方/z7(9/7/mga undata)、暮瓦 KBruchus rufimanus)、紙良 KBruchus pisorum)、鳥瓦象(Bruchus /βπίζ))、蘋果卷葉象甲 (jBjdbc似 0eiw/ae)、甜菜大龜甲、 豆葉甲 (Cerotoma trifurcata)、 甘藍莢象曱 [Ceuthorrhynchus assimilis)、I I "f (Ceuthorrhynchus ⑽ρζ·)、甜菜脛跳曱、煙草金針蟲 {Conoderus vespertinus)、天冬負 H 气{Crioceris asparagf)、 長角葉曱、十二星葉甲 (Diabrotica 12_punctata)、玉米根葉甲 virgifera)、墨西哥立瓢義(Epilachna varivestis)、煙萆 跳甲(五pz’Wx /n>iz>enms)、巴西艾美爾球蟲(五 似以)、松樹象甲(丑α6ζ·βί^)、埃及苜藉象 甲(//^era ⑽、苜蓿葉象甲;?〇扣ca)、 雲杉八齒小蠹(/γ 、具條負泥蟲(kma bilineata)、票、苒負泥氣(Lema melanopus)、馬铃集罗备 (Leptinotarsa decemlineata)、甜茱金針备(Limonius californicus)、箱 I 气{Lissorhoptrus oryzophilus)、普 通叩甲(Me/αποίι^ commi/mi)、油菜露尾曱(Me/igei/zes 128642.doc -52- 200838429 aeneus)、忽、_ 魏龟金 HMelolontha hippocastani)、西 方 l H 魏金亀^ [Melolontha melolontha)、稻% 泥备 oryzae)、槽象甲、草 莓根象甲ovaiws)、辣根猿葉甲(P/rnedo" cochleariae)、油茱歡跳 Ψ (Phyllotreta chrysocephala)、 金龜屬sp.)、庭園麗金龜(P/zj/Zc^eri/^ /2(9r"c<9/(2)、宪菁淡足跳甲«emorwrn)、黃曲 條跳甲(尸/^/Mirda 、曰本麗金龜
/apow/ca)、婉豆葉象甲(57ίο⑽ lineatus) Sl 數篆 (Sitophilus granaria) \ •雙楚 U (dipterans,Diptera),例如埃及伊蚊(deda 、刺擾伊蚊(deda vexans) ^墨西哥橘實繩 [Anastrepha ludens)、丘斑按蚊(Anopheles maculipennis)、 地中海實绳(Orai"以c叩ζ’ίαία)、姐症金蜗 bezziana)、美洲金繩/zomz’m’vorax)、稻金繩 (Chrysomya macellaria)、高粱癭蚊(Contarinia sorghicola)、亀波鐵(Cordylobia anthropophaga)、1 ♦ 淡色庫蚊(Cw/ex ⑼s)、瓜實绳(Dacws ei/cwrZi/iae)、 油橄欖實蠅(乃加似o/eae)、蕓苔莢癭蚊 办rawz’cae)、黃腹廄绳(FimTz/a c^nz’cw/arb)、大馬胃繩 (G似ierop/n7⑽ ζ>7ία"·/ζ\)、刺舌绳、 騷擾角繩如)、蝴蝶蘭潛繩 [Haplodiplosis equestris)、後緣(Hylemyia platura)、故 I 規[Hypoderma /beak)、美洲斑潛繩(Z^Wom;;% 128642.doc •53- 200838429 «yai/vM)、三葉斑潛繩、山羊綠繩 (Lucilia caprina)、銅綠織(Lucilia cuprina)、絲、先綠織 (Zwcz’/k 、白揚花繩(jLycork 以)、黑森 麥桿繩(Majei/o/a (iairwcior)、 廄腐繩似)、羊鼻繩ov/s)、瑞 典麥稈绳/Wi)、甜菜潛葉繩 、蔥地草種繩(P/zorWa 、甘藍草種 纖(P/zorHa 、麥地草種繩(P/zorWa c<9arciaia)、
櫻桃實蠅(及如〜化沿cerasz·)、蘋果實繩 pomonella) ^ 牛 it ⑽feov/wws)、甘藍大蚊(T7;?w/a oleracea )反歡洲:K 故(Tipula paludosa、·, •纓翅目(i/2r(ps,,例如煙草褐薊馬 (Frankliniella fusca)、售辕餘馬{Frankliniella occidentalism、 花薊馬irii/cz·)、橘實薊馬(S^zrioi/zrz·/^ c/irz·)、稻莉馬(TTzrz·/^ oryzae)、南黃薊馬(77zn·/^ ρα/mz·) 及煙薊馬(TTzn·/^ iahcz·); • 膜翅目則,,例如黃翅菜葉 蜂rwae)、大頭美切葉蟻(^4ίία cep/za/oies)、南 美切葉蟻(Αία 、德州切葉蟻iex⑽α)、小 梨實葉蜂(丹mhwia)、蘋葉蜂(/fop/ocampa testudinea)、廚犧{Monomorium pharaonis)、火犧 (Solenopsis invicta)及红火織(Solenopsis invicta) ·, •異翅目{heteropterans ,Heteroptera) ’ 例如喜綠蝽 {Acrosternum hilare)、^ ^ {Blissus leucopterus、、 128642.doc -54- 200838429 煙草黑斑盲蝽、棉紅蝽 chgw/aiws)、中介紅蝽(AyWercws hiermed/ws)、麥爲盾 4# (Eurygaster integriceps)、棉褐 _ (Euschistus impictiventris)、葉足緣锋(Leptoglossus phyllopus)、美 國牧草盲蝽(Z^ygws //weo/ark)、牧草盲蝽 、稻綠蝽(iVezara virzWa)、甜菜撿網培 (Piesma quadrata)、侮% 蜂{Solubea insularis)反锋 l {Thyanta perditor) \
• 同翅目,//omopkra),例如紅豆草無網長 管虫牙(Jcyri/zc^/p/zcm 、落葉松球財 /βΓζϋ)、鼠李馬鈴薯财«ρ/nWa nwiwri/z·)、蠢豆虫牙 {Aphis fabae) ^ ^ % {Aphis forbesi) ^ {Aphis pomi)、棉虫牙{Aphis gossypii)、醋栗虫牙{Aphis groww/ar/ae)、鼠李均1 、繡線菊財 «ρ/π·χ Miraea/a)、接骨木财 «p/zk samZ^cz·)、婉豆虫牙 (Acyrthosiphon pisum)、馬龄暮長鬚缉(Aulacorthum wMwz·)、莉短尾財cardwi)、圓尾虫牙 (Brachycaudus helichrysl)、桃票、短 I 场(Brachycaudus persicae) x # ^ (Brachycaudus prunicola)、甘藍财 {Brevicoryne brassicae)、角釘毛財(Capitophorus ftorm·)、方翅網蜂(Cerosip/m gc^sypiz·)、草莓毛管财 [Chaetosiphon fragaefolii)、茶藤 f亀瘤額[Cryptomyzus r/Z?^)、諾曼尼椎球财nordwa训/a似e)、雲杉 椎球辑(Drey/似piceae)、根瘤财(jDj^op/n’vS* 、 128642.doc -55- 200838429
綠箸场(Dysaulacorthum pseudosolani)、頻粉紅劣虫牙 p/ankgMea)、梨葉蚜ργζ·)、蠶豆 微葉蟬(五/αόαβ)、梅大尾蚜似 prwm·)、茶蘼苦菜所/aciwcae)、麥長管财 {Macrosiphum avenae)、大戟長管財 ewpAor6/ae)、薔薇長管財(AfacroWp/zon rowe)、蠶豆修 尾虫牙(Megowra v/cz’ae)、梨草虫牙、 I 藏參场(Metopolophium dirhodum)、^ (Myzodes perdcae)、冬蒽瘤額輯、櫻桃黑瘤 額虫牙cerwz·)、核黃瘤額财(M;/z似vahcms)、萵苣 财(Nasonovia ribis-nigri)、場稻 1 (Nilaparvata 、囊柄癭綿财(PempWgws 、蔗飛風 {Perkinsiella saccharicida)、蛇麻夜額財(Phorodon /zizmw//)、蘋木風(尸π//α ma/z·)、梨木風pzW)、冬 1 絡瘤场(Rhopalomyzus aMa/oWcws)、玉米!益管財 (Rhopalosiphum maidis)、木数激管场(Rhopalosiphum padV)、辕專緣管场(Rhopalosiphum ζ·似eriwm)、苗圓尾 虫牙(iS^/Tpap/ni ma/a)、蘋果圓尾財(iSappap/ni ma//)、麥 二又攝(Schizaphis graminum)、输梨绵场(Schizoneura lanuginosa) ^ φ- ^ ^ (Sitobion avenae) ^ 溫室白粉氮 {Trialeurodes vaporariorum) Λ 大洁场{Toxoptera aurantiiand) 及葡萄根瘤虫牙(w v"(/b"z·); •白蟻目(iermz’ies ’ /sopiera) ’ 例如乾木白蟻 /7(^化(9"以)、黃足白蟻/7αν(ρα)、南歐網 128642.doc -56 - 200838429 紋白蟻(及/wd/wg似)及南非戰白蟻 natalensis) \ •直翅目 〇ri/zo/7ier<2似,(9ri/2〇/?iera),例如家總蟀(dc/zeia domesifca)、東方蜚蠊(jB/βίία 、德國小蠊 (Blattella germanica)、歡洲珠竣(Forficula auricularia)、 歐洲螻蛄(Gr;;//oia/;7(2 δτγ/Μία/ρα)、飛虫皇 m^raiork)、雙帶蚱猛(Me/⑽op/似 赤腿蚱
