MXPA06009067A - Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the spores germination or mycelium growth by acting on different metabolic routes - Google Patents

Abstract

A composition comprising at least a pyridylethylbenzamide derivative of general formula (I) (a) and a compound capable of inhibiting the spores germination or mycelium growth by acting on different metabolic routes (b) in a (a) / (b) weight ratio of from 0.01 to 20. A composition further comprising an additional fungicidal compound. A method for preventively or curatively combating the phytopathogenic fungi of crops by using this composition.

Description

FUNGICIDE COMPOSITION COMPRISING A PYRIDILETILBENZAMIDE DERIVATIVE AND A COMPOUND CAPABLE OF INHIBITING THE GERMINATION OF SPPORES OR THE GROWTH OF THE MICELLY ACTING ON DIFFERENT METABOLIC ROUTES FIELD OF THE INVENTION The present invention relates to new fungicidal compositions comprising a pyridyl methylbenzamide derivative and a compound capable of inhibiting spore germination or mycelial growth by acting on different metabolic pathways. The present invention also relates to a method for combating or controlling phytopathogenic fungi by applying to a site infested or susceptible to being infested with such a composition. BACKGROUND OF THE INVENTION In international patent application WO 01/11965, numerous pyridylethylbenzamide derivatives are generically described. The possibility of combining one or more of these numerous pyridylethylbenzamide derivatives with known fungicidal products to develop a fungicidal activity is described in general terms, without a specific example or biological data. It is always of great interest in agriculture to use novel pesticidal mixtures that show a synergistic effect to avoid or to control remarkably the development of REF: 173870 strains resistant to the active ingredients or to the mixtures of ingredients - known active ingredients used by the farmer while minimizing the doses of chemical products spread in the environment and reduce the cost of treatment. Now, some novel fungicidal compositions have been discovered which possess the characteristics mentioned above. DETAILED DESCRIPTION OF THE INVENTION Accordingly, the present invention relates to a composition comprising: a) a pyridylethylbenzamide derivative of the general formula (I) wherein: - p is an integer equal to 1, 2, 3 or 4; - q is an integer equal to 1, 2, 3, 4 or 5; - each substituent X is chosen, independently of the others, as halogen, alkenyl or haloalkyl; - each substituent Y is chosen, independently of the others, as: halogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, amino, phenoxy, alkylthio, dialkylamino, acyl, cyano, ester, hydroxy, aminoalkyl, benzyl, haloalkoxy, halosulfonyl, halothioalkyl, alkoxyalkenyl, alkylsulfonamide, nitro, alkylsulfonyl, phenylsulfonyl or benzylsulfonyl; as well as its 2-pyridine N-oxides; and b) a compound capable of inhibiting spore germination or mycelial growth by acting on different metabolic pathways; in a weight ratio of (a) / (b) from 0.01 to 20. In the context of the present invention: halogen means: chlorine, bromine, iodine or fluorine; - each of the alkyl or acyl radicals present in the molecule contains from 1 to 10 carbon atoms, preferably from 1 to 7 carbon atoms, more preferably from 1 to 5 carbon atoms and can be linear or branched; - each of the alkenyl or alkynyl radicals present in the molecule contains from 2 to 10 carbon atoms, preferably from 2 to 7 carbon atoms, more preferably from 2 to 5 carbon atoms and can be linear or branched. The composition according to the present invention provides a synergistic effect. This synergistic effect allows a reduction of the chemical substances that are scattered in the environment and a reduction of the cost of the fungal treatment.

