EP1523472A1 - Cis-alkoxy-substituted spirocyclic 1-h-pyrrolidine-2,4-dione derivatives serving as pesticides - Google Patents

Abstract

The invention relates to novel cis-alkoxy-substituted spirocyclic 1-H-pyrrolidine-2,4-dione derivatives of formula (I), in which A, G, X and Y have the meanings as cited in the description, to a number of methods for producing these derivatives and to their use as pesticides.

Description

CIS ALKOXY-SUBSTITUTED SPIROCYCLIC 1-H-PYRROLIDIN-2, 4-DI0N DERIVATIVES AS A PEST CONTROL

The present invention relates to new cis-alkoxy-substituted spirocyclic 1-H-pyrrohdin-2,4-dione derivatives, several processes for their preparation and their

Use as a pesticide.

Alkoxy-substituted spirocyclic 1H-pyrrolidine-2,4-dione derivatives with acaricidal, insecticidal and herbicidal activity are known: EP-A 596 298, WO 95/26954, WO 95/20572, EP-A 668 267, WO 96/25395, WHERE

96/35664, WO 97/01535, WO 97/02243, WO 97/36868, WO 98/05638, WO 99/43649, WO 99/48869, WO 99/55673, WO 01/23354, WO 01/74770.

Due to the manufacturing process, the known Nerbindungen occur in the form of cis / trans isomer mixtures, the cis / trans ratios of which fluctuate.

New compounds of the formula (I)

found in which

X represents alkyl, halogen, alkoxy, haloalkyl or haloalkoxy,

Y represents hydrogen, alkyl, alkoxy, halogen, haloalkyl or haloalkoxy, where only one of the radicals X or Y is halogenoalkyl or haloalkoxy,

A represents C _r C ₆ alkyl,

G for hydrogen (a) or for one of the groups

((bb)) ooddeerr (C)

stands,

wherein

M represents oxygen or sulfur,

R ¹ for each optionally substituted by halogen C ₁ -C ₂₀ alkyl, C ₂ -C ₂₀ alkenyl, -Cs-alkoxy-Ci-Cs-aJkyl, Ci-Cs-alkylthio-Ci-Cs-alkyl or poly-Ci -Cs-alkoxy-Ci-Cs-alkyl or for C ₃ -C ₈ -cycloalkyl optionally substituted by halogen, -Ce-alkyl or CrC ₆ -alkoxy, in which optionally one or two not directly adjacent methylene groups by oxygen and / or sulfur are replaced,

represents phenyl which is optionally substituted by halogen, cyano, nitro, CrCo-alkyl, C Ce-alkoxy, -Ce-haloalkyl, Ci-Ce-haloalkoxy, -Co-alkylthio or CrC _ό -alkylsulfonyl, or represents thienyl,

R ² represents in each case optionally halogen-substituted C ₁ -C ₂ o alkyl, G ₂ -C ₂₀ - alkenyl, Cι-C ₈ -alkoxy-C 2 -C ₈ -alkyl or poly-C ₁ -C ₈ -alkoxy-C ₂ -C ₈ alkyl, for C ₃ -C ₈ cycloalkyl optionally substituted by halogen, Ci-Cβ-alkyl or -C _ό- alkoxy or

for each optionally by halogen, cyano, nitro, -Cβ-alkyl, CrC ₆ - alkoxy, Ci-C _ö -haloalkyl or Cι _. -C ₆ -Halogenalkoxy substituted phenyl or benzyl.

Including the different meanings (a), (b) and (c) of group G, the following main structures (I-a) to (I-c) (cis isomer) result:

Furthermore, it was found that the new compounds of the formula (T) can be obtained by one of the processes described below:

(A) Compounds of the formula (I-1-a) are obtained

in which

A, X and Y have the meanings given above,

if

Compounds of formula (H)

A, X and Y have the meanings given above,

and

R ^{8 stands} for alkyl (preferably CC _ö alkyl), intramolecularly condensed in the presence of a diluent and in the presence of a base.

It was also found

(B) that the compounds of the formula (Ib) shown above, in which A, R ¹ , X and Y have the meanings given above, are obtained if compounds of the formula (Ia) shown above, in which A, X and Y have the meanings given above,

α) with acid halides of the formula (HT)

Shark Y- .R 'P)

O in what

R ^{1 has} the meaning given above and

Shark represents halogen (especially chlorine or bromine)

or

β) with carboxylic anhydrides of the formula (IN)

R ^ CO-O-CO-R ¹ (TV)

in which

R has the meaning given above, if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder;

(C) that the compounds of the formula (Ic) shown above, in which A, R ² ,

M, X and Y have the meanings given above, if compounds of the formula (I-a) shown above, in which A, X and Y have the meanings indicated above, are obtained in each case

with chloroformic acid esters or chloroformic acid thioesters of the formula (V)

in which

R and M have the meanings given above,

if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder;

(D) that the compounds of the formulas (fa) to (Ic) shown above are obtained if cis / trans isomer mixtures of the formulas (Ia ¹ ) to (I-c ') are known, for example, from WO 98/05638 or WO 01 / 74770

in which

A, X, Y, M, R ¹ and R ^{2 have} the meaning given above using physical separation processes such as, for example, column chromatography or fractional crystallization.

(E) It has furthermore been found that compounds of the formula (I-a) are obtained if compounds of the formulas (I-b) or (I-c) in which A, M, X, Y,

R ¹ and R ^{2 have} the meaning given above, for example hydrolyzed with aqueous bases and then acidified.

It has also been found that the new compounds of the formula (I) have good activity as pesticides, preferably as insecticides and / or acaricides, and moreover are often very well tolerated by plants, in particular by crop plants.