^XMelanoplus femur-rubrum)、暮西胥辦瘦(Melanoplus 、遷徙虫专猛(Me/a^7<9/?/z^ 、落磯 山蚱猛spretus)、红楚造(Nomadacris septemfasciatcT)、矣洲大綠(Periplaneta americana)、矣 洲蚱虫孟、棕尾蚱猛(Sc/niiocerca peregrina) ^ ^ ^ ^ M {Stauronotus maroccanus)反溫^ 室虫悉螽; •蛛形綱(yirac/znoic/ea),諸如(例如)隱嗓蜱科 (drga以、蜱科(/xc^/d以)及济蜗科之虫知 蛛類(arac/zm·心)(蜱蜗目(dcar//^)),諸如美洲花蜱 {Amblyomma americanum)、彩飾花碑(Amblyomma variegatum) ^波斯隱ϋ彖蜱pem’cw)、具環方頭蜱 [Boophilus annulatus)、無故牛缉[Boophilus decoloratus)、 微小牛蜱(56>c^/n7w«y mkro/7/似)、森林革蜱(DamaceWor silvarum)、長蝝璃眼蜱(//ya/omma 、羊硬蜱 {Ixodes ricinus) 、 {Ixodes rubicundus) 、 口彖碑 {Ornithodorus moubata)、异後兔缉(Otobius megninf)、 128642.doc -57 - 200838429
雞皮刺蜗、羊癢蜗 ovis)、俯加島頭缉[Rhipicephalus appendiculatus)、參工 腿扇頭蜱(Rhipicephaius evertsi)、疥虫茜(Sarco尸ία scaZnW);及癭·蜗屬(五spp.),諸如蘋刺癭蜗 {Ac ulus schlechtendali) 橘鐘虫茜{Phyllocoptrata o/e/vora)及掛桔癭瞒Me/(io/7/);跗線蜗屬 (Tarsonemidae spp·、,議如台蛾(Phytonemus pallidus)反 多食附線蜗(尸/如⑽);細鬚蜗屬 (Tenuipalpidae spp·、,諸如紫偽葉瞒 ρΛαβπζϋ);葉蜗屬(ZWra^ye/n-c/ae ,諸如朱砂葉 虫高ez·⑽akrMws)、神澤氏葉蜗 、太平洋紅葉瞒、棉 紅葉蜗telarius)反梅葉織[Tetranychus urticae) \蘋果紅虫知蛛w/mz·)、橘全爪虫茜 (户⑽⑽少以似dW)及草地小瓜瞒(O/z’gonj/c/zi^ prai⑼以、)。 此外,其適用於控制以下有害線蟲,尤其植物寄生線 蟲,諸如根結線蟲類··北方根結線蟲(Me/o/办gyM /mp/a)、南方根結線蟲(Me/oMo幻;加爪口圭根結 線蟲/avam’ea)及其他根結線蟲屬 (Me/cn·而gj;心)種;形成胞囊之線蟲類··馬鈴薯金線蟲 (G/okAra 及其他胞囊線蟲屬(G/(9^<^ra) 種;小麥禾穀胞囊線蟲(iiWerodera “VMM)、大豆胞囊線 赢(Heterodera g/ycka)、甜菜胞囊線蟲 sc/zae/ziz·/)、三葉草胞囊線蟲⑺·)及其他異 128642.doc -58 - 200838429
皮線蟲(T/eierodera)種;種子癭·線蟲類:粒線蟲 種;莖及葉線蟲類:滑刃線蟲種;刺線蟲 類:刺線蟲(5e/o㈣及其他刺線蟲 種;松材線蟲類:松材線蟲(5w/^a/7/2e/e?7c/z⑽ 工3;/〇;7/?//1^)及其他傘滑刃線蟲(51^($|(2/7/^/6加/22^)種;環形 線蟲類:環線蟲(CWcc^ema)種、環紋線蟲(CWco"eme//a) 種、輪線蟲(Cr/cc^emozWes)種、中環線蟲(Mesocr/crcmema) 種;莖及球莖線蟲類:馬鈴薯腐爛莖線蟲(/)/〇;/⑼c/zw (ieWrwcic^)、玉米莖線蟲(i^pwcz·)及其他雙墊 刃(Diiy/eM/zws)種·,錐線蟲類··錐線蟲(Dd/c/zc^ori^)種; 螺旋象義類··香集螺、旋形象蟲XHeliocotylenchus multicinctus) 及其他螺旋線蟲種;稍及擬勒線蟲類: 勒線蟲(//em/cj;c"c^/2〇ra)種及半輪線蟲 種;潛根線蟲種;槍線蟲類:搶線蟲 種;偽根瘤線蟲類:珍珠線蟲(iVacc^Z>z/*y) 種;針線蟲類:橫帶長針線蟲e/owgaiw)及其 他長針線蟲(Ic^g/而rw)種;腐線蟲類:落選短體線蟲 (Praij/endws neg/eciz/s)、穿刺短體線蟲 peweiraw)、彎曲短體線蟲(iVai;;/⑼ c/zws cwrWiai ⑽)、古氏 短體線蟲及其他草地墊刃線蟲 (/Vaiy/enc/zMS)種;穿孔線蟲類··香蕉穿孔線蟲(Λβί/ορ/ιο/ι^ Wmz7以)及其他内侵線蟲種;腎形線蟲類:強 狀盤旋線蟲⑼似iws)及其他盤旋線蟲 種;盾線蟲種;殘根線蟲類: 128642.doc •59- 200838429 原始毛刺線蟲(7>/c如办及其他毛刺線蟲 (TWc/2〇办rw*y)種、擬毛刺線蟲似)種;矮化 線蟲類·克萊頓矮化線蟲c/ayi6^/)、不 疋矮化線蟲而6/似)及其他矮化線蟲 (Tylenchorhynchus)種;柑橘線螽類·,墊刃線螽(Ty!enchu!us) 種,劍線蟲類:劍線蟲(尤仏心㈣幻種;及其他植物寄生線 蟲種。
目、同翅目、等翅目及直翅目之害蟲。 胞 其亦適用於控制以下植物寄生線蟲,諸如根結線蟲屬、 囊線蟲屬、異皮線蟲屬、内侵線蟲屬、盤旋線蟲屬、草 地墊刃線蟲屬及其他屬。 對於種子處理而言,合適目標為各種作物種子、水果 類、蔬菜、香辛料及勸告姑^ 及野。二 種子,例如玉米/玉蜀黍(甜 及野生)、硬質小麥、大豆、小麥、大麥 黑小麥、香蒸、水稻、棉花、向曰;… 宿車卓皮、鬲糸、油菜籽、芸苔屬(BrA · 菜、痴子、番茄、葛苣、I # ass!ca spp·)、甜 甜瓜、豆、乾豆、碗豆、驻菜、大π瓜、南瓜、 蘿蔔、塊莖(諸如甘蔗)、 77年〜、、甘藍菜、胡 ^ } 煙草、咖啡、钴丄 花科、葫蘆、葡萄藤、胡 卓皮及草料、十字 鳳仙花屬植(impatiens)、 木油菜、三色堇、 释聿牛花及天怂 術語種子處理包含此項技術中已^。 理技術’諸如(但不限於)拌 ::有合適之種子處 主佈、種子噴粉、浸 128642.doc 200838429 種、種子塗膜、種子多層塗佈 子粒化。 種子包殼、種子滴液及種 發月之活性成份混合物對於油菜a、、, 夕大麥、燕麥、高樑、向日葵、水稻、夕王米黑 草料、棉花、甜菜、豆、碗豆 、玉蜀黍、草皮及 (諸如韻蘆、番莊、霖子、馬鈐宴、觀賞植物及蔬菜 菜、胡蘿*5、+ — 馬7薯、胡椒、萵t、甘藍 蕹自十子化科)之種子處理尤為有利。
竿尤::佳為油菜、小麥、豆…、大豆、棉花、高 〆、未水心、蔬菜及觀賞植物之種子處理。 本發明之混合物最佳用於油菜之種子處理。 此外,本發明之混合物亦可用於因繁殖(包括遺傳工程 化方法)之故而财受除草劑或殺真菌劑或殺蟲劑之作用的 作物。 舉例而言’本發明之混合物可用於轉殖基因作物,其對 來自由磺醯脲類、味唑啉酮類、草銨膦(咖― ammonium)或嘉麟塞異丙胺鹽(glyph〇sateis〇pr〇pyiam_ium) 及類似活性物質組成之群的除草劑具有抗性(參見例如Ep_ A 242 236、ΕΡ·Α 242 246)(W〇 92/00377)(EP-A 257 993、 US 5,013,659),或可用於例如棉花之轉殖基因作物植物, 其具有產生穌力卤毋素(Bacillus thuringiensis toxin,Bt毒 素)之能力,此使得該等植物對某些害蟲具有抗性(ep-a 142 924、EP-A 193 259) 〇 此外,本發明之混合物亦可用於處理與現存植物相比具 有改質特徵之植物’後者可藉由(例如)傳統繁殖方法及/或 128642.doc •61 - 200838429 產生突變體,或藉由重組程序而產生。舉例而言,為改質 在植物中所合成之澱粉(例如WO 92/11376、WO 92/14827、 WO 9 1/19806)或為具有改質脂肪酸組成之轉殖基因作物植 物(WO 91/1 3972)的目的,已描述關於作物植物之重組改 質的若干案例。 式I化合物及化合物II以及視情況之其他活性成份可同時 (亦即聯合地或分別地)或連續地加以施用;在分別施用之 情況下,次序一般對控制措施之結果無任何影響。 式I化合物及化合物II通常係以有效量施用,其重量比較 佳為100:1至1:100,尤其為⑼:丨至!:;^,較佳為1〇:1至 式I化合物及其他殺真菌劑通常係以有效量施用,其重 量比較佳為1000:1至1:1000。 視所要效果而定,尤其在農業栽培領域之情況下,本發 明混合物之施用率為5至2000 g/ha,較佳為5〇至15〇〇 g/ha,尤其為 50至 750 g/ha。 此處式I化合物之施用率為1 g至1 kg/ha,較佳為1 〇至 9〇〇 g/ha,尤其為 20至 75〇 g/ha。 相應地,化合物π之施用率為! 8至1 kg/ha,較佳為至 750 g/ha,尤其為 20至 500 g/ha。 相應地,其他殺真菌劑之施用率為! §至1 kg/ha,較佳 為 5至 900 g/ha,尤其為 1〇 至 750 g/ha。
在處理種子中, g a.i./100 kg ^ 100 128642.doc 62- 200838429 kg或1 g : 100g a.i./ΙΟΟ kg。對於一些特定作物種子(諸如 萬苣或洋蔥)而言,施用率可較高。 本發明之另一實施例係針對正經本發明之混合物進行處 理之種子。 該等新穎活性成份混合物具有極為有利之治療性、預防 ί·生及系統性殺真菌特性以保護栽培植物。如已提及,該等 • 雜成份混合物可用於抑制或破壞不同作物或有用植物之 植物或植物部分(果實、花、葉、莖、塊莖、根)上所出現 的病原體,而同時彼等後來生長出之植物部分亦得到保護 而不受該等病原體侵襲。活性成份混合物具有對抗主要出 現於植物發育早期之土壤中的疾病具高度活性之特殊優 勢。 士在控制植物病原性有害真菌及/或有害昆蟲及/或線蟲 如’尤其在控制植物病原性有害真菌及/或# #昆蟲時, 式I化合物及化合物Π以及視情況其他活性成份或本發明之 鲁⑽合物的分別或聯合施用係藉由在植物播種前後或在植物 出苗前後處理種子、植物或土壌而進行。 活!·生化合物及本發明之混合物可例如經製備成直接可噴 . 轉液、散劑及懸浮液之形式或經製備成高度濃縮水性、 油1·生或其他懸浮液、分散液、乳液、油分散液、糊狀物、 粉劑、適於散布之組合物或顆粒的形<,且可藉由喷霧、 霧化、撒布、播撒或灌水,或以原樣或以水基漿料形式經 種子處理機器施用之著色懸浮液、溶液、乳液而加以施 用。使用形式視特定目的而定;在各種情況下,其應確保 128642.doc -63· 200838429 本發明之混合物儘可能精細且均勻之分布。 活性化合物及混合物可轉化為習知調配物,例如溶液、 乳液、懸浮液、粉劑、散劑、糊狀物及顆粒。使用形式視 特定意欲目的而定;在各種情況下,其應確保本發明之化 合物精細且均句之分布。