In the context of the present invention, Colby defines the terminology "synergistic effect" according to the article entitled "Calculation of the synergistic and antagonistic responses of herbicide combinations" Weeds, (1967), 15, pages 20-22. The last article mentions the formula: Ec = x +, y? * Y- 100 wherein E represents the predicted percentage of inhibition of the disease by the combination of the two fungicides in the defined doses (for example, equal to x and y respectively), x is the percentage of inhibition observed for the disease by the compound (I) at a defined dose (equal to x) and is the percentage of inhibition observed for the disease by the compound (II) at a defined dose (equal to y). When the percentage of inhibition observed for the combination is greater than E, there is a synergistic effect. The composition according to the present invention comprises a pyridylethylbenzamide derivative of general formula (I). Preferably, the present invention relates to a composition comprising a pyridylethylbenzamide derivative of general formula (I) in which the different characteristics can be chosen singly or in combination as: - relative to p, p is 2; - in relation to q, q is 1 or 2. More preferably, q is 2; as regards X, X is chosen, independently of the others, as halogen or haloalkyl. More preferably, X is chosen, independently of the others, as a chlorine atom or a trifluoromethyl group; - in relation to Y, Y is chosen, independently of the others, as halogen or haloalkyl. More preferably, Y is chosen, independently of the others, as a chlorine atom or a trifluoromethyl group; More preferably, the pyridylethylbenzamide derivative of the general formula (I) present in the composition of the present invention is: - N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (compound 1); - N- { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-iodobenzamide (compound 2); or N-. { 2- [3,5-dichloro-2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (compound 3). Even more preferably, the pyridylethylbenzamide derivative of the general formula (I) present in the composition of the present invention is N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (compound 1). The composition according to the invention comprises a compound capable of inhibiting the germination of spores or the growth of the mycelium by acting on different metabolic routes. Preferably, the present invention relates to a composition comprising a compound capable of inhibiting spore germination or. mycelial growth acting on different metabolic pathways selected from dicarboximide derivatives, phthalimide derivatives, 2-butoxy-6-iodo-3-propyl-benzopyran-4-one, 2,6-dichloro-N-. { [3-chloro-5- (trifluoromethyl) -2-pyridinyl] methyl} benzalaida, (Z) -N- [a- (cyclopropylmethoxyimino) -2,3-difluoro-6- (trifluoromethyl) benzyl] -2-phenylacetamide, (RS) -2- (4-chlorophenyl) -N- [ 3-methoxy-4- (prop-2-ynyloxy) phenethyl] -2- (prop-2-ynyloxy) acetamide, 6-iodo-2-propoxy-3-propylquinazolin-4 (3H) -one, benalaxyl, benthiavalicarb, chlorothalonil, copper hydroxide, copper oxychloride, copper sulfate, copper sulfate (tribasic), cuprous oxide, cymoxanil, diclomezine, diclofluanid, dithianon, dimetomorph, dodine, etaboxam, fenpiclonil, fentin, ferbam, fluazinam, fludioxonil, flusulfamide, guazatine, iminoctadine, mancobre, mancozeb, maneb, metalaxyl, metalaxyl-M, metiram, metasulfocarb, nabam, nickel bis (dimethyldithiocarbamate), iprovalicarb, oxina-copper, propamocarb, propineb, quinoxifen, sulfur, siltiofam, thiram, tolylfluanide, triazoxide , validamicin, zineb, ziram, phosphorous acid and fosetyl-Al. 2-Butoxy-6-iodo-3-propyl-benzopyran-4-one, 2,6-dichloro-β- are preferred. { [3-chloro-5- (tri-fluoromethyl) -2-pyridinyl] ethyl} benzamide, chlorothalonil, iprovalicarb, mancozeb, propamocarb and fosetyl-Al. According to the present invention, the dicarboximide derivatives can be for example clozolinate, iprodione, procymidone or vinclozolin. Irodione is still preferred. According to the present invention, the phthalimide derivatives can be for example captafol, captan, folpet, thiochlorfenfim. They prefer captan and folpet. The composition according to the present invention comprises (a) at least one derivative. of pyridylethylbenzamide of general formula (I) and (b) a compound capable of inhibiting spore germination or mycelial growth by acting on different metabolic pathways in a weight ratio (a) / (b) from 0.01 to 20; preferably from 0.05 to 10; even more preferably from 0.1 to 5. The composition of the present invention may further comprise at least one other fungicidal active ingredient different (c). The fungicidal active ingredient (c) can be selected from azaconazole, azoxystrobin, (Z) -N- [u- (cyclopropylmethoxyimino) -2, 3-difluoro-6- (trifluoromethyl) benzyl] -2-phenylacetamide, 6-iodo-2 -propoxy-3-propylquinazolin-4 (3H) -one, 6-iodo-2-propoxy-3-propylquinazolin-4 (3H) -one, benalaxyl, benomyl, benthiavalicarb, biphenyl, bitertanol, blasticidin-S, boscalide, borax , bromuconazole, bupirimate, sec-butylamine, calcium polysulfide, captafol, captan, carbendazim, carboxy, carpropamid, quinomethionate, chlorothalonil, clozolinate, copper hydroxide, copper octanoate, oxychloride. copper, copper sulfate, cuprous oxide, cysoxamid, cymoxanil, cyproconazole, cyprodinil, dazomet, debacarb, diclofluanide, dichlorophen, diclobutrazol, diclocimet, diclomezine, dichloram, dietofencarb, diphenoconazole, diphenzoquat methylisulfate, difenzoquat, diflumetorim, dimethirimol, dimetomorph, diniconazole, dinobuton, dinocap, diphenylamine, dithianon, dodemorf, dodemorf acetate, dodine, edifenfos, epoxiconazole, etaconazole, ethaboxam, etirimol, ethoxyquin, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamide, fenpiclonil, fenoxanil, fenpropidin, fenpropimorf, fentina, fentina hydroxide, fentina acetate, ferbam, ferimzona, fluazinam, fludioxonilo, fluoroimida, fluoxastrobina, fluquinconazole, flusilazol, flusulfamida, flutolanil, flutriafol, folpet, formaldehyde, fosetil, fosetil-aluminio, fuberidazol, furalaxilo, furametpyr, guazatine, guazatin acetates, hexachlorobenzene, hexaconazole, 8-hydroxyquinoline sulfate, hydroxyquinolinesulphate d potassium, himexazole, imazalil