Synergistic fungicidal mixtures for fungal control in cereals

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SYNERGISTIC FUNGICIDAL MIXTURES FOR FUNGAL CONTROL IN CEREALS

Cross Reference to Related Applications j β

[0001] This application claims the benefit of U.S, Provisional Patent Application A

Serial No. 61/249479, filed October 07, 2009. g

Field of the Invention [0002] This invention concerns a synergistic fungicidal composition containing (a) a : compound of Formula 1, Π, III, IV or V and (b) at least one fungicide selected from the group consisting of epoxiconazole, prothioconazole, azoxystrobin, pyraclostrobin, penthiopyrad, |g

isopyrazam, bixafen, boscalid, prochloraz, and chlorothalonil. T

Background of the Invention

[0003] Fungicides are compounds, of natural or synthetic origin, which act to protect T plants against damage caused by fungi. Current methods of agriculture rely heavily on the use of fungicides. In fact, some crops cannot be grown usefully without the use of fungicides.

Using fungicides allows a grower to increase the yield and the quality of the crop, and

consequently, increase the value of the crop. In most situations, the increase in value of the T crop is worth at least three times the cost of the use of the fungicide.

[0004] However, no one fungicide is useful in all situations and repeated usage of a single fungicide frequently leads to the development of resistance to that and related fungicides. Consequently, research is being conducted to produce fungicides and combinations of fungicides that are safer, that have better performance, that require lower dosages, that are easier to use, and that cost less. λ [0005] Synergism occurs when the activity of two or more compounds exceeds the activities of the compounds when used alone.

Summary of the Invention 1 WO 2011/044213 PCT/US2010/051598 [0006] It is an object of this invention to provide synergistic compositions comprising fungicidal compounds. It is a further object of this invention to provide processes that use these synergistic compositions. The synergistic compositions are capable of preventing or curing, or both, diseases caused by fungi of the classes Ascomycetes and Basidiomycetes. In addition, the synergistic compositions have improved efficacy against the Ascomycete and Basidiomycete pathogens, including leaf blotch and brown rust of wheat. In accordance with this invention, synergistic compositions are provided along with methods for their use.

[0007]

Detailed Description of the Invention [0008] The present invention concerns a synergistic fungicidal mixture comprising an fungi cidally effective amount of (a) a compound of Formula I, II, III, IV or V, and (b) at least one fungicide selected from the group consisting of epoxiconazole, prothioconazole, azoxystrobin, pyraclostrobin, penthiopyrad, isopyrazam, bixafen, boscalid, prochloraz and chlorothalonil. O.x ί

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IV 3 WO 2011/044213 PCT/US2010/051598

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[0009] Azoxystrobin is the common name for methyl (a£r)-2-[[6-(2-cyanophenoxy)- 4-pyrimidinyl]oxy]-a-(methoxymethylene)benzeneacetate. Its fungicidal activity is described in The Pesticide Manual, Fourteenth Edition, 2006, Azoxystrobin controls a variety of pathogens at application rates between 100 and 375 grams/hectare (g/ha).

[0010] Bixafen is the common name for 7V-(3',4'-dichloro-5-fluoro[l,l'-biphenyl]-2- yl)-3-(difluoromethy 1)-1 -methyl-1 if-pyrazole-4-carboxamide, Bixafen controls a variety of pathogens such as Septoria trilici and rust.

[0011] Boscalid is the common name for 2-chloro-/V-(4’-chIorobiphenyl-2- yl)nicotinamide. Its fungicidal activity is described in The Pesticide Manual, Fifteenth Edition, 2009. Boscalid provides control of powdery mildews, Alternaria, Botrytis, Sclerotinia, Mycoshpaerella and Monilinia on fruit, turf, cereals, rape, peanuts and potatoes.

[0012] Chlorothalonil is the common name for telrachlorisophthalonitrile. Its fungicidal activity is described in The Pesticide Manual, Fifteenth Edition, 2009, Chlorothalonil controls a wide variety of pathogens at application rates between 1000 to 2500 g/ha, [0013] Epoxiconazole is the common name for reZ-l-[[(2R,35)-3-(2-chlorophenyl)-2- (4-fluorophenyl)oxiranyl]methyl]-lff-l,2,4-triazole. Its fungicidal activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Epoxiconazole provides broad-spectrum 4

·· - ·%Ί.·:χ .,.ν- — X ·, · X WO 2011/044213 PCT/US2010/051598 fungicidal control, with preventative and curative action, of diseases caused by Ascomycetes, Basidiomycetes and Deuteromycetes in cereals and sugar beet.

[0014] Isopyrazam is the common name for 3-(difluoromethyl) -1 -methyl-A-[1,2,3,4- tetrahydro-9-(l-methylethyl)-l,4-niethanonaphthalen-5-yl]-l//-pyrazole-4-carboxainidc. Its fungicidal activity is described in The Pesticide Manual, Fifteenth Edition, 2009. Isopyrazam provides control of Septoria and rusts in wheat, as well as Ramularia in barley.

[0015] Penthiopyrad is the common name for#-(2-(1,3-dimethylbutyl)-3-thienyl]-l- methyl-3-(trifluoromethyl)-lH-pyrazole-4-carboxamide. Its fungicidal activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Penthiopyrad provides control of rust and Rhizoctonia diseases, as well as grey mold, powdery mildew and apple scab.