調配物係以已知方式製備(關於綜述,參見例如us 3,060,084、EP-A 707 445(關於液體濃縮物),Browning, ’’Agglomeration’’,Chemical Engineering,1967年 12月 4 日, 147-48,Perry’s Chemical Engineer’s Handbook,第 4版, McGraw-Hill,New York,1963,第 8-57頁以及下列各者: WO 91/13546、US 4,172,714、US 4,144,050、US 3,920,442、US 5,180,587、US 5,232,701、US 5,208,030、 GB 2,095,558、US 3,299,566、Klingman,Weed Control as a Science,John Wiley及 Sons,Inc” New York,1961,Hance 等人,Weed Control Handbook,第 8 版,Blackwell Scientific Publications, Oxford, 1989 及 Mollet, H·, Grubemann, A., Formulation technology, Wiley VCH Verlag GmbH,Weinheim (Germany),2001,2. D. A. Knowles, Chemistry and Technology of Agrochemical Formulations, Kluwer Academic Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8)),舉例而言,藉由以適用於調配農業化學製 品之助劑(諸如溶劑及/或載劑、(若必要)乳化劑、界面活 性劑及分散劑、防腐劑、消泡劑、防涞劑、對於種子處理 調配物而言視情況以及著色劑及/或黏合劑及/或膠凝劑)補 128642.doc -64- 200838429 充活性化合物來進行製備。
合適溶劑之實例A 、】為水、方族溶劑(例如S〇1veSSO產品、二 (例如礦物油館份)、醇類(例如甲醇、丁醇、 :醇$醇)_類(例如環己酮、丫·丁内酮 (ΝΜΡ、ΝΟΡ)、乙酸gt — 私 分足酮類 G I I曰類(二乙酸乙二醇酯)、二 肪酸二甲醯胺類、护妝祕4 員知肪酸類及脂肪酸酯類。原則上亦可使 用溶劑混合物。
合適礼化劑為非離子及陰離子乳化劑(例如聚環氧乙烧 脂肪醇醚、烷基磺酸酯及芳基磺酸酯)。 分散劑之實例為木質素亞硫酸鹽廢液及f基纖維素。 /斤用之合適界面活性劑為木f續酸、萘績酸、苯紛石黃 ,、二丁基萘磺酸之鹼金屬鹽、鹼土金屬鹽及銨鹽、烷基 方基磺酸鹽、烷基硫酸鹽、烷基磺酸鹽、脂肪醇硫酸鹽、 月曰肪駄及;^酸化脂肪醇二醇醚,此外為磺化萘及萘衍生物 與甲醛之縮合物、萘或萘磺酸與苯酚及甲醛之縮合物、聚 裱氧乙烷辛基酚醚、乙氧基化異辛基苯酚、辛基苯酚、壬 基苯紛、烧基酚聚乙二醇醚、三丁基苯基聚乙二醇醚、三 硬月曰醯基苯基聚乙二醇醚、烷基芳基聚醚醇、醇及脂肪醇 %氧乙烷縮合物、乙氧基化蓖麻油、聚環氧乙烷烷基醚、 乙氧基化聚環氧丙烷、月桂醇聚乙二醇醚縮醛、山梨糖醇 酯、木質素亞硫酸鹽廢液及甲基纖維素。 適用於製備直接可喷霧溶液、乳液、糊狀物或油分散液 之物質為中等;弗點至面佛點之礦物油顧份,諸如煤油或柴 油,此外為煤焦油及植物源油或動物源油、脂族烴、環烴 128642.doc -65- 200838429 j芳族煙,例如曱苯、二甲笨、石壤、四氮化蔡、烧基化 奈或其衍生物、曱醇、乙醇、丙醇、丁醇、環己醇'環己 酮、異佛爾酮、高極性溶劑(例如二甲亞颯、N_甲基吡咯 咬酮或水)。 亦可將防凍劑(諸如甘油、乙二醇、丙二醇)及殺菌劑添 加至調配物中。 合適消泡劑為(例如)以矽或硬脂酸鎂為主之消泡劑。 合適防腐劑為(例如)雙氯酚及苄醇半曱縮醛。 種子處理調配物可另外包含黏合劑及視情況之著色劑。 可添加黏合劑以改良在處理之後活性材料於種子上之黏 著性。合適黏合劑為嵌段共聚物EQ/PO界面活性劑,以及 聚乙烯醇、聚乙烯吡咯啶酮、聚丙烯酸酯、聚曱基丙烯酸 酉曰、聚丁烯、聚異丁烯、聚苯乙烯、聚乙烯胺、聚乙烯醯 胺、來乙稀亞胺(Lupasol®、P〇lymin㊣)、聚醚、聚胺基甲 酉文S曰ΛΚ乙酸乙烯酯、經乙基纖維素(tylose)及由此等聚合 物衍生之共聚物。 在調配物中視情況亦可包括著色劑。適用於種子處理調 配物之著色劑或染料為若丹明B(Rhodamin b)、c.I·顏料紅 112、C·1·溶劑紅1、顏料藍15:4、顏料藍15:3、顏料藍 15:2、顏料藍15:1、顏料藍80、顏料黃1、顏料黃13、顏料 紅U2、顏料紅48··2、顏料紅48:1、顏料紅57:1、顏料紅 5 3 · 1顏料撥4 3、顏料撥34、顏料燈5、顏料綠36、顏料 綠7、顏料白6、顏料棕25、鹼性紫10、鹼性紫49、酸性紅 5 1、酸性紅52、酸性紅14、酸性藍9、酸性黃23、驗性紅 128642.doc -66- 200838429 10、鹼性紅108。 膠凝劑之一實例為角又菜(Satiagel®)。 散劑、適於散布之材料及可撒布產品可藉由將活性物質 與固體載劑混合或伴隨研磨來製備。 顆粒例如L塗佈顆粒、浸潰顆粒及均質顆粒,可藉由 使活性化合物黏合至固體載劑來製備。 固體載劑之實例為確土,諸如料、㊉酸鹽、滑石、高 嶺土、鎂質黏土、石灰石、石灰、白堊、紅玄武土、黃 土、黏土、白雲石、矽藻土、硫酸鈣、硫酸鎂、氧化鎂、 粉狀合成材料;肥料,諸如硫酸鏔、磷酸銨、硝酸銨、尿 素,及植物源產品,諸如穀粉、樹皮粉、木粉及堅果殼 粉、纖維素粉末及其他固體載劑。 一般而言,調配物包含重量%、較佳〇丨至列重 量%之活性化合物。在此情況下,活性化合物係以9〇重量 %至100重量%、較佳95重量%至100重量%之純度(根據 NMR光譜)使用。 出於種子處理之目的,相應調配物可經稀釋丨〇倍,從 而在即用型製劑中得到以重量計〇.〇1重量%至6〇重量。/〇、 較佳〇·1重量%至40重量%之活性化合物濃度。 式I彳匕合物及混合物可以原樣、以其調配物形式或以自 其製備之使用形式來使用,例如以直接可噴霧溶液、散 劑、懸浮液或分散液、乳液、油分散液、糊狀物、可撒布 產品、適於散布之材料或顆粒之形式藉助於噴霧、霧化、 撒布、散布或傾倒來使用。使用形式完全視意欲目的而 128642.doc -67- 200838429 情況下確保本發明之活性化合物的最精 用形式可藉由添加水由乳液濃縮物、糊狀物戋可 ㈣散劑(可嘴霧散劑、油分散液)來製備。為製備乳液、 糊狀物或油分散液,可藉助於濕潤劑、增黏劑、分散劑或 =ϋ吏呈原狀或溶解於油或溶劑中之物質在水中句化。 然而’亦可能製備由活性物質、濕潤劑、增黏劑、分散劑
或礼化剑及(右適當)溶劑或油構成之濃縮物,且該等濃縮 物適於用水稀釋。 即用型製劑中之活性化合物濃度可在相對寬的範圍内變 化 般而a,其為0·〇〇〇ι重量。/〇至ίο重量%,較佳為0 01 重量%至1重量%。 亦可以超低容量法(ULV)成功地使用活性化合物,有可 能施用包含超過95重量%之活性化合物的調配物或甚至施 用無添加劑之活性化合物。
定;希望其在各種 細可能之分布。 以下為調配物之實例·· ^用於葉面施用之水稀釋型產品。為種子處理之目的, 該等產品可在經稀釋或未經稀釋之情況下施用於種子。 A)水溶性濃縮物(SL、LS) 將10重量份活性化合物溶解於9〇重量份之水或水溶性溶 劑中。或者,添加濕潤劑或其它助劑。活性化合物在經水 稀釋後即溶解,藉此獲得具有1 〇% (w/w)活性化合物之調 配物。 B)可分散濃縮物(〇〇) 128642.doc -68- 200838429 將20重量份活性化合物溶解於7〇重量份之環己顚1中,同 時添加1 0重量份之分散劑,例如聚乙稀α比哈咬酮。經水稀 釋得到分散液,藉此獲得具有20% (w/w)活性化合物之調 配物。 C) 可乳化濃縮物(EC)
將1 5重量份活性化合物溶解於7重量份之二甲苯中,同 時添加十二烷基苯磺酸鈣及萬麻油乙氧化物(在各種情況 下均為5重量份)。經水稀釋得到乳液,藉此獲得具有丨5〇/〇 (w/w)活性化合物之調配物。 D) 乳液(EW、EO、ES) 將25重量份活性化合物溶解於35重量份之二甲苯中,同 時添加十二烷基苯磺酸鈣及t麻油乙氧化物(在各種情況 下均為5重量份)。將此混合物藉助於乳化機(例如
Ultraturrax)引入30重量份水中且將其製成均質乳液。經水 稀釋得到乳液,藉此獲得具有25% (w/w)活性化合物之調 配物。 E)懸浮液(SC、OD、FS) 在攪動式球磨機中,將20重量份活性化合物粉碎,同時 =加10重量份分散劑、濕潤劑及7〇重量份水或有機溶劑: 付到精細活性化合物懸浮液。經水稀釋得到活性化合物之 L疋懸〉予液,藉此獲得具有2〇% (w/w)活性化合物之 物。 σ j目d F) 水分散性顆粒及水溶性顆粒(WG、sG) 將50重量份活性化合物精細研磨,同時添加π重量份之 128642.doc -69- 200838429 为政劑及濕潤劑’且藉助於技術設備(例如擠壓機、噴霧 塔、流體化床)將其製成水分散性或水溶性顆粒。經水稀 釋得到活性化合物之穩定分散液或溶液,藉此獲得具有 50% (w/w)活性化合物之調配物。 G)水分散性散劑及水溶性散劑(WP、SP、SS、WS) 將75重量份活性化合物於轉子_定子研磨機中研磨,同 日寸添加25重ϊ份之分散劑、濕潤劑及矽膠。經水稀釋得到 活性化合物之穩定分散液或溶液,藉此獲得具有 (w/w)活性化合物之調配物。 凝膠調配物(GF) 在攪動式球磨機中,將20重量份活性化合物粉碎,同時 添加10重量份之分散劑、!重量份之膠凝劑、濕潤劑及7〇 重量份之水或有機溶劑以得到精細活性化合物懸浮液。經 水稀釋得到活性化合物之穩定懸浮液,藉此獲得具有20% (w/w)活性化合物之調配物。 2.用於葉面施用之不經稀釋施用型|。口口。為種子處理之 目的,該等產品可經稀釋後施用於種子。 I) 可撒布散劑(DP、DS) 將5重量份活性化合物精細研磨且與95重量份之細粉狀 高嶺土均句混合。此得到具有5% (w/w)活性化合物之可粉 化產品。 J) 顆粒(GR、FG、GG、VIG) 將0.5重量份活性化合物精細研磨且連同⑴重量份之載 劑-起,藉此獲得具有〇.5% (w/w)活性化合物之調配物。 128642.doc -70- 200838429 現有方法為擠壓、噴霧乾燥或流體化床法。此得到可不經 稀釋即施用於葉面使用之顆粒。 K) ULV溶液(UL) 將ή份活性化合物溶解⑽重量份之有機溶劑⑼ 甲苯)中。此得到具有1 0〇/〇 (w/w)活性化合物之產品, 其係不經稀釋即施用於葉面使用。 