sulfate, imazalil, ibenconazole, iminoctadine, iminoctadine triacetate, ipconazole, iprobenfos, iprodione, iprovalicarb, isoprothiolane, asugamycin, hydrated kasugamycin hydrochloride, kresoxim-methyl, mancobre, mancozeb, maneb, mepanipyrim, mepronil , mercuric chloride, mercuric oxide, mercuric chloride, metalaxyl, metalaxyl-M, metam-sodium, meta, metconazole, metasulfocarb, methyl isothiocyanate, metiram, methominostrobin, mildiomycin, myclobutanil, naba, nickel bis (dimethyldithiocarbamate), nitrotal-isopropyl , nuarimol, octylinone,. ofurace, oleic acid, oxadixyl, oxina-copper, oxpoconazole fumarate, oxycarboxin, pefurazoate, penconazole, pencicuron, pentachlorophenol, sodium pentachlorophenoxide ,. pentachlorophenyl laurate, phenylmercury acetate, sodium 2-phenylphenoxide, 2-phenylphenol, phosphorous acid, phthalide, picoxystrobin, piperalin, polyoxinspolioxin B, polyoxin, polyoxorim, probenazole, prochloraz, procymidone, propamocarb hydrochloride, propamocarb, propiconazole, propineb, protioconazole, piradostrobin, pyrazophos, pyributicarb, pirifenox, pyrimethanil, pyroquilon, quinoxifen, quintozene, silthiopham, simeconazole, spiroxamine, sulfur, tar oils, tebuconazole, tecnazene, tetraconazole, thiabendazole, thifluzamide, thiophanate-methyl, strip, tolclofos-methyl, tolylfluanide, triadimefon, triadimenol, triazoxide, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamycin, vinclozolin, zineb, ziram and zoxamide. Preferably, the fungicidal active ingredient (c) is selected from dietofencarb, hexaconazole, cyprodinil, tebuconazole and bromuconazole. When the third active ingredient (c) is present as defined above, in the composition, this compound may be present in a weight ratio amount (a): (b): (c) of 1: 0.01. 0.01 to 1: 20 :. 20 varying the ratios of the compound (a) and the compound (c) independently of one another. Preferably ', the weight ratio (a): (b): (c) can be from 1: 0.05: 0.05 to 1: 10: 10. The following compositions can be cited to illustrate in a non-limiting manner the present invention: compound 1 with 2-butoxy-6-iodo-3-propyl-benzopyran-4-one, compound 1 with 2,6-dichloro-N-. { [3-chloro-5- (trifluoromethyl) -2-pyridinyl] methyl} benzamide, compound 1 with (Z) -N- [OL- (cyclopropylmethoxyimino) -2,3-difluoro-6- (trifluoromethyl) benzyl] -2-phenylacetamide, compound 1 with (RS) -2- (4-chlorophenyl) -N- [3-methoxy-4- (prop-2-ynyloxy) phenethyl] -2- (prop-2-ynyloxy) acetamide, compound 1 with 6-iodo-2-propoxy-3-propylquinazolin- (3H) - ona, compound 1 with benalaxyl, compound 1 with benthiavalicarb, compound 1 with chlorothalonil, compound 1 with copper hydroxide, compound 1 with copper oxychloride, compound 1 with copper sulfate, compound 1 with copper sulfate (tribasic), compound 1 with cuprous oxide, compound 1 with ci oxanil, compound 1 with diclomezine, compound 1 with diclofluanid, compound 1 with dithianon, compound 1 with dimetomorf, compound 1 with dodin, compound 1 with etaboxam, compound 1 with phenpiclonil, compound 1 with fentin, compound 1 with ferbam, compound 1 with fluazinam, compound 1 with fludioxonil, compound 1 with flusulfamide, compound 1 with guazatine, compound 1 with iminoctadine, compu this 1 with mancobre, compound 1 with mancozeb, compound 1 with maneb, compound 1 with metalaxyl, compound 1 with metalaxyl-M, compound. 1 with metiram, compound 1 with metasulfocarb, compound 1 with nabam, compound 1 with nickel bis (dimethyldithiocarbamate), compound 1 with iprovalicarb, compound 1 with oxine-copper, compound 1 with propamocarb, compound 1 with propineb, compound 1 with quinoxifen , compound 1 with sulfur, compound 1 with siltiofam, compound 1 with thiram, compound 1 with tolylfluanide, compound 1 with triazoxide, compound 1 with validamycin, compound 1 with zineb, compound 1 with ziram, compound 1 with phosphorous acid, compound 1 with fosetyl-Al, compound 1 with clozolinate, compound 1 with iprodione, compound 1 with procymidone, compound 1 with vinclozolin, compound 1 with captafol, compound 1 with captan, compound 1 with folpet, compound 1 with thiochlorfenfim, compound 2 with 2-butoxy -6-iodo-3-propyl-benzopyran-4-one, compound 2 with 2,6-dichloro-N-. { [3-chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} benzamide, compound 2 with (Z) -N- [- (cyclopropylmethoxyimino) -2,3-difluoro-6- (trifluoromethyl) benzyl] -2-phenylacetamide, compound 2 with (RS) -2- (4-chlorophenyl) - N- [3-methoxy-4- (prop-2-ynyloxy) phenethyl] -2- (prop-2-ynyloxy) -acetamide, compound 2 with 6-iodo-2-propoxy-3-propylquinazolin-4 (3H) -one, compound 2 with benalaxyl, compound 2 with benthiavalicarb, compound 2 with chlorothalonil, compound 2 with copper hydroxide, compound 2 with copper oxychloride, compound 2 with copper sulfate, compound 2 with copper sulfate (tribasic), compound 2 with cuprous oxide, compound 2 with cymoxanil, compound 2 with diclomezine, compound 2 with diclofluanid, compound 2 with dithianon, compound 2 with dimetomorf, compound 2 with dodin, compound 2 with etaboxam, compound 2 with phenpiclonil, compound 2 with fentin, compound 2 with ferbam, compound 2 with fluazinam, compound 2 with fludioxonil, compound 2 with flusulfamide, compound 2 with guazatine, compound 2 with iminoctadine, comp pair 2 with mancobre, compound 2 with mancozeb, compound 2 with maneb, compound 2 with metalaxyl, compound 2 with metalaxyl-M, compound 2 with metiram, compound 2 with metasulfocarb, compound 2 with nabam, compound 2 with bis (dimethyldithiocarbamate) nickel, compound 2 with iprovalicarb, compound 2 with oxina-copper, compound 2 with propamocarb, compound 2 with propineb, compound 2 with quinoxifen, compound 2 with sulfur, compound 2 with siltiofam, compound 2 with thiram, compound 2 with tolylfluanide, compound 2 with triazoxide, compound 2 with validamycin, compound 2 with zineb, compound 2 with ziram, compound 2 with phosphorous acid, compound 2 with fosetyl-Al, compound 2 with clozolinate, compound 2 with iprodione, compound 2 with procymidone, compound 2 with vinclozolin, compound 2 with captafol, compound 2 with captan, compound 2 with folpet, compound 2 with thiochlorfenfim, compound 3 with 2-butoxy-6-iodo-3-propyl-benzopyran-4-one, compound 3 with 2,6-dichloro-N-. { [3-chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} benzamide, compound 