FI80441B - 3-PHENYL-4-CYANOPYRROLDERIVAT, FOERFARANDE FOER DERAS FRAMSTAELLNING OCH DERAS ANVAENDNING SOM MIKROBICIDER. - Google Patents

Description

The present invention relates to novel N-alkylated 3-phenyl-4-cyanopyrrole derivatives and to their use as microbicides. The present invention relates to novel N-alkylated 3-phenyl-4-cyanopyrrole derivatives and to their use as microbicides. , of formula (I) below, their preparation and microbicides containing at least one of the title compounds as active ingredient. The invention also relates to the preparation of said substances and to the use of new active substances and substances for controlling harmful microorganisms, in particular fungi harmful to plants.

This invention relates to novel compounds of general formula (I)

Riy- \

N · -.- * - CN / rS

JX / Il II (I)

R2 V

R3-CH - Y

wherein R 1 and R 2 are, independently, hydrogen, halogen, methoxy or methylthio; R 3 represents hydrogen or C 1 -C 8 haloalkyl; Y represents hydroxy, halogen or -O-C (O) -R4, where R4 represents hydrogen, C1-C4-alkyl, C1-C3-haloalkyl, C2-C3-alkenyl, 2-tetrahydrofuryl, C1-C2-alkoxycarbo -yl or -CH2ORg, wherein

R 9 represents C 1-4 alkyl, 2-methoxyethyl, allyl, propargyl or unsubstituted or chlorine-substituted phenyl.

The term alkyl, alone or as part of another substituent, is to be understood as meaning, depending on the number of carbon atoms always given, for example the following groups: methyl, ethyl, propyl, butyl, pentyl, hexyl, etc., and their isomers, e.g. isopropyl, isobutyl, tert-butyl, isopentyl, etc. Haloalkyl means alkyl substituents which are simply halogenated - perhalogenated, such as e.g. CH 2 Cl 2, CHCl 2, CCl 3, CH 2 Br, CHBr 3, CB 3, CH 2 F, CHF 2, CF 3, CCl 2 CCL2-CHCl2, CH2CH2F, CJ3, etc. Halogen is to be understood herein as follows to mean fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine. Alkenyl means, for example, vinyl, propenyl (1), allyl, etc., as well as alkyl chains which are cleaved by several C = C double bonds.

The compounds of formula (I) are normally stable oils, resins or generally crystalline solids which have very valuable microbicidal properties. They can be used, above all, in open-air conditions in the agricultural sector or in nearby areas for the curative and, in particular, preventive control of microorganisms harmful to plants. The active compounds of the formula (I) according to the invention have a high fungicidal activity over a wide range of application concentrations and there are no problems with their use in the open air.

Due to their considerable microbicidal activity, the following groups of compounds are increasingly preferred in ascending order: a) Compounds of formula (I) in which the phenyl ring is in the 2-position and R 2 is in the phenyl ring in the 3-position and independently represent hydrogen, halogen, nitro or methylthio; R 3 represents hydrogen or C 1 -C 4 haloalkyl; and Y represents hydroxy, halogen or the group -O-C (O) -R 1, wherein R 4 represents C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, 2-tetrahydrofuryl, C 1 -C 4 alkoxycarbonyl or the group - CH 2 OR 8, wherein R 8 represents C 1 -C 4 alkyl, 2-methoxyethyl, allyl, propargyl or unsubstituted or chlorine-substituted phenyl.

II: 3 80441 b) Compounds of formula (I) wherein Rx represents hydrogen, 2-chloro, 2-methoxy or 2-methylthio; R 2 represents hydrogen or 3-chlorine; R 3 represents hydrogen or C 1 -C 4 haloalkyl; and Y represents hydroxy, chlorine or the group -OC (O) -R 4, wherein R 4 represents C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, 2-tetrahydrofuryl, C 1 -C 2 alkoxycarbonyl or the group -CH 2 OR 6, where R 8 represents C1-C4 alkyl, 2-methoxyethyl, allyl, propargyl or unsubstituted or chlorine-substituted phenyl.

c) Compounds of formula (I) wherein R 1 represents hydrogen, 2-chloro, 2-methoxy or 2-methylthio; R 2 represents hydrogen or 3-chlorine; R 3 represents hydrogen or CCl 3 and Y represents hydroxy, chlorine or the group -O-C (O) -R 4, wherein R 4 represents C 1 -C 4 alkyl, C 1-4 haloalkyl, 2-tetrahydrofuryl, methoxycarbonyl or the group -CH 2 OR 6 , wherein R 9 represents C 1 -C 4 alkyl, 2-methoxyethyl, allyl, propargyl, phenyl or chlorine-substituted phenyl.

Particularly preferred individual compounds are, for example: the following individual compounds a to 1 are particularly preferred due to their strong plant fungicidal action in the open air: a) N- (hydroxymethyl) -3- (3-chlorophenyl) -4-cyanopyrrole; b) N- (1-acetyloxy-2,2,2-trichloroethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, c) N- (1-hydroxy-2,2,2-trichloroethyl) ) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, d) N- (1-methoxyacetyloxy-2,2,2-trichloroethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, e) N- (methoxyacetyloxymethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, 4 80441 f) N- (1-hydroxy-2,2,2-trichloroethyl) -3- (2-chlorophenyl) - 4-cyanopyrrole, g) N- [1- (n-butylcarbonyloxy) -2,2,2-trichloroethyl] -3- (2,3-dichlorophenyl) -4-cyanopyrrole, h) N- [1- (n- propoxyacetyloxy) -2,2,2-trichloroethyl] -3- (2,3-dichlorophenyl) -4-cyanopyrrole, i) N- [1- (n-butoxyacetyloxy) -2,2,2-trichloroethyl] -3- (2,3-dichlorophenyl) -4-cyanopyrrole, j) N- [1- (isopropo xacetyloxy) -2,2,2-trichloroethyl] -3- (2-chlorophenyl) -4-cyanopyrrole, k) N- [1- (propargyloxyacetyloxy) -2,2,2-trichloroethyl] -3- (2,3 -dichlorophenyl) -4-cyanopyrrole, 1) N- (acetyloxymethyl) -3- (2-chlorophenyl) -4-cyanopyrrole.

The novel compounds of formula (I) are prepared according to the invention in that the 3-phenyl-4-cyanopyrrole derivative of formula (II) E2 \ - \ l \ ™ (II) S · m · · ·

R2 Y

i

B

by conversion with an aldehyde of formula (III) R3 - CHO (III) is converted into a hydroxy derivative of formula (Ia) ------ CN »>

> / n II

/ · = · «·

R2 Y

/ C \

OH

80 5 80441 and the latter is converted, if desired, into another product of formula (I) by replacing the free OH group with another residue Y, this exchange taking place by converting either the compound of formula (Ia) with an acid of formula (IV) R 4 - COOH (IV) or, preferably, a reactive acid derivative thereof, in particular an acid halide, such as an acid chloride of formula (IVa) [R4COCl], or an acid bromide or an acid anhydride of formula (ivb) [(R4CO) 2 O] [ For the acyloxy product according to Ib) R, v ______C »X / Il II (Ib) S% s · · ·

R2 V

k 0 r / \) - l! -R,

3 A

wherein in formulas (Ia), (Ib), (II), (III), (IV), (iva), (ivb) and (V) the substituents have the same meaning as in formula (I).

The reaction of compounds of formula (II) with aldehydes of formula (III) may be carried out in the presence or absence of a reaction-inert solvent or solvent mixture. Suitable are, for example, aromatic hydrocarbons, such as benzene, toluene or xylene; halogenated hydrocarbons such as chlorobenzene; aliphatic hydrocarbons such as petroleum ether; ethers and ethereal compounds such as dialkyl ethers (diethyl ether, diisopropyl ether, tert-butyl methyl ether, etc.), furan, dimethoxyethane, dioxane, tetrahydrofuran; dimethylformamide, etc.

The reaction of the compounds of formula (II) with the compounds of formula (III) is preferably carried out without 6 80441 solvent, but using an excess of aldehyde of formula (III). Depending on the aldehyde of formula (III), work is done in solution or melt. In this case, the addition of an acidic or basic catalyst advantageously affects the reaction rate. Suitable acid catalysts are, for example, anhydrous hydrogen halides and mineral acids, such as hydrogen chloride, hydrogen bromide or sulfuric acid, but also concentrated hydrochloric acid. Alkali catalysts which can be used are, for example, tri-10-alkylamines (trimethylamine, triethylamine, dimethylethylamine, etc.), alkali and alkaline earth metal carbonates (such as »BaCO2 / MgCO2, I2CO2 / etc.) Or alkali alcoholates (such as NaOCH N, NaCl (H 2 O, KO (iso-C 1 H 2 O), KO (t-butyl)). The temperatures in this reaction are generally in the range of 0 ° C to 200 ° C, preferably 0 ° C to 160 ° C, and the reaction time is 1 to 24 hours, especially 1 to 4 hours.