The compounds of the invention are generally defined by the formula (T). Preferred substituents or ranges of those mentioned in the above and below

The residues listed in formulas are explained below: X preferably represents chlorine, bromine, methyl, ethyl, propyl, trifluoromethyl, methoxy, difluoromethoxy or trifluoromethoxy,

Y preferably represents hydrogen, chlorine, bromine, methoxy, methyl, ethyl, propyl, trifluoromethyl or trifluoromethoxy,

where only one of the radicals X or Y may represent trifluoromethyl, difluoromethoxy or trifluoromethoxy,

A preferably represents C _r C ₆ alkyl,

G preferably represents hydrogen (a) or one of the groups

in which

M represents oxygen or sulfur,

R ¹ preferably represents C ₁ -C 6 -alky !, C ₂ -C ₁₆ -alkenyl, C ₁ -C 6 -alkoxy-CrCe-alkyl, -Ce-alkyltMo-Cβ-alkyl or poly, each optionally mono- to trisubstituted by fluorine or chlorine - -Cö-alkoxy-CrCö-alkyl or for optionally single to double by fluorine, chlorine, Ci-Cs-alkyl or C1 _. -C ₅ - alkoxy-substituted C ₃ -C -cycloalkyl, in which one or two not directly adjacent methylene groups are optionally replaced by oxygen and or sulfur,

for phenyl which is optionally monosubstituted to trisubstituted by fluorine, chlorine, bromine, cyano, nitro, Cr -alkyl, C ₁ -C ₄ -alkoxy, Ci-Cs-haloalkyl, CrCr-haloalkoxy, d-C -alkylthio or -C alkylsulfonyl or for thienyl . R particularly preferably represents in each case optionally mono- to trisubstituted by fluorine or chlorine-substituted Cι-Ci6-alkyl, _C2 -Ci6 alkenyl, Cι-C ₆ alkoxy C ₂ -C ₆ -alkyl or poly-CrC alkoxy _ö C ^ Ce-alkyl,

for C ₃ -C cycloalkyl which is optionally mono- to disubstituted by fluorine, chlorine, Q-Gr alkyl or -Gralkoxy or

for phenyl or benzyl substituted in each case optionally once or twice by fluorine, chlorine, bromine, cyano, nitro, C ₁ -C ₄ alkyl, C ₁ -C ₃ alkoxy, d-Cs-haloalkyl or C ₃ ~ C ₃ - haloalkoxy.

X particularly preferably represents chlorine, bromine, methyl, ethyl, methoxy, trifluoromethyl, trifluoromethoxy or difluoromethoxy,

Y particularly preferably represents chlorine, bromine, methyl, ethyl, propyl, methoxy,

Trifluoromethyl or trifluoromethoxy, where only one of the radicals X or Y may represent trifluoromethyl, trifluoromethoxy or difluoromethoxy,

A particularly preferably represents C ₁ -C ₄ -alkyl,

G very particularly preferably represents hydrogen (a) or one of the groups

in which

M represents oxygen or sulfur, R ¹ particularly preferably represents in each case optionally mono- to trisubstituted by fluorine or chlorine -C ₈ -AJkyl, C ₂ -C ₈ alkenyl, Cι-C ₂ alkoxy-Cι- C ₂ alkyl, C ₁ -C ₂ -alkylthio -C ₁ -C ₂ alkyl or for C ₃ -C ₆ cycloalkyl which is optionally mono- to disubstituted by fluorine, chlorine, methyl or methoxy and in which a methylene group is optionally replaced by oxygen and / or sulfur,

for phenyl which is optionally mono- to disubstituted by fluorine, chlorine, bromine, cyano, nitro, methyl, methoxy, trifluoromethyl or trifluoromethoxy or for thienyl,

R ² particularly preferably represents C ₁ -C ₈ -alkyl, C ₂ -C ₈ -alkenyl or CrQ-alkoxy- C ₂ -C ₃ -alkyl, C ₅ -C ₆ -cycloalkyl,

for each optionally simply by fluorine, chlorine, cyano, nitro, methyl,

Methoxy, trifluoromethyl or trifluoromethoxy substituted phenyl or benzyl.

X very particularly preferably represents chlorine, bromine, methyl or trifluoromethyl (emphasized chlorine, bromine or methyl),

Y very particularly preferably represents chlorine, bromine or methyl, (highlighted for methyl),

A very particularly preferably represents methyl, ethyl, propyl, butyl or isobutyl,

(highlighted for methyl or ethyl),

G very particularly preferably represents hydrogen (a) or one of the groups

M represents oxygen or sulfur (highlighted for oxygen),

R ¹ very particularly preferably represents Cι _. -C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₁ -C ₂ alkoxy-

C Ca-aJkyL C ₁ -C ₂ alkylthio-C ₁ -C ₂ alkyl, for each optionally simply by fluorine, chlorine ,. Methyl or methoxy substituted cyclopropyl, cyclopentyl or cyclohexyl,

for optionally simply by fluorine, chlorine, bromine, cyano, nitro, methyl,

Methoxy, trifluoromethyl or trifluoromethoxy substituted phenyl or for thienyl,

R ² very particularly preferably represents C ₁ -C ₈ -alkyl, C ₂ -C ₆ -alkenyl or CrC ₃ - alkoxy-C ₂ -C ₃ -alkyl,

for cyclopentyl or cyclohexyl

or for phenyl or benzyl which is optionally simply substituted by fluorine, chlorine, cyano, nitro, methyl, methoxy, trifluoromethyl or trifluoromethoxy.

The general definitions or explanations of residues or explanations listed above or in preferred areas can be combined with one another, that is to say also between the respective areas and preferred areas. They apply accordingly to the end products as well as to the preliminary and intermediate products. According to the invention, preference is given to the compounds of the formula (T) in which there is a combination of the meanings listed above as preferred (preferred).

According to the invention, particular preference is given to the compounds of the formula (T) in which there is a combination of the meanings listed above as being particularly preferred.

According to the invention, very particular preference is given to the compounds of the formula (T) in which there is a combination of the meanings listed above as being particularly preferred.

Saturated or unsaturated hydrocarbon residues such as alkyl or alkenyl can also be used in connection with heteroatoms, e.g. in alkoxy, where possible, be straight-chain or branched.

Optionally substituted radicals can be mono- or polysubstituted, and in the case of multiple substitutions the substituents can be the same or different.

n In addition to the compounds mentioned in the preparation examples, the following compounds of the formula (I-a) may be mentioned individually:

Table 1 A = CH ₃

Table 3 A = CH ₃

Table 4 A = CH ₃

Table 5 A = CH ₃

Table 6 A = CH ₃

Table 7 A = CH ₃

Table 8 A = C ₂ H ₅

Table 9 A = C ₂ H ₅

Table 10 A - C ₂ H ₅

Table 11 A = C ₂ H ₅

Table 12 A = C ₂ H ₅

Table 13 A = CH ₃ M = O

Table 14 A = CH ₃ M = O

4/007448

• 25-

Table 15 A = CH, M = O

Table 16 A = CH ₃ M = O

Table 17 A = CH, M = O

Table 18 A = C ₂ H ₅ M = O

Table 19 A = C ₂ H ₅ M = O

Table 20 A = C ₂ H ₅ M = O

Table 21 A = C ₂ H ₅ M = O

04/007448

32

Table 22 A = C ₂ H ₅ M = O

Table 23 A = CH ₃ M = S

TabeUe 24 A = CH ₃ M = S

TabeUe 25 A = CH ₃ M = S

Table 26 A = CH, M = S

Table 27 A = CH ₃ . M = S

Table 28 A = C ₂ H ₅ M = S

Table 29 A = C ₂ H ₅ M = S

Table 30 A = C ₂ H ₅ M = S

Table 31 A = C ₂ H ₅ M = S

Table 32 A = C ₂ H ₅ M = S

If, for example, according to process (A) cis-N - [(2,5-dimethyl) - phenylacetyl] -1-amino-4-methoxy-cyclohexane-carboxylic acid ethyl ester is used as starting material, the course of the process according to the invention can be represented by the following reaction scheme :