習知種子處理調配物包括例如可流動濃縮物FS、溶液 LS、乾燥處理用散劑DS、漿料處理用水分散性散劑、 水溶性散劑SS及乳液ES與EC及凝膠調配物(^。該等調配 物可在經稀釋或未經稀釋之情況下施用於種子。在播種前 進行針對種子之施用,或直接施用於種子上。 在一較佳實施例中,FS調配物係用於種子處理。通常, FS調配物可包含1-800 gA之活性成份、1-200 g/i之界面活 性劑、0至200 g/Ι之防凍劑、〇至400 g/Ι之黏合劑、〇至2〇〇 g/Ι之顏料及至多1公升之溶劑,較佳為水。 即用型製劑中之活性化合物濃度可在相對寬的範圍内變 化。一般而言,其為0.0001%至10%,較佳為0 01%至1%。 亦可以超低容量法(ULV)成功地使用活性化合物,有可 月色施用包含超過9 5重量%之活性化合物的調配物或甚至施 用無添加劑之活性化合物。 可將各種類型之油、濕潤劑、佐劑、除草劑、殺真菌 劑、其他殺蟲劑或殺菌劑添加至活性化合物中,若適當則 直至即刻使用之前(槽混製劑)。該等藥劑可以1:100至 100:1 '較佳1:10至10:1之重量比與本發明之藥劑混合。 128642.doc -71- 200838429 在此意義上,合適佐劑尤其為:經有機改質之聚矽氧 烧,例如Break Thru S 240⑧;醇烧氧基化物,例如Atplus 245®、Atplus MBA 1303®、Plurafac LF 300φ&Lutensol ON 30® ; EO/PO嵌段聚合物,例如Pluronic RPE 2035®及 Genapol B® ;醇乙氧基化物,例如Lutensol XP 80® ;及二 辛基績基琥拍酸鈉,例如Leophen RA®。 本發明混合物之測試展示該等混合物有效控制真菌及/ 或昆蟲及/或線蟲且有效改良植物之健康狀況。 使用實例 化合物及混合物之殺真菌作用係由以下測試得以證明: 温室 製備··以若干步驟製備喷霧溶液: 製備儲備溶液:將丙酮及/或DMSO與濕潤劑/乳化劑 Uniperol(其係基於乙氧基化烷基苯酚)之混合物(溶劑-乳化 劑之比為99:1(體積))添加至25 mg化合物中,總共得到10 ml。接著添加水直至總體積為100 ml。 用所述溶劑·乳化劑-水混合物將此儲備溶液稀釋至給定 濃度。 使用實例1 -控制由番蘇晚疫病菌⑽ 引起之番茄的晚疫病(late blight) 使番蘇植物之幼苗生長於盆中。用含有下表中所提及濃 度之活性成份或其混合物的水性懸浮液對該等植物進行喷 霧至溢流(run-off)。次曰,將經處理之植物用番茄晚疫病 菌孢子囊之水性懸浮液接種。在接種之後,立即將試驗植 128642.doc -72- 200838429 物轉移至’朝濕、至。在l8〇c至2〇。。及接近㈣之相對濕度 下6天後,視覺評估葉片上之真菌侵襲程度,以害病葉片 面積之%計。 將目測之受感染葉片面積百分比轉化為以佔未經處理對 照組之百分比計的功效: 如下使用Abbot氏公式計算功效(E): " E = (1-α/β)*1〇〇 _ α對應於經處理植物之真菌感染❶/。,且 β對應於未經處理(對照)植物之真菌感染% ; 功效為0意謂經處理植物之感染程度相當於未經處理之 對妝植物的感染程度;功效為1 〇〇意謂經處理之植物未受 感染。 使用 Colby 氏公式(Colby,S.R· "Calculating synergistic and antagonistic responses of herbicide combinations^, Weeds,15, 20-22, 1967)測定活性化合物組合之預期功效且 φ 與觀測功效相比較。
Colby氏公式: E = X + y-x*y/l 〇〇 E 當使用濃度為a與b的活性化合物A與B之混合物時,以 ' 佔未經處理對照組之百分比表示的預期功效; X 當使用濃度為a之活性化合物A時,以佔未經處理對照 組之百分比表不的功效, y 當使用濃度為b之活性化合物B時,以佔未經處理對照 組之百分比表示的功效。 128642.doc -73- 200838429
表1A -個別活性化合物 編號 活性化合物 活性化合物在喷霧 功效,以佔未經處理 液中之濃度[ppm] 對照組之百分比計 1 對照組(未經處理) - (90%感染) 2 表 1,#1-245 16 0 3 表1,#1-113 4 22 4 氟蟲腈 63 0 5 16 0 6 益達胺 16 22 7 加保扶 16 0 表1B -本發明之來自表1A之活性化合物的混合物
編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 8 表1,# 1-245+氟蟲腈 16+63 ppm 1:4 22 0 9 表1,#1-113+氟蟲腈 4+16 ppm 1:4 78 22 10 表1,#1-113+益達胺 4+16 ppm 1:4 78 40 11 表1,#1-113+加保扶 4+16 ppm 1:4 89 22 使用實例2 -預防性控制青椒葉上之灰黴(灰黴孢菌) 使青椒幼苗於盆中生長至2至3片葉期。用含有下表中所 提及濃度之活性成份或其混合物的水性懸浮液對該等植物 進行喷霧至溢流。次日,將經處理之植物用灰黴孢菌於 2%生物麥芽(biomalt)水溶液中之孢子懸浮液接種。接著, 立即將試驗植物轉移至黑暗潮濕室。在22°C至24°C及接近 128642.doc 74- 200838429 100%之相對濕度下5天後,視覺評估葉片上之真菌侵襲程 度,以害病葉片面積之%計。 類似於實例1進行評估。 表2 A -個別活性化合物 編號 活性化合物 活性化合物在喷霧 液中之濃度[ppm] 功效,以佔未經處理 對照組之百分比計 12 對照(未經處理) - (90%感染) 13 表卜#1-290 16 0 14 氟蟲腈 63 10 表2B -本發明之來自表2A之活性化合物的混合物 編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 15 表卜#1-290+氟蟲腈 16+63 ppm 1:4 30 10 使用實例3 -治療性控制大豆上由大豆鏽菌 引起之大豆錄病 將盆植大豆籽苗之葉用大豆鏽菌孢子接種。為確保人工 接種成功,將植物轉移至相對濕度為約95%且溫度為23°C 至27°C之潮濕室中歷時24 h。次日,用含有如下所述濃度 之活性成份的水性懸浮液對該等植物進行喷霧至溢流。使 植物風乾。接著將試驗植物於溫度為23-27°C且相對濕度 介於60%與80%之間的溫室中培育14天。視覺評估葉片上 之真菌侵襲程度,以害病葉片面積之%計。 類似於實例1進行評估。 將化合物N-R’-2,2-二鹵基-1-R”環丙烷甲醯胺-2-(2,6-二 128642.doc -75- 200838429 氣- ct,a,(x-二氣-對甲苯基)踪(其中R’為乙基^ _基為氯基^ 且R"為甲基)編號為A.23-1。 表3 A -個別活性化合物 編號 活性化合物 活性化合物在噴霧 液中之濃度[ppm] 功效,以佔未經處理 對照組之百分比計 16 對照(未經處理) - (90%感染) 17 表1,#1-245 16 0 18 4 0 19 A.23-1 63 0 20 加保扶 16 0 表3B -本發明之來自表3 A之活性化合物的混合物 編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 21 表卜 #Ι-245+Α.23·1 16+63 ppm 1:4 33 0 22 表1,# 1-245+加保扶 4+16 ppm 1:4 56 0 使用實例4 -殺真菌性控制由葡萄生單軸黴引起之葡萄霜 黴病 使葡萄插枝於盆中生長至4至5葉片期。用含有下表中所 提及濃度之活性成份或其混合物的水性懸浮液對該等植物 進行喷霧至溢流。使植物風乾。次日,將其用葡萄生單軸 黴之水性孢子懸浮液藉由將該懸浮液喷於較低葉面處來接 種。接著,立即將試驗植物轉移至溫度為22-24°C且相對 濕度接近於100%的潮濕室中歷時24 h。隨後在溫度為20-25°C且相對濕度為約50%-80%的温室中培育5天之時段。 128642.doc -76- 200838429 為刺激疾病症狀之發作,再次將植物轉移至潮濕室中歷時 24小時。接著視覺評估較低葉片表面上之真菌侵襲程度, 以害病葉片面積之%計。 類似於實例1進行評估。 表4 A -個別活性化合物
編號 活性化合物 活性化合物在喷霧 液中之濃度[ppm] 功效,以佔未經處理 對照組之百分比計 23 對照(未經處理) • (90%感染) 24 表 1,#1-9 4 0 25 表 1,#1-290 16 56 26 4 0 27 亞滅培 16 0 28 α-賽滅寧 63 0 29 氟蟲腈 16 0 30 氰氟蟲胺 16 0 表4B -本發明之來自表4 A之活性化合物的混合物 編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 31 表1,#1-9+氟蟲腈 4+16 ppm 1:4 22 0 32 表1,#1-9+氰氟蟲胺 4+16 ppm 1:4 22 0 33 表1,# 1-290+亞滅培 4+16 ppm 1:4 22 0 34 表1,# I-290+α-賽滅寧 16+63 ppm 1:4 83 56 微量測試 128642.doc •77· 200838429 使用實例5 -在微量滴定測試中對抗晚疫病病原體番茄晚 疫病菌之活性 製備10000 mg a.iVl 1 DMSO。將儲備溶液移取於微量滴 定盤(MTP)上且使用真菌的基於豌豆汁之水性營養培養基 稀釋,並在第二步驟中用番茄晚疫病菌之水性遊動孢子懸 浮液稀釋至規定活性化合物濃度。將培養盤置於溫度為18 °C的充滿水蒸氣之室中。在接種後第7天,使用吸收光度 計在405 nm下量測MTP。
將所量測之參數與不含活性化合物之對照型式的生長以 及不含真菌及活性化合物之空白值進行比較以確定相對生 長率,以個別活性化合物中病原體之%表示。 類似於實例1進行評估。 表5 A -個別活性化合物
128642.doc -78- 200838429
