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    Publication numberCA2458163 A1
    Publication typeApplication
    Application numberCA 2458163
    PCT numberPCT/US2002/030302
    Publication date27 Mar 2003
    Filing date10 Sep 2002
    Priority date21 Sep 2001
    Also published asCA2458163C, CN1713819A, CN100539840C, DE60221994D1, DE60221994T2, EP1427285A1, EP1427285B1, US7696232, US8637552, US9173400, US20040209923, US20100152194, US20130031677, US20140141972, WO2003024222A1
    Publication numberCA 2458163, CA 2458163 A1, CA 2458163A1, CA-A1-2458163, CA2458163 A1, CA2458163A1, PCT/2002/30302, PCT/US/2/030302, PCT/US/2/30302, PCT/US/2002/030302, PCT/US/2002/30302, PCT/US2/030302, PCT/US2/30302, PCT/US2002/030302, PCT/US2002/30302, PCT/US2002030302, PCT/US200230302, PCT/US2030302, PCT/US230302
    InventorsRichard Alan Berger, John Lindsey Flexner
    ApplicantE. I. Du Pont De Nemours And Company, Richard Alan Berger, John Lindsey Flexner
    Export CitationBiBTeX, EndNote, RefMan
    External Links: CIPO, Espacenet
    Anthranilamide arthropodicide treatment
    CA 2458163 A1
    Abstract
    This invention pertains to methods for protecting a propagule or a plant grown therefrom from invertebrate pests comprising contacting the propagule or the locus of the propagule with a biologically effective amount of a compound of Formula I: its N-oxide or an agriculturally suitable salt thereof wherein A
    and B and R1 through R8 are as defined in the disclosure. This invention also relates to propagules treated with a compound of Formula I and compositions comprising a Formula I compound for coating propagules.
    Description  available in
    Claims(23)
    1. A method for protecting from a propagule or a plant grown therefrom from an invertebrate pest, comprising:
    contacting the propagule or the locus of the propagule with a biologically effective amount of a compound of Formula I, an N-oxide thereof or an agriculturally suitable salt thereof wherein A and B are independently O or S;
    R1 is H, C1-C6 alkyl, C2-C6 alkoxycarbonyl or C2-C6 alkylcarbonyl;
    R2 is H or C1-C6 alkyl;
    R3 is H; C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, or C3-C6 cycloalkyl, each optionally substituted with one or more substituents selected from the group consisting of halogen, CN, NO2, hydroxy, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyl, C3-C6 trialkylsilyl, phenyl, phenoxy, 5-membered heteroaromatic rings, and 6-membered heteroaromatic rings;
    each phenyl, phenoxy, 5-membered heteroaromatic ring, and 6-membered heteroaromatic ring optionally substituted with one to three substituents independently selected from the group consisting of C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C3-C6 cycloalkyl, C1-C4 haloalkyl, C2-C4 haloalkenyl, C2-C4 haloalkynyl, C3-C6 halocycloalkyl, halogen, CN, NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylamino, C2-C8 dialkylamino, C3-C6 cycloalkylamino, C4-C8 (alkyl)(cycloalkyl)amino, C2-C4 alkylcarbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkylaminocarbonyl, C3-C8 dialkylaminocarbonyl and C3-C6 trialkylsilyl; C1-C4 alkoxy; C1-C4 alkylamino; C2-C8 dialkylamino; C3-C6 cycloalkylamino; C2-C6 alkoxycarbonyl or C2-C6 alkylcarbonyl;

    R4 is H, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, CN, halogen, C1l-C4 alkoxy, C1-C4 haloalkoxy or NO2;
    R5 is H, C1-C6 alkyl, C1-C6 haloalkyl, C1-C4 alkoxyalkyl, C1-C4 hydroxyalkyl, C(O)R10, CO2R10, C(O)NR10R11, halogen, C1-C4 alkoxy, C1-C4 haloalkoxy, NR10R11, N(R11)C(O)R10, N(R11)CO2R10 or S(O)n R12;
    R6 is H, C1-C6 alkyl, C1-C6 haloalkyl, halogen, CN, C1-C4 alkoxy or C1-C4 haloalkoxy;
    R7 is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C2-C6 haloalkenyl, C2-C6 haloalkynyl or C3-C6 halocycloalkyl;
    or R7 is a phenyl ring, a benzyl ring, a 5- or 6-membered heteroaromatic ring, a naphthyl ring system or an aromatic 8-, 9- or 10-membered fused heterobicyclic ring system, each ring or ring system optionally substituted with one to three substituents independently selected from R9;
    R8 is H, C1-C6 alkyl, C1-C6 haloalkyl, halogen, C1-C4 alkoxy or C1-C4 haloalkoxy;
    each R9 is independently C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, C3-C6 cycloalkyl, C1-C4 haloalkyl, C2-C4 haloalkenyl, C2-C4 haloalkynyl, C3-C6 halocycloalkyl, halogen, CN, NO2, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 alkylamino, C2-C8 dialkylamino, C3-C6 cycloalkylamino, C4-C8 (alkyl)(cycloalkyl)amino, C2-C4 alkylcarbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkylaminocarbonyl, C3-C8 dialkylaminocarbonyl or C3-C6 trialkylsilyl;
    R10 is H, C1-C4 alkyl or C1-C4 haloalkyl;
    R11 is H or C1-C4 alkyl;
    R12 is C1-C4 alkyl or C1-C4 haloalkyl; and n is 0, 1 or 2.