[0016] Prochloraz is the common name for #-propyl-7V-[2,4,6- trichlorophenyoxy)ethyl]imidazole-l-carboxamide. Its fungicidal activity is described in The Pesticide Manual, Fifteenth Edition, 2009. Prochloraz provides control against a wide variety of pathogens at application rates between 400 to 600 g a.i./ha.

[0017] Prothioconazole is the common name for 2-[2-(l-chlorocyclopropyl).-3-(2- chlorophenyl)-2-hydroxypropyl]-l,2-dihydro-3H-1,2,4-triazole-3-thione. Its fungicidal activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Prothioconazole is used for control of diseases such as eyespot, Fusarium ear blight, leaf blotch, rust and powdery mildew by foliar application in wheat, barley and other crops.

[0018] Pyraclostrobin is the common name for methyl [2-[[[l-(4-chioropheny 1)-177- pyrazol~3-yl]oxy]methyl]phenyl]methoxycarbamate. Its fungicidal activity is described in The Pesticide Manual, Fourteenth Edition, 2006. Pyraclostrobin controls major plant pathogens, such as Septoria tritici, Puccinia spp., Drechslera tritici-repentis and Pyrenophora teres in cereals, [0019] In the composition of this invention, the weight ratio of the compounds of

Formula I-V to epoxiconazole at which the fungicidal effect is synergistic lies within the range of between about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to prothioconazole at which the fungicidal effect is synergistic lies within the range of between about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to azoxystrobin at which the fungicidal effect is synergistic lies within the range of between 5 &lt; Z - A ,.. W:- L AlZ z- ' -- WO 2011/044213 PCT/US2010/051598 about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to pyraclostrobin at which the fungicidal effect is synergistic lies within the range of between about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to penthiopyrad at which the fungicidal effect is synergistic lies within the range of between about 1:10 and about 10:1. The weight ratio of the compound of Formula I to isopyrazam at which the fungicidal effect is synergistic lies within the range of between abouL 1:10 and about 10:1. The weight ratio of the compound of Formula I to bixafen at which the fungicidal effect is synergistic lies within the range of between about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to boscalid at which the fungicidal effect is synergistic lies within the range of between about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to prochloraz at which the fungicidal effect is synergistic lies within die range of between about 1:10 and about 10:1. The weight ratio of the compounds of Formula I-V to chlorothalonil at which the fungicidal effect is synergistic lies within the range of between about 1:50 and 1:1.

[0020] The rate at which the synergistic composition is applied will depend upon the particular type of fungus to be controlled, the degree of control required and the timing and method of application, In general, the composition of the invention, can be applied at an application rate of between about 65 grams per hectare (g/ha) and about 2300 g/ha based on the total amount of active ingredients in the composition. Epoxiconazole is applied at a rate between about 30 g/ha and about 125 g/ha and the compound of Formula FV is applied at a rate between about 35 g/ha and about 300 g/ha. Prothioconazole is applied at a rate between about 50 g/ha and about 200 g/ha and the compound of Formula I-V is applied at a rate between about 35 g/ha and about 300 g/ha. Azoxystrobin is applied at a.rate between about 50 g/ha and about 250 g/ha and the compound of Formula I-V is applied at a rate between about 35 g/ha and about 300 g/ha. Pyraclostrobin is applied at a rate between about 50 g/ha and about 250 g/ha and the compound of Formula I-V is applied at a rate between about 35 g/ha and about 300 g/ha. Penthiopyrad is applied at a rate between about 50 g/ha and about 300 g/ha and the compound of Formula I-V is applied at a rate between about 35 g/ha and about 300 g/ha. Isopyrazam is applied at a rate between about 30 g/ha and about 125 g/ha and the compound of Formula I is applied at a rate between about 35 g/ha and about 300 g/ha Bixafen is applied at a rate between about 30 g/ha and about 125 g/ha and the compound of Formula I is applied at a rate between about 35 g/ha and about 300 g/ha. Boscalid is applied at a rate between about 50 g/ha and about 350 g/ha and the compound of Formula I-V is 6 is? ·- -UX"- U -/'··?/.,.. .-..w WO 2011/044213 PCT/US2010/051598 applied at a rate between about 35 g/ha and about 300 g/ha. Prochloraz is applied at a rate between about 50 g/ha and about 450 g/ha and the compound of Formula I-V is applied at a rate between about 35 g/ha and about 300 g/ha. Chlorothalonil is applied at a rate between about 100 g/ha and about 2000 g/ha and the compound of Formula I-V is applied at a rate between about 35 g/ha and about 300 g/ha.

[0021] The components of the synergistic mixture of the present invention can be applied either separately or as part of a multipart fungicidal system.