3 with (Z) -N- [- (cyclopropylmethoxyimino) -2,3-difluoro-6- (trifluoromethyl) benzyl] -2-phenylacetamide, compound 3 with (RS) -2- (4-chlorophenyl) - N- [3-methoxy-4- (prop-2'-ynyloxy) phenethyl] -2- (prop-2-ynyloxy) acetamide, compound 3 6-iodo-2-propioxy-3-propylquinazolin-4 (3H) - ona, compound 3 with benalaxyl, compound 3 with benthiavalicarb, compound 3 with chlorothalonil, compound 3 with copper hydroxide, compound 3 with copper oxychloride, compound 3 with copper sulfate, compound 3 with copper sulphate (tribasic), compound 3 with cuprous oxide, compound 3 with cymoxanil, compound 3 with diclomezine, compound 3 with diclofluanid, compound 3 with dithianon, compound 3 with dimetomorf, compound 3 with dodin, compound 3 with etaboxam, compound 3 with phenpiclonil, compound 3 with fentin, compound 3 with ferbam, compound 3 with fluazinam, compound 3 with fludioxonil, compound 3 with flusulfamide, compound 3 with guazatine, compound 3 with iminoctadine, compound or 3 with mancobre, compound 3 with mancozeb, compound 3 with maneb, compound 3 with metalaxyl, compound 3 with metalaxyl-M, compound 3 with methyram, compound 3 with metasulfocarb, compound 3 with nabam, compound 3 with bis (dimethyldithiocarbamate) of nickel, compound 3 with iprovalicarb, compound 3 with oxina-copper, compound 3 with propamocarb, compound 3 with propineb, compound 3 with quinoxifen, compound 3 with sulfur, compound 3 with siltiofam, compound 3 with strip, compound 3 with tolylfluanide, compound 3 with triazoxide, compound 3 with validamycin, compound 3 with zineb, compound 3 with ziram, compound -3 with phosphorous acid, compound 3 with fosetyl-Al, compound 3 with clozslinate, compound 3 with iprodione, compound 3 with procymidone, compound 3 with vinclozolin, compound 3 with captafol, compound 3 with captan, compound 3 with folpet, compound 3 with thiochlorfenfim The composition according to the present invention may further comprise another additional component as a support, vehicle or material of acceptable load from the agricultural point of view. In the present specification, the term "support" refers to an organic or inorganic material, natural or synthetic, with which the active material is combined to make it more easily applicable, mainly on the parts of the plant. Thus, this support is generally inert and should be acceptable from the agricultural point of view. The support can be a solid or a liquid. Examples of suitable supports include clays, natural or synthetic silicates, silica, resins, waxes, solid fertilizers, water, alcohols, in particular butanol, organic solvents, mineral and vegetable oils and derivatives thereof. Mixtures of such supports can also be used. The composition may also comprise other additional components. In particular, the composition may also comprise a surfactant. The surfactant can be an emulsifier, a dispersing agent or a wetting agent, of ionic or non-ionic type or a mixture of these surfactants. Mention may be made, for example, of poly (acrylic acid) salts, salts of lignosulfonic acid, salts of phenolsulfonic or naphthalenesulfonic acid, polycondensates of ethylene oxide with fatty alcohols or fatty acids or fatty amines, substituted phenols (in particular alkylphenols) or arylphenols), salts of esters of sulfosuccinic acid, taurine derivatives (in particular alkyl taurates), phosphoric esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols and derivatives of the compounds described above containing sulfate, sulfonate and phosphate. The presence of at least one surfactant is generally essential when the active material and / or the inert support are insoluble in water and when the vector agent for the application is water. Preferably, the surfactant content may be between 5% and 40% by weight of the composition. Additional components may also be included, for example, protective colloids, adhesives, thickeners, thixotropic agents, penetrating agents, stabilizers, sequestering agents. More generally, the active materials can be combined with any solid or liquid additive, which is adapted to conventional formulation techniques. In general, the composition according to the invention can contain from 0.05 to 99% (by weight) of active material, preferably from 10 to 70% by weight. The compositions according to the present invention can be used in various forms such as aerosol diffuser, capsule suspension, cold fog concentrate, powder, emulsifiable concentrate, oil in water emulsion, water in oil emulsion, encapsulated granule, fine granule, Self-suspending concentrate for seed treatment, gas (pressurized), gas generating product, granules, hot fog concentrate, macrogranules, microgranules, oil dispersible powder, autosuspensible concentrate miscible with oil, liquid miscible with oil, paste, vegetable rod , powder for dry treatment of seeds, seeds coated with a pesticide, soluble concentrate, soluble powder, solution for treatment of seeds, concentrate in suspension (self-suspending concentrate), ultra-low volume liquid (ulv), ultra low volume suspension (ulv), granules or tablets dispersible in water, water dispersible powder for treatment of slurries, granules or tablets soluble in water, water soluble powder for seed treatment and wettable powder. These compositions include not only compositions that are readily applied to the plant or seed to be treated by a suitable device such as a spray or dusting device, but also concentrated commercial compositions that must be diluted before being applied to the culture. The fungicidal compositions of the present invention can be used to curatively or preventively control crop phytopathogenic fungi. In this way, according to a further aspect of the present invention, a method is provided for preventively or curatively controlling phytopathogenic fungi of crops characterized in that a fungicidal composition as described above is applied to the seed, the plant and / or the fruit of the plant or to the soil in which the Plant is growing or where you want it to grow. The composition such as that used against phytopathogenic fungi of crops comprises an effective and / or phytotoxic amount of an active material of general formula (I).