    2. The method of Claim 1 wherein A and B are both O;
    R7 is a phenyl ring or a 5- or 6-membered heteroaromatic ring selected from the group consisting of each ring optionally substituted with one to three substituents independently selected from R9;
    Q is O, S, NH or NR9;

    W, X, Y and Z are independently N, CH or CR9, provided that in J-3 and J-4 at least one of W, X, Y or Z is N.
    3. The method of Claim 2 wherein R1, R2 and R8 are all H;
    R3 is C1-C4 alkyl optionally substituted with halogen, CN, OCH3 or S(O)n CH3;
    R4 group is attached at position 2;
    R4 is CH3, CF3, OCF3, OCHF2, CN or halogen;
    R5 is H, CH3 or halogen;
    R6 is CH3, CF3 or halogen;
    R7 is phenyl or 2-pyridinyl, each optionally substituted; and p is 0, 1 or 2.
    4. The method of Claim 3 wherein R3 is C1-C4 alkyl and R6 is CF3.
    5. The method of Claim 3 wherein R3 is C1-C4 alkyl and R6 is Cl or Br.
    6. A propagule contacted with a biologically effective amount of a compound of Formula I according to Claim 1, an N-oxide thereof or an agriculturally suitable salt thereof.
    7. The propagule according to Claim 6 which is a seed.
    8. The propagule of Claim 7 which is a seed of wheat, durum wheat, barley, oat, rye, maize, sorghum, rice, wild rice, cotton, flax, sunflower, soybean, garden bean, lima bean, broad bean, garden pea, peanut, alfalfa, beet, garden lettuce, rapeseed, cole crop, turnip, leaf mustard, black mustard, tomato, potato, pepper, eggplant, tobacco, cucumber, muskmelon, watermelon, squash, carrot, zinnia, cosmos, chrysanthemum, sweet scabious, snapdragon, gerbera, babys-breath, statice, blazing star, lisianthus, yarrow, marigold, pansy, impatiens, petunia, geranium or coleus.
    9. The propagule of Claim 8 which is a seed of cotton, maize, soybean or rice.
    10. The propagule of Claim 6 which is a rhizome, tuber, bulb or corm, or viable division thereof.
    11. The propagule of Claim 10 which is a rhizome, tuber, bulb or corm, or viable division thereof, of potato, sweet potato, yam, garden onion, tulip, gladiolus, lily, narcissus, dahlia, iris, crocus, anemone, hyacinth, grape-hyacinth, freesia, ornamental onion, wood-sorrel, squill, cyclamen, glory-of the-snow, striped squill, calla lily, gloxinia or tuberous begonia.
    12. The propagule of Claim 11 which is a rhizome, tuber, bulb or corm, or viable division thereof, of potato, sweet potato, garden onion, tulip, daffodil, crocus or hyacinth.
    13. The propagule of Claim 6 which is a stem or leaf cutting.
    14. The propagule of Claim 6 coated with a composition comprising (1) a biologically effective amount of a compound of Formula I, an N-oxide thereof or an agriculturally suitable salt thereof, and (2) a film former or adhesive agent.
    15. A propagule comprising a biologically effective amount of a compound of Formula I according to Claim 1, an N oxide thereof or an agriculturally suitable salt thereof.
    16. An invertebrate pest control composition for coating a propagule, the composition comprising (1) a biologically effective amount of a compound of Formula I
    according to Claim 1, an N-oxide thereof or an agriculturally suitable salt thereof, and (2) a film former or adhesive agent.
    17. The composition according to Claim 16 wherein the film former or adhesive agent is selected from the group consisting of polyvinyl acetates, polyvinyl acetate copolymers, hydrolyzed polyvinyl acetates, polyvinylpyrrolidone-vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers, polyvinyl methyl ether, polyvinyl methyl ether-maleic anhydride copolymer, waxes, latex polymers, celluloses including ethylcelluloses and methylcelluloses, hydroxymethylcelluloses, hydroxypropylcellulose, hydroxymethylpropylcelluloses, polyvinylpyrrolidones, alginates, dextrins, malto-dextrins, polysaccharides, fats, oils, proteins, karaya gum, jaguar gum, tragacanth gum, polysaccharide gums, mucilage, gum arabics, shellacs, vinylidene chloride polymers and copolymers, lignosulfonates, acrylic copolymers, starches, polyvinylacrylates, zeros, gelatin, carboxymethylcellulose, chitosan, polyethylene oxide, acrylimide polymers and copolymers, polyhydroxyethyl acrylate, methylacrylimide monomers, alginate, ethylcellulose, polychloroprene and syrups or mixtures thereof.
    18. The composition according to Claim 17 wherein the film former or adhesive agent is selected from polymers and copolymers of vinyl acetate, polyvinylpyrrolidone-vinyl acetate copolymer and water-soluble waxes.