[0022] The synergistic mixture of the present invention can be applied in conjunction with one or more other fungicides to control a wider variety of undesirable diseases. When used in conjunction with other fungicide(s), the presently claimed compounds may be formulated with the other fungicide(s), tank mixed with the other fungicide(s) or applied sequentially with the other fungicide(s). Such other fungicides may include 2-(thiocyanatomethylthio)-benzothiazole, 2-phenylphenol, 8-hydroxyquinoline sulfate, ametoctradin, amisulbrom, antimycin, Ampelomyces quisqualis, azaconazole, azoxystrobin, Bacillus subtilis, Bacillus subtilis strain QST713, benalaxyl, benomyl, ben thiavali carb -isopropyl, benzyl aminobenzene-sulfonate (BABS) salt, bicarbonates, biphenyl, bismerthiazol, bitertanol, bixafen, blasticidin-S, borax, Bordeaux mixture, boscalid, bromuconazole, bupirimate, calcium polysulfide, captafol, captan, carbendazim, carboxin, carpropamid, carvone, chlazafenone, chloroneb, chlorothalonil, chlozolinate, Coniothyrium minitans, copper hydroxide, copper octanoate, copper oxychloride, copper sulfate, copper sulfate (tribasic), cuprous oxide, cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dazomet, debacarb, diammonium ethylenebis-(dithiocarbamate), dichlofiuanid, dichlorophen, diclocymet, diclomezine, dichloran, diethofencarb, difenoeonazole, difenzoquat ion, diflumetorim, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinobuton, dinocap, diphenylamine, dithianon, dodemorph, dodemorph acetate, dodine, dodine free base, edifenphos, enestrobin, enestroburin, epoxiconazole, ethaboxam, ethoxyquin, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil, fenpiclonil, fenpropidin, feiipropimorph, fenpyrazamine, fentin, fentin acetate, fentin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, flumorph, fluopicolide, fluopyram, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil, flutolanil, flutriafol, fluxapyroxad, folpet, formaldehyde, fosetyl, fosetyl-aluminium, fuberidazole, furalaxyl, furametpyr, guazatine, guazatine acetates, GY’81, 7 WO 2011/044213 PCT/US2010/051598 hexachlorobenzene, hexaconazole, hymexazol, imazalil, imazalil sulfate, imibenconazole, iminoctadine, iminoctadine triacetate, iminoctadine tris(albesilate), iodocarb, ipconazole, ipfenpyrazolone, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isopyrazam, isotianil, kasugamycin, kasugamycin hydrochloride hydrate, kresoxim-methyl, laminarin, mancopper, mancozeb, mandipropamid, maneb, mefenoxam, mepanipyrim, mepronil, meptyl-dinocap, mercuric chloride, mercuric oxide, mercurous chloride, metalaxyl, metalaxyl-M, metam, metarn-ammonium, metam-potassium, metam-sodium, metconazole, methasulfocarb, methyl iodide, methyl isothiocyanate, metiram, metominostrobin, metrafenone, mildiomycin, myclobutanil, nabam, nitrothal-isopropyl, nuarimol, octhilinone, ofurace, oleic acid (fatty acids), oiysastrobin, oxadixyl, oxine-copper, oxpoconazole fumarate, oxycarboxin, pefurazoate, penconazole, pencycuron, penflufen, pentachlorophenol, pentachlorophenyl laurate, penthiopyrad, phenylmercury acetate, phosphonic acid, phthalide, picoxystrobin, polyoxin B, polyoxins, polyoxorim, potassium bicarbonate, potassium hydroxyquinoline sulfate, probenazole, prochloraz, procymidone, propamocarb, propamocarb hydrochloride, propiconazole, propineb, proquinazid, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrazophos, pyribencarb, pyributicarb, pyrifenox, pyrimethanil, pyriofenone, pyroquilon, quinoclamine, quinoxyfen, quintozene, Reynoutria sachalinensis extract, sedaxane, silthiofam, simeconazole, sodium 2-phenylphenoxide, sodium bicarbonate, sodium pentachlorophenoxide, spiroxamine, sulfur, SYP-Z048, tar oils, tebuconazole, tebufloquin, tecnazene, tetraconazole, thiabendazole, thifluzamide, thiophanate-methyl, thiram, tiadinil, tolclofos-methyl, Colylfluanid, triadimefon, triadimenol, triazoxide, tricyclazole, tridemorph, trifloxystrobin, trifiumizole, triforine, triticonazole, validamycin, valifenalate, valiphenal, vinclozolin, zineb, ziram, zoxamide, Candida oleophila, Fusarium oxysporum, Gliocladium spp., Phlebiopsis gigantea, Streptomyces griseoviridis, Trichoderma spp., (RS)-N~G>,5-dichlorophenyl)-2-(methoxymethyl)-succinimide, 1,2-di chloropropane, 1,3-dichloro-l, 1,3,3-tetrafluoroacetone hydrate, l-chloro-2,4-dinitronaphthalene, l-chloro-2-nitropropane, 2-(2-heptadecyl-2-imidazolin-l-yI)ethanol, 2,3-dihydro-5-phenyl-l,4-dithi-ine 1,1,4,4-tetraoxide, 2-methoxyethylmercury acetate, 2-methoxyethylmercury chloride, 2-methoxyethylmercury silicate, 3-(4-chlorophenyl)-5-methylrhodanine, 4-(2-nitroprop-l-enyl)phenyl thiocyanateme, ampropylfos, anilazine, azithiram, barium polysulfide, Bayer 32394, benodanil, benquinox, bentaluron, benzamacril; benzamacril-isobutyl, benzamorf, binapacryl, bis(methylmercury) sulfate, bis(tributyltin) oxide, buthiobate, cadmium calcium copper zinc chromate sulfate, carbamorph, CECA, chlobenthiazone, chloraniformethan, chlorfenazole, chlorquinox, 8 '<<5 PCT/US2010/051598 WO 2011/044213 climbazole, copper bis(3-phenylsalicylate), copper zinc chromate, cufraneb, cupric hydrazinium sulfate, cuprobam, cyclafuramid, cypendazole, cyprofuram, decafentin, dichlone, dichlozoline, diclobutrazol, dimethirhnol, dinocton, dinosulfon, dinoterbon, dipyrithione, ditalimfos, dodicin, drazoxolon, EBP, ESBP, etaconazole, etem, ethirim, fenaminosulf, fenapanil, fenitropan, fluotrimazole, furcarbanil, furconazole, furconazole-cis, furmecyclox, furophanate, glyodine, griseofulvin, halacrinale, Hercules 3944, hexyllhiofos, ICIA0858, isopamphos, isovaledione, mebenil, mecarbinzid, metazoxolon, methfuroxam, methylmercury dicyandi amide, metsulfovax, milneb, mucochloric anhydride, myclozolin, V-3,5-dichlorophenyl-succinimide, V-3-mtrophenylitacommide, natamycin, N-ethylmercurio-4-toluenesulfonanilide, nickel bis(dimethyldiLhiocarbamate), OCH, phenylmercury dimethyldithiocarbamate, phenylmercury nitrate, phosdiphen, prothiocarb; prothiocarb hydrochloride, pyracarbolid, pyridinitril, pyroxychlor, pyroxyfur, quinacetol; quinacetol sulfate, quinazamid, quinconazole, rabenzazole, salicylanilide, SSF-109, sultropen, tecoram, thiadifluor, thicyofen, thiochlorfenphim, thiophanate, thioquinox, Lioxymid, triamiphos, triarimol, triazbutil, trichlamide, urbacid, zarilamid, and any combinations thereof.