The term "effective and non-phytotoxic amount" refers to an amount of composition according to the invention that is sufficient to combat or destroy the fungi present or that may appear in the cultures, and which does not carry any appreciable symptom "of phytotoxicity for said crops. Such amount may vary within a wide range depending on the fungi to be controlled or controlled, the type of crop, the climatic conditions and the compounds included in the fungicide composition, according to the invention. Systematic field tests, which are within the capabilities of a person skilled in the art The treatment method according to the present invention is useful for treating propagation material such as tubers and rhizomes, but also seeds, seedlings or transplanted seedlings and plants or plants that are transplanted.This treatment procedure can also be useful For treating roots, the treatment method according to the present invention can also be used to treat aerial parts of the plant, such as trunks, stems or stems, leaves, flowers and fruits of the plant in question. Among the plants that can be protected by the method according to the invention, cotton can be mentioned; linen; vine; fruit crops such as Rosaceae sp. (for example, fruits with pips such as apples and pears, but also stone fruits such as apricots, almonds and peaches), Ribesioidae sp. , Juglandaceae sp. , Betulaceae sp. , Anacardiaceae sp. , Fagaceae sp. , Moraceae sp. , Oleaceae sp. , Actinidaceae sp. , Lauraceae sp. , Musaceae sp. (for example, bananas and plantains), Rubiaceae sp. , Theaceae sp. , Sterculiceae sp. and Rutaceae sp. (for example lemons, oranges and grapefruit); legume crops such as Solanaceae sp. (for example, tomatoes), Liliaceae sp. , Asteraceae sp. (for example, lettuce), Umbelliferae sp. , Cruciferae sp. , Chenopodiaceae sp. , Cucurbitaceae sp. , Papilionaceae sp. (for example, peas), Rosaceae sp. (for example, strawberries); large crops, such as Graminae sp. (for example, corn, cereals such as wheat, rice, barley and triticale), Asteraceae sp. (for example, sunflower), Cruciferae sp. (for example, rapeseed), Papilionaceae sp. (for example, soybean), Solanaceae sp. (for example, potatoes) and Chenopodiaceae sp. (for example, beet); horticultural and arboreal crops; as well as the genetically modified homologs of these crops. Among the plants and the possible diseases of these plants protected by the process according to the present invention, the following should be mentioned: - wheat, as it relates. to the fight against the following diseases of the seeds: fusariosis (Microdochium nivale and Fusarium roseum), covered coal of the wheat (Tilletia caries, Tilletia controversa or Tilletia indica), septoriosis (Septoria nodorum) and naked coal; - Wheat, as regards the fight against the following diseases of the aerial parts of the plant: ocular spot of the cereal (Tapesia yallundae, Tapesia acuiformis), foot disease (Gaeumannomyces graminis), foot blight (F. culmorum , F. graminearum), black spots (Rhizoctonia cerealis), powdery mildew (Erysiphe graminis forma specie tritici), rusts (Puccinia striiformis and Puccinia recóndita) and septoriosis (Septoria tri tici and Septoria nodorum); - wheat and barley, as regards the fight against bacterial and viral diseases, for example yellow mosaic of barley; - barley, as regards the control of the following seed diseases: reticular spots (Pyrenophora graminea, Pyrenophora teres and Cochliobolus sativus), naked charcoal (Ustilago nuda) and fusaria (Microdochium nivale and Fusariupi roseum); - barley, as regards the fight against the following diseases of the aerial parts of the plant: ocular spot of. cereal (Tapesia yallundae), reticulate spots (Pyrenophora teres and Cochliobolus sativus), powdery mildew (Erysiphe graminis forms specie hordei), dwarf rust (Puccinia hordei) and scald of barley (Rhynchosporium secalis); potato, in relation to the control of diseases of the tubers (in particular Helminthosporium solani, Phoma tuberosa, Rhizoctonia solani, Fusarium solani) and mildew (Phytopthora infestans) and certain viruses (Y virus); - potato, as regards the fight against the following diseases of the leaves: early blight (Alternarla solani), mildew (Phytophthora infestans); - cotton, as regards the control of the following diseases of shoots obtained from seeds: fall of mastic and basal rot (Rhyzoctonia solani, Fusarium oxisporum) and black rot of the root (Thielaviopsis basicola); protein-producing crops, for example peas, in relation to the control of the following seed diseases: anthracnose (Ascochyta pisi, Mycosphaerella pinodes), fusariosis (Fusarium oxisporum), gray mold (Botrytis cinerea) and mildew (Peronospora pisi); oil-producing crops, for example, rapeseed, with respect to the control of the following seed diseases: Phoma lingam, Al ternarla brassicae and Sclerotinia solero tiorum; - corn, as regards the control of seed diseases: (Rhizopus sp., Penicillium sp., Trichoderma sp., Aspergillus sp., and Gibberella fujikuroi); - flax, in what refers to the fight against the diseases of the seeds: When ternarla linicola; - forest trees, as regards the fight against the fall of mastic (Fusarium oxisporum, Rhizoctonia solani); - rice, in relation to combating the following diseases of the aerial parts: parasitic Bruzzone (Magnaporthe grisea), spots on the edges of the pods (Rhizoctonia solani); crops "of legumes, in relation to combating the following diseases of seeds or outbreaks that come from seeds: fall of mastic and basal rot (Fusarium oxisporum, Fusarium roseum, Rhizoctonia solani, Pythium sp.) - Leguminous crops, as regards the fight against the following diseases of the aerial parts: gray mold (Botrytis sp.), powdery mildew (in particular Erysiphe cichoracearum, Sphaerotheca fuliginea and Leveillula táurica), fusaria (Fusarium oxisporum, Fusarium roseum), leaf spots (Cladosporium sp.), Alternating (Al ternarla sp.), Anthracnose (Colletotrichum sp.), Septoria (Septoria sp.), Black spots (Rhizoctonia solani) and mildew (for example, Bremia lactucae, Peronospora sp., Pseudoperonospora sp. , Phytophthora sp.); - fruit trees, in relation to diseases of the aerial parts: diseases by monilia (Monilia fructigenae, M. laxa), scab (Venturia inaequalis) and oídio (Podos) phaera leucotricha); - vine, in relation to diseases of leaves: in particular gray mold (Botrytis cinerea), powdery mildew (Uncinula necator), black scab (Guignardia biwelli) and mildew (Plasmopara vi tícola); beet, in relation to combating the following diseases of the aerial parts: blight (Cercospora beticola), powdery mildew (Erysiphe beticola), leaf spots (Ramularia beticola). The fungicidal composition according to the present invention can also be used against fungal diseases that can grow on or within the wood. The term "wood" refers to all types of wood species, and to all types of wood work intended for construction, for example, solid wood, high density wood, laminated wood and plywood. The process for treating the wood according to the invention comprises essentially bringing it into contact with one or more compounds of the present invention, or a composition according to the invention; this includes, for example, direct application, spraying, immersion, injection or any other suitable means. The fungicidal composition according to The present invention can also be used in the treatment of genetically modified organisms with the compounds according to the invention or the agrochemical compositions according to the invention. Genetically modified plants are plants in whose genome a heterologous gene encoding a protein of interest has been stably integrated. The term "heterologous gene encoding a protein of interest" basically means genes that contribute to the transformed plant new agronomic properties, or genes to improve the agronomic quality of the transformed plant. The dose of active material normally applied in the treatment according to the present invention is generally and advantageously between 10 and 2,000 g / ha, preferably between 20 and 1,500 g / ha for applications in leaf treatment. The dose of active substance applied is generally and advantageously between 1 and 200 g per 100 kg of seeds, preferably between 2 and 150 g per 100 kg of seeds in the case of seed treatment. It is clearly understood that the doses indicated above are given as illustrative examples of the invention. A person skilled in the art will know how to adapt the application dose according to the nature of the crop to be treated. The compositions according to the present invention can also be used for the preparation of a composition useful to curatively or preventively treat fungal diseases in humans and animals such as, for example, mycosis, dermatosis, trichophyton and candidiasis diseases or diseases caused by Aspergillus spp. or Candida spp. , for example Aspergillus fumigatus or Candida albicans, respectively. The present invention will now be illustrated with the following examples: Example 1: Efficacy against Botrytis cinerea of a mixture containing N-. { 2- [3-chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2- trifluorom tilbenzamide (compound 1) and mancozeb The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert de Paris variety) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per L) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of KH2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when compound 1 and mancozeb are tested alone and in mixtures of different weight ratios.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 2: Efficacy against Botrytis cinerea of a mixture containing? -. { 2- [3-chloro-5- (trifluorosmethyl) -2-pyridinyl] ethyl} -2- trifluoromethylbenza ida (compound 1) and propineb The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert variety of Paris) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of KH2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when compound 1 and mancozeb are tested alone and in mixtures of different weight ratios.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 3: Effectiveness against Puccinia recondite of a mixture containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} - 2-trxfluoromethylbenzamide (compound 1) and captan The active ingredients tested were prepared by crucible homogenization in a mixture of acetone / tween / water. This suspension was then diluted with water to obtain the desired concentration of active material. Wheat plants (Scipion variety), in seedbeds, seeded in a 50/50 peat-pozzolana substrate and maintained at 12 ° C, are treated in the 1-leaf stage (10 cm high), spraying them with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants were contaminated by spraying their leaves with an aqueous suspension of Puccinia spores (100,000 spores per ml). The spores are harvested from contaminated wheat ten days old and suspended in water containing 2.5 ml / 1 of 10% tween 80. The contaminated wheat plants are incubated for 24 hours at 20 ° C and 100% relative humidity and then for 10 days at 202 ° C and 70% relative humidity. The classification is carried out 10 days after the contamination, comparing with the control plants. The following table summarizes the results obtained when testing compound 1 and capture alone and in mixtures of different weight ratios.