    19. The composition according to Claim 16 further comprising an effective amount of at least one additional biologically active compound or agent.
    20. The composition according to Claim 19 wherein at least one additional biologically active compound or agent is selected from arthropodicides of the group consisting of pyrethroids, carbamates, neonicotinoids, neuronal sodium channel blockers, insecticidal macrocyclic lactones, .gamma.-aminobutyric acid (GABA) antagonists, insecticidal areas and juvenile hormone mimics.
    21. The composition according to Claim 19 wherein at least one additional biologically active compound or agent is selected from the group consisting of abamectin, acephate, acetamiprid, amidoflumet (S-1955), avermectin, azadirachtin, azinphos-methyl, bifenthrin, binfenazate, buprofezin, carbofuran, chlorfenapyr, chlorfluazuron, chlorpyrifos, chlorpyrifos-methyl, chromafenozide, clothianidin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, cypermethrin, cyromazine, deltamethrin, diafenthiuron, diazinon, diflubenzuron, dimethoate, diofenolan, emamectin, endosulfan, esfenvalerate, ethiprole, fenothicarb, fenoxycarb, fenpropathrin, fenproximate, fenvalerate, fipronil, flonicamid, flucythrinate, tau-fluvalinate, flufenerim (UR-50701), flufenoxuron, fonophos, halofenozide, hexaflumuron, imidacloprid, indoxacarb, isofenphos, lufenuron, malathion, metaldehyde, methamidophos, methidathion, methomyl, methoprene, methoxychlor, monocrotophos, methoxyfenozide, nithiazin, novaluron, noviflumuron (XDE-007), oxamyl, parathion, parathion-methyl, permethrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb, profenofos, pymetrozine, pyridalyl, pyriproxyfen, rotenone, spinosad, spiromesifin (BSN
    2060), sulprofos, tebufenozide, teflubenzuron, tefluthrin, terbufos, tetrachlorvinphos, thiacloprid, thiamethoxam, thiodicarb, thiosultap-sodium, tralomethrin, trichlorfon and triflumuron, aldicarb, oxamyl, fenamiphos, amitraz, chinomethionat, chlorobenzilate, cyhexatin, dicofol, dienochlor, etoxazole, fenazaquin, fenbutatin oxide, fenpropathrin, fenpyroximate, hexythiazox, propargite, pyridaben, tebufenpyrad; and biological agents such as Bacillus thuringiensis including ssp. aizawai and kurstaki, Bacillus thuringiensis delta endotoxin, baculovirus, and entomopathogenic bacteria, virus and fungi.
    22. The composition according to Claim 19 wherein at least one additional biologically active compound or agent is selected from fungicides of the group consisting of acibenzolar, azoxystrobin, benomyl, blasticidin-S, Bordeaux mixture (tribasic copper sulfate), bromuconazole, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, copper oxychloride, copper salts, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, (S)-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-4-methylbenzamide (RH 7281), diclocymet (S-2900), diclomezine, dicloran, difenoconazole, (S)-3,5-dihydro-5-methyl-2-(methylthio)-5-phenyl-3-(phenylamino)-4H-imidazol-4-one (RP 407213), dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dodine, edifenphos, epoxiconazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fencaramid (SZX0722), fenpiclonil, fenpropidin, fenpropimorph, fentin acetate, fentin hydroxide, fluazinam, fludioxonil, flumetover (RPA 403397), flumorf/flumorlin (SYP-L190), fluoxastrobin (HEC
    5725), fluquinconazole, flusilazole, flutolanil, flutriafol, folpet, fosetyl-aluminum, furalaxyl, furametapyr (S-82658), hexaconazole, ipconazole, iprobenfos, iprodione, isoprothiolane, kasugamycin, kresoxim-methyl, mancozeb, maneb, mefenoxam, mepronil, metalaxyl, metconazole, metominostrobin/fenominostrobin (SSF-126), metrafenone (AC
    375839), myclobutanil, neo-asozin (ferric methanearsonate), nicobifen (BAS 510), orysastrobin, oxadixyl, penconazole, pencycuron, probenazole, prochloraz, propamocarb, propiconazole, proquinazid (DPX-KQ926), prothioconazole (JAU 6476), pyrifenox, pyraclostrobin, pyrimethanil, pyroquilon, quinoxyfen, spiroxamine, sulfur, tebuconazole, tetraconazole, thiabendazole, thifluzamide, thiophanate-methyl, thiram, tiadinil, triadimefon, triadimenol, tricyclazole, trifloxystrobin, triticonazole, validamycin and vinclozolin.
    23. The composition according to Claim 19 wherein at least one additional biologically active compound or agent is selected from fungicides in the group consisting of thiram, maneb, mancozeb and captan.
    Classifications
    International ClassificationA01N43/56, A01N25/12, A01N43/40, A01N25/04, A01N25/14, A01P7/00
    Cooperative ClassificationA01N43/54, A01N43/86, A01N43/58, A01N43/56
    European ClassificationA01N43/56
    Legal Events
    DateCodeEventDescription
    29 Aug 2006EEERExamination request