[0023] The compositions of the present invention are preferably applied in the form of a formulation comprising a composition of (a) a compound of Formula I and (b) at least one fungicide selected from the group consisting of epoxiconazole, prothioconazole, azoxystrobin, pyraclostrobin, penthiopyrad, isopyrazam, bixafen, boscalid, prochloraz, and chlorothalonil, together with a phytologically acceptable carrier.

[0024] Concentrated formulations can be dispersed in water, or another liquid, for application, or formulations can be dust-like or granular, which can then be applied without further treatment, The formulations are prepared according to procedures which are conventional in the agricultural chemical art, but which are novel and important because of the presence therein of a synergistic composition.

[0025] The formulations that are applied most often are aqueous suspensions or emulsions. Either such water-soluble, water-suspend able, or emulsifiable formulations are solids, usually known as weltable powders, or liquids, usually known as emulsifiable concentrates, aqueous suspensions, or suspension concentrates. The present invention contemplates all vehicles by which the synergistic compositions can be formulated for delivery and use as a fungicide. 9 WO 2011/044213 PCT/US2010/051598 [0026] As will be readily appreciated, any material to which these synergistic compositions can be added may be used, provided they yield the desired utility without significant interference with the activity of these synergistic compositions as antifungal agents.

[0027] Wettable powders, which may be compacted to form water-dispersible granules, comprise an intimate mixture of the synergistic composition, a carrier and agriculturally acceptable surfactants. The concentration of the synergistic composition in the ! wettable powder is usually from about 10% to about 90% by weight, more preferably about 25% to about 75% by weight, based on the total weight of the formulation. In the preparation of wettable powder formulations, the synergistic composition can be compounded with any of the finely divided solids, such as prophyllite, talc, chalk, gypsum, Fuller's earth, bentonite, attapulgite, starch, casein, gluten, montmorillonite clays, diatomaceous earths, purified silicates or the like. In such operations, the finely divided carrier is ground or mixed with the synergistic composition in a volatile organic solvent. Effective surfactants, comprising from about 0.5% to about 10% by weight of the wettable powder, include sulfonated lignins, naphthalenesulfonates, alkylbenzenesulfonates, alkyl sulfates, and non-ionic surfactants, such as ethylene oxide adducts of alkyl phenols.

[0028] Emulsifiable concentrates of the synergistic composition comprise a convenient concentration, such as from about 10% to about 50% by weight, in a suitable liquid, based on the total weight of the emulsifiable concentrate formulation. The components of the synergistic compositions, jointly or separately, are dissolved in a carrier, which is either a ! water-miscible solvent or a mixture of waLer-inuniscible organic solvents, and emulsifiers. ,

The concentrates may be diluted with water and oil to fonn spray mixtures in the form of oil- ! in-water emulsions. Useful organic solvents include aromatics, especially the high-boiling naphthalenic and olefinic portions of petroleum such as heavy aromatic naphtha. Other organic solvents may also be used, such as, for example, terpenic solvents, including rosin ,; derivatives, aliphatic ketones, such as cyclohexanone, and complex alcohols, such as 2- !> ethoxyethanol. i;\ [0029] Emulsifiers which can be advantageously employed herein can be readily determined by those skilled in the art and include various nonionic, anionic, cationic and | amphoteric emulsifiers, or a blend of two or more emulsifiers. Examples of nonionic | emulsifiers useful in preparing the emulsifiable concentrates include the polyalkylene glycol | 10 ί • · <: _ r -- . ·'········ ·-; .:.i; WO 2011/044213 PCT/US2010/051598 ethers and condensation products of alkyl and aryl phenols, aliphatic alcohols, aliphatic amines or fatty acids with ethylene oxide, propylene oxides such as the ethoxylated alkyl phenols and carboxylic esters solubilized with die polyol or polyoxyalkylene. Cationic emulsifiers include quaternary ammonium compounds and fatty amine salts. Anionic emulsifiers include the oil-soluble salts (e.g., calcium) of alkylaryl sulfonic acids, oil-soluble salts or sulfated poly glycol ethers and appropriate salts of phosphated poly gly col ether, [0030] Representative organic liquids which can be employed in preparing the emulsifiable concentrates of the present invention are the aromatic liquids such as xylene, propyl benzene fractions, or mixed naphthalene fractions, mineral oils, substituted aromatic organic liquids such as dioctyl phthalate, kerosene, dialkyl amides of various fatty acids, particularly the dimethyl amides of fatty glycols and glycol derivatives such as the ra-butyl ether, ethyl ether or methyl ether of diethylene glycol, and the methyl ether of triethylene glycol. Mixtures of two or more organic liquids are also often suitably employed in the preparation of the emulsifiable concentrate. The preferred organic liquids are xylene, and propyl benzene fractions, with xylene being most preferred. The surface-active dispersing agents are usually employed in liquid formulations and in the amount of from 0.1 to 20 percent by weight of the combined weight of the dispersing agent with the synergistic compositions. The formulations can also contain other compatible additives, for example, plant growth regulators and other biologically active compounds used in agriculture.