編號 活性化合物 活性化合物在喷霧液 中之濃度[ppm] 功效,以佔未經處理 對照組之百分比計 50 加保扶 16 12 51 4 8 52 1 6 53 可尼丁 16 11 54 4 2 55 1 2 56 A.23-1 16 15 57 4 15 58 1 10 59 氰氟蟲胺 16 12 60 4 6 表5B-本發明之來自表5 A之活性化合物的混合物 編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 61 表卜 #Ι-9+Α·23-1 1+4 ppm 1:4 91 69 62 表1,#1-110+氟蟲腈 1+4 ppm 1:4 92 22 63 表1,#1-110+益達胺 1+4 ppm 1:4 94 13 64 表1,#1-110+亞滅培 1+4 ppm 1:4 96 14 65 表1,#Ι-110+α-賽滅寧 1+4 ppm 1:4 93 14 66 表1,#1-110+加保扶 1+4 ppm 1:4 96 15 128642.doc -79- 200838429
編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 67 表1,#1-110+可尼丁 1+4 ppm 1:4 93 10 68 表1,#Μ10+Α·23·1 1+4 ppm 1:4 96 21 69 表1,#1-110+氰氟蟲胺 1+4 ppm 1:4 93 13 70 表1,#1-113+氟蟲腈 4+16 ppm 1:4 96 28 71 表1,#1-113+益達胺 4+16 ppm 1:4 78 21 72 表1,#1-113+亞滅培 4+16 ppm 1:4 85 19 73 表卜#Ι-113+α-賽滅寧 4+16 ppm 1:4 92 19 74 表1,#1-113+加保扶 4+16 ppm 1:4 84 22 75 表1,#1-113+可尼丁 4+16 ppm 1:4 84 21 76 表1,#Ι-113+Α·23-1 4+16 ppm 1:4 99 24 77 表1,#1-113+氰氟蟲胺 4+16 ppm 1:4 71 22 78 表1,# 1-245+氟蟲腈 0.25+1 ppm 1:4 67 10 128642.doc -80 - 200838429 編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 79 表1,#Ι·245+益達胺 0.25+1 ppm 1:4 48 14 80 表1,#Ι·245+加保扶 0.25+1 ppm 1:4 50 15 81 表1,# 1-245+可尼丁 0.25+1 ppm 1:4 41 12 82 表卜 # I-245+A.23-1 0.25+1 ppm 1:4 54 20 使用實例6 -在微量滴定測試中對抗小麥殼針孢菌之活性 製備10000 mg a.i./l 1 DMSO。將儲備溶液移取於微量滴 定盤(MTP)上且使用真菌的基於生物麥芽之水性營養培養 基稀釋,並在第二步驟中用小麥殼針孢菌之水性遊動孢子 懸浮液稀釋至規定活性化合物濃度。將培養盤置於溫度為 18°C的充滿水蒸氣之室中。在接種後第7天,使用吸收光 度計在405 nm下量測MTP。 將所量測之參數與不含活性化合物之對照型式的生長以 及不含真菌及活性化合物之空白值進行比較以確定相對生 長率,以個別活性化合物中病原體之%表示。 類似於實例1進行評估。 128642.doc -81- 200838429
表6 A -個別活性化合物 編號 活性化合物 活性化合物在喷霧 液中之濃度[ppm] 功效,以佔未經處理 對照組之百分比計 83 表1,#1-9 16 12 84 表1,#1-245 16 4 85 (X-赛滅寧 63 9 86 氰氟蟲胺 63 0 表6B -本發明之來自表6 A之活性化合物的混合物 編號 活性化合物之混合物 濃度 混合比 觀測功效 計算功效* 87 表1,#1-9+氰氟蟲胺 16+63 ppm 1:4 39 12 88 表1,# I-245+α-賽滅寧 6+63 ppm 1:4 37 13 89 表1,# 1-245+氰氟蟲胺 6+63 ppm 1:4 36 4 測試結果展示由於增效作用,與使用Colby氏公式所預 測相比,本發明之混合物顯著更為有效。 128642.doc -82-
Claims (1)
- 200838429 十、申請專利範圍: 1 · 種農藥混合物,其包含 a)至少一種式1之唑并嘧啶胺:其中各取代基係如下定義: R gc3-c12烧基、(VC12烯基、c5-C12烧氧基烧基、c3- • C6環烧基、苯基或苯基烷基; R為^(:12烷基、C2-C12烯基、CVC4鹵烷基或(VC4烷 氧基-C1-C4烧基; 其中R1及/或R2中之脂族鏈可經1至4個相同或不同之 Ra基團取代: Ra為鹵素、氰基、羥基、巯基、d-Cw烷基、Cr c10鹵烷基、c3-c_烷基、c2-c10烯基、C2-Ci〇快 基、CVC6烷氧基、Cl-C6烷基硫基、CVC6嫁氧 • 基-CVC6烧基或NRARB ; RA、RB為氫或cvc6烷基; - 其中R1及/或Ra中之環狀基團可經1至4個Rb基團取 代: Rb為鹵素、氰基、羥基、酼基、硝基、NRARB、 烧基、CVC6鹵烷基、C2-C6烯基、C2-C’ 基或Ci_C6烧氧基; R3為氫、鹵素、氰基、nrarb、羥基、酼基、CrC:6 128642.doc 烷基、烷基、c3-c8環烷基、(ν(:6烷氧 基、eve:6统基硫基、C3_C8環烧氧基、C3-C8環烷 基硫基、羧基、曱醯基、Cl_Cl0烷基羰基、Ci_Cl〇 烧氧基戴基、C2_c1G烯氧基羰基、C2_Ci(^氧基羰 基、苯基、苯氧基、苯硫基、苄氧基、苄硫基或 CVC6烷基-s(o)m-; m為0、1或2 ; 為CH或N ; 至少一種化合物II,其係選自以下族群: Α· 1 ·有機(硫代)罐酸酉旨類:歐殺松(acephate)、甲 基 D比 °惡填(azamethiphos)、益棉鱗(azinphos-ethyl) 毅速松(azinphos-methyl)、氯氧填 (chlorethoxyfos)、毒蟲畏(chi〇rfenvinphos)、氯曱 硫磷(chlormephos)、毒死蜱(chl〇rpyrifos)、甲基毒 死蜱(chlorpyrifos-methyl)、場毒填(coumaphos)、 殺模腈(cyanophos)、滅賜松(demeton-S_methyl)、 大利松(diazinon)、敵敵畏(dichlorvos)/DDVP、雙 特松(dicrotophos)、大滅松(dimethoate)、甲基毒蟲 畏(dimethylvinphos)、乙拌石粦(disulfoton)、EPN、 乙硫填(ethion)、普伏松(ethoprophos)、伐滅麟 (famphur)、苯線填(fenamiphos)、殺填硫鱗 (fenitrothion)、倍硫鱗(fenthion)、吼 It 硫填 (flupyrazophos)、福賽絕(fosthiazate)、飛達松 200838429(heptenophos)、異 σ惡唆麟(isoxathion)、馬拉松 (malathion)、滅加松(mecarbam)、甲胺雄 (methamidophos)、滅大松(methidathion)、速滅填 (mevinphos)、久效填(monocrotophos)、二漠填 (naled)、氧樂果(omethoate)、滅多松(oxydemeton-methyl)、對硫碟(parathion)、甲基對硫鱗 (parathion-methyl)、賽達松(phenthoate)、甲拌構 (phorate)、伏殺填(phosalone)、亞胺硫石粦 (phosmet)、鱗胺(phosphamidon)、巴賽松 (phoxim)、亞特松(pirimiphos-methyl)、丙溴石粦 (profenofos)、撲達松(propetamphos)、丙硫碌 (prothiofos)、白克松(pyraclofos)、必芬松 (pyridaphenthion) ' 拜裕松(quinalphos)、硫特普 (sulfotep)、丁 續硫麟(tebupirimfos)、亞培松 (temephos)、託福松(terbufos)、殺蟲畏 (tetrachlorvinphos)、硫滅松(thiometon)、三落松 (triazophos)、三氯松(trichlorfon)、繁米松 (vamidothion); A·2·胺基甲酸酯類:得滅克(aldicarb) '阿蘭克 (alanycarb)、免敵克(bendiocarb)、免扶克 (benfuracarb)、丁酮威(butocarboxim)、丁 g同石風威 (butoxycarboxim)、加保利(carbaryl)、加保扶 (carbofuran)、丁基加保扶(carbosulfan)、乙硫苯威 (ethiofencarb)、丁基滅必乱(fenobucarb)、覆滅蜗 128642.doc 200838429 (formetanate)、夫硫克(furathiocarb)、滅必風 (isoprocarb)、滅賜克(methiocarb)、納乃得 (methomyl)、治滅乱(metolcarb)、歐殺滅 (oxamyl)、比力tr 普(pirimicarb)、安丹(propoxur)、 硫地克(thiodicarb)、久效威(thiofanox)、混殺威 (trimethacarb)、XMC、滅殺威(xylylcarb)、嗤財威 (triazamate);Α·3·擬除蟲菊酯類(Pyrethroid): 阿納寧 (acrinathrin)、亞列寧(allethrin)、d-順反式亞列 寧、d-反式亞列寧、畢芬寧(bifenthrin)、百亞列寧 (bioallethrin)、S-環戊烯基百亞列寧(bioallethrin S-cylclopentenyl)、百列滅寧(bioresmethrin)、乙氰菊 酯(cycloprothrin)、賽扶寧(cyfluthrin)、β-賽扶寧 (betacyHuthrin)、賽洛寧(cyhalothrin)、λ-賽洛寧 (lambda-cyhalothrin)、γ_賽洛寧(gamma-cyhalothrin) 、賽滅寧(cypermethrin)、α·賽滅寧、β-賽滅寧、Θ-賽滅寧、ζ-赛滅寧、赛齡寧(cyphenothrin)、第滅寧 (deltamethrin)、益避寧(empenthrin)、益化利 (esfenvalerate)、依芬寧(etofenprox)、芬普寧 (fenpropathrin) > 芬化利(fenvalerate)、護賽寧 (flucythrinate)、氣氯苯菊 1旨(flumethrin)、r -福化 利(tau-fluvalinate)、合芬寧(halfenprox)、依普寧 (imiprothrin)、百滅寧(permethrin)、盼 丁滅乱 (phenothrin)、普亞列寧(prallethrin)、異列滅寧 128642.doc (resmethdn)、RU 15525、西拉福芬(silafluofen)、 七氟 酉旨(tefluthrin)、胺菊 g旨(tetraniethrin)、泰滅 争(tralomethrin)、四氟苯菊醋(transfiuthrin)、ZXI 8901 ; Α·4.