Patent Application
20070149588
The present invention relates to 6-(2,3,6-trifluorophenyl)triazolopyrimidines of the formula I
in which the substituents are as defined below:
Moreover, the invention relates to a process for preparing these compounds, to compositions comprising them and to their use for controlling phytopathogenic harmful fungi.
5-Halo-6-(2,3,6-trifluorophenyl)triazolopyrimidines are known in the general manner from EP-A 945 453. 5-Cyano- and 5-alkoxytriazolopyrimidines are disclosed in WO 02/083677. Triazolopyrimidines having optically active amino substituents in the 7-position are proposed in a general manner in WO 02/38565.
The compounds described in the publications mentioned above are suitable for controlling harmful fungi.
However, they are not always entirely satisfactory. Using this as a basis, it is an object of the present invention to provide compounds having improved activity and/or a broader activity spectrum.
Accordingly, we have found the compounds defined at the outset. Furthermore, we have found a process for their preparation, compositions comprising them and methods for controlling harmful fungi using the compounds I.
The compounds according to the invention differ from the compounds described in the abovementioned publication by the substitution in the 5-position of the triazolopyrimidine skeleton.
Compared to the known compounds, the compounds of the formula I have increased activity and/or a broader activity spectrum against harmful fungi.
The compounds according to the invention can be obtained by different routes. Advantageously, they are obtained from the 5-halo-6-(2,3,6-trifluorophenyl)triazolo-pyrimidines of the formula II known from EP-A 945 453 by reaction with compounds M-X (formula III). Depending on the meaning of the group X to be introduced, the compounds III are inorganic cyanides or alkoxides. The reaction is advantageously carried out in the presence of an inert solvent. The cation M in formula III is of little importance; for practical reasons, preference is usually given to ammonium, tetraalkylammonium or alkali metal or alkaline earth metal salts.
The reaction temperature is usually from 0 to 120° C., preferably from 10 to 40° C. [cf. J. Heterocycl. Chem., Vol. 12, pp. 861-863 (1975)].
If R2 is hydrogen, a removable protective group is advantageously introduced prior to the reaction with III [cf. Greene, Protective Groups in Organic Chemistry, J. Wiley & Sons, (1981)].
Suitable solvents comprise ethers, such as dioxane, diethyl ether and, preferably, tetrahydrofuran, alcohols, such as methanol or ethanol, halogenated hydrocarbons, such as dichloromethane, and aromatic hydrocarbons, such as toluene or acetonitrile.
Compounds of the formula I in which X is C1-C4-alkyl can be obtained advantageously by the synthesis route below:
The 5-alkyl-7-hydroxy-6-phenyltriazolopyrimidines VI are obtained from 2-aminotriazole IV and keto esters V where R is C1-C4-alkyl. In the formulae V and VI, X1 is C1-C4-alkyl. Using the easily obtainable 2-phenylacetoacetic esters (V where X1=CH3), the 5-methyl-7-hydroxy-6-phenyltriazolopyrimidines, which are a preferred subject-matter of the invention, are obtained [cf. Chem. Pharm. Bull., 9, 801, (1961)]. 2-Aminotriazole IV is commercially available. The starting materials V are advantageously prepared under the conditions described in EP-A 10 02 788.
The 5-alkyl-7-hydroxy-6-phenyltriazolopyrimidines obtained in this manner are, using halogenating agents [HAL], converted under the conditions known from WO-A 94/20501 into the halopyrimidines of the formula VII in which Hal is a halogen atom, preferably a bromine or a chlorine atom, in particular a chlorine atom. Advantageous halogenating agents [HAL] are chlorinating or brominating agents, such as phosphorus oxybromide, phosphorus oxychloride, thionyl chloride, thionyl bromide or sulfuryl chloride.
This reaction is usually carried out at from 0° C. to 150° C., preferably at from 80° C. to 125° C. [cf. EP-A 770 615].
The reaction of VII with amines VIII in which R1 and R2 are as defined for formula I is advantageously carried out at from 0° C. to 70° C., preferably from 10° C. to 35° C., preferably in the presence of an inert solvent, such as an ether, for example dioxane, diethyl ether or, in particular, tetrahydrofuran, a halogenated hydrocarbon, such as dichloromethane, or an aromatic hydrocarbon, such as, for example, toluene [cf. WO-A 98/46608].