If, for example, according to process (B-α) cis-3 - [(2,5-dimethyl) - phenyl] -5,5- (3-methoxy) pentamethylene-pyrrolidine-2,4-dione and pivaloyl chloride are used as starting materials, the course of the process according to the invention can be represented by the following reaction scheme:

If, for example, according to process (B-β) cis-3 - [(2,5-dimethyl) - ρhenyl] -5,5- (3-memoxy) pentamethylene-pyrroHdin-2,4-dione and acetic anhydride are used as starting compounds, the course of the process according to the invention can be represented by the following reaction scheme:

For example, according to process (C) cis-3 - [(2-bromo-5-methyl) - phenyl] -5,5- (3-methoxy) -pentamethylene-pyrrolidine-2,4-dione and chloroformic acid ethyl ester are used as Starting compounds, the course of the process according to the invention can be represented by the following reaction scheme:

If, for example, process (E) cis-3 - [(2,5-dimethyl) phenyl] - is used

5,5- (3-me oxy) pentame ylen-4-emoxycarbonyl-Δ ³ -pyrrolin-2-one and aqueous bases as starting compounds, the course of the process according to the invention can be represented by the following reaction scheme:

The compounds of the formula (H) required as starting materials in process (A) according to the invention

in which

A, X, Y and R ^{δ have} the meanings given above,

are new.

The acylamino acid esters of the formula (IT) are obtained, for example, if cis-amino acid derivatives of the formula (VI)

in which

A, B and R ^{8 have} the meanings given above,

with substituted phenylacetic acid halides of the formula (VII)

in which

X and Y have the meanings given above and Shark represents chlorine or bromine,

acylated (Chem. Reviews 52, 237-416 (1953); Bhattacharya, Indian J. Chem. 6, 341-5, 1968)

or if you have acylamino acids of the formula (VflT)

in which

A, X and Y have the meanings given above,

esterified (Chem. Ind. (London) 1568 (1968)).

The compounds of the formula (VIfl)

in which

A, X and Y have the meanings given above are new. The compounds of the formula (VIU) are obtained if cis-amino acids of the formula (IX)

in which

A has the meanings given above,

with substituted phenylacetic acid halides of the formula (VH)

in which

X and Y have the meanings given above and

Shark represents chlorine or bromine,

acylated according to Schotten-Baumann (Organikum, VEB Deutscher Verlag der Wissens- schatten, Berlin 1977, p. 505).

The compounds of the formula (VH) are known (WO 98/05638, WO 01/74770) or can be prepared by the processes described there.

The compounds of the formulas (VT) and (EX) are known (WO 02/02532) or can be prepared by the processes described there. The acid halides of the formula (Ifl), carboxylic acid anhydrides of the formula (TV) and chloroformic acid esters or chloroformic acid thioesters of the formula (V) which are also required as starting materials for carrying out the processes (B) and (C) according to the invention are generally known compounds of organic or inorganic Chemistry.

Process (A) is characterized in that compounds of the formula (ET), in which A, X, Y and R ^{8 have} the meanings given above, are subjected to an intramolecular condensation in the presence of a diluent and in the presence of a base.

In the process (A) according to the invention, all organic solvents which are inert to the reactants can be used as diluents. Hydrocarbons such as toluene and xylene are preferably usable, furthermore ethers such as dibutyl ether, tetrahydrofuran, dioxane, glycol dimethyl ether and

Diglycol dimethyl ether, and also polar solvents, such as dimethyl sulfoxide, sulfolane, dimethylformamide and Ν-methyl-pyrroüdon, as well as alcohols such as methanol, ethanol, propanol, iso-propanol, butanol, iso-butanol and tert-butanol.

All the usual proton acceptors can be used as the base (deprotonating agent) when carrying out process (A) according to the invention. Alkali metal and alkaline earth metal oxides, hydroxides and carbonates, such as sodium hydroxide, potassium hydroxide, magnesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate, which can also be used in the presence of phase transfer catalysts such as, for example, triethylbenzylammonium chloride, tetrabutylammonium bromide (methylene chloride, adogen 46, C ₈ -C ₁₀ ) ammonium chloride) or TDA 1 (= tris (me oxyemoxye yl) amine) can be used. Alkali metals such as sodium or potassium can also be used. Alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodium hydride and calcium hydride, and also alkali metal alcoholates, such as sodium methylate, sodium ethylate and potassium tert-butoxide, can also be used. The reaction temperature can be varied within a substantial range when carrying out process (A) according to the invention. In general, temperatures between 0 ° C and 250 ° C, preferably between 50 ° C and 150 ° C.

Process (A) according to the invention is generally carried out under normal pressure.

When carrying out process (A) according to the invention, the reaction component of the formula (III) and the deprotonating base are generally employed in equimolar to approximately double-equimolar amounts. However, it is also possible to use one or the other component in a larger excess (up to 3 moles).

Process (Bα) is characterized in that compounds of the formula (I-a) are reacted with carboxylic acid halides of the formula (Tfl), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.

Diluents which can be used in process (B-α) according to the invention are all solvents which are inert to the acid halides. Hydrocarbons such as gasoline, benzene, toluene, xylene and tetralin are preferably usable, furthermore halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, and also ketones such as acetone and

Methyl isopropyl ketone, furthermore ethers, such as diethyl ether, tetrahydrofuran and dioxane, in addition carboxylic acid esters, such as ethyl acetate, and also strongly polar solvents, such as dimethylformamide, dimethyl sulfoxide and sulfolane. If the hydrolysis stability of the acid halide permits, the reaction can also be carried out in the presence of water. Suitable acid binders for the reaction according to process (Bα) according to the invention are all customary acid acceptors. Tertiary amines, such as triethylamine, pyridine, diazabicyclooctane (DABCO), diazabicycloundecene (BU), diazabicyclonones (DBN), Hunig base and N, N-dimethylaniline, and also alkaline earth metal oxides, such as magnesium oxide and calcium oxide, are preferably usable. Moreover

Alkali and alkaline earth metal carbonates, such as sodium carbonate, potassium carbonate and calcium carbonate, and also alkali hydroxides, such as sodium hydroxide and potassium hydroxide.