保幼激素擬似物:烯蟲乙醋(hydroprene)、烯 蟲炔酯(kinoprene)、美賜年(methoprene)、芬諾克 (fenoxycarb)、百利普芬(pyriproxyfen); A.5·菸鹼受體促效劑/拮抗劑化合物:亞滅培 (acetamiprid)、免速達(bensuhap)、培丹鹽酸鹽 (cartap hydrochloride)、可尼丁(clothianidin)、呋 蟲胺(dinotefuran)、益達胺(imidacloprid)、噻蟲嗪 (thiamethoxam)、烯啶蟲胺(nitenpyram)、菸鹼、賜 諾殺(spinosad)(別位促效劑)、售蟲琳(thiacloprid)、 殺蟲環(thiocyclam)、殺蟲雙(thiosultap-sodium)、 式(Γ1)之噻唑化合物:A.6. GABA門控氯離子通道拮抗劑化合物:可氯丹 (chlordane)、安殺番(endosulfan)、γ-HCH(靈丹 (lindane))、乙酞蟲脂(acetoprole)、乙蟲清(ethiprole) 、氟蟲腈(fipronil)、°比氟普羅(pyrafluprole)、吼普 羅(pyriprole)、凡利普羅(vaniliprole)、5-胺基-1- 200838429 (2,6-二氯-4-三氟甲基-苯基)-4-三氯曱烷亞磺醯基-1H-吡唑_3·硫代碳酸醯胺; Α·7·氯離子通道活化劑:阿巴汀(abamectin)、因 滅汀苯甲酸鹽(emamectin benzoate)、密滅丁 (milbemectin)、樂匹滅汀(lepimectin);Α·8· METI I化合物:啥蜗醚(fenazaquin)、芬普蜗 (fenpyroximate)、,瞒醚(pyrimidifen)、比達本 (pyridaben)、响蜗胺(tebufenpyrad)、♦蟲醯胺 (tolfenpyrad)、啼蟲胺(flufenerim)、魚藤精 (rotenone); Α·9_ METI II 及 III化合物··亞 g昆蜗(acequinocyl)、 氟阿西普(fluacyprim)、伏蟻腙(hydramethylnon); Α·10·氧化填酸化解偶聯劑:蟲蜗腈(chlorfenapyr) 、DNOC ;A. 11 ·氧化構酸化抑制劑:亞環錫(azocyclotin)、 錫瞒丹(cyhexatin)、汰芬隆(diafenthiuron)、苯丁 錫(fenbutatin oxide)、克蜗特(propargite)、得脫蜗 (tetradifon); Α·12·蜆皮破壞劑:賽滅淨(cyromazine)、環轰醯 肼(chromafenozide)、氣蟲醯肼(halofenozide)、甲 氧蟲酸肼(methoxyfenozide)、蟲醢肼(tebufenozide); Α·13·增效劑:增效醚(piperonyl butoxide)、脫葉 填(tribufos); Α·14·鈉離子通道阻斷劑化合物:因得克 128642.doc 200838429 (indoxacarb)、氰敗蟲胺(metaflumizone); Α·15·燻蒸劑:甲基溴、氯化苦(chloropicrin)硫醯 氟; Α· 1 6.選擇性攝食阻斷劑:可羅替(crylotie)、11比財 酮(pymetrozine)、氟唆蟲醯胺(flonicamid); A.17.蜗生長抑制劑:克芬蜗(clofentezine)、合賽 多(hexythiazox)、依殺虫茜(etoxazole);Α· 1 8·甲殼素合成抑制劑:布芬淨(buprofezin)、雙 三氟蟲脲(bistrifluron)、克福隆(chlorfluazuron)、 二福隆(diflubenzuron)、氟環脲(flucycloxuron)、 氟芬隆(flufenoxuron)、六伏隆(hexaflumuron)、祿 芬隆(lufenuron)、諾華隆(novaluron)、多氟脲 (noviflumuron)、得福隆(teflubenzuron)、殺蟲隆 (triflumuron);Α·19·脂質生物合成抑制劑:螺瞒酯(spirodiclofen) 、螺曱虫茜酯(spiromesifen)、螺蟲乙醋(spirotetramat); Α·20.章魚胺促效劑(octapaminergic agonsit) ··三 亞蜗(amitraz); A.21.蘭尼定(ryanodine)受體調節劑··氟蟲醯胺 (flubendiamide); Α·22·各種殺蟲劑:填化铭、醯胺氟美(amidoflumet) 、苯克洛嗔(benclothiaz)、西脫蜗(benzoximate)、 聯苯肼酯(bifenazate)、 侧砂、新殺蜗 (bromopropylate)、氰化物、赛諾 11 比芬(cyenopyrafen) 128642.doc 200838429 、丁氟蜗酉旨(cyflumetofen)、滅蜗猛(chinomethionate) 、大克蜗(dicofol)、氟乙酸鹽、膦、唆蟲丙醚 (pyridalyl)、比氟奎宗(pyrifluquinazon)、硫、吐酒 石(tartar emetic); Α·23· Ν-ΚΛ2,2-二鹵基-1-R”環-丙烷曱醯胺·2-(2,6-二氯-α,α,α-三氟-對曱苯基)腙或N-RL2,2-二(R,,,)丙 酿胺-2-(2,6-二氯-α,α,α·三氟-對甲苯基)-腙,其中 R’為甲基或乙基,鹵基為氣基或溴基,R”為氫或曱 基,且R"’為甲基或乙基; Α·24.丙二腈化合物:CF3(CH2)2C(CN)2CH2(CF2)3CF2H、 cf3(ch2)2c(cn)2ch2(cf2)5cf2h、 CF3(CH2)2C(CN)2(CH2)2C(CF3)2F、 CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3、 CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H、 CF3(CH2)2C(CN)2CH2(CF2)3CF3、 cf3(cf2)2ch2c(cn)2ch2(cf2)3cf2h 及 CF3CF2CH2C(CN)2CH2(CF2)3CF2H ; Α·25·微生物破壞劑:蘇力菌以色列亞種 thuringiensis subsp. /srae/e似/)、球形芽孢桿菌 {Bacillus sphaericus)、篆 tj 議綠澤生後{Bacillus ί/zwrkgk似subsp. 、蘇力菌庫斯塔克亞 種i/zi/rhgz’e 似以 subsp· [wrsia 禽 ζ·)、蘇力菌 擬步行曱亞種(Bac"/⑽ thuringiensis subsp· Tenebrionis) ° 128642.doc 200838429 2.如請求項1之農藥混合物 義: 其中該式I化合物具有以下含 為C3'Cl2院基、C5-Ci2燒氧基炫基、苯基或苯基-Cl· 2 C4燒基’其中苯基可經1至3個Rb基團取代; R為cvc12烧基、Cl_c4齒燒基、Ci-C4烧氧基々 基; r3為氫或nh2。 3. 參 4. 5. 月求項1或2之辰藥混合物,其中該式工化合物係選自由 以:各者組成之群:6_(m苯基)_5m2,4]三 坐并[l’5-a]哺咬_7_基胺、6·^·第三丁基苯基)巧·甲基、 [1,2,4]三唑并[1,5#密啶I基胺、5-甲基-6-(3,5,5-三甲 土己基)_[1,2,4]二口坐并以,%^♦咬_7基胺、%甲基^辛 基[1,2,4]二唾并以,、]响啶_7_基-胺、&甲基巧_辛基-[一1’2’4]二唾开[aa]哺咬1基胺、卜乙基辛基-三嗤并[1,5-十密冬7·基胺、5-乙基冬辛基·Π,2,4]三嗤并 [1,5_a]喷咬I基胺、%乙基-Μ3,5,5-三甲基-己基)· [一1’2’4]二嗤开[Wa]鳴咬^基胺、卜辛基_5_丙基 三唾并[1,5_a]哺咬1基胺、5-甲氧基一甲基冬辛基_ Π,2,4]三唾并[u.a]喷咬基胺、6-辛基_5_三氣甲基-[1,2,4]二唾并[i,5-a]哺咬基胺及5_三氟甲基冬㈡ 三曱基-己基)-[1,2,4]三σ坐并[aa]喷咬:7基胺。 如請求項⑴中任一項之農藥混合物,其中該化合㈣ 係選自由如請求項1之胺基甲酸酯類組成之群。 如請求項4之農藥混合物,纟中該化合物π係選自由加保 128642.doc 200838429 土加保扶及硫地克組成之群。 6.如請求項 #、g6 、中任一項之農藥混合物,其中該化合物π 7二、由如請求項1之擬除盘菊酯類組成之群。 宣、塞胃=辰藥&合物’纟中該化合物11係選自由畢芬 8如试出扶,、赛滅寧、α_賽滅寧及七氟菊酯組成之群。 係;、項1至3中任一項之農藥混合物,其中該化合物11 自由如明求項1之菸鹼受體促效劑/拮抗劑化合物組 成之群。 ^明,項8之農藥混合物,其中該化合物以係選自由亞滅 σ可尼丁、呋蟲胺、益達胺、賜諾殺、噻蟲嗪及噻蟲 啉組成之群。 1(>·如:求項1至3中任一項之農藥混合物,其中該化合物Η 係k自由如請求項iiGABA門控氣離子通道拮抗劑化合 物組成之群。 U·如請求項10之農藥混合物,其中該化合物„為氟蟲腈。 12·如請求項丨至丨丨中任一項之農藥混合物,其包含增效有 效量之式I化合物及化合物Η。 如明求項1至12中任一項之農藥混合物,其包含重量比 為100:1至1·· 100之式I化合物及化合物Η。 14·如請求項1至13中任一項之農藥混合物,其進一步包含 殺真菌劑。 15. —種改良植物健康狀況之方法,其包含依任何所要次 序’同時(亦即聯合或分開)或連續施用有效量之如請求 項1至14中任一項之混合物。 128642.doc -10 - 200838429 16. -㈣制或預防植物、植物部分、種子或其生長位點處 ’、菌仏木的方法’其包含依任何所要次序,同時(亦即 聯合或分開)或連續施用増效有效量之如請求項⑴钟 任一項之混合物。 17. -種控制或預防植物、植物部分、種子或其生長位點處 之有害昆蟲或線蟲的方法’其包含依任何所要次序,同 時(亦即聯合或分開)或連續地施用增效有效量之如請求 項1至14中任一項之混合物。 18. 如請求項15、16或17之方法’其中該如請求項⑴斗之 混合物係以〇.lg/ha至2000 g/ha之量施用。 19. -種保護種子之方法’其包含在播種前及/或在催芽後使 該等種子舆增效有效量之如請求項之混合物接 觸。 2〇·如請求項19之方法,其中該如請求項^之混合物係 以每100 kg種子0.1 g至5 kg之量施用。 21. —種植物繁殖材料,其係經如請求項丨至14之混合物處 理。 22. 如請求項21之植物繁殖材料,其中種子為該繁殖材料。 23. -種種子,其+每100 _子包含〇」g至5 “之量的如 請求項1至14之混合物。 24. —種農藥組合物,其包含液體或固體載劑及如請求項】 至14中任一項之混合物。 25· —種藉由以溶劑及/或載劑補充該等式1之活性化合物及 化合物II來製備如請求項24之組合物的方法。 128642.doc -11- 200838429 七、指定代表圖: (一) 本案指定代表圖為:(無) (二) 本代表圖之元件符號簡單說明: 八、本案若有化學式時,請揭示最能顯示發明特徵的化學式:128642.doc