Preference is given to using a base, such as a tertiary amine, for example triethylamine, or an inorganic amine, such as potassium carbonate; it is also possible for excess amine of the formula VIII to serve as base.
Alternatively, compounds of the formula I in which X is C1-C4-alkyl can also be prepared from compounds I in which X is halogen, in particular chlorine, and malonates of the formula IX. In formula IX, X is hydrogen or C1-C3-alkyl and R is C1-C4-alkyl. They are converted into the compounds of the formula X and decarboxylated to compounds I [cf. U.S. Pat. No. 5,994,360].
The malonates IX are known from the literature [J. Am. Chem. Soc. 64 (1942), 2714; J. Org. Chem. 39 (1974), 2172; Helv. Chim. Acta 61 (1978), 1565], or they can be prepared in accordance with the literature cited.
The subsequent hydrolysis of the ester X is carried out under generally customary conditions; depending on the different structural elements, alkaline or acidic hydrolysis of compounds X may be advantageous. Under the conditions of ester hydrolysis, there may already be complete or partial decarboxylation to I.
The decarboxylation is usually carried out at temperatures of from 20° C. to 180° C., preferably from 50° C. to 120° C., in an inert solvent, if appropriate in the presence of an acid.
Suitable acids are hydrochloric acid, sulfuric acid, phosphoric acid, formic acid, acetic acid, p-toluenesulfonic acid. Suitable solvents are water, aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, such as methylene chloride, chloroform and chlorobenzene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles, such as acetonitrile and propionitrile, ketones, such as acetone methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide; with particular preference, the reaction is carried out in hydrochloric acid or acetic acid. It is also possible to use mixtures of the solvents mentioned.
Compounds of the formula I in which X is C1-C4-alkyl can also be obtained by coupling 5-halotriazolopyrimidines of the formula I in which X is halogen with organometallic reagents of the formula XI. In one embodiment of this process, the reaction is carried out with transition metal catalysis, such as Ni or Pd catalysis.
In formula XI, M is a metal ion of valency Y, such as, for example, B, Zn or Sn, and X″ is C1-C3-alkyl. This reaction can be carried out, for example, analogously to the following methods: J. Chem. Soc. Perkin Trans. 1, (1994), 1187, ebid. 1 (1996), 2345; WO-A 99/41255; Aust. J. Chem. 43 (1990), 733; J. Org. Chem. 43, (1978), 358; J. Chem. Soc. Chem. Commun. (1979), 866; Tetrahedron Lett. 34 (1993), 8267; ebid. 33 (1992), 413.
The reaction mixtures are worked up in a customary manner, for example by mixing with water, separating the phases and, if appropriate, chromatographic purification of the crude products. Some of the intermediates and end products are obtained in the form of colorless or slightly brownish viscous oils which can be purified or freed from volatile components under reduced pressure and at moderately elevated temperature. If the intermediates and end products are obtained as solids, purification can also be carried out by recrystallization or digestion.
If individual compounds I cannot be obtained by the routes described above, they can be prepared by derivatization of other compounds I.
If the synthesis yields mixtures of isomers, a separation is generally not necessarily required since in some cases the individual isomers can be interconverted during work-up for use or during application (for example under the action of light, acids or bases). Such conversions may also take place after use, for example in the treatment of plants in the treated plant, or in the harmful fungus to be controlled.
In the definitions of the symbols given in the formulae above, collective terms were used which are generally representative of the following substituents:
The scope of the present invention includes the (R)- and (S)-isomers and the racemates of compounds of the formula I having chiral centers.
With a view to the intended use of the triazolopyrimidines of the formula I, particular preference is given to the following meanings of the substituents, in each case on their own or in combination:
Preference is given to compounds I in which R1 is C1-C4-alkyl, C2-C6-alkenyl or C1-C8-haloalkyl.
Preference is given to compounds I in which R1 is a group A:
in which
Moreover, preference is given to compounds I in which R1 is C3-C6-cycloalkyl which may be substituted by C1-C4-alkyl.
Especially preferred are compounds I in which R2 is hydrogen.
Preference is likewise given to compounds I in which R2 is methyl or ethyl.
If R1 and/or R2 comprise haloalkyl or haloalkenyl groups having a center of chirality, the (S)-isomers are preferred for these groups. In the case of halogen-free alkyl or alkenyl groups having a center of chirality in R1 or R2, preference is given to (R)-configured isomers.