The reaction temperature in process (Bα) according to the invention can be varied within a substantial range. In general, temperatures between -20 ° C and + 150 ° C, preferably between 0 ° C and 100 ° C.

When carrying out process (Bα) according to the invention, the starting materials of the formula (I-a) and the carboxylic acid halide of the formula (Tfl) are generally in each case used in approximately equivalent amounts. However, it is also possible that

Use a large excess of carboxylic acid halide (up to 5 mol). The processing takes place according to usual methods.

The process (Bß) is characterized in that compounds of the formula (I-a) with carboxylic anhydrides of the formula (IN), if appropriate in the presence of a

Nerdünnungsmittel and optionally in the presence of an acid binder.

Diluents which can be used in the process (Bß) according to the invention are preferably those diluents which are also preferred when using acid halides. In addition, an excess of carboxylic acid anhydride can also act as a diluent. Suitable acid binders which may be added in process (Bß) are preferably those acid binders which are also preferred when using acid halides.

The reaction temperature can be varied within a substantial range in the process (Bß) according to the invention. In general, temperatures between -20 ° C and + 150 ° C, preferably between 0 ° C and 100 ° C.

When carrying out the process (Bß) according to the invention, the starting materials of the formula (I-a) and the carboxylic anhydride of the formula (TV) are generally used in approximately equivalent amounts in each case. However, it is also possible to use the carboxylic anhydride in a larger excess (up to 5 mol). The processing takes place according to usual methods.

The general procedure is to remove diluent and excess carboxylic acid anhydride and the carboxylic acid formed by distillation or by washing with an organic solvent or with water.

Process (C) is characterized in that compounds of the formula

(I-a) with chloroformate or chloroformate thiol ester of the formula (V) if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.

Acid binders used in process (C) according to the invention are all conventional

Acid acceptors into consideration. Tertiary amines, such as triethylamine, pyridine, DABCO, DBU, DBA, Hunig base and N, N-dime l-aniline, furthermore alkaline earth metal oxides, such as magnesium and calcium oxide, and also alkali and alkaline earth metal carbonates, such as sodium carbonate, are preferably usable. KaHum carbonate and calcium carbonate as well as AH aH hydroxides such as sodium hydroxide and KaHum hydroxide. Diluents which can be used in process (C) according to the invention are all solvents which are inert to the chloroformic acid esters or chloroformic acid thiolestem esters. Hydrocarbons such as gasoline, benzene, toluene, xylene and tetraHn are preferably usable, furthermore halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, furthermore ketones such as acetone and methyl propyl ketone, furthermore ethers such as diethyl ether, tetrahydrofuran and in addition carboxylic acid esters, such as ethyl acetate, also nitriles, such as acetonitrile, and also strongly polar solvents, such as dimethylformamide, dimethyl sulfoxide and sulfo oil.

The reaction temperature can be varied within a substantial range when carrying out process (C) according to the invention. The reaction temperature is generally between -20 ° C and + 100 ° C, preferably between 0 ° C and 70 ° C.

Process (C) according to the invention is generally carried out under normal pressure.

When carrying out process (C) according to the invention, the starting materials of the formula (I-a) and the corresponding chloroformate or chloroformate thioester of the formula (V) are generally in each case used in approximately equivalent amounts. However, it is also possible to use one or the other component in a larger excess (up to 2 mol). The processing takes place according to usual methods. In general, one proceeds by removing precipitated salts and removing the remaining reaction mixture by removing the

Nourishing agent constricts.

Process (E) according to the invention is characterized in that compounds of the formulas (Ib) or optionally (Ic) are hydrolyzed in the presence of a solvent and in the presence of a base in an aqueous medium and then acidified with acids. In production process (E), about 1 to 10 mol, preferably 1 to 3 mol, of base are reacted at 0 to 150 ° C., preferably 20 ° to 80 ° C., per mole of the starting compounds of the formula (Ib).

Possible diluents that are added are all water-miscible organic solvents such as alcohols, ethers, amides, sulfones or sulfoxides.

Methanol, ethanol, propanol, isopropanol, butanol, isobutanol,

Tetrahydrofuran, dioxane, dimethylformamide, dimethylacetamide, N-MeÜiylpyrrolidon, sulfolane or dimethyl sulfoxide used.

Acidification was preferably carried out as inorganic acids such as hydrochloric acid, sulfuric acid, phosphoric acid or nitric acid and as organic acids such as formic acid,

Acetic acid or sulfonic acids are used.

Process (D) according to the invention is characterized in that cis / trans isomer mixtures of the formulas (Ib ¹ ) or (I-c ') are separated by chromatographic methods, preferably by column chromatography on silica gel.

In the production process (D), about 10 g to 200 g, preferably 50 to 100 g, of silica gel are used per gram of starting compound.

Mixed solvents of different polarities are used as eluents. Solvent mixtures of halogenated hydrocarbons in combination with are preferred

Ketones, esters or alcohols.

Process (D) according to the invention is generally carried out under normal pressure. It is also possible to work at higher pressures such as those that occur during separation using MPLC or HPLC systems. With good plant tolerance and favorable toxicity to warm-blooded animals, the active substances are suitable for controlling animal pests, in particular insects, arachnids and nematodes, which occur in agriculture, in forests, in the protection of stored goods and materials, and in the hygiene sector. They can preferably be used as pesticides. They are effective against normally sensitive and resistant species as well as against all or individual stages of development. The pests mentioned above include:

From the order of the Isopoda e.g. Oniscus asellus, Armadillidium vulgare, Porcellio scaber.

From the order of the Diplopoda e.g. Blaniulus guttulatus.

From the order of the Chilopoda e.g. Geophilus carpophagus, Scutigera spp ..

From the order of the Symphyla e.g. Scutigerella immaculata.

From the order of the Thysanura e.g. Lepisma saccharina.

From the order of the Collembola e.g. Onychiurus armatus.

From the order of the Orthoptera e.g. Acheta domesticus, Gryllotalpa spp., Locusta migratoria migratorioides, Melanoplus spp., Schistocerca gregaria.

From the order of the Blattaria e.g. Blatta orientaHs, Periplaneta americana,

Leucophaea maderae, Blattella germanica.