The replacement of the free hydroxyl group in the compounds of formula (Ia) with a group Y is preferably carried out in a reaction-inert solvent. Examples of such solvents include: aromatic and aliphatic hydrocarbons such as benzene, toluene, xylene, petroleum ether, Igro or cyclohexane; halogenated hydrocarbons such as chlorobenzene, methylene chloride, ethylene chloride, chloroform, carbon tetrachloride or tetrachlorethylene; Ethers and ethereal compounds such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dimethoxyethane, dioxane, tetrahydrofuran or anisole; esters such as ethyl acetate, propyl acetate or butyl acetate; nitriles such as acetonitrile; or compounds such as dimethyl sulfoxide, dimethylformamide; and mixtures of such solvents with each other.

The coupling of group Y takes place according to conventional methods. When Y represents chlorine, for example, phosphorus oxychloride, phosphorus trichloride, phosphorus pentachloride or, preferably, thionyl chloride is used as the reagent. Usually work at temperatures between 0 ° C and + 120 ° C. When Y is bromine, phosphorus tribromide or phosphorus pentabromide is preferably used and the reaction is carried out at 50 ° C to + 50 ° C. When Y is -O-C (O) -R 1, the corresponding acid halide, especially the acid chloride, is usually used as the reagent. In this case, it is expedient to carry out the reaction at a temperature of -20 ° C to + 50 ° C, preferably in the presence of -10 ° C to + 30 ° C and a weak base such as pyridine or triethylamine. Furthermore, 4-dialkylaminopyridines such as 4-dimethylamin or 4-diethylaminopyridine can be added as catalysts to accelerate the reaction.

The reaction of compounds of formula (I) in which Y represents halogen, in particular chlorine or bromine, with salts of formula (V) takes place in the customary manner in the presence of a customary, inert solvent or solvent mixture. Examples of such solvents include: aromatic and aliphatic hydrocarbons such as benzene, toluene, xylene, petroleum ether, ligroin or cyclohexane; ethers and ethereal compounds such as dialkyl ethers, e.g. diethyl ether, diisopropyl ether, tert-butyl methyl ether, dimethoxyethane, dioxane, tetrahydrofuran or anisole; esters such as ethyl acetate, propyl acetate or butyl acetate; nitriles such as acetonitrile; or compounds such as dimethyl sulfoxide, dimethylformamide and mixtures of such solvents.

Addition of a catalytic amount of a crown ether, such as, e.g., 18-crown-6 or 15-crown-5, 30 in this reaction preferably affects the reaction rate. Reaction temperatures are generally in the range of 0 ° C to 150 ° C, preferably 20 ° C to 80 ° C. The reaction takes 1 to 24 hours.

8 80441

In a preferred embodiment, the preparation of the compounds of formula (Ib), in particular those in which = CCl.j or = H, starting from the compounds of formula (II), is carried out by the so-called one-pot process. In this case, it is preferable to work in one of the abovementioned inert solvents or diluents, for example, ethereal compounds such as tetrahydrofuran and in the presence of a weak base such as trialkylamine (triethylamine) or pyridine. Chloral or para-formaldehyde is used as reagents. The reaction can be accelerated by the addition of a catalyst such as 1,8-diazabicyclo (5.4.0.) - undec-7-ene (= DBu). The temperatures in this first reaction step are -20 ° C to + 100 ° C, preferably 0 ° C to 50 ° C, and the reaction time is 0.5 to 2 hours. The intermediate gives a hydroxy derivative of formula (Ia) which is not isolated but is reacted in the same reaction solution at -30 ° C to + 30 ° C, preferably at -10 ° C to 0 ° C and a catalytic amount of 4-dialkylaminopyridine, preferably at 20 ° C. 4-dimethylaminopyridine in the presence of a compound of formula (IV). The reaction time in this 2nd step is 0.5 to 16 hours.

The starting materials of formulas (III), (IV) and (V) are generally known or are prepared according to known methods.

Some of the pyrrole compounds of formula (II) are known in the literature. Thus, for example, the process for preparing 4-cyano-3-phenylpyrrole and its chemical properties are described in Tetrahedron Letters No.

30 52, pp. 5337-5340 (1972). The biological activity of the compound is not mentioned.

N-acylated, substituted 3-phenyl-4-cyanopyrrole 9 80441 derivatives are known from the literature, so there are, for example, pyrroles of the formula (VI) • - · mx y ~ \\ i, rCN (vi), / ta · · ·

Xn Y

O = C-CH3 wherein X represents a halogen atom, a lower alkyl or halo-lower alkyl group and n is 0, 1 or 2, described in DE-OS 2,927,480 as fungicides.

Also pyrrole derivatives of the formula (VII) R10 "ffR9 (VII) γ \ R7 with acyl, alkoxycarbonylalkyl, ...

Rg, R9 is hydrogen, aryl, - R10 is hydroxy, mercapto, ...

10 are known from GB patent 2,078,761 as heat and light aging inhibitors for PVC plastics.

Further pyrrole derivatives of formula (VIII) R5-H H-R5 (VIII) <V \ R1 wherein R1 is alkyl, optionally substituted by acyloxy ...

15 Rj is hydrogen, alkyl, cyano, ...

80441 are mentioned as polymerization catalysts for vinyl chloride in DE-OS 2,028,363.

Known pyrrole derivatives are either ineffective against plant pathogens or show clear phytosanitary activity only in the greenhouse, which, however, is not reproducible in the open air due to the instability of the compounds with respect to environmental effects. Thus, they are not useful in agriculture, horticulture or nearby applications. In contrast, the novel pyrrole derivatives of the formula (I) according to the invention represent a valuable enrichment in the prior art, since it has surprisingly been found that the novel pyrroles of the formula (I) have the highly advantageous microbicidal spectrum against phytopathogenic fungi and bacteria. . They can be used not only in agriculture or similar areas of application to control harmful microorganisms on crops, but also to store perishable products in warehouses. The compounds of formula (I) have very advantageous healing, systemic and in particular preventive properties and can be used for the protection of several crops, in particular in open crops. The active compounds of the formula (I) can be used to reduce or eliminate microorganisms present in plants or plant parts (fruits, flowers, foliage, stems, tubers, roots) of various useful crops, so that later growing plant parts are also spared from such microorganisms.

The active ingredients are effective, for example, against phytopathogenic fungi belonging to the following 30 classes: Ascomycetes, e.g. Erysiphe, Sclerotinia,. . Fusarium, Monilinia, Helminthosporium; parent fungi (Bacidiomycetes) such as Puccinia, Tilletia, 11 80441

Rhizoctonia; and Oomycetes species belonging to the category of algae (Phycomycetes), such as Phytophtora. As plant protection products, the compounds of the formula (I) can be used with particularly good results against important pests belonging to the genus Fungi imper-5 fecti, such as, for example, Cercospora, Piricularia and, above all, Botrytis. Botrytis species (B. cinerea, B. allii) cause gray mold pollution on vines, strawberries, apples, red onions and other fruit-10 and vegetable species, which is a significant economic disadvantage. In addition, certain compounds of formula (I), e.g. compound 1.2, can be used successfully to protect perishable flora or fauna products. They control fungi such as Penicillium, Aspergillus, Rhizopus, Fusarium, Helminthosporium, Nigrospora and Alternaria, as well as bacteria such as butyric acid bacteria and fungi such as Candida.

As plant protection products, the compounds of formula (I) have a very advantageous spectrum of action in agricultural use for the protection of crops without the use of harmful undesirable side effects.

They can also be used as pickling agents in the treatment of seed cereals (cereals, tubers, grains) and plant cuttings to protect against fungal infections and against phytopathogenic fungi present in the soil.

The invention thus also relates to microbicidal substances and to the use of the compounds of the formula (I) for controlling phytopathogenic microorganisms, in particular fungi harmful to plants, or for preventing pollution in plants and in containers containing plant or animal products.

12 80 441

In addition to the above, the present invention also relates to the preparation of (agro) chemical agents, which is characterized in that the active ingredient is mixed well with one or more of the substances or groups of substances described herein. The invention 5 also relates to a process for the treatment of plants or storage products which takes place using compounds of the formula (I) or new substances on plants, parts of plants, their growing medium or substrate.