A preferred embodiment of the invention relates to compounds of the formula I.1:
in which
A further preferred embodiment of the invention relates to compounds of the formula I.2.
in which Y is hydrogen or C1-C4-alkyl, in particular methyl and ethyl, and X is defined according to formula I, in particular is cyano, methoxy or ethoxy.
A further preferred embodiment of the invention relates to compounds in which R1 and R2 together with the nitrogen atom to which they are attached from a five- or six-membered heterocyclyl or heteroaryl which is attached via N and may contain a further heteroatom from the group consisting of O, N and S as ring member and/or may carry one or more substituents from the group consisting of halogen, C1-C6-alkyl, C1-C6-halo-alkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C3-C6-alkenyloxy, C3-C6-haloalkenyloxy, C1-C6-alkylene and oxy-C1-C3-alkyleneoxy. These compounds correspond in particular to formula I.3,
in which
Preference is furthermore given to compounds I in which R1 and R2 together with the nitrogen atom to which they are attached form a piperidinyl, morpholinyl or thio-morpholinyl ring, in particular a piperidinyl ring, which, if appropriate, is substituted by one to three groups halogen, C1-C4-alkyl or C1-C4-haloalkyl. Particular preference is given to the compounds in which R1 and R2 together with the nitrogen atom to which they are attached form a 4-methylpiperidine ring.
The invention furthermore preferably provides compounds I in which R1 and R2 together with the nitrogen atom to which they are attached form a pyrazole ring which, if appropriate, is substituted by one or two groups halogen, C1-C4-alkyl or C1-C4-haloalkyl, in particular by 3,5-dimethyl or 3,5-di-(trifluoromethyl).
In addition, particular preference is also given to compounds of the formula I in which R1 is CH(CH3)—CH2CH3, CH(CH3)—CH(CH3)2, CH(CH3)—C(CH3)3, CH(CH3)—CF3, CH2C(CH3)═CH2, CH2CH═CH2, cyclopentyl or cyclohexyl; R2 is hydrogen or methyl; or R1 and R2 together are —(CH2)2CH(CH3)(CH2)2—, —(CH2)2CH(CF3)(CH2)2— or —(CH2)2O (CH2)2—.
Particular preference is furthermore given to compounds I in which X is cyano, methoxy or ethoxy, in particular cyano or methoxy.
In another preferred embodiment of the compounds of the formula I, X is C1-C4-alkyl, in particular methyl.
In particular with a view to their use, preference is given to the compounds I compiled in the tables below. Moreover, the groups mentioned for a substituent in the tables are per se, independently of the combination of which they are mentioned, a particularly preferred embodiment of the substituent in question.
Table 1
Compounds of the formula I in which X is cyano and the combination of R1 and R2 corresponds for each compound to one row of table A
Table 2
Compounds of the formula I in which X is methoxy and the combination of R1 and R2 corresponds for each compound to one row of table A
Table 3
Compounds of the formula I in which X is ethoxy and the combination of R1 and R2 corresponds for each compound to one row of table A
Table 4
Compounds of the formula I in which X is methyl and the combination of R1 and R2 corresponds for each compound to one row of table A
The compounds I are suitable as fungicides. They are distinguished by an outstanding effectiveness against a broad spectrum of phytopathogenic fungi, especially from the classes of the Ascomycetes, Deuteromycetes, Oomycetes and Basidiomycetes. Some are systemically effective and they can be used in plant protection as foliar and soil fungicides.
They are particularly important in the control of a multitude of fungi on various cultivated plants, such as wheat, rye, barley, oats, rice, corn, grass, bananas, cotton, soybean, coffee, sugar cane, vines, fruits and ornamental plants, and vegetables, such as cucumbers, beans, tomatoes, potatoes and cucurbits, and on the seeds of these plants.
They are especially suitable for controlling the following plant diseases:
The compounds I are also suitable for controlling harmful fungi, such as Paecilomyces variotii, in the protection of materials (e.g. wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products.
The compounds I are employed by treating the fungi or the plants, seeds, materials or soil to be protected from fungal attack with a fungicidally effective amount of the active compounds. The application can be carried out both before and after the infection of the materials, plants or seeds by the fungi.
The fungicidal compositions generally comprise between 0.1 and 95%, preferably between 0.5 and 90%, by weight of active compound.
When employed in plant protection, the amounts applied are, depending on the kind of effect desired, between 0.01 and 2.0 kg of active compound per ha.