From the order of the Dermaptera e.g. Forficula auricularia.

From the order of the Isoptera, for example Reticuliterm.es spp .. From the order of the Phthiraptera, for example Pediculus humanus corporis, Haematopinus spp., Linognathus spp., Trichodectes spp., Damalinia spp ..

From the order of the Thysanoptera e.g. Hercinothrips femoralis, Thrips tabaci, Thrips pal i, Frankliniella accidentalis.

From the order of the Heteroptera e.g. Eurygaster spp., Dysdercus intermedius, Piesma quadrata, Cimex lectularius, Rhodnius prolixus, Triatoma spp.

From the order of the Homoptera e.g. Aleurodes brassicae, Bemisia tabaci,

Trialeurodes vaporariorum, Aphis gossypii, Brevicoryne brassicae, Cryptomyzus ribis, Aphis fabae, Aphis pomi, Eriosoma lanigerum, Hyalopterus aiτmdinis, Phylloxera vastatrix, Pemphigus spp., Macrosiphum avenae, Myzus spp., Phorodonppi , Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Laodelphax striatellus, Nilaparvata lugens, Aonidiella aurantii, Aspidiotus hederae, Pseudococcus spp., Psylla spp.

From the order of the Lepidoptera e.g. Pectinophora gossypiella, Bupalus pimarius, Cheimatobia brumata, Lithocolletis blancardella, Hyponomeuta padella, Plutella xylostella, Malacosoma neustria, Euproctis chrysorrhoea, Lymantria spp.,

Bucculatrix thurberiella, Phyllocnistis citrella, Agrotis spp., Euxoa spp., Feltia spp., Earias insulana, HeHothis spp., Mamestra brassicae, Panolis flammeä, Spodoptera spp., Trichoplusia ni, Carpocapsa pomonella, Pierilo s., Pierilo s nubilalis, Ephestia kuehniella, Galleria mellonella, Tineola bisselHella, Tinea pelHonella, Hofmannophila pseudospretella, Cacoecia podana, Capua reticulana,

Choristoneura fumiferana, Clysia ambiguella, Homona magnanima, Tortrix viridana, Cnaphalocerus spp., Oulema oryzae.

From the order of the Coleoptera e.g. Anobium punctatum, Rhizopertha dominica, Bruchidius obtectus, Acanthoscelides obtectus, Hylotrupes bajulus, Agelastica alni,

Leptinotarsa decemlineata, Phaedon cochleariae, Diabrotica spp., Psylliodes chrysocephala, Epilachna varivestis, Atomaria spp., Oryzaephilus surinamensis, Anthonomus spp., Sitophilus spp., Otiorrhynchus sulcatus, Cosmopolites sordidus, Ceuthorrhynchus assimiHs, Hypera postica, Dermestes sppus, spp., Trog. spp., Trog ., Mehgethes aeneus, Ptinus spp., Niptus hololeucus, Gibbium psylloides, TriboHum spp., Tenebrio molitor, Agriotes spp.,

Conoderus spp., Melolontha melolontha, Amphimallon solstitialis, Costelytra zealandica, Lissorhoptrus oryzophilus.

From the order of the Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.

From the order of the Diptera e.g. Aedes spp., Anopheles spp., Culex spp., Drosophila melanogaster, Musca spp., Fannia spp., Calliphora erythrocephala, Lucilia spp., Chrysomyia spp., Cuterebra spp., Gastrophilus spp., Hyppobosca spp., Stomoxys Oestrus spp., Hypoderma spp., Täbanus spp., Tannia spp., Bibio hortulanus, Oscinella frit, Phorbia spp., Pegomyia hyoscyami, Ceratitis capitata, Dacus oleae, Tipula paludosa, Hylemyia spp., Liriomyza spp ..

From the order of the Siphonaptera e.g. Xenopsylla cheopis, Ceratophyllus spp .. From the Arachnida class e.g. Scorpio maurus, Latrodectus mactans, Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hyalommxodes spp., .Ϊ. Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Bryobia praetiosa, Panonychus spp., Tetranychus spp., Hemitarsonemus spp., Brevipalpus spp ..

The plant-parasitic nematodes include, for example, Pratylenchus spp., Radopholus simiHs, Ditylenchus dipsaci, Tylenchulus semipenetrans, Heterodera spp., Globodera spp., Meloidogyne spp., Aphelenchoides spp., Longidorus spp., Tripusichus spp., Xiphinema spp. , If appropriate, the compounds according to the invention can also be used in certain concentrations or application rates as herbicides and microbicides, for example as fungicides, antifungals and bactericides. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active compounds.

According to the invention, all plants and parts of plants can be treated. Plants are understood here to mean all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants). Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant cultivars which can or cannot be protected by plant breeders' rights. Under plant parts, all above-ground and underground

Parts and organs of plants, such as shoots, leaves, flowers and roots, are to be understood, examples being leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds as well as roots, tubers and rhizomes. The plant parts also include crops and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.

The treatment of the plants and parts of plants with the active compounds according to the invention takes place directly or by acting on their surroundings, living space or storage space according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, scattering, spreading and, in the case of propagation material, in particular in the case of seeds, furthermore by coating in one or more layers.

The active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, solvent-free powders, granules, suspension-emulsion concentrates and impregnated materials

Natural and synthetic substances as well as very fine encapsulation in polymeric substances. These formulations are prepared in a known manner, for example by mixing the active ingredients with extenders, that is to say liquid solvents and / or solid carriers, optionally using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-producing agents

Means.

If water is used as an extender, e.g. organic solvents can also be used as auxiliary solvents. The following are essentially suitable as liquid solvents: aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chlorethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, e.g. Petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar

Solvents such as dimethylformamide and dimethyl sulfoxide, and water.

The following are suitable as solid carriers:

e.g. Ammonium salts and natural rock flours, such as kaolins, clays,

Talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock flour, such as highly disperse silica, aluminum oxide and silicates, are suitable as solid carriers for granules: e.g. broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic Granules from inorganic and organic flours and granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stems; suitable emulsifiers and / or foam-generating agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolyzates; The following may be used as dispersants: for example lignin sulfite waste liquor and methyl cellulose. Adhesives such as carboxymethyl cellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalene and lecithme and synthetic phospholipids can be used in the formulations. Further

Additives can be mineral and vegetable oils.

Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes, such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt,

Molybdenum and zinc can be used.

The formulations generally contain between 0.1 and 95% by weight of active compound, preferably between 0.5 and 90%.