According to the Colby method, a synergistic effect has been observed in the mixtures tested.

Example 4: Efficacy against Botrytis cinerea of a mixture containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2- trifluoramethylbenzamide (compound 1) and folpet The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert variety, Paris) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated at the Zll cotyledon stage by spraying with the aqueous suspension described above. . The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of H2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% effectiveness) was carried out 5 to 7 days after the contamination, compared to the control plants. The following table summarizes the results obtained when compound 1 and folpet are tested alone and in mixtures of different weight ratios.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 5: Efficacy against Botrytis cinerea of a mixture containing N-. { 2- [3-chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (compound 1) and iprodione The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert variety of Paris) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material.

After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - I g / l of H2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and at a relative humidity of 80%. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when compound 1 and iprodione are tested alone and in mixtures of different weight ratios.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 6: Efficacy against Botrytis cinerea of a mixture containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2- trifluoroethylbenzamide (compound 1) and fludioxonil The tested active ingredients were prepared by crucible homogenization in a mixture of acetone / tween / water. This suspension was then diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert variety of Paris) in seedbeds, planted on a 50/50 peat-pozzolana substrate and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar ~ 2 g / l of NH4N03 - 1 g / l of KH2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when testing compound 1 and fludioxonil "" alone and in mixtures of different weight ratios.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 7: Efficacy against Botrytis cinerea of a mixture containing N-. { 2- [3-chloro-5- (trifluoro-etxl) -2-pyridinyl] etxl} -2-trifluoromethylbenzamide (compound 1) and benalaxyl The tested active ingredients were prepared by crucible homogenization in a mixture of acetone / tween / water. This suspension was then diluted with water to obtain the desired concentration of active material.