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| BRPI0806347A2 (pt) | 2007-01-19 | 2011-09-06 | Basf Se | misturas fungicidas, agente fungicida, método para combater fungos nocivos fitopagênicos, semente, e, processo para preparar um agente |
| WO2008092836A2 (en) * | 2007-01-30 | 2008-08-07 | Basf Se | Method for improving plant health |
| EA019915B1 (ru) | 2007-09-20 | 2014-07-30 | Басф Се | Фунгицидная композиция для борьбы с фитопатогенными вредными грибами |
| WO2010043553A1 (en) * | 2008-10-16 | 2010-04-22 | Basf Se | Pesticidal mixtures comprising metaflumizone and a fungicidal compound |
| WO2010043639A2 (en) * | 2008-10-16 | 2010-04-22 | Basf Se | Pesticidal mixtures |
| CN201712857U (zh) | 2010-05-10 | 2011-01-19 | S.C.约翰逊父子公司 | 用于挥发性材料的散发装置及其壳体和散发片 |
| CN102415403B (zh) * | 2010-09-28 | 2013-12-25 | 南京华洲药业有限公司 | 一种含呋虫胺和速灭威的复合杀虫组合物及其用途 |
| EP2460407A1 (de) | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Wirkstoffkombinationen umfassend Pyridylethylbenzamide und weitere Wirkstoffe |
| CN102630693A (zh) * | 2012-03-28 | 2012-08-15 | 联保作物科技有限公司 | 一种杀虫组合物及其制剂和应用 |
| US9205163B2 (en) | 2012-11-27 | 2015-12-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
| US9278151B2 (en) | 2012-11-27 | 2016-03-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
| CN103828821B (zh) * | 2012-11-27 | 2016-01-13 | 陕西汤普森生物科技有限公司 | 一种含唑嘧菌胺与甲氧基丙烯酸酯类的杀菌组合物 |
| CN103250742B (zh) * | 2013-05-23 | 2014-08-06 | 苏州谷力生物科技有限公司 | 一种杀虫剂组合物 |
| KR102377395B1 (ko) * | 2021-11-05 | 2022-03-22 | 주식회사 에스비티제약 | 살충제 및 이를 이용한 해충 구제 방법 |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| 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 |
| DE3130633A1 (de) * | 1981-08-01 | 1983-02-17 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)pyrimidine und diese enthaltende fungizide |
| DE3338292A1 (de) * | 1983-10-21 | 1985-05-02 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)-pyrimidine und diese enthaltende fungizide |
| ATE67493T1 (de) * | 1985-02-04 | 1991-10-15 | Bayer Agrochem Kk | Heterocyclische verbindungen. |
| US5013659A (en) * | 1987-07-27 | 1991-05-07 | E. I. Du Pont De Nemours And Company | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
| KR900003088B1 (ko) * | 1988-03-26 | 1990-05-07 | 재단법인 한국화학연구소 | 5-하이드록시피라졸 유도체 |
| US5180587A (en) * | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
| EP0777964B1 (en) * | 1989-08-30 | 2001-11-14 | Kynoch Agrochemicals (Proprietary) Limited | Preparation of a dosage device |
| ES2091878T3 (es) * | 1990-10-11 | 1996-11-16 | Sumitomo Chemical Co | Composicion plaguicida. |
| FR2684519B1 (fr) * | 1991-12-06 | 1994-01-28 | Rhone Poulenc Agrochimie | Association d'un fongicide de la famille des triazoles et d'imidacloprid. |
| ATE433442T1 (de) * | 1997-04-07 | 2009-06-15 | Nihon Nohyaku Co Ltd | Pyrazolderivate, verfahren zu ihrer herstellung, zwischenprodukte und schädlingsbekämpfungsmittel, das diese als aktiven bestandteil enthält |
| US6277856B1 (en) * | 1998-09-25 | 2001-08-21 | American Cynamid Co. | Fungicidal mixtures |
| US6221890B1 (en) * | 1999-10-21 | 2001-04-24 | Sumitomo Chemical Company Limited | Acaricidal compositions |
| ES2283626T3 (es) * | 2001-07-26 | 2007-11-01 | Basf Aktiengesellschaft | 7-aminotriazolpirimidinas para controlar hongos nocivos. |
| PL1725561T3 (pl) * | 2004-03-10 | 2010-12-31 | Basf Se | 5,6-Dialkilo-7-aminotriazolopirymidyny, sposób ich wytwarzania i ich zastosowanie do zwalczania szkodliwych grzybów oraz środki zawierające te związki |
| WO2005087771A2 (de) * | 2004-03-10 | 2005-09-22 | Basf Aktiengesellschaft | 5,6-dialkyl-7-amino-triazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
| BRPI0508337A (pt) * | 2004-03-10 | 2007-07-24 | Basf Ag | compostos, processos para a preparação dos mesmos, agente fungicida, semente, e, processo para o combate de fungos nocivos fitopatogênicos |
| US20080076785A1 (en) * | 2004-09-28 | 2008-03-27 | Carsten Blettner | 7-Aminomethyl-1,2,4-Triazolo[1,5-A]Pyrimidine Compounds And Their Use For Controlling Pathogenic Fungi |