The active compounds according to the invention, as such or in their formulations, can also be used in a mixture with known fungicides, bactericides, acaricides, nematicides or insecticides, in order, for example, to to broaden the spectrum of activity or to prevent the development of resistance. In many cases, synergistic effects are obtained, i.e. the effectiveness of the mixture is greater than the effectiveness of the individual components.

The following connections can be considered as mixed partners:

fungicides:

Aldimorph, ampropylfos, ampropylfos-KaHum, andoprim, anilazine, azaconazole, azoxystrobin,

Benalaxyl, benodanil, benomyl, benzamacril, benzamacrylic isobutyl, bialaphos,

Binapacryl, biphenyl, bitertanol, blasticidin-S, bromuconazole, bupirimate, buthiobate, Calcium polysulfide, capsimycin, captafol, captan, carbendazim, carboxin, carvone, quinomethionate (quinomethionate), chlobenthiazon, chlorfenazol, chloroneb, chloropicrin, chlorothalonil, chlozoHnat, clozylacon, cufraneb, cymoxazilol, cyodamilanilof, cyproconilanil, cyprooxilil, cypinoxanil, cypinoxanil, cypinoxanil, cyproconil

Debacarb, dichlorophene, diclobutrazole, diclofluanide, diclomezin, dicloran, diethofencarb, difenoconazole, DimetMrimol, Dimethomorph, Diniconazol, Diniconazol-M, Dinocap, Diphenylamine, Dipyrithione, Ditalimfos, Dorphianzolodon, Dithianononodon

Ediphenphos, Epoxiconazole, Etaconazole, Ethirimol, Etridiazole,

Famoxadone, fenapanil, fenarimol, fenbuconazole, fenfuram, fenitropan, fenpiclonil, fenpropidin, fenpropimorph, fentin acetate, fentin hydroxide, ferbam, ferimzone,

Fluazinam, Flumetover, Fluoromid, Fluquinconazole, Flurprimidol, Flusilazol, Flusulfamid, Flutolanil, Flutriafol, Folpet, Fosetyl-Aiminium, Fosetyl-Sodium, FthaHd, Füberidazol, Furalaxyl, Furametpyr, Furcarbonol, Furazoloxolol, Furazazoloxol

guazatine,

Hexachlorobenzene, hexaconazole, hymexazole,

lrnazaHl, Imibenconazol, hmnoctadin, Jminoctadinealbesilat, Iminoctadinetriacetat,

Iodocarb, ipconazole, iprobefos (IBP), iprodione, lfumamycin, isoprothiolan, isovaledione,

Kasugamycin, Kresoxim-methyl, copper preparations, such as: copper hydroxide, copper naphthenate, copper oxychloride, copper sulfate, copper oxide, oxy-copper and Bordeaux mixture, Mancopper, Mancozeb, Maneb, Meferimzone, Mepampyrim, Mepronil, Metalaxyl, Metconazol, Methasulfocarb, Methfuroxam, Metiram, Metomeclam, Metsulfovax, Mildiomycin, Myclobutanil, Myclozolin,

Nickel dimethyldithiocarbamate, nitrothal isopropyl, Nuarimol,

Ofurace, Oxadixyl, Oxamocarb, Oxolinicacid, Oxycarboxim, Oxyfenthiin,

Paclobutrazole, pefurazoate, penconazole, pencycuron, phosdiphen, picoxystrobin,

Pimaricin, piperalin, polyoxin, polyoxorim, probenazole, prochloraz, procymidon, propamocarb, propanosine sodium, propiconazole, propineb, pyraclostrobin, pyrazophos, pyrifenox, pyrimethanil, pyroquilon, pyroxyfur,

Quinconazole, quintozen (PCNB),

Sulfur and sulfur preparations,

Tebuconazole, Teclofϊalam, Tecnazen, Tetcyclacis, Tetraconazol, Thiäbendazol, Thicyofen, Thifluzamide, Thiophanate-methyl, Thiram, Tioxymid, Tolclofos-methyl,

Tolylfluanid, Triadimefon, Triadimenol, Triazbutil, Triazoxid, Trichlamid, Tricyclazol, Tridemorph, Trifloxystrobin, Triflumizol, Triforin, Triticonazol,

uniconazole

VaHdamycin A, VinclozoHn, Viniconazole,

Zarilamid, Zineb, Ziram as well

Dagger G, OK 8705,

OK 8801,

α- (l, 1-dimethylethyl) -ß- (2-phenoxyethyl) - 1H-1, 2,4-triazole-1-ethanol, α- (2,4-dichlorophenyl) -ß-fluoro-b-propyl- 1 H- 1, 2,4-triazole-1-ethanol, α- (2,4-dichlorophenyl) -ß-methoxy-a-methyl-1 H-1, 2,4-triazole-1-ethanol, α- (5-methyl-1,3-dioxan-5-yl) -ß - [[4- (1-rifluoromethyl) phenyl] methylene] - 1H-1, 2,4-triazol-1-ethanol,

(5RS, 6RS) -6-hydroxy-2,2,7,7-teframethyl-5- (1H-l, 2,4-triazol-l-yl) -3-octanone, (E) -a- (methoxyimmo ) -N-methyl-2-ρhenoxy-ρhenylacetamid,

{2-Methyl-1 - [[[1 - (4-memylphenyl) ethyl] amino] carbonyl] propyl} carbamic acid 1-isopropyl ester

l- (2,4-DicMorphenyl) -2- (lH-l, 2,4-triazol-l-yl) -emanone-O- (phenylmemyl) -oxime, l- (2-methyl-l-naphthalenyl) - lH-ρyrrol-2,5-dione, l- (3,5-dicmorphenyl) -3- (2-propenyl) -2,5-pyrrodinedione, 1 - [(diiodomethyl) sulfonyl] -4-methyl-benzene, l - [[2- (2,4-DicMorphenyl) -1, 3-dioxolan-2-yl] -memyi] -IH-imidazole, l - [[2- (4-chlorophenyl) -3-phenyloxiranyl] methyl ] -lH-l, 2,4-triazole, l- [l- [2 - [(2,4-DicUorphenyl) methoxy] phenyl] ethenyl] -lH-imidazole, l-memyl-5-nonyl- 2- (phenylmethyl) -3-pvrroHdinol, 2 ', 6'-dibromo-2-memyl-4'-triflu ^