Target crops for plant protection within the scope of the present invention include, for example, the following plant species: cereals (wheat, barley, rye, oats, rice, sorghum and related); beets (sugar beet and turnips); soft-hearted fruits, stone fruits and berries (apple, pear, plum, peach, almond, cherry, strawberry, raspberry and bear-15 whip); legumes (beans, lentils, sugar peas, soybeans); oilseeds (canola, mustard, poppy, olive, sunflower, coconut, castor, cocoa, peanut); cucumbers (pumpkin, cucumbers, melons); fiber plants (cotton, flax, hemp, jute); citrus fruits 20 (orange, lemon, pompom, mandarin); vegetable species (spinach, lettuce, asparagus, cabbage, carrot, onion, tomato, potato, paprika); bay plants (avocado, cinnamon, camphor) or plants such as maize, tobacco, walnut, coffee, sugar cane, tea, wine-25 vine, hops, banana and natural rubber plants and ornamentals (Composite).

As storage preservatives, the compounds of formula (I) are used in unmodified form or preferably in combination with excipients commonly used in the preparation process and are prepared, for example, as emulsion concentrates, brushable pastes, directly sprayable or dilutable solutions, dilute emulsions, spray powders, spray powders, or they are encapsulated in polymeric materials in a known manner. The method of application, such as spraying, atomizing, dusting, spraying, brushing or watering, and the form of the substance depend on the objectives set and the prevailing conditions. Preferred application rates are generally 0.01 to at most 2 kg of active ingredient / 100 kg of substrate to be protected; however, the amounts depend quite substantially on the quality of the substrate (surface size, solidity, moisture content) and its environmental effects.

For the purposes of this invention, storage and storage products are to be understood as meaning natural products of flora and / or fauna and their further processed products, for example the following naturally occurring plants, their parts (stems, leaves, tubers, seeds, fruits, grains) which: have just been harvested or are still in processed form (pre-dried, moistened, crushed, ground, roasted). Examples which are in no way limiting in scope within the scope of this invention include the following crops: cereals (such as wheat, barley, rye, oats, rice, sorghum and related); beets (such as carrots, sugar beets and turnips); soft-hearted 25 fruits, stone fruits and berries (such as apple, pear, plum, peach, almond, cherry, strawberry, raspberry and blackberry); legumes (such as beans, lentils, sugar peas, soybeans); oilseeds (such as canola, mustard, poppy, olive, sunflower, coconut, castor-30 plant, cocoa, peanut); cucumbers (such as pumpkin, cucumbers, melons); fibrous plants (such as cotton, flax, hemp, jute, nettle); citrus fruits; vegetable species (such as spinach, lettuce, asparagus, cabbage, red onion, tomato, potato, paprika); bay plants (such as avocado, 14 80 441 cinnamon, camphor) or corn, tobacco, walnut, coffee, sugar cane, tea, bunch of grapes, chestnut, hops, banana, grass and hay.

As natural products of animal origin, mention may be made in particular of dried fish and meat products, such as dried meat, dried fish, meat concentrates, bone meal, fishmeal and animal dry fodder.

The treated stock product is protected from harmful contamination by mold fungi or other undesired microorganisms 10 by treatment with compounds of formula (I). Thus, the formation of toxic and partially carcinogenic molds (aflatoxins and ochratoxins) is prevented, the product remains unpolluted and its quality is maintained longer. The method according to the invention can be used for all dry and moist storage and storage products which are exposed to microorganisms such as yeasts, bacteria and in particular molds.

A preferred method of applying the active agent is based on spraying or wetting the substrate with a liquid preparation or mixing the substrate with a solid active agent preparation. The preservation method described is part of this invention.

The active compounds of the formula (I) are usually used in the form of compositions and can be applied simultaneously or sequentially to the surfaces, plants or substrates to be treated with the other active compounds. These other active ingredients can be fertilizers, trace element preparations or other preparations which affect the growth of the plant. 30 They can also be selective herbicides, insecticides, fungicides, bactericides, nematicides, molar

II

15 80441 lusicides or mixtures of several such preparations, together with possibly other carriers, surfactants and other additives which are customary in the art.

Suitable carriers and additives can be solid or liquid and correspond to substances suitable for the production process, such as natural or regenerated minerals, solvents, dispersing, wetting, fixing, thickening agents, binders or fertilizers.

One preferred method of applying an active agent of formula (I) or a (agrochemical) containing at least one such active agent is application to leaves (leaf application). The number of applications and the application rate then depend on the contamination pressure of the respective agent (fungal species). However, the active compounds of the formula (I) can be applied to the plants via the soil by means of the root system (systemic effect) by wetting the plant growth site with a liquid preparation 20 or by applying the substance to the soil in solid form, e.g.

in granules (soil dosage). The compounds of formula (I) may also be added to seed grains (pickling) by either wetting the liquid with a liquid preparation of the active ingredient or coating it with a solid preparation. In addition to the above, in certain cases other dosage forms are possible, such as treatment on a plant stem or buds.

The compounds of formula (I) are thus used in unmodified form or preferably in combination with customary excipients and are thus prepared, e.g. or encapsulated, e.g., in polymeric materials, in a known manner. The method of application, such as spraying, atomizing, dusting, spraying, brushing or wetting, as well as the quality of the substance, are selected depending on the objectives set and the prevailing conditions. Preferred application rates are generally from 50 g to 5 kg of active ingredient (AS) per hectare; preferably 100 g - 2 kg AS / ha, secretion-10 ti 200 g - 600 g AS / ha.

Preparations, i.e. substances, products and compositions containing an active ingredient of the formula (I) and optionally a solid or liquid additive are prepared in a known manner, e.g. by mixing well and / or grinding the active ingredient with excipients such as solvents, solid carriers and optionally surfactants ( surfactants).

Suitable solvents are: aromatic hydrocarbons, preferably fractions such as, for example, xylene mixtures or substituted naphthalenes, phthalic acid esters such as dibutyl or dioctyl phthalate, aliphatic hydrocarbons such as cyclohexane or paraffin, esters and their glycols, alcohols and glycols , ethylene glycol monomethyl or ethyl ether, ketones such as cyclohexanone, strongly polar solvents such as N-methyl-2-pyrrolidone, dimethyl sulfoxide or dimethylformamide, and optionally epoxidized vegetable oils such as epoxidized coconut oil or coconut oil; or water.

As solid carriers, e.g. for dusts and dispersible powders, natural stone powders, such as lime slag, talc, kaolin, tl 17 80 441 montmorillonite or attapulgite, are generally used. Highly dispersed silicic acid or highly dispersed absorbent polymer may also be added to improve physical properties. Suitable granular, adsorptive granulate-5 carriers are porous substances, such as pumice stone, crushed brick, seaweed or bento-rivet, and non-adsorbent carriers are, for example, lime or sand. In addition to the above, a number of inorganic or organic pre-granulated substances can be used, such as, in particular, dolomite or crushed plant residues, such as, for example, cork flour or sawdust.

Particularly preferred spreading aids which can lead to a significant reduction in the amount of use are also natural (animal or plant) or synthetic phospholipids of the cephalin and lecithin series, such as, for example, phosphatidylethanolamine, phosphatidylserine, phosphatidylcholine, phosphatidylcholine, sphingidylcholine; lysolecithin, plasma-20 logene, or cardiolipin, which can be obtained, for example, from animal or plant cells, in particular the brain, heart, lungs, liver, scrambled eggs or soybeans. Useful commercial mixtures are, for example, phosphatidylcholine mixtures. Synthetic phospholipids include, for example, dioctanoylphosphatidylcholine and dipalmititoylphosphatidylcholine.

Suitable surfactants, depending on the type of compound of formula (I) to be prepared, are non-ionic, cationic or anionic surfactants which have good emulsifying, dispersing and wetting properties. Surfactants also mean mixtures of surfactants.

18 80441

Suitable anionic surfactants can be both so-called water-soluble soaps and also water-soluble synthetic surfactants.

Among the soaps, mention may be made of the alkaline or optionally substituted ammonium salts of the higher fatty acids, such as, for example, the sodium or potassium salts of oleic or stearic acid or of mixtures of natural fatty acids which may be formed from coconut or tallow oil. Mention may also be made of the lauric salts of fatty acid methyl-10.

More generally, however, so-called synthetic surfactants are used, in particular fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkyl sulfonates.

Fatty sulfonates or sulphates are generally in the form of alkali, alkaline earth or optionally substituted ammonium salts and contain an alkali residue having 8 to 22 carbon atoms, the alkyl also comprising the alkyl part of an acyl residue, e.g. lignin sulphonic acid, dodecyl sulfuric acid ester or natural the sodium or calcium salt of a fatty alcohol sulphate mixture prepared from fatty acids. These also include salts of sulfuric acid esters and sulfonic acids of fatty alcohol-ethylene oxide adducts. The sulfonated benzimidazole derivatives preferably contain 25 2-sulfonic acid groups and one fatty acid residue having 8 to 22 carbon atoms. Alkylarylsulfonates are, for example, the sodium, calcium or triethanolamine salts of dodecylbenzenesulfonic acid, dibutylnaphthalenesulfonic acid or the naphthalenesulfonic acid-formaldehyde condensation product.