[0031] Aqueous suspensions comprise suspensions of one or more water-insoluble compounds, dispersed in an aqueous vehicle at a concentration in the range from about 5% to about 70% by weight, based on the total weight of the aqueous suspension formulation. Suspensions are prepared by finely grinding the components of the synergistic combination either together or separately, and vigorously mixing the ground material into a vehicle comprised of water and surfactants chosen from the same types discussed above. Other ingredients, such as inorganic salts and synthetic or natural gums, may also be added to increase the density and viscosity of the aqueous vehicle. It is often most effective to grind and mix at the same time by preparing die aqueous mixture and homogenizing it in an implement such as a sand mill, hall mill, or piston-type homogenizer.

[0032] The synergistic composition may also be applied as a granular formulation, which is particularly useful for applications to the soil. Granular formulations usually contain from about 0.5% to about 10% by weight of the compounds, based on the total weight of the 11 >Vv,WA ·-?« WO 2011/044213 PCT/US2010/051598 granular formulation, dispersed in a carrier which consists entirely or in large part of coarsely divided attapulgitc, bentonite, diatomite, clay or a similar inexpensive substance. Such formulations are usually prepared by dissolving the synergistic composition in a suitable solvent and applying it to a granular carrier which has been preformed to the appropriate particle size, in the range of from about 0.5 to about 3 mm. Such formulations may also be prepared by making a dough or paste of the carrier and the synergistic composition, and crushing and drying to obtain the desired granular particle.

[0033] Dusts containing the synergistic composition are prepared simply by intimately mixing the synergistic composition in powdered form with a suitable dusty agricultural carrier, such as, for example, kaolin clay, ground volcanic rock, and the like. Dusts can suitably contain from about 1% to about 10% by weight of the synergistic compos ition/carrier combination.

[0034] The formulations may contain agriculturally acceptable adjuvant surfactants to enhance deposition, wetting and penetration of the synergistic composition onto the target crop and organism. These adjuvant surfactants may optionally be employed as a component of the formulation or as a tank mix. The amount of adjuvant surfactant will vary from 0.01 percent to 1.0 percent volume/volume (v/v) based on a spray-volume of water, preferably 0.05 to 0.5 percent, Suitable adjuvant surfactants include ethoxylated nonyl phenols, ethoxylated synthetic or natural alcohols, salts of the esters or sulfosuccinic acids, ethoxylated organosilicones, ethoxylated fatty amines and blends of surfactants with mineral or vegetable oils.

[0035] The formulations may optionally include combinations that can comprise at least 1% by weight of one or more of the syneTgistic compositions with another pesticidal compound. Such additional pesticidal compounds may be fungicides, insecticides, nematocides, miticides, arthropodicides, bactericides or combinations thereof that are compatible with the synergistic compositions of the present invention in the medium selected for application, and not antagonistic to the activity of the present compounds. Accordingly, in such embodiments the other pesticidal compound is employed as a supplemental toxicant for the same or for a different pesticidal use. The pesticidal compound and the synergistic composition can generally be mixed together in a weight ratio of from 1:100 to 100:1. 12 Γ· - Ξ’ΤΓ?--· WO 2011/044213 PCT/US2010/051598 [0036] The present invention includes within its scope methods for the control or prevention of fungal attack. These methods comprise applying to the locus of the fungus, or to a locus in which the infestation is to be prevented (for example applying to wheat or barley plants), a fungicidally effective amount of the synergistic composition. The synergistic composition is suitable for treatment of various plants at fungicidal levels, while exhibiting low phytotoxicity. The synergistic composition is useful in a protectant or eradicant fashion. The synergistic composition is applied by any of a variety of known techniques, either as the synergistic composition or as a formulation comprising the synergistic composition. For example, the synergistic compositions may be applied to the roots, seeds or foliage of plants for the control of various fungi, without damaging the commercial value of the plants. The synergisLic composition is applied in the form of any of the generally used formulation types, for example, as solutions, dusts, wettable powders, flowable concentrates, or emulsifiable concentrates, These materials are conveniently applied in various known fashions.

[0037] The synergistic composition has been found to have significant fungicidal effect, particularly for agricultural use. The synergistic composition is particularly effective for use with agricultural crops and horticultural plants, or with wood, paint, leather or carpet backing.