| BRPI0517432A (pt) * | 2004-12-17 | 2008-10-07 | Basf Ag | composto, uso dos mesmos, agente para combater fungos fitopatogênicos, processo para combater fungos fitopatogênicos, e, semente |
| MX2007008999A (es) * | 2005-02-16 | 2007-09-18 | Basf Ag | 5-alcoxialquil-6-alquil-7-amino-azolopirimidinas, un procedimiento para su obtencion y el uso de las mismas para combatir hongos nocivos, asi como productos que las contienen. |
| DE102005007160A1 (de) * | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| BRPI0607498A2 (pt) * | 2005-03-01 | 2016-11-01 | Basf Ag | compostos, processo para a preparação dos mesmos, agente, semente, e, processo para combater fungos nocivos fitopatogênicos |
| BRPI0607496A2 (pt) * | 2005-03-01 | 2016-11-01 | Basf Ag | compostos, processo para a preparação dos mesmos, agente, semente, e, processo para combater fungos nocivos fitopatogênicos |
| BRPI0607502A2 (pt) * | 2005-03-01 | 2016-11-01 | Basf Ag | compostos processo para a preparação dos mesmos, agente, semente, e, processo para combater fungos nocivos fitopatogênicos |
| TW200714602A (en) * | 2005-03-01 | 2007-04-16 | Basf Ag | 5,6-dialkyl-7-aminoazolopyrimidines, their preparation and their use for controlling harmful fungi, and compositions comprising these compounds |
| EP1876899A2 (de) * | 2005-04-25 | 2008-01-16 | Basf Aktiengesellschaft | Verwendung von 5-alkyl-6-phenylalkyl-7-amino-azolopyrimidinen, neue azolopyrimidine, verfahren zu ihrer herstellung und sie enthaltende mittel |
| AU2006274075A1 (en) * | 2005-07-27 | 2007-02-01 | Basf Se | Fungicide 6-phenyl-triazolopyrimidinyl amines |
| CN101228165A (zh) * | 2005-07-27 | 2008-07-23 | 巴斯福股份公司 | 杀真菌的5-甲基-6-苯基吡唑并嘧啶-7-基胺 |
| JP2009502862A (ja) * | 2005-07-27 | 2009-01-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌剤5−アルキル−6−フェニルピラゾロピリミジン−7−イルアミン |
| US8679514B2 (en) * | 2005-07-27 | 2014-03-25 | Basf Se | Fungicidal mixtures based on azolopyrimidinylamines |
| HRP20141028T1 (hr) * | 2005-08-05 | 2014-12-19 | Basf Se | Fungicidne smjese koje sadrže supstituirane anilide 1-metil-pirazol-4-ilkarboksilne kiseline |
| JP5227950B2 (ja) * | 2006-05-03 | 2013-07-03 | ビーエーエスエフ ソシエタス・ヨーロピア | 種子処理のためのアリールカルボン酸ビフェニルアミドの使用 |
| JP2009542768A (ja) * | 2006-07-13 | 2009-12-03 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌性アゾロピリミジン、それらの製造方法及び有害菌の防除のためのそれらの使用、並びにそれらを含む物質 |
| BRPI0806347A2 (pt) * | 2007-01-19 | 2011-09-06 | Basf Se | misturas fungicidas, agente fungicida, método para combater fungos nocivos fitopagênicos, semente, e, processo para preparar um agente |
| EP1952690A3 (en) * | 2007-01-31 | 2009-04-22 | Basf Se | Pesticidal mixtures based on triazolopyrimidines and insecticides |
-
2008
- 2008-01-18 BR BRPI0806766-0A patent/BRPI0806766A2/pt not_active IP Right Cessation
- 2008-01-18 US US12/523,793 patent/US20100093531A1/en not_active Abandoned
- 2008-01-18 WO PCT/EP2008/050559 patent/WO2008092759A2/en not_active Ceased
- 2008-01-18 CN CN200880003226XA patent/CN101588719B/zh not_active Expired - Fee Related
- 2008-01-18 CA CA002674533A patent/CA2674533A1/en not_active Abandoned
- 2008-01-18 EP EP08701571A patent/EP2114159A2/en not_active Withdrawn
- 2008-01-18 KR KR1020097018014A patent/KR20090105974A/ko not_active Ceased
- 2008-01-18 JP JP2009546719A patent/JP5351047B2/ja not_active Expired - Fee Related
- 2008-01-18 MX MX2009007207A patent/MX2009007207A/es not_active Application Discontinuation
- 2008-01-29 CL CL200800240A patent/CL2008000240A1/es unknown
- 2008-01-29 AR ARP080100363A patent/AR065082A1/es not_active Application Discontinuation
- 2008-01-30 PE PE2008000214A patent/PE20081697A1/es not_active Application Discontinuation
- 2008-01-30 TW TW097103586A patent/TW200838429A/zh unknown
-
2009
- 2009-07-21 CR CR10945A patent/CR10945A/es unknown
- 2009-08-18 EC EC2009009587A patent/ECSP099587A/es unknown
- 2009-08-28 MA MA32180A patent/MA31195B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR20090105974A (ko) | 2009-10-07 |
| BRPI0806766A2 (pt) | 2011-09-13 |
| US20100093531A1 (en) | 2010-04-15 |
| WO2008092759A3 (en) | 2009-01-29 |
| EP2114159A2 (en) | 2009-11-11 |
| JP5351047B2 (ja) | 2013-11-27 |
| PE20081697A1 (es) | 2009-01-25 |
| WO2008092759A2 (en) | 2008-08-07 |
| CL2008000240A1 (es) | 2008-05-30 |
| CR10945A (es) | 2009-09-14 |
| CN101588719B (zh) | 2013-07-17 |
| CA2674533A1 (en) | 2008-08-07 |
| AR065082A1 (es) | 2009-05-13 |
| JP2010516726A (ja) | 2010-05-20 |
| MA31195B1 (fr) | 2010-02-01 |
| ECSP099587A (es) | 2009-09-29 |
| CN101588719A (zh) | 2009-11-25 |
| MX2009007207A (es) | 2009-08-12 |
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