Gherkin plants (Petit vert de Paris variety) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated, with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous spore suspension of -Botrytis cinerea (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and are placed - in suspension in a solution - of nutrients composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of KH2P0 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when compound 1 and benalaxyl are tested alone and in a 1: 3 weight ratio mixture.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 8: Efficacy against ~ Botrytis cinerea of a mixture containing N-. { 2- [3-chloro-5- (trifluoraethyl) -2-pyridinyl] ethyl} -2- trifluoromethylbenzamide (compound 1) and matalaxyl-M The active ingredients tested were prepared by crucible homogenization in a mixture of acetone / tween / water. This suspension was then diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert de Paris variety) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per L) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of KH2P0 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when compound 1 and matalaxyl-M are tested alone and in a 1: 3 weight ratio mixture.

According to the Colby method, a synergistic effect has been observed in the mixtures tested.

Example 9: Efficacy against Botrytis cinérea de tina mixture containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2- trifluoromethylbenzamide (compound 1) and propamocarb-HCl The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert de Paris variety) in seedbeds, seeded on a 50/50 substrate of peat-pozzolana and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea 'spores (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of KH2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out 5 to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when testing compound 1 and propamocarb-HCl alone and in a 1: 9 weight ratio mixture.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 10: Efficacy against Botrytis cinerea of a mixture containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoramethylbenzamide (compound 1) and fosetyl-Al The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (Petit vert variety of Paris) in seedbeds, planted on a 50/50 peat-pozzolana substrate and maintained at 18-20 ° C, were treated in the Zll cotyledon stage by spraying with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by depositing drops of an aqueous suspension of Botrytis cinerea spores (150,000 spores per mL) on the upper surface of the leaves. The spores are collected from a 15-day culture and suspended in a nutrient solution composed of: - 20 g / l of gelatin - 50 g / l of cane sugar - 2 g / l of NH4N03 - 1 g / l of KH2P04 The contaminated gherkin plants were deposited for 5/7 days in a climatic chamber at 15-11 ° C (day / night) and 80% relative humidity. The classification (% efficiency) was carried out from 5 - to 7 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when testing compound 1 and fosetyl-Al alone and in a 1: 9 weight ratio mixture.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 11: Efficacy against Sphaerotheca fuliginea of a composition containing N-. { 2- [3-chloro-5- (trifluoramethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (Compound 1) and tolylfluanide The formulated compounds were diluted with water to obtain the. concentration of active material desired. Gherkin plants (variety Vert petit de Paris) in seedbeds, seeded on a 50/50 peat-pozzolana substrate and maintained at 20 ° C / 23 ° C, were treated in the 2-leaf stage by spraying with the aqueous suspension described previously. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants were contaminated by spraying with an aqueous spore suspension of Sphaerotheca fuliginea (100,000 spores per ml). The spores were collected from contaminated plants. The contaminated gherkin plants were incubated at approximately 20 ° C / 25 ° C and at a relative humidity of 60/70%. The classification (% of efficacy) was carried out 21 days after the contamination, in comparison with the control plants. The following table summarizes the results obtained when compound 1 and tolylfluanide are tested alone and in mixtures of different ratios by weight.

According to the Colby method, a synergistic effect has been observed in the mixtures tested. Example 12: Efficacy against parasitic Peronospora of a composition containing N-. { 2- [3-chloro-5- (trifluoramethyl) -2-pyridinyl] et l} -2-trifluorome-ilbenzamide (compound 1) and 2,6-dichloro-N-. { [3-chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} Enzyme (compound A) The active ingredient tested is prepared by homogenizing Potter in a suspension-type formulation concentrated at 100 g / L. This suspension is then diluted with water to obtain the desired concentration of active material. The cabbage plants (Eminence variety), in seedbeds, seeded in a 50/50 peat-pozzolana substrate and maintained at 18-20aC, are treated in the cotyledon stage by spraying them with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants are contaminated by spraying them with an aqueous suspension of spores of Peronospora brassicae (50,000 spores per ml). The spores are collected from the infected plant. The contaminated cabbage plants are incubated for 5 days at 20 ° C, in a humid atmosphere. The classification is carried out 5 days after the contamination, comparing with the control plants The following table summarizes the results obtained when testing compound 1 and compound A alone and in a 1: 1 weight ratio mixture.

According to the Coiby method, a synergistic effect has been observed in the mixtures tested.

Example 13: Efficacy against Sphaerotheca fuliginea of a composition containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (Compound 1) and iprovalicarb The formulated compounds were diluted with water to obtain the desired concentration of active material. Gherkin plants (variety Vert petit de Paris) in seedbeds, planted on a 50/50 peat-pozzolan substrate and maintained at 20 ° C / 23 ° C, were treated in the 2-leaf stage by spraying with the suspension aqueous described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants were contaminated by spraying with an aqueous spore suspension of Sphaerotheca fuliginea (100,000 spores per ml). The spores were collected from contaminated plants. The contaminated gherkin plants were incubated at approximately 20 ° C / 25 ° C and at a relative humidity of 60/70%. The classification (% of efficiency) was carried out 21 days after contamination, compared to control plants. The following table summarizes the results obtained when testing compound 1 and iprovalicarb alone and in a 1: 9 weight ratio mixture.

According to the Coiby method, a synergistic effect has been observed in the mixtures tested. Example 14: Efficacy against Erysiphe graminis f. sp. tritici of a composition containing N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide (compound 1) and chlorothalonil The formulated compounds were diluted with water to obtain the desired concentration of active material. Wheat plants (variety Audace) in seedbeds, seeded in a 50/50 substrate of peat-pozzolan and maintained at 12aC, are treated in the 1-leaf stage (10 cm high), spraying them with the aqueous suspension described above. The plants, used as controls, are treated with an aqueous solution that does not contain the active material. After 24 hours, the plants were contaminated by sprinkling them with Erysiphe graminis spores. F. sp. tritici, dusted using contaminated plants.