Corresponding phosphates, such as

II

19 80441 e.g. phosphoric acid ester salts of the p-nonylphenol- (4-14-ethylene oxide) adduct.

Suitable nonionic surfactants are, in particular, polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, optionally saturated or unsaturated fatty acids and alkylphenols, which may contain from 3 to 30 glycol ether groups in the case of alkylene groups and 8 to 20 carbon atoms.

Other suitable nonionic surfactants include water-soluble polyethylene oxide adducts containing from 20 to 250 ethylene glycol ether groups and from 10 to 100 propylene glycol ether groups with propylene glycol, ethylenediaminopolypropylene glycol and alkyl glycol, and alkyl polyethylene.

Said compounds usually contain 1 to 5 ethylene glycol units per propylene glycol unit.

Examples of nonionic surfactants include nonylphenol polyethoxyethanols, castor oil polyglycol ethers, polypropylene-polyethylene oxide adducts, tributylphenoxypolyethylene ethanol, polyethylene glycol and octylphenoxypolyethoxyethanol.

Further fatty acid esters of polyoxyethylene sorbitan, such as polyoxyethylene sorbitan trioleate, are also possible.

Cationic surfactants are, in particular, quaternary ammonium salts which contain, as N-substituents, at least one alkyl residue having 8 to 22 carbon atoms and, as other substituents, lower, optionally halogenated, alkyl, benzyl or lower hydroxyalkyl residues. The salts are preferably in the form of halides, methyl sulphates or ethyl sulphates, e.g. stearyltrimethylammonium chloride or benzyldi (2-chloroethyl) ethylammonium bromide. In storage protection, 5 non-hazardous additives for human and animal food are preferred.

Surfactants useful in the manufacturing technique have been shown e.g. in "Mc Cutcheon's Detergents and Emulsifiers Annual" BC 10 Publishing Corp., Ridgewood New Jersey, 1981.

Helmut Stache "Tensid-Taschenbuch" Carl Hanser-Verlag, Munich / Vienna 1981.

Agrochemical preparations generally contain from 0.1 to 99%, in particular from 0.1 to 95%, of the active compound of the formula (I), from 99.9 to 1%, in particular from 99.8 to 5%, of solid or liquid additives and from 0 to 25%. , especially 0.1 to 25% surfactant.

Concentrated substances are preferred as a commodity, while dilute substances are usually used by the consumer.

The substances may also contain other additives, such as stabilizers, antifoams, viscosity regulators, binders, binders and fertilizers or other active ingredients to achieve specific effects.

Such (agro) chemical agents are also a subject of this invention.

The following examples are intended to further illustrate the invention without, however, limiting it. Temperatures are given in degrees Celsius. Percentages and parts are calculated by weight. In addition, the following symbols are used: h = hour, min = minute.

21 80441

Preparation Examples: Example H1: Preparation of N-hydroxymethyl-3- (2-chlorophenyl) -4-cyanopyrrole of formula 1.1 is

S S

\ / ", | ίΊ_εΝ (Compound No. 1.1) • · ·

Y

CH20H

60.8 g of 3- (2-chlorophenyl) -4-cyanopyrrole, 9.9 g of paraformaldehyde and 0.8 g of triethylamine are mixed well, followed by heating at a bath temperature of 90 ° with stirring. After 1 h 15 min, the melt formed is cooled to room temperature, whereupon this glassy mixture hardens. Recrystallization from toluene gives the above product as brownish crystals, m.p. 15 94-97 °.

Example H2: Preparation of N-chloromethyl-3- (2-chlorophenyl) -4-cyanopyrrole of formula 2.1 • • ·

· 'N · - · - * - CN

\ / Il II,,,.

· = ·. v. · (Compound No. 2.1)

Cl Y

To 60 ml of thionyl chloride is added in several portions, while stirring vigorously, 48 g of N-hydroxymethyl-3- (2-chlorophenyl) -4-cyanopyrrole, so that a reasonable gas evolution occurs throughout. When gas evolution ceases, the mixture is stirred for a further 2 h at room temperature and finally for 2.5 h at 35-40 °. After cooling to room temperature, toluene is added and the mixture is evaporated. The residue is recrystallized from diethyl ether / petroleum gasoline to give the product described above as beige crystals, m.p. 97-99 °.

Example H3: Preparation of N-acetyloxymethyl-3- (2-chlorophenyl) -4-cyanopyrrole of formula 10 3.2 is • - «

<N.-.-— CN

\ / Il II

• S · · · [io (Compound No. 3.2) ch2-oc-ch3 41.4 g of N-hydroxymethyl-3- (2-chlorophenyl) -4-cyanopyrrole are dissolved in 350 ml of pyridine and 1.8 g are added. 4-dimethylaminopyridine. 21.4 ml of acetic anhydride 15 are then slowly added dropwise at 0 ° to 7 ° and the mixture is stirred at 0 ° to 7 ° for 12 h, then the reaction mixture is poured into ice water and extracted twice with ethyl acetate. The extracts are washed twice with dilute, ice-cold hydrochloric acid and twice with half-saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and the filtrate is evaporated. The residue is recrystallized from diethyl ether / hexane to give the above product as colorless crystals, m.p. 91-95 °.

Example H4: Preparation of N- (1-acetyloxy-2,2,2-trichloroethyl) -2- 3- (2,3-dichlorophenyl) -4-cyanopyrrole of formula 3.4 11 23 80 441 • - ·

<rCN

· «» T · 1 1 \ / n r 1 q (Compound No. 3.4)

Cl O-C-CH

To a mixture of 2.4 g of 3- (2,4-dichlorophenyl) -4-cyanopyrrole in 50 ml of tetrahydrofuran are added dropwise successively 1.2 ml of chloral and 1.8 ml of triethylamine. The reaction mixture is stirred for 1.5 h at 25 °, after which 0.1 g of 4-dimethylaminopyridine is added and cooled to -10 °. At -10 ° to -5 °, a solution of 0.9 ml of acetyl chloride in 10 ml of tetrahydrofuran is added dropwise very slowly, and finally the reaction mixture is stirred for 30 min at 0 °, then for 1 h at room temperature, filtered and the filtrate is evaporated. The residue is dissolved in diethyl ether, the ether solution is washed twice with half-saturated sodium chloride solution, dried over sodium sulfate, filtered and the filtrate is evaporated.

. . The crude product is recrystallized from diethyl ether / petroleum gasoline to give the above product as colorless crystals, m.p. 111-113 °.

Example H5: Preparation of N-chloromethyl-3- (2,3-dichlorophenyl) -4-cyanopyrrole of formula 2.4

I IJ

ci. - »- CN

I IJ II w

Cl (Compound No. 2.4) H 2 Cl 2 23.7 g of 3- (2,3-dichlorophenyl) -4-cyanopyrrole are dissolved in 300 ml of tetrahydrofuran, 7.5 g of para-formaldehyde are added and finally 1.5 and 1, 8-diazabicyclo (5,5,0) - 24 80441 undec-7-ene. Stir for 3 h at room temperature.

21.7 ml of thionyl chloride are then added dropwise, with stirring, at 20 ° to 30 ° to form a hydroxymethyl derivative. The reaction mixture is stirred for 5 to 16 h at room temperature, after which it is poured into ice water and the resulting mixture is extracted twice with ethyl acetate. The combined organic extracts are washed twice more with brine, dried over sodium sulfate, filtered and evaporated. The residue is crystallized from ether / petroleum gasoline to give the above product as beige crystals, m.p. 132-133 °.

Example H6: Preparation of N- (1-hydroxy-2,2,2-trichloroethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole 15 having the formula 1.3 (Compound No. 1.3)

A

C13C OH

To a mixture of 64.1 g of 3-cyano-4- (2,3-dichlorophenyl) pyrrole and 1.2 ml of triethylamine in 400 ml of tetrahydrofuran is added dropwise at 20 ° to 29 ° 39.6 ml of chloral. Finally, a further 2.4 ml of triethylamine are added, followed by 1.2 ml of diazabicyclo (5.4.0) undec-7-ene and the clear solution is stirred for 2 h at room temperature, then for 14 h at 0 ° to 5 °. . The solution is then poured into dilute hydrochloric acid and ice and the mixture is extracted twice with ethyl acetate. The organic extracts are washed three times with cold, half-saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. Crystallization of the residue from ether / petroleum gas gives the desired product as colorless crystals, m.p. 117 ° (dec.).