In seed treatment, amounts of active compound of 1 to 1000 g, preferably 5 to 100 g, per 100 kilogram of seed are generally required.
When used in the protection of materials or stored products, the amount of active compound applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are, for example, 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active compound per cubic meter of treated material.
The compounds I can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules. The application form depends on the particular purpose; in each case, it should ensure a fine and uniform distribution of the compound according to the invention.
The formulations are prepared in a known manner, for example by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants. Solvents/auxiliaries which are suitable are essentially:
Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalene-sulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxy-ethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.
Suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydro-naphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strongly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water.
Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound. The active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
The following are examples of formulations:
1. Products for Dilution with Water
A Water-soluble Concentrates (SL)
10 parts by weight of a compound according to the invention are dissolved in water or in a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound dissolves upon dilution with water.
B Dispersible Concentrates (DC)
20 parts by weight of a compound according to the invention are dissolved in cyclohexanone with addition of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion.
C Emulsifiable Concentrates (EC)
15 parts by weight of a compound according to the invention are dissolved in xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5%). Dilution with water gives an emulsion.
D Emulsions (EW, EO)
40 parts by weight of a compound according to the invention are dissolved in xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5%). This mixture is introduced into water by means of an emulsifying machine (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion.
E Suspensions (SC, OD)
In an agitated ball mill, 20 parts by weight of a compound according to the invention are comminuted with addition of dispersants, wetters and water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound.
F Water-dispersible Granules and Water-soluble Granules (WG, SG)
50 parts by weight of a compound according to the invention are ground finely with addition of dispersants and wetters and made into water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound.
G Water-dispersible Powders and Water-soluble Powders (WP, SP)
75 parts by weight of a compound according to the invention are ground in a rotor-stator mill with addition of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound.
2. Products to be Applied Undiluted
H Dustable Powders (DP)
5 parts by weight of a compound according to the invention are ground finely and mixed intimately with 95% of finely divided kaolin. This gives a dustable product.
Granules (GR, FG, GG, MG)
0.5 part by weight of a compound according to the invention is ground finely and associated with 95.5% carriers. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted.
J ULV Solutions (UL)
10 parts by weight of a compound according to the invention are dissolved in an organic solvent, for example xylene. This gives a product to be applied undiluted.
The active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; the intention is to ensure in each case the finest possible distribution of the active compounds according to the invention.
Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.
The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1%.
The active compounds may also be used successfully in the ultra-low-volume process (ULV), by which it is possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
Various types of oils, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the agents according to the invention in a weight ratio of 1:10 to 10:1.
The compositions according to the invention can, in the use form as fungicides, also be present together with other active compounds, e.g. with herbicides, insecticides, growth regulators, fungicides or else with fertilizers. Mixing the compounds I or the compositions comprising them in the application form as fungicides with other fungicides results in many cases in an expansion of the fungicidal spectrum of activity being obtained.
The following list of fungicides, in conjunction with which the compounds according to the invention can be used, is intended to illustrate the possible combinations but does not limit them:
With appropriate modification of the starting compounds, the procedures given in the synthesis examples below were used to obtain further compounds I. The compounds obtained in this manner are listed in the tables below, together with physical data.
A solution of 0.2 g (0.5 mmol) of 5-chloro-6-(2,3,6-trifluorophenyl)-7-(2-methyl-piperidinyl)-1,2,4-triazolo[1,5a]pyrimidine [cf. EP-A 945 453] and 0.5 g (3.3 mmol) of tetrabutylammonium cyanide in 2 ml of acetonitrile was stirred at 20-25° C. for 14 hours. The reaction mixture was then evaporated under reduced pressure and the residue was purified by preparative MPLC on silica gel RP-18 using acetonitrile/water mixtures. The eluate gave 0.13 g of the title compound as a colorless solid of m.p. 173-177° C.
1H-NMR (CDCl3, δ in ppm): 8.5 (s, 1H); 7.4 (m, 1H); 7.1 (m, 1H); 4.65 (m, 1H); 3.1-3.4 (m, 2H); 1.8-1.9 (m, 1H); 1.6-1.8 (m, 3H); 1.5 (m, 2H); 1.25 (m, 3H).