The classification was carried out 7 to 14 days after the contamination, comparing with the control plants. The following table summarizes the results obtained when testing compound 1 and chlorothalonil. alone and in mixtures of different weight ratios.

According to the Coiby method, a synergistic effect has been observed in the mixtures tested. It is noted that in relation to this date, the best method known to the applicant to carry out the aforementioned invention, is that which is clear from the present description of the invention.

Claims (18)

2. Having described the invention as above, the content of the following claims is claimed as property: 1. A composition characterized by comprises: a) a pyridylethylbenzamide derivative of the general formula (I) - wherein: - p is an integer equal to 1, 2, 3 or 4; - q is an integer equal to 1, 2, 3, 4 or 5; - each substituent X is chosen, independently of the others, as halogen, alkenyl or haloalkyl; - each substituent Y is chosen, independently of the others, as: halogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, amino, phenoxy, alkylthio, dialkylamino, acyl, cyano, ester, hydroxy, aminoalkyl, benzyl, haloalkoxy, halosulfonyl, halothioalkyl, alkoxyalkenyl, alkylsulfonamide, nitro, alkylsulfonyl, phenylsulfonyl or benzylsulfonyl; as well as its N-oxides of 2-pyridine; and b) a compound capable of inhibiting spore germination or mycelial growth by acting on different metabolic pathways; in a weight ratio of (a) / (b) from 0.01 to 20. 2. - A composition according to claim 1, characterized in that p is 2.
3. 3. - A composition according to claim 1 or 2, characterized in that q is 1 or 2.
4. 4. A composition according to any of claims 1 to 3, characterized in that X is chosen, independently of the others, as halogen or haloalkyl.
5. 5. - A composition according to any of claims 1 to 4, characterized in that X is independently chosen from the others, such as a chlorine atom or a trifluoromethyl group.
6. 6. - A composition according to any of claims 1 to 5, characterized in that Y is chosen, independently of the others, as halogen or haloalkyl.
7. 7. A composition according to any of claims 1 to 6, characterized in that Y is chosen, independently of the others, as a chlorine atom or a trifluoromethyl group.
8. 8. - A composition according to any of claims 1 to 7, characterized in that the compound of general formula (I) is: - N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide; - N- { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-iodobenzamide or N-. { 2- [3,5-dichloro-2-pyridinyl] ethyl} -2- trifluoromethylbenzamide.
9. 9. - A composition according to claim 8, characterized in that the compound of general formula (I) is N-. { 2- [3-Chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2-trifluoromethylbenzamide.
10. 10. A composition according to any of claims 1 to 9, characterized in that the compound capable of inhibiting the germination of spores or the growth of the mycelium acting on different metabolic pathways is a dicarboximide derivative.
11. 11. - A composition according to claim 10, characterized in that the dicarboximide derivative is clozolinate, iprodione, procymidone or vinclozolin.
12. 12. - A composition according to any of claims 1 to 9, characterized in that the compound capable of inhibiting the germination of spores or the growth of the mycelium acting on different metabolic pathways is a derivative of phthalimide.
13. 13. - A composition according to claim 12, characterized in that the phthalimide derivative is captafol, captan, folpet or thiochlorfenfim.
14. 14. A composition according to any of claims 1 to 9, characterized in that the compound capable of inhibiting the germination of spores or the growth of the mycelium acting on different metabolic pathways is 2-butoxy-6-iodo-3-propyl- benzopyran-4-one, 2,6-dichloro-N-. { [3-chloro-5- (trifluoromethyl) -2-pyridinyl] methyl} benzamide, (Z) -N- [a- (cyclopropylmethoxyimino) -2,3-difluoro-6- (trifluoromethyl) benzyl] -2-phenylacetamide, (RS) -2- (4-chlorophenyl) ~ N- [3- methoxy-4- (prop-2-ynyloxy) phenethyl] -2- (prop-2-ynyloxy) acetamide, 6-iodo-2-propoxy-3-propylquinazolin-4 (3H) -one, benalaxyl, benthiavalicarb, chlorothalonil, copper hydroxide, copper oxychloride, copper sulfate, copper sulfate (tribasic), cuprous oxide, cymoxanil, diclomezine, diclofluanid, dithianon, dimetomorph, dodine, etaboxam, fenpiclonil, fentin, ferbam, fluazinam, fludioxonil, flusulfamide, guazatin, iminoctadine, mancobre, mancozeb, maneb, metalaxyl, metalaxyl-M, metiram, metasulfocarb, naba, bis (dimethyldithiocarbamate) of nickel, iprovalicarb, oxina-copper, propamocarb, propineb, quinoxifen, sulfur, siltiofam, thiram, tolylfluanid, triazoxide, validamycin, zineb, ziram, phosphorous acid and fosetyl-Al.
15. 15. - A composition according to any one of claims 1 to 14, characterized in that it also comprises a fungicidal compound (c).
16. 16. A composition according to claim 15, characterized in that the fungicidal compound (c) is selected from dietofencarb, hexaconazole, cyprodinil, tebuconazole and bromuconazole.
17. 17. A composition according to any of claims 1 to 16, characterized in that it also comprises a support, vehicle, material and / or surfactant acceptable from the agricultural point of view.
18. 18. A method for preventively or curatively controlling phytopathogenic fungi of crops, characterized in that an effective and non-phytotoxic amount of a composition according to any of claims 1 to 17 is applied to the seed, the plant and / or the fruit of the plant or soil in which it grows or in which it is desired that the plant grows.