2,2-DicMor-N- [l- (4-cMhenyl) -emyl] -l-emyl-3-memyl-cyclopropanecarboxamide,

2,6-DicMor-5- (memylMo) -4-pyrimidmyl thiocyanate,

2,6-DicMor-N- (4-trifluoromethylberιzyl) -benzamide,, 6-DicMor-N - [[4- (trifluoromethyl) -phenyl] -memyl] -benzamide, - (2,3,3-triiodo- 2-ρropenyl) -2H-tetrazole, - [(l-memylemyl) sulfonyl] -5- (tricωorme l) -l, 3,4-tmadiazole, 2 - [[6-Deoxy-4-O- (4-O-yl-ß-p-glycopyranosyl) -aD-glucoρyranosyl] -amino] -4- me oxy-lH-pyιrolo [2,3-d] pyrimidm-5-carbonitrile,

2-Aιrώιobutan,

2-bromo-2- (bromine yl) pentandinitrile, 2-chloro-N- (2,3-dmydro-l, l, 3-trimemyl-lH-mden-4-yl) -3-pyrid

2-CUor-N- (2,6-dime ylphenyl) -N- (isothiocyanatomethyl) acetamide,

2-phenylphenol (OPP),

3,4-dichloro-l- [4- (fluoromethoxy) phenyl] -IH-pyrrole-2,5-dione,

3,5-DicUor-N- [cyan [(l-yl-2-propynyl) -oxy] -methyl] -berιzamid, 3- (l, 1-dimethylpropyl-1-oxo-lH-indene-2-carbonitrile .

3- [2- (4-C orphenyl) -5-ethoxy-3-isoxazoH (hnyl] pyridine,

4-CMor-2-cyan-N, N-dimethyl-5- (4-methylphenyl) - 1H-imidazole-1 -sulfonamide,

4-Memyl-tetrazolo [l, 5-a] quinazolin-5 (4H) -one,

8- (1,1-dimemylethyl) -N-ethyl-N-propyl-1,4-dioxaspiro [4.5] decane-2-memanamine, 8-hydroxyquinoline sulfate,

9H-xan-1-9-carboxylic acid 2 - [(henylarnino) carbonyl] hydrazide, bis- (l-methylyl) -3-memyl-4 - [(3-memylbenzoyl) -oxy] -2,5-t ophendicar ^ eis- 1 - (4-chlorophenyl) -2- (lH- 1, 2,4-triazol-1-yl) -cycloheptanol, cis-4- [3- [4- (l, l-dimemylpropyl) - phenyl-2- ^ hydrochloride,

Ethyl - [(4-chlorophenyl) azo] cyanoacetate,

KaHumhydrogencarbonat,

Methantetrathiol sodium salt,

Methyl-l- (2,3-dmydro-2,2-dimemyl-lH-mden-l-yl) -lH-inή methyl-N- (2,6-dimemylphenyl) -N- (5-isoxazolylcarbonyl) -DI _^ alaninate,

Methyl N- (cMoracetyl) -N- (2,6-dimemylphenyl) -DI _^ alaninate,

N- (2,3-DicMor-4-hydroxyphenyl) -l-memyl-cyclohexanecarboxamide.

N- (2,6-Dimemylphenyl) -2-memoxy-N- (tettahydro-2-oxo-3-fOTanyl) -acetam

N- (2,6-dimethylphenyl) -2-methoxy-N- (tettahydro-2-oxo-3-1hienyl) acetam ^ N- (2-CMor-4-rhttophenyl) -4-me yl-3-nitto benzenesulfonamide,

N- (4-Cyclohexyl-phenyl) -l, 4,5,6-tettahydro-2-pyrimidin (Hnanιm N- (4-Hexylphenyl) -l, 4,5,6-tettahydro-2-pyrirm ^* dinamine, N- (5-C or-2-memylρhenyl) -2-me oxy-N- (2-oxo-3 -oxazoHά ^ yl) -acetamide, N- (6-methoxy) -3-pyridmyl) -cycloprop.mcarboxamide, N- [2,2,2-trichloro-1 - [(cMoracetyl) -amino] -ethyl] -benzamide , N- [3-CMor-4,5-bis (2-ρrop yloxy) -ρhenyl] -N'-m

N-forrnyl-N-hydroxy-DL-alanine sodium salt,

O, O-Diethyl- [2- (mpropylammo) -2-oxoemyl] ethylphosphoramidol oat _^ O-methyl-S-phenyl-phenylpropylphosphoramidothioat, S-methyl-1, 2,3-benzotMadiazol-7-carbothioate, spiropITJ-l -Berizopyran ^ _j l S '^ - isabeiizofuranj-S'-on,

4- [3,4-dimethoxyphenyl) -3- (4-fluorophenyl) acryloyl] morpholine

bactericides:

Bronopol, dichlorophene, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin,

Octhilinone, furan carboxylic acid, oxytetracycline, probenazole, streptomycin, tecloftalam, copper sulfate and other copper preparations.

Insecticides / acaricides / nematicides:

Abamectin, Acephate, Acetamiprid, Acrinathrin, Alanycarb, Aldicarb, Aldoxycarb, Alpha-cypermethrin, Alphamethrin, Amitraz, Avermectin, AZ 60541, AzadHachtin, Azamethiphos, Azinphos A, Azinphos M, Azocyclotin,

Bacillus popilliae, Bacillus sphaericus, Bacillus subtiHs, Bacillus thuringiensis,

Baculoviruses, Beauveria bassiana, Beauveria tenella, bendiocarb, Berifuracarb, bensultap, benzoximate, betacyfluthrin, bifenazate, bifenthrin, Bioemanomethrin, Biopermethrin, bistrifluron, BPMC, bromophos A, Bufencarb, buprofezin, Butathiofos, Butocarboxim, Butylpyridaben ^' Cadusafos, Carbaryl, Carbofuran, Carbophenothion, Carbosulfan, Cartap, Chloethocarb, Chlorethoxyfos, Chlorfenapyr, Chlorfenvinphos, Chlorfluazuron, Chlormephos, Chlorpyrifos, Chlorpyrifos M, C ovaporthrin, Chromafenozide, Cis- Resmethrhrin, Clofethethrin, Clofethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispenthrhrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clofethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clispethethrin, Clofethethrin, Clispethethrin, Clispethethrin, Clispytethin Cycloprene, cycloprothrin, cyfluthrin, cyhalothrin, cyhexatin,

Cypermethrin, cyromazine,

Deltamethrin, Demeton M, Demeton S, Demeton-S-methyl, Diafenthiuron, Diazinon, Dichlorvos, Dicofol, Diflubenzuron, Dimethoat, Dimethylvinphos, Diofenolan, Disulfoton, Docusat-sodium, Dofenapyn,