After addition of 0.12 g of 30% strength sodium methoxide solution, a solution of 0.2 g (0.5 mmol) of 5-chloro-6-(2,3,6-trifluorophenyl)-7-cyclopentylamino-1,2,4-triazolo[1,5a]pyrimidine [cf. EP 945 453] in 5 ml of methanol was stirred at 20-25° C. for 24 hours, then at 50° C. for 3 hours, after addition of a further 0.12 g of 30% strength sodium methoxide solution at 50° C. for 8 hours, after further addition of 0.2 g of 30% strength sodium methoxide solution at 60° C. for 4 hours, then at 20-25° C. for 18 hours. The reaction mixture was then evaporated under reduced pressure and the residue was purified by preparative MPLC on silica gel RP-18 using acetonitrile/water mixtures. The eluate gave 0.13 g of the title compound as a yellow resin.
1H-NMR (CDCl3, δ in ppm): 8.2 (s, 1H); 7.3 (m, 1H); 6.95 (m, 1H); 6.2 (d, 1H); 4.0 (s, 3H); 3.55 (m, 1H); 1.65 (m, 4H); 1.5 (m, 4H)
A solution of 0.6 g (1.6 mmol) of 5-chloro-6-(2,3,6-trifluorophenyl)-7-(2-methylpiperidinyl)-1,2,4-triazolo[1,5a]pyrimidine [cf. EP 945 453] and 0.6 g (4 mmol) of sodium dimethylmalonate in 5 ml of acetonitrile was stirred at 80° C. for about 5 hours. A yellow solid precipitated out. The reaction mixture was then filtered off with suction through silica gel, the yellow solid was taken up in methylene chloride and dilute hydrochloric acid and the suspension was stirred at 20-25° C. for about 15 min. The phases were then separated and the organic phase was dried and freed from the solvent.
The residue obtained was—without purification—taken up in 10 ml of conc. hydrochloric acid, and the reaction mixture was stirred at 80-90° C. for 3 hours. The reaction mixture was then diluted with water and the aqueous phase was extracted with methylene chloride. The combined organic phases were dried and freed from the solvent. The residue was purified by preparative MPLC on silica gel RP-18 using acetonitrile/water mixtures and digestion in hexane. This gave 0.2 g of the title compound as a bright solid of m.p. 108-110° C.
1H-NMR (CDCl3, δ in ppm): 8.4 (s, 1H); 7.3 (m, 1H); 7.0 (m, 1H); 4.2 (m, 1H); 3.05-3.25 (m, 2H); 2.4 (s, 3H); 1.25-1.75 (m, 6H); 1.05 (m, 3H)
The fungicidal action of the compounds of the formula I was demonstrated by the following tests:
The active compounds were prepared as a stock solution with 25 mg of active compound which was made up to 10 ml using a mixture of acetone and/or DMSO and the emulsifier Uniperol® EL (wetting agent having emulsifying and dispersing action based on ethoxylated alkylphenols) in a volume ratio of solvent/emulsifier of 99 to 1. The mixture was then made up with water to 100 ml. This stock solution was diluted with the solvent/emulsifier/water mixture described to the concentration of active compound stated below.
Leaves of potted barley seedlings of the cultivar “Hanna” were sprayed to runoff point with an aqueous suspension having the concentration of active compound stated below. 24 hours after the spray coating had dried on, the test plants were inoculated with an aqueous spore suspension of Pyrenophora [syn. Drechslera] teres, the net blotch pathogen. The test plants were then placed in a greenhouse at temperatures between 20 and 24° C. and 95 to 100% atmospheric humidity. After 6 days, the extent of the development of the disease was determined visually in % infection of the entire leaf area. In this test, the plants which had been treated with 250 ppm of the compound I-1, I-2, I-3 or I-4 showed an infection of not more than 7%, whereas the untreated plants were 100% infected.
Bell-pepper seedlings of the cultivar “Neusiedler Ideal Elite” were, after 2 to 3 leaves were well developed, sprayed to runoff point with an aqueous suspension having the concentration of active compound stated below. The next day, the treated plants inoculated with a spore suspension of Botrytis cinerea, which contained 1.7×106 spores/ml in a 2% aqueous biomalt solution. The test plants were then placed in a dark climatized chamber at 22 to 24° C. and high atmospheric humidity. After 5 days, the extent of the fungal infection on the leaves could be determined visually in %.
In this test, the plants which had been treated with 250 ppm of the compound I-1, I-2, I-3 or I-4 showed no infection, whereas the untreated plants were 90% infected.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10359442.6 | Dec 2003 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP04/14206 | 12/14/2004 | WO | 6/15/2006 |