[0038] In particular, the synergistic composition is effective in controlling a variety of undesirable fungi that infect useful plant crops. The synergistic composition may be used against a variety of Ascomycete and Basidiomycete fungi, including for example the following representative fungi species: wheat brown rust (Puccinia recondita; Bayer code PUCCRT); stripe rust of wheat (Puccinia striiformis; Bayer code PUCCST); leaf blotch of wheat (Mycosphaerella graminicola; anamorph: Septoria tritici; Bayer code SEPTTR); glume blotch of wheat (Leptosphaeria nodorum; Bayer code LEPTNO; anamorph: Stagonospora nodorum); spot blotch of barley (Cochliobolus sativum; Bayer code COCHSA; anamorph: Helminthosporium sativum); leaf spot of sugar beets (Cercospora beticola; Bayer code CERCBE); leaf spot of peanut (Mycosphaerella arachidis; Bayer code MYCOAR; anamorph: Cercospora arachidtcola); cucumber anthracnose (Glomerella lagenarium; anamorph: Colietotrichum lagenarium; Bayer code COLLLA) and black sigatoka disease of banana (Mycosphaerella ftjiensis; BAYER code MYCOFI). It will be understood by those in the art that the efficacy of the synergistic compositions for one or more of the foregoing fungi establishes the general utility of tire synergistic compositions as fungicides. 13 iWWiSi .. WO 2011/044213 PCT/US2010/051598 [0039] The synergistic compositions have a broad range of efficacy as a fungicide.

The exact amount of the synergistic composition to be applied is dependent not only on the relative amounts of the components, but also on the particular action desired, the fungal species to be controlled, and the stage of growth thereof, as well as the part of the plant or other product to be contacted with the synergistic composition. Thus, formulations containing the synergistic composition may not be equally effective at similar concentrations or against the same fungal species.

[0040] The synergistic compositions are effective in use with plants in a disease- inhibiting and phytologically acceptable amount. The term "disease-inhibiting and phytologically acceptable amount" refers to an amount of the synergistic composition that kills or inhibits the plant disease for which control is desired, but is not significantly toxic to the plant. The exact concentration of synergistic composition required varies with the fungal disease Lo be controlled, the type of formulation employed, the method of application, the particular plant species, climate conditions, and the like.

[0041 ] The present compositions can be applied to fungi or their locus by the use of conventional ground sprayers, granule applicators, and by other conventional means known to those skilled in the art.

[0042] The following examples are provided to further illustrate the invention. They are not meant to be construed as limiting the invention.

Examples

Evaluation of Curative and Protectant Activity of Fungicide Mixtures vs. Leaf Blotch of

Wheat (Mycosphaerella sraminicola', anamorph: Septoria tritich Bayer code: SEPTTR) [0043] Wheat plants (variety Yuma) were grown from seed in a greenhouse in plastic pots with a surface area of 27.5 square centimeters (cm2) containing 50% mineral soil/50% soil-less Metro mix, with 8-12 seedlings per pot, The plants were employed for testing when first leaf was fully emerged, which typically took 7 to 8 days after planting. Test plants were inoculated with an aqueous spore suspension of Septoria tritici either 3 days prior to (3-day curative test) or 1 day after fungicide treatments (1-day protectant test). After inoculation the plants were kept in 100% relative humidity (one day in a dark dew chamber followed by two 14 SSidF V-; -;sl..'L .;£££?· WO 2011/044213 PCT/US2010/051598 days in a lighted mist chamber) to permit spores to germinate and infect the leaf. The plants were then transferred to a greenhouse for disease to develop.

[0044] Evaluation of Curative Activity of Fungicide Mixtures vs. Wheat Brown Rust (Puccinia reconditcr, Bayer code: PUCCRT) [0045] Yuma wheaL seedlings were grown as described above, and inoculated with an aqueous spore suspension of Puccinia recondita 3 days prior to or 1-day after fungicide treatment. After inoculation, plants were kept in 100% relative humidity for 24 hours in a dark dew room to allow spores to germinate and infect plants. The plants were then transferred to a greenhouse for disease to develop.

[0046] Treatments consisted of fungicides compound I, Π, ΙΠ, IV, V, epoxiconazole, prothioconazole, azoxystrobin, pyraclostrobin, penthiopyrad, boscalid, prochloraz, and chlorothalonil, either using individually or as two-way mixture with compounds I-V. For compound I, isopyrazam and bixafen were also included in the studies. Technical grades of materials were dissolved in acetone to make stock solutions, which were then used to perform dilutions in acetone either for each individual fungicide component or for the two-way mixture. Desired fungicide rates were obtained after mixing dilutions with 9 volumes of water containing 110 parts per million (ppm) Triton X-100. Twenty milliliter (mL) fungicide solutions were applied onto 12 pots of plants using an automated booth sprayer, which utilized two 6218-1/4 JAUPM spray nozzles operating at 20 pounds per square inch (psi) set at opposing angles to cover both leaf surfaces. All sprayed plants weTe allowed to air dry prior to further handling. Control plants were sprayed in the same manner with the solvent blank.

[0047] When disease fully developed on the control plants, infection levels were assessed on treated plants visually and scored on a scale of 0 to 100 percent. Percentage of disease control was then calculated using the ratio of disease on treated plants relative to control plants.