25 80441

Example H7; Preparation of N- (Ί- (methoxyacetyloxy) -2,2,2-tria-5-chloroethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole of formula 3.5

I II

RFV '---- CN

(Compound No. 3.5) Y n Cl3C-CH-OC-CH2-OCH3 4.8 g of 3-cyano-4- (2,3-dichlorophenyl) pyrrole are dissolved in 50 ml of tetrahydrofuran and 0.2 ml of DBU are added at room temperature, followed by 2.3 ml of chloral. The solution is cooled to -5 °, after which 3.3 ml of triethylamine are added dropwise. Stir for 1 hour at -5 °, then slowly add dropwise at -10 ° to 5 ° 2.2 ml of methoxyacetic acid chloride dissolved in any tetrahydrofuran. Stir for 1 h under external cooling, then pour into ice water and extract the mixture twice with ethyl acetate. The organic extracts are washed twice with cold dilute hydrochloric acid and twice with cold, half-saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. Crystallization of the residue from petroleum gasoline gives the above product as colorless crystals, m.p. 88-90 °.

Example H8; Preparation of N - [(methoxyacetyloxy) methyl] -3- (2,3-dichlorophenyl) -4-cyanopyrrole of formula 3.22 26 8 0 4 41 • ·

I IJ

d Y Y-r-CH

Cl · · (Compound No. 3.22)

n I

CH.-OC-CH OCH II 0 4.5 g of 3-cyano-4- (2,3-dichlorophenyl) pyrrole are dissolved in 50 ml of tetrahydrofuran and 0.65 g of paraformaldehyde, 3.0 ml of triethylamine and 0, 5 ml DBU. The mixture is stirred for 2 h at room temperature to give a clear solution. 2.0 ml of ethoxyacetic acid chloride are then slowly added dropwise at 5 °, while stirring. Stir for a further 2.5 h at 0 ° to 5 °, then filter and evaporate the filtrate. Crystallization of the residue from ether / petroleum gas 10 gives the above product as colorless crystals, m.p. 72-75 °.

The compounds shown in the following tables can be prepared in a similar manner:

Table 1: Compounds of formula

R1V

V -% ------ CN

X / Il II

S · s · · ·

R2 Y

R 3 £ h Y

15 wherein Y is OH.

ii 27 80 441 R1 K? r-3 Physics. constants

te no ^ J

1 · 1 2_cl H H sul.p. 94-97 ° 1'2 H 3-C1 H m.p. 72-74 ° 1-3 2-Cl 3 “Cl CC13 117 ° dec.

l '** H 2-SCH3 CC13 85 ° h.

· 5 2-C1 H CC13 70-76 ° m.p.

! · 6 2_cl 3-C1 H m.p. 137-140 ° 1-7 H 3-Cl CCl 3

1.8 2-SCH3 H H

1.9 2-OCH3 H H resin 1.10 2-OCH3 H CC1 1Λ1 H H H m.p. 81-84 °

1.12 H 3-OCH 3 H

1.13 H 3-OCH3 CC13 resin 1.14 H 3-SCH3 CC13 1.15 H 3-SCH3 H resin

1.16 2-OCH3 3-OCH3 H

1.17 2-OCH3 3-OCH3 CC13 1.18 H 3-Br H m.p. 65-69 ° 1.19 H 3-Br CC13 1.20 H 3-F H m.p. 75-77 °

1.21 2-F H H

t 1.22 H 3-F CC13 1.23 H 3-J CC13

1.24 H 3-J H

Table 2: Compounds of formula 28 80 441

R1V

>> -i — rCK

/ »At · ·

R2 Y

r3-ch-y wherein Y is Cl.

Compound R. R ~ R_ Physics. constants

te No. J

2.1 2-C1 H H m.p. 97-99 ° 2-2 H 3-Cl H m.p. 77-79 ° 2.3 2-C1 H CC13 2.-4 2-C1 3-C1 H m.p. 132-133 ° 2-5 2-Cl 3 -Cl CCl 3 m.p. 152-157 ° 2-6 H 3-Cl CCl 3

2.7 2-SCH3 H H

2.8 2-SCH3 H CC13

2.9 2-0CH3 H H

2.10 2-OCH3 H CC13 2.11 h 3-0CH3 h resin 2.12 H 3-OCH3 CC13 resin

2.13 H 3-SCH3 H

2.14 H 3-SCH3 CC13

2.15 2-OCH3 3-OCH3 H

2.16 2-OCH3 3-OCH3 CC13 2.17 H 3-Br H m.p. 71-74 ° 2.18 H 3-Br CC13 half to dry 2.19 H 3-F H m.p. 80-83 ° 11

Table 2; (continued) 29 80441

2.20 2-F H H

2.21 H 3-F CC13 2.22 H 3-J CC13 2.23 H 3-J H m.p. 59-65 ° 2.24 H 3-OCELj CHCl 2 2.25 H 3-OCH 3 CHCl 2 resin 2.26 H 3-SCH3 CH2C1

Table 3; Compounds of formula

V

• · - · -.- CN

X / Il II

/ # = · · ·

R2 Y

r 3 -ch-y wherein Y is -OC (O) R 2.

Compound R. R_ R_ R. Physics. Constant te No. 1 ^ 4 3.1 2-C1 H CC13 CH3 m.p. 100-108 ° 3.2 2-C1 H H CH3 m.p. 91-95 ° 3.3 H 3-Cl CC13 CH3 m.p. 118-120 ° 3.4 2-C1 3-Cl CC13 CH3 m.p. 111-113 ° 3.5 2-C1 3-Cl CC13 CH2OCH3 m.p. 88-90 ° 3.6 2-SCH3 H CC13 CH3 m.p. 139-141 ° 3.7 2-OCH3 H CC13 CH3 m.p. 106-108 ° 3.8 2-C1 H H CC13 3.9 2-C1 H CH2OCH3 m.p. 112-114 ° 3.10 H 3-Cl CC13 CH (CH3) 2 3.11 H 3-C1 CC13 (CH2) 3CH3 resin

Table 3: (continued) 30 80441 3.12 H 3 -Cl CC13 C ^ Br 3.13 H 3-C1 CC13 CF3 3.14 H 3-C1 H CH3 3.15 H 3-C1 H CHCl2 3.16 2-C1 3-Cl CC13 m.p. 137-141 ° 3.17 2-Cl 3 -Cl CCl 3 (CH) CH 2 R 1.5548 3.18 2-Cl 3 -Cl CCl 3 CH 2 Cl m.p. 143-151 ° 3.19 2-C1 3-C1 CC13 H resin 3.20 2-C1 3-C1 H CH3 m.p. 95-99 ° 3.21 2-C1 3-C1 H C (CH) m.p. 86-88 ° 3.22 2-C1 3-C1 H CH2OCH3 m.p. 72-75 ° 3.23 2-Cl 3-Cl H CCl 3

3.24 2-C1 3-C1 H H

3.25 2-OCH3 H CC13 C (CH3) 3 3.26 2-OCH3 H CC13 C ^ Cl Hold

3.27 2-OCH3 H CC13 H

3.28 2-OCH3 HH CC13 3.29 2-OCH3 HH CH3 3.30 2-OCH3 HH CH2OCH3 ^ crystalline 3.31 2-SCH3 H CC13 3.32 2-SCH3 H CC13 CH2C1 3.33 2-SCH3 H CC13 CH20CH3 semi-crystalline 3.34 2-SCH3 HH CH3 3.35 2- SCH3 HH C2H5 3.36 2-SCH3 HH CC13 3.37 2-C1 3-C1 H CH2C1 m.p. 113-115 ° 3.38 2-C1 3-C1 H resin 11

Table 3: (continued) 31 80441 3.39 2-Cl 3 -Cl HCl Hg-n 1¾0 1-5571 3.40 2-Cl 3 -Cl CCl 3 C (CH 3> 3 mp 146-147 ° 3.41 HH CCl 3 CH 2 OCH 3 m.p. 121-122 ° 3.42 2-C1 3 -Cl CC13 C2H5 semicrystalline 3.43 2-C13-C1H CH2Br mp 88-90 ° 3.44 2-C13-C1 CC13 CH2Br mp 132-125 ° 3.45 2-Cl 3 -Cl CCl 3 CH 2 Cl 2 H 5 mp 115-117 ° 3.46 2-Cl 3 -Cl H CH 2 Cl 2 mp 83-85 ° 3.47 2-Cl H CCl 3 CH 2 OCH 3 mp 116 -118 ° 3.48 HHH CH2OCH3 mp 78-79 ° 3.49 2-C1-3-C1H CH2OCH-m.p. 87-88 ° 3.50 2-Cl3-C1 CC13 CH2OCH-m.p. 76-78 ° 3.51 2-Cl 3 -Cl H CH.0C.H - n m.p. 71-74 ° 2 4 9 * 3.52 2-Cl 3 -Cl CCl, CH.OC.H-n m.p. pp. 89-91 J 2 A 9 3.53 2-Cl 3 -Cl H CH.OC.H-n