Eflusilanate, Emamectin, Empenthrin, Endosulfan, Entomopfthora spp., Esfenvalerate, Ethiofencarb, Ethion, Ethoprophos, Etofenprox, Etoxazole, Etrimfos,

Fenamiphos, fenazaquin, fenbutatin oxide, fenitrothion, fenothiocarb, fenoxacrim,

Fenoxycarb, fenpropathrin, fenpyrad, fenpyrithrin, fenpyroximate, fenvalerate, fipronil, fluazinam, fluazuron, flubrocythrinate, flucycloxuron, flucythrinate, flufenoxuron, flumethrin, flutenzine, fluvalinate, fonophan, furosfiazol, fosarbiazil, fosti methofiazole

granulosis

Halofenozide, HCH, Heptenophos, Hexaflumuron, Hexythiazox, Hydroprene,

Imidacloprid, indoxacarb, isazofos, isofenphos, isoxathion, ivermectin,

nucleopolyhedroviruses

Lambda cyhalothrin, lufenuron Malathion, Mecarbam, Metaldehyde, Methamidophos, Metharhician anisopliae, Metharhician flavoviride, Methidathione, Methiocarb, Methoprene, Methomyl, Methoxyfenozide, Metolcarb, Metoxadiazone, Mevinphos, Milbemectin, Milbemycin, Monocrotophos,

Naled, itenpyram, nithiazine, novaluron

Omethoate, oxamyl, oxydemethone M

Paecilomyces fumosoroseus, Parathion A, Parathion M, Permethrin, Phenthoat,

Phorat, Phosalone, Phosmet, Phosphamidon, Phoxim, Pirimicarb, Pirimiphos A, Pirimiphos M, Profenofos, Promecarb, Propargite, Propoxur, Prothiofos, Prothoat, Pymetrozine, Pyraclofos, Pyresmethrin, Pyrethrum, Pyridroxy, Pyridfenip, Pyridifen, Pyridfenipion

quinalphos,

Pdbavirin

Salithion, Sebufos, Silafluofen, Spinosad, Spirodiclofen, Sulfotep, Sulprofos,

Tau fluvaHnate, tebufenozide, tebufenpyrad, Tebupirimiphos, teflubenzuron, tefluthrin, temephos, Temivinphos, terbufos, TettacMorvinphos, tetradifon theta cypermethrrn, oxalate hydrogen thiacloprid, thiamethoxam, Thiapronil, Thiatriphos thiocyclam, thiodicarb, thiofanox, thuringiensin, Tralocythrin, tralomethrin,

Triärathen, Triazamate, Triazophos, Triazuron, Tric ophenidine, Trichlorfon, Triflumuron, Trimethacarb,

Vamidothion, Vaniliprole, Verticillium lecanii

YI 5302 Zeta-cypermethrin, zolaprofos

(lR-cis) - [5- (Thenylmethyl) -3-fLirmyl] methyl-3 - [(dmydro-2-oxo-3 (2H) -fm methyl] -2,2-dimethylcyclopropane carboxylate

(3-phenoxyphenyl) methyl-2,2,3,3-tetramethylcyclopropanecarboxylat

1 - [(2-Chloro-5-thiazolyl) methyl] tetrahydro-3,5-dimethyl-N-nitro-1,3,5-triazine-2 (1H) - imine

2- (2-chloro-6-fluorophenyl) -4- [4- (l, l-dimemylethyl) phenyl] -4,5-dihydro-oxazol

2- (Acetlyoxy) -3-dodecyl-l, 4-naphthaHndion

2-Chloro-N - [[[4- (l-phenylethoxy) phenyl] amino] carbonyl] benzamide 2-chloro-N - [[[4- (2,2-ώcMor-l, l-difluoremoxy ) phenyl] -ammo] carbonyl] benzamide

3-methylphenyl propylcarbamate

4- [4- (4-ethoxyphenyl) -4-methylpentyl] -l-fluoro-2-phenoxy-benzene

4-chloro-2- (l, 1-dimethylethyl) -5 - [[2- (2,6-mmethyl-4-phenoxyphenoxy) e yl] tM

3 (2H) pyridazinone 4-cmor-2- (2-chloro-2-methylρropyl) -5 - [(6-iodo-3-pyridinyl) methoxy] -3 (2H) pyridazinone

4-Chloro-5 - [(6-c or-3-pyridinyl) me1hoxy] -2- (3,4-dicWorphenyl) -3 (2H) -pyridazinone

Bacillus thuringiensis strain EG-2348

Benzoic acid [2-benzoyl-1 - (1,1-dimethylethyl) hydrazide butanoic acid 2,2-dimethyl-3- (2,4-dichlorophenyl) -2-oxo-l-oxaspir ^' o [4.5] dec-3- en-4-yl ester

[3 - [(6-CMOR-3-pyridmyl) meτhyl] -2-tMazoHdmyHden] -cyananή

Dihydro-2- (nitromethylene) -2H- 1,3 -thiazine-3 (4H) -carboxaldehyde

Emyl- [2 - [[l, 6-d ydro-6-oxo-l- (ρhenylmethyl) -4-pyridazmyl] oxy] emyl] -caΛ N- (3,4,4-trifluoro-l-oxo-3 -butenyl) glycine N- (4-CMoφhenyl) -3- [4- (αHfluormethoxy) phenyl] -4,5-dihydro-4-ρhenyl-lH-ρyrazol-

1-carboxamide

N - [(2-C or-5-tMazolyl) memyl] -N'-memyl-N '' - nitto-guanidine

N-methyl-N '- (1-methyl-2-propenyl) - 1, 2-hydrazinedicarbothioamide

N-Memyl-N'-2-propenyl-l, 2-hydrazmdicarbotrήoamid

O, O-Diemyl- [2- (mpropylammo) -2-oxoemyl] -ethylρhosphoramidothio

N-Cyanomemyl-4-trifluoromethyl-m ^ otinamid

3,5-DicMor-l- (3,3-dicrύor-2-propenyloxy) -4- [3- (5-trifluoromethylpyridin-2-yloxy) propoxyj-benzene

A mixture with other known active ingredients, such as herbicides or with fertilizers and growth regulators, is also possible.

When used as insecticides, the active compounds according to the invention can furthermore be present in their commercially available formulations and in the use forms prepared from these formulations in a mixture with synergists. Synergists are compounds that increase the effectiveness of the active ingredients without the added synergist itself being active.

The active substance content of the use forms prepared from the commercially available formulations can vary within wide ranges. The active substance