[0048] Colby’s equation was used to determine the fungicidal effects expected from the mixtures. (See Colby, S. R. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 1967,15, 20-22.) 15 WO 2011/044213 PCT/US2010/051598 [0049] The following equation was used to calculate the expected activity of mixtures containing two active ingredients, A and B:

Expected = A + B - ( A x B/100) A = observed efficacy of active component A at the same concentration as used in the mixture; B = observed efficacy of active component B at the same concentration as used in the mixture.

[0050] Representative synergistic interactions are presented in the following Tables 1-12. %DC Obs= Percent disease control observed %DC Exp= Percent disease control expected

Synergism factor = %DC Obs/%DC Exp

Table 1: Synergistic interactions of compound I and other fungicides in 3-day curative (3DC) Septoria tritici (SEPTTR) tests

Rate ppm %DC obs %DC exp Synergism factor Compound I+epoxiconazole 0.4 + 0.1 71 43 1,64 Compound I+epoxiconazole 0.15+0.13 97 48 2.02 Compound I+prothioconazole 0.4 + 25 99 72 1.38 Compound I+prothioconazole 1.35+1.S 99 83 1.19 Compound I+prothioconazole 0.45+0.6 69 7 10.50 Compound I+azoxystrobin 6.25 +0.4 100 89 1.12 Compound I+azoxystrobin 1.35+2.25 99 83 1.19 Compound I+azoxystrobin 0.45+0.75 72 15 4.78 Compound I+pyraclostrobin 0.1 + 0.4 92 80 1.15 Compound I+penthiopyrad 6.25 + 0.1 98 90 1.08 Compound I+penthiopyrad 0.15+0.2 31 4 7.08 Compound I+isopyrazam 6.25 + 0.1 99 89 1,11 Compound I+isopyrazam 0.4 + 6.25 68 55 1.23 Compound I+isopyrazam 0.1 + 6.25 86 57 1.50 16 PCT/US2010/051598 λ’’:ν;®ϊ?ί;^^ϊ2ΐ¥ϊ__ί+?ΐ·:;;++ι>7χ>7><<ς>Λ-::;+-+3. _ΧχχΐΧΤί;:.' WO 2011/044213

Table 2: Synergistic interactions of compound I and other fungicides in 1-day protectant (1DP) SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound I+epoxiconazole 0.1 + 0.1 92 74 1.24 Compound I+epoxiconazole 0,1 + 0.025 85 55 1,53 Compound I+prothioconazole 0.1 + 1.56 94 70 1.34 Compound I+prothioconazole 0.15+0,2 46 15 3.01 Compound 1+azoxystrobin 0.1 + 1.56 91 66 1.38 Compound I+azoxystrobin 0,1 + 0.4 72 43 1.66 Compound I+azoxystrobin 0.1 + 0.1 80 61 1.31 Compound I+pyraclostrobin 0.1 + 0.1 99 92 1.08 Compound I+pyraclostrobin 0.05+0.08 68 30 2.27 Compound I+penthiopyrad 0.4 + 0.4 96 90 1.07 Compound I+penthiopyrad 0.1 + 0.4 56 47 1.19 Compound I+isopyrazam 0.15+0.13 49 9 5,68 Compound I+bixafen 0.15+0.2 30 12 2.50 Compound I+boscalid 0.15+0.33 25 14 1.81 Compound I+prochloraz 0,15+0.45 35 7 5.00 Compound 1+chlorothalonil 0.15+0.6 16 9 1.83

Table 3: Synergistic interactions of compound I and other fungicides in 3DC Puccinia recondita (PUCCRT) tests

Rate ppm %DC obs %DC exp Synergism factor Compound I+epoxiconazole 0.4 + 0.1 100 87 1.15 Compound I+epoxiconazole 0.1 + 0.1 100 82 1.22 Compound I+prothioconazole 0.4+ 1,56 100 91 1.10 Compound I+prothioconazole 1.35+1.8 94 39 2.43 17 PCT/US2010/051598 WO 2011/044213

Compound I+azoxystrobin 0.4 + 0.4 90 84 1.07 Compound I+azoxystrobin 0.15+0,25 43 14 3.14 Compound I+pyraclostrobin 0.4 + 0.1 74 55 1.34 Compound I+pyraclostrobin 0.1+0.4 74 64 1.15 Compound I+isopyrazam 0.4+1.56 100 95 1.05 Compound I+isopyrazam 0.45+0.38 33 29 1.13

Table 4: Synergistic interactions of compound I and other fungicides in 1DP PUCCRT tests

Rate ppm %DC obs %DC exp Synergism factor Compound I+prolhioconazole 0.15+0.2 78 69 1.14 Compound I+prochloraz 0,15+0.45 93 69 1.35

Table 5: Synergistic interactions of compound II and other fungicides in 1DP SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound Π+epoxiconazole 0.45+0,2 54 33 1.67 Compound Π+pyraclostrobin 0.45+0,1 80 61 1.32 Compound II+boscalid 0.45+5 44 21 2.04 Compound Il+prochloraz 0.45+5 55 36 1.54

Table 6: Synergistic interactions of compound II and other fungicides 3DC SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound II+prothioconazole 1.35+1.8 95 38 2.49 Compound II+prothioconazole 0.45+0.6 38 14 2.65 Compound II+azoxystrobin 1.35+2.25 98 72 1.36 Compound Π+azoxystrobin 0.45+0.75 71 52 1.36 Compound II+pyraclostrobin 0,15+0.25 95 50 1.89 Compound Π+pyraclostrobin 0.05+0.08 29 16 1.78 Compound II+boscalid 1.35+3 100 57 1.75 18 WO 2011/044213 PCT/US2010/051598