L D 1J

3.54 2-Cl 3-Cl CC1, CH.OC.H-n i 2 o li 3.55 2-Cl H H CH2 OCH (CH) 3.56 2-Cl H CC13 CH2OCH (CH3) 2 m.p. 69-76 ° 3.57 2-Cl 3 -Cl H CH 2 OCH (CH 3) 2 m.p. 74-75 ° 3.58 2-Cl 3 -Cl CCl 3 CH 2 OCH (CH 3) 2 m.p. 112-115 ° 3.59 2-Cl 3 -Cl H CH 2 OCH (CH 3) C 2 H 5 m.p. 71-73 ° 3.60 2-Cl 3 -Cl CCl 3 CH 2 CH (CH 2 Cl 2 mp 70-74 ° 3-61 2-Cl 3 -Cl H CH 2 O (CH) 3.62 2-Cl 3 -Cl CCl 3 CH 2 OH (CH 3) 3 3.63 2-Cl HH CH 2 OCH 2 CH 2 OCH 3 3.64 2-Cl H CCl 3 CH 2 OCH 2 CH 2 OCH 3 3.65 2-Cl 3 -Cl H CH 2 OCH 2 CH 2 OCH 3 mp 99-101 ° 32 80441

Table 3: (continued) 3.66 2-Cl 3 -Cl CCl 3 CH 2 OCH 2 CH 2 OCH 3 r ^ ° 1.5472 3.67 2-Cl 3 -Cl H CH 2 OCH 2 CH = CH 2 m.p. 65-67 ° 3.68 2-Cl 3-Cl CCl 3 CH 2 OCH 2 CH = CH 2 m.p. 86-88 ° 3.69 2-Cl 3-Cl H CH OCH CHCH m.p. 109-111 ° C 3.70 2-Cl 3 -Cl; CC13 CH2OCH2CeCH 1.5732 3.71 2-Cl 3-Cl H CH0CcH ,. mp 119-121 ° I 265 en 3.72 2-Cl 3 -Cl CCl 3 CH 2 OC 6 H 5 η ^ υ 1.5803 3.73 2-Cl 3 -Cl and H CH 2 OC 6 H 3 Cl 2 (3.5) m.p. 125-127 ° 3.74 2-Cl 3 -Cl CCl 3 CH 2 O 6 H 3 Cl 2 (3.5) m.p. 154-156 ° 3.75 2-Cl 3 -Cl H O 2 O 2 Cl 2 (2.4) m.p. 102-104 ° 3.76 2-Cl 3-Cl CCl 3 CH 2 OC 6 H 3 Cl 2 (2,4) m.p. 157-159 ° 3.77 2-Cl H and H 2-tetrahydrofuryl 1.5672 3.78 2-Cl H CCl 3 2-tetrahydrofuryl m.p. 142-149 ° 3.79 2-Cl 3 -Cl H 2 -tetrahydrofuryl m.p. 96-98 ° 3.80 2-Cl 3 -Cl CCl 3 2-tetrahydrofuryl m.p. 156-160 ° 3.81 2-Cl HH CH2SCH3 3.82 2-Cl H CC13 O ^ SCl · ^ 3.83 HHH CH2SCH3 3.84 HH CC13 CH2SCH3 3.85 2-Cl 3-Cl H CH2SCH3 3.86 2-Cl 3-Cl CC13 CH2SCH3 3.87 2-Cl 3-Cl H CH2SCH (CH3) C2H5 resin 3.88 2-Cl 3-Cl CC13 CH2SCH (CH3) C2H5 3.89 2-Cl HH CH „SCH (CH0) C« H [.

Z 6 Z ό 3.90 2-Cl H CC13 CH2SCH (CH3) C2H5 3.91 2-Cl 3-Cl H CH „SC.H0-n 2 4 9 3.92 2-Cl 3-Cl CC1_ CH0SC.Hn-n 3 2 4 9 il

Table 3: (continued) 33 8 0 4 41 3.93 2-C1 3-C1 H CH 2 SCiCH) 3.94 2-C1 3-Cl CC13 CH2SC (CH) 3.95 2-C1 3-C1 H 0 (0) 00 ^ m.p. . 111-113 ° 3.96 2-C1 H H CH.SC, Hc L o 5 3.97 2-C1 H CC1. CH SC £ Hc 5 O 5 3.98 2-Cl 3 -Cl H CH0SC ^ Hc 2 6 5 3.99 2-Cl 3 -Cl CCl. CH SC.H.

j 2. o 5 3.100 2-C1 H H CH = CH2 3.101 2-C1 H CC13 CH = CH2 3.102 2-C1 3-C1 H CH = CH2 3.103 2-C1 3-C1 CC13 CH = CH2 m.p. 106-108 ° 3.104 2-C1 3-C1 H CH = CH-CH3 3.105 $ -Cl 3 -Cl CC13 CH = CH-CH3 m.p. 107-109 ° 3.106 2-C1 H H CH = CH-CH3 3.107 2-C1 H CC13 CH = CH-CH3 3 · 108 H H H CH2Cl m.p. 83-84 °

3.109 H 3-0CH H CH

3 3 3 · 110 H 3-0CH3 CC13 CH3 3-m h 3-och3 cci3 ch3 3 · 112 H 3-OCH3 H CH3 resin 3.113 2-OCH 3-OCH H CH OCH resin J 3 2 3

3.114 2-0CH 3-0CH. H CH

3 3 3 3.115 H 3-Br CC13 CH2OCH3 3.Π6 H 3-Br H CH3 3 · 117 H 3-F H CH3 3.118 2-F H H CH20CH3 3-H9 H 3-F CC13 CH3 34 80 441

Preparation examples for liquid active ingredients of formula (I) (% = weight percent) F1: Emulsion concentrates a) b) c) active ingredient from the tables 25% 40% 50% 5 Ca-dodecylbenzenesulfonate 5% 8% 6% castor oil polyethylene glycol ether (36% ethylene oxide) 5% tributylphenoyl-polyethylene glycol ether (30 moles of ethylene-10 oxide) - 12% 4% cyclohexanone - 15% 20% xylene mixture 65% 25% 20% Such concentrates can be prepared by diluting with water to give the desired concentration.

F2: Solutions. .. v - a) b) c) d) active ingredient from the tables 80% 10% 5% 95% ethylene glycol monomethyl ether 20% - - 20 polyethylene glycol MG 400 - 70% - N-methyl-2-pyrrolidone - 20% - epoxidized coconut oil - - 1% 5% petrol (boiling range 25,160 - 190 °) - - 94% - (MG = molecular weight) 35 8 0 4 41 F3; Granules a) b) active ingredient from the tables 5% 10% kaolin 94% highly dispersed silicic acid 1% 5 attapulgite - 90%

The active ingredient is dissolved in methylene chloride, applied to a carrier and finally the solvent is evaporated off in vacuo.

F4: Dusts a) b) 10 active substance from tables 2% 5% highly dispersed silicic acid 1% 5% talc 97% kaolin - 90%

By mixing the active ingredient well with the carrier, ready-to-use dusts are obtained.

Preparation examples for active compounds of formula (I) (% = weight percent) F5; Spray powders a) b) c) active ingredient from the tables 25% 50% 75% 20 Na-lignin sulfonate 5% 5%

Na-lauryl sulphate 3% to 5%

Na-diisobutylnaphthalene sulfonate - 6% 10% octylphenol polyethylene glycol ether - 2% - (7-8 moles of ethylene oxide) highly dispersed silicic acid 5% 10% 10% kaolin 62% 27% 36 80441

The active ingredient is mixed well with the additives and ground in a very suitable mill. Spray powders are obtained which can be diluted with water to suspensions in each case.

5 F6; Emulsion concentrate active ingredient from the tables 10% octylphenol polyethylene glycol ether (4-5 moles of ethylene oxide) 3%

Ca-dodecylbenzenesulfonate 3% castor oil polyglycol ether (35 moles ethylene oxide) 4% cyclohexanone 30% xylene mixture 50% Emulsions of the desired concentration can be prepared from this concentrate with water at a dilution of 15.

F7: Dusts a) b) active substance from the tables 5% 8% talc 95% kaolin - 92% 20 Ready-to-use dusts are obtained by mixing the active substance with the carrier by grinding in a suitable mill.

F8: Extruded granulate active ingredient from tables 10%

Na-lignin sulfonate 2% 25 carboxymethylcellulose 1% kaolin 87%

II

The active ingredient is mixed with additives, ground and moistened with water. This mixture is extruded and finally air dried.

37 80441 F9: Coated granulate 5 active ingredient from tables 3% polyethylene glycol (MG 200) 3% kaolin 94% (MG = molecular weight)

The finely ground active ingredient is uniformly applied in a mixer to kaolin moistened with polyethylene glycol. In this way, dust-free coated granules are obtained.