Compound Π+boscalid 0.45+1 60 22 2.73 Compound II+prochloraz 1.35+4.05 95 53 1.81 Compound H+prochloraz 1.5+3 75 63 1.20 Compound II+chlorothalonil 1.35+5.4 92 42 2.17 Compound II+chlorothalonil 0.45+1.8 58 18 3.22

Table 7: Synergistic interactions of compound ΙΠ and other fungicides in 1DP SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound III+epoxiconazole 0.3+0.2 61 36 1.69 Compound ΠΙ+prothioconazole 1,35+1.8 98 90 1.09 Compound III+azoxystrobin 0,15+0.25 38 27 1.42 Compound ΠΙ+pyraclostrobin 0.3+0.1 76 63 1.21 Compound Hl+penthiopyrad 0.3+3 53 42 1.25- Compound HF+penthiopyrad 1.35+1.8 95 89 1.07 Compound El+boscalid 1.35+3 97 91 1.07 Compound III+boscalid 0.3+5 56 25 2.22 Compound ΠΙ+prochloraz 1.35+4.05 98 91 1.07 Compound III+prochloraz 0.3+5 62 39 1.60 Compound III+chlorothalonil 1.35+5,4 95 86 1.11 Compound III+chlorothalonil 0.15+0.6 40 21 1.93 'Fable 8: Synergistic interactions of compound ΙΠ and other fungicides in 3DC SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound III+epoxiconazole 0.5+0.03 73 60 1.21 Compound ΠΙ+prothioconazole 0,45+0.6 88 33 2.69 Compound ΠΙ+prothioconazole 0.15+0.2 50 42 1.20 Compound III+azoxystrobin 0.45+0.75 95 63 1.51 Compound III+azoxystrobin 0.15+0.25 63 43 1.44 Compound ΠΙ+pyraclostrobin 0.5+0.15 75 56 1.33 19 WO 2011/044213 PCT/US2010/051598

Compound ΠΙ+penthiopyrad 0.45+0.6 97 69 1.41 Compound m+boscalid 0.45+1 83 39 2.13 Compound III+boscalid 0.15+0.33 35 29 1.23 Compound ΠΙ+prochloraz 0,45+1.35 71 42 1.68 Compound ΠΙ+prochloraz 0.15+0.45 67 22 3.08 Compound III+chlorothalonil 0.45+1.8 58 36 1.62

Table 9: Synergistic interactions of compound IV and other fungicides in 1DP SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound IV+epoxiconazole 2+0.2 42 37 1.14 Compound IV+prothioconazole 4.2+5.6 90 78 1.15 Compound IV+boscalid 2+5 31 26 1.19 Compound IV+chlorothalonil 4.2+16.8 84 67 1.26 Compound IV+chlorothalonil 1.35+5.4 33 23 1.44

Table 10: Synergistic interactions of compound IV and other fungicides in 3DC SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound IV+prothioconazolc 4.2+5,6 97 64 1.52 Compound IV+azoxystrobin 4.2+7 96 84 1.14 Compound IV+azoxystrobin 1.35+2.25 70 57 1.23 Compound IV+pyraclostrobin 6+0.15 97 62 1.56 Compound IV+pyraclostrobin 0.05+0.08 30 22 1.40 Compound IV+penthiopyrad 4.2+5.6 98 81 1.21 Compound IV+penthiopyrad 1.35+1.8 74 15 4.86 Compound IV+boscalid 1.35+3 65 52 1.25 Compound IV+prochloraz 6+3 72 63 1.15 Compound IV+chlorothalonil 4.2+16.8 67 10 7.05 20 WO 2011/044213 PCT/US2010/051598

Table 11: Synergistic interactions of compound V and other fungicides in 1DP SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound V+epoxiconazole 2+0.2 97 87 1.11 Compound V+epoxiconazole 0.15+0.13 28 17 1.61 Compound V+prothioconazole 0.45+0.6 20 14 1.39 Compound V+azoxystrobin 0.45+0.75 38 12 3.09 Compound V+pyraclostrobin 2+0.1 99 93 1.07 Compound V+pyraclostrobin 0,05+0.08 50 17 3.00 Compound V+penthiopyrad 0.45+0,6 23 14 1.56 Compound V+boscalid 2+5 92 85 1.09 Compound V+prochloraz 1.35+4.05 87 38 2.28 Compound V+prochloraz 0.45+1.35 38 5 7.23 Compound V+chlorothalonil 1.35+5.4 57 25 2.26

Table 12: Synergistic interactions of compound V and other fungicides in 3DC SEPTTR tests

Rate ppm %DC obs %DC exp Synergism factor Compound V+epoxiconazole 2+0.03 61 44 1.41 Compound V+prothioconazole 1.35+1,8 78 52 1.51 Compound V+pyraclostrobin 2+0.15 86 38 2.30 Compound V+penthiopyrad 2+1 50 33 1.50 Compound V+penthiopyrad 1.35+1.8 67 37 1.81 Compound V+boscalid 2+2 50 41 1.22 Compound V+prochloraz 2+3 56 38 1.45 Compound V+prochloraz 0.15+0.45 50 40 1.26 Compound V+chlorothalonil 4.2+16.8 97 71 1.38 Compound V+chlorothalonil 1,35+5.4 54 34 1.59

For all tables, %DC = % Disease Control 21