F10: Suspension concentrate active substance from tables 40% 15 ethylene glycol 10% nonylphenol polyethylene glycol ether 6% (15 moles ethylene oxide) N-lignin sulphonate 10% carboxymethylcellulose 1% 20 37% aqueous silicone solution 0.2% aqueous formaldehyde solution%% formaldehyde solution water 32%

The finely ground active ingredient is mixed well with the additives. This gives a suspension concentrate, from which suspensions of the desired concentration can be prepared by dilution with water.

3β 80441

Biological examples;

Example B1: Action against wheat against Puccinia graminis a) Residual protective effect 5 Wheat plants are sprayed 6 days after sowing with a spray made of powder of the active ingredient (0.06% of active ingredient). After 24 hours, the treated plants are infected with a spore suspension of the fungus. Incubate for 48 hours at a relative humidity of 95-100% and a temperature of about 20 °, after which the infected plants are transferred to a greenhouse at about 22 °. The development of rust spots is assessed 12 days after infection.

b) Systemic impact

5 days after sowing, a spray made of spray powder of active substance (0.006% of active substance based on soil volume) is poured onto the wheat plants. After 48 hours, the treated plants are infected with a spore suspension of the fungus. Incubate for 48 hours at a relative humidity of 95-100% and a temperature of about 20 °, after which the infected plants are transferred to a greenhouse at about 22 °. The development of rust spots is assessed 12 days after infection.

The compounds of Tables 1-3 show not only in the above greenhouse experiment but also in the open field a good activity against Puccinia fungi. Untreated but infected control plants became 100% Puccinia infected. Among others, compounds Nos. 1.2 to 1.5, 1.9, 1.13, 2.11, 2.12, 2.18, 3.2, 3.4 to 3.7, 3.37 to 3.40, 3.42 to 3.46, 3.51, 3.52, 3.57, 3.70, 3.73 to 3.76 and 3.94 limited the 39 80 441 habits. Puccinia infection O - 10%.

Example B2: Effect on peanut plants against Cercospora arachidicola a) Residual protective effect Peanut plants 5 to 15 cm high are sprayed with a spray of active ingredient spray powder (0.006% of active ingredient) and 48 hours later are infected with a fungal conidia suspension. The infected plants are incubated for 72 hours at about 21 ° C and high humidity, after which they are kept in a greenhouse until typical leaf spots appear. The fungicidal effect is evaluated 12 days after infection and is based on the number and size of spots present.

b) Systemic effect For peanut plants 15 to 15 cm high, a spray made of spray powder of the active substance (0.06% of active compound based on the volume of the soil) is poured. After 48 hours, the treated plants are infected with a fungal conidia suspension and incubated for 72 hours at about 21 ° C with high humidity. Finally, the plants are transferred to a greenhouse and fungal infection is assessed after 11 days.

Compared to untreated but infected control plants (number and size of spots = 100%), 25 peanut plants treated in the greenhouse or outdoors with the active ingredients of Tables 1-3 had significantly less Cercospora infection. Thus, compounds 1.3, 1.6, 3.4, 3.5, 3.17, 3.18, 3.20, 3.49, 3.51, 3.52, 3.57, 3.67, 3.69, 3.70, 3.75 and 3.95 inhibit Cercospora 80 80441 infection almost completely (8%).

Example B3; Effect on beans against Botrytis cinerea Residual protective effect

Beans about 10 cm high are sprayed with a spray made of active ingredient rye-5 weft powder (0.02% active ingredient). After 48 hours, the treated plants are infected with a fungal conidia suspension. Infected plants are incubated for 3 days at a relative humidity of 95-100% and a temperature of 21 °, after which fungal infection is assessed. The compounds in Tables 1-3 inhibit fungal infection very strongly not only in the model experiment presented above but also in the open field. At a concentration of 0.02%, for example, compounds Nos. 1.1 to 1.6, 1.9, 1.11, 1.13, 1.15, 1.18, 1.20, 2.1, 2.2, 2.4, 2.5, 2.11, 2.12, 2.17, 2.18, 2.19, 2.23, 31.1 - 3.7, 3.9, 3.16 to 3.22, 3.26, 3.30, 3.33, 3.37, 3.38, 3.39 to 3.52, 3.56 to 3.60, 3.65 to 3.80, 3.95, 3.103, 3.105, 3.108, 3.112 and 3.113 fully effective (0-5% of cases) . Some compounds also had this effect at half the amount of substance. Infection of untreated-20 but infected beans increased 100%. Intermediates 16 and 24 are equally effective.

Example B4; Effect on apples against Botrytis cinerea

Artificially damaged apples are treated by instilling 25 syringes of active ingredient spray powder on the damaged areas. The treated fruits are then inoculated with a spore suspension of Botrytis cinerea and incubated for one week at high humidity and about 20 °.

li 41 80441

In the interpretation, rot-defective, damaged sites are calculated and the fungicidal effect of the test compound is derived from this. Among others, compounds Nos. 1.1 to 1.6, 1.9, 1.11, 1.13, 1.15, 1.18, 1.20, 2.1, 2.2, 2.4, 2.5, 2.11, 2.12, 5 2.17, 2.18, 2.19, 2.23, 31.1 to 3.7, 3.9, 3.16 to 3.22 , 3.26, 3.30, 3.33, 3.37, 3.38, 3.39 to 3.52, 3.56 to 3.60, 3.65 to 3.80, 3.95, 3.103, 3.105, 3.108, 2.112 and 3.113 prevent fungal infection almost completely compared to untreated control fruits (100% infection). 10 Intermediates Nos 16 and 24 have an equally good effect.

Example B5: Effect on rice against Piricularia oryzae

After two weeks of growth, the rice plants are sprayed with a spray made of 15 active substance spray powders (0.02% active substance). After 48 hours, the treated plants are infected with a fungal conidia suspension. Incubate for 5 days at a humidity of 95 to 100% and a temperature of 24 °, after which fungal infection is assessed. The compounds of formula 20 (I) show good inhibition

Piricularia infection, such as compounds Nos. 1.3, 1.6, 2.2, 2.4, 3.1 to 3.5, 3.7, 3.17, 3.18, 3.20, 3.21, 3.44 to 3.47, 3.49, 3.51, 3.52, 3.57, 3.67, 3.70, 3.75 and 3.95 reduce infection by less than 10%, so that this effect could also be achieved in open field conditions.

Example B6: Action against cabbage against Rhizoctonia solani

Effect after soil application

The mushroom is cultured with sterile millet grains and added to a 30 soil-santa mixture. In the infected soil, containers 42 80 441 are filled and cabbage seed is sown. Immediately after sowing, the test preparation prepared as a spray powder is poured into the ground as an aqueous suspension (20 ppm of active ingredient based on the volume of soil). The soil containers are then placed in a greenhouse at about 24 ° for 2-3 weeks and kept evenly moist by light spraying. The evaluation of the test determines the growth of cabbage plants. After treatment with spray powder containing one of the compounds No. 1.3, 2.1, 3.20 or 3.37 as active ingredient, more than 80% of the cabbage-10 seeds grow after the plants and the plants are healthy in appearance.

Example B7: Residual protective effect on apple trees

Venturia inaequalis1

Apple cuttings with new growths 10 to 20 cm long are sprayed with 15 sprays (0.006% of active substance) of powdered powder of active ingredient. After 24 hours, the treated plants are infected with a fungal conidia suspension. The plants are then incubated for 5 days at a relative humidity of 90-100% and for 10 days in a greenhouse at 20-24 °. Scabies infection is assessed 15 days after 20 infections. The compounds of formula (I) have a good activity against Venturia, in particular compounds Nos. 1.2, 1.3, 3.4, 3.5, 3.17, 3.18, 3.20, 3.22, 3.37, 3.39, 3.71 and 3.95 prevent scab infection compared to untreated control plants, reducing it to less than 25%. 20%. Compounds Nos. 1.3, 3.4, 3.5 and 3.17 achieve this result in the open, even at a dosage of 0.002%.

Example B8: Action against Helminthosporium gramineum 30 Wheat grains are contaminated with a spore suspension of a fungus and re-dried. The contaminated grains are covered with a suspension of test substance 43 80441, spray powder (600 ppm of active ingredient based on the weight of the seeds). After two days, the grains are placed in suitable culture vessels and after the next four days, the development of 5 fungal colonies around the grains is assessed. The number and size of fungal colonies are used to evaluate the test product. In this case, the compounds of Tables 1 to 3, in particular the compounds of Table 3, inhibit fungal infection extensively (0 to 10%).

10 Example B9: Action against Fusarium nivale

Wheat grains are contaminated with a spore suspension of the fungus and dried again. The contaminated grains are covered with a suspension of the test substance in powder spray (600 ppm of active ingredient based on the weight of the seeds).

15 After two days the grains are placed in suitable culture vessels and after four days the development of fungal colonies around the grains is assessed. The number and size of fungal colonies are used to evaluate the test product.

In grains treated with spray powder containing one of the compounds of Tables 1 to 3 as active ingredient, the development of fungal colonies is almost completely reduced (0 to 5%).

Example B10; Grain protection: (Grainpreservative Test) 25 a) Short-term test against wet fungi in moist maize

Dry maize grains for animal feed (portions 80 g) are mixed in a well-sealed plastic container with the active ingredients of Tables 1-3 in the form of an aqueous suspension, emulsion or solution.

The treatment of the substance is dimensioned so that the concentration of active substance becomes 0.06%, calculated on the dry weight of the maize. A moistened piece of paper takes care of the moisture-saturated environment in a container filled with corn and finally sealed. Incubate for 2-3 weeks at about 20 °, after which only water-treated maize samples spontaneously develop a mixed culture of molds. No artificial infection is required. The amount of fungal-10 inhibition after 3 weeks serves as a measure of the evaluation of the efficacy of the compounds of formula (I).

(b) Long-term test on moist maize against molds I. Samples of maize which, after 3 weeks, are free from fungal infection shall be further incubated for two months. After each month, a visual assessment is performed according to the criteria presented in the a-test.

II. The test is carried out in essentially the same way as in (a) and (b), except that the test compound is tested for 6 months using 2000, 600 and 200 ppm of active substance (calculated on the dry weight of the maize).

Treatment with the compounds of formula (I) according to Tables 1 to 3 completely inhibits the formation of mold fungi in moist maize in all three tests a, bl and bll, both short-term (3 weeks) and long-term (6 months).

Thus, for example, compounds 1.1 to 1.6, 1.9, 1.11, 1.13, 1.15, 1.18 and 1.20, as well as some of the compounds in Tables 2 and 3 in all three tests a, bl and bll, inhibit test fungus at 600 ppm of active substance.

II

45 8 0 4 41 nan almost completely (O - 5% infection).

In similar experiments, in which feed grain (oats), hay, root-cut or kidney beans are optionally used instead of feed maize, parallel results are observed in protection for several months when treated with the above-mentioned active ingredients of formula (I).

Claims (15)

46 80 441 Compounds of formula (I) V \ _____ CN (I) y / li n t1 '/ · »· · · R2 Y r3-Ch-y wherein and R2 are, independently of one another, hydrogen, halogen, methoxy or methylthio ; R 3 represents hydrogen or C 1 -C 6 haloalkyl; Y represents hydroxy, halogen or -O-C (O) -R4, where R4 represents hydrogen, C1-C4-alkyl, C1-C3-haloalkyl, C2-C3-alkenyl, 2-tetrahydrofuryl, C 1-4 alkoxycarbonyl or the group -CH 2 OR 6, wherein R 6 represents C 1 -C 4 alkyl, 2-methoxyethyl, allyl, propargyl or unsubstituted or chlorine-substituted phenyl. Compounds of formula (I) according to Claim 1, characterized in that R 1 is attached to the 2-position of the phenyl ring and R 2 to the 3-position of the phenyl ring and represents, independently of one another, hydrogen, halogen, methoxy or methylthio; R 3 represents hydrogen or C 1 -C 4 haloalkyl; and Y represents hydroxy, halogen or -O-C (O) -R4, wherein R4 represents C1-C4-alkyl, C1-haloalkyl, 2-tetrahydrofuryl, C1-C2-alkoxycarbonyl or -CH2ORg, where Rg means C 1 -C 4 alkyl, 2-methoxyethyl, allyl, propargyl or unsubstituted or chlorine-substituted phenyl. Compounds of formula (I) according to Claim 2, characterized in that R 1 represents hydrogen, 2-chloro, 2-methoxy or 2-methylthio; R 2 represents hydrogen II 80441 or 3-chloro; R 3 represents hydrogen or C 1 -C 4 haloalkyl; and Y represents hydroxy, chlorine or the group -OC (O) -R 4, wherein R 4 represents C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, 2-tetrahydrofuryl, C 1 -C 2 alkoxycarbonyl or the group -CH 2 OR 8, where R 8 means C 1 -C 4 alkyl, 2-methoxyethyl, allyl, propargyl or unsubstituted or chlorine-substituted phenyl. Compounds of formula (I) according to Claim 3, characterized in that R 1 represents hydrogen, 2-chloro, 2-methoxy or 2-methylthio; R 2 represents hydrogen or 3-chlorine; R 3 represents hydrogen or CCl 3 and Y represents hydroxy, chlorine or the group -O-C (O) -R 4, wherein R 4 represents C 1 -C 4 alkyl, C 1-4 haloalkyl, 2-tetrahydrofuryl, methoxycarbonyl or the group -CH 2 OR 9, wherein Rg is C1-C4 alkyl, 2-methoxyethyl, allyl, propargyl, phenyl or chloro-substituted phenyl. A compound of formula (I) according to claim 1, which is: N- (hydroxymethyl) -3- (3-chlorophenyl) -4-cyanopyrrole. A compound of formula (I) according to claim 2, which is: N- (1-acetyloxy-2,2,2-trichloroethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, N- ( 1-hydroxy-2,2,2-trichloroethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, N- (1-methoxyacetyloxy-2,2,2-trichloroethyl) -3- (2,3- dichlorophenyl) -4-cyanopyrrole, N- (methoxyacetyloxymethyl) -3- (2,3-dichlorophenyl) -4-cyanopyrrole, N- [1- (n-butylcarbonyloxy) -2,2,2-trichloroethyl] -3 - ( 2,3-dichlorophenyl) -4-cyanopyrrole, N- [1- (n-propoxyacetyloxy) -2,2,2-trichloroethyl] -3- (2,3-dichlorophenyl) -4-cyanopyrrole, 48 80441 N - [ 1- (n-butoxyacetyloxy) -2,2,2-trichloroethyl] -3- (2,3-dichlorophenyl) -4-cyanopyrrole, N- [1- (propargyloxyacetyloxy) -2,2,2-trichloroethyl] -3 - (2,3-dichlorophenyl) -4-cyanopyrroles. A compound of formula (I) according to claim 1, which is: N- (1-hydroxy-2,2,2-trichloroethyl) -3- (2-chlorophenyl) -4-cyanopyrrole, N- [1- (isopropoxyacetyloxy) ) -2,2,2-trichloroethyl] -3- (2-chlorophenyl) -4-cyanopyrrole, N- (acetyloxymethyl) -3- (2-chlorophenyl) -4-cyanopyrrole. Process for the preparation of compounds of formula (I) as defined in claim 1, characterized in that in the presence or absence of a solvent, at a temperature of from 20 ° C to 90 ° C, the 3-phenyl-4-cyanopyrrole derivative of formula (II) By the reaction of R2 y H with an aldehyde of formula (III) in the presence or absence of an acidic or basic catalyst R3 to CHO (III) is converted to the hydroxy derivative of formula (Ia)> V .-- -CN (Ia) y / n ij * 2 Y r 'oh and the latter is, if desired, converted into another derivative of formula II 49 80 441 (I) by replacing the free OH group with another residue Y, the substituents in formulas (Ia), (II ) and (III) and Y have the same meaning as in formula (I). Process according to Claim 8, characterized in that the compound of the formula (Ia), either in the presence or absence of a customary inert solvent, with an acid anhydride of the formula (IVa) or an acid chloride of the formula (IVb) (R 4 CO) 20 (IVa) R 4 CO ) at a temperature of -10 ° C to 7 ° C is directly converted to the acyloxy product of formula (Ib) R 1 -> -rCM (1b) * 2 V „/ K 8 ec-% where the substituents in formulas (Ib) , (IVa) and (IVb) have the same meaning as in formula (I). A microbicidal agent for controlling or reducing the infection of live plants and / or for preserving perishable plant or animal products, characterized in that it contains a compound of the formula (I) as at least one active component. Substance according to Claim 10, characterized in that it contains as active component at least one compound as defined in Claims 5 to 7. Substance according to Claim 11, characterized in that it contains 0.1 to 99% of active ingredient of the formula (I), 99.9 to 1% of solid or liquid additive and 0 to 25% of surfactant. bo 80441 Substance according to Claim 12, characterized in that it contains 0.1 to 95% of active ingredient of the formula (I), 99.8 to 5% of solid or liquid additive and 0. to 25% of surfactant. A method for controlling or reducing infection by phytopathogenic microorganisms in crops, characterized in that a compound of the formula (I) is applied to the plants, parts of plants or their medium. A method for preserving or protecting flora and / or fauna storage and storage products from harmful microorganisms, characterized in that the article is treated with at least a microbicidally effective amount of a compound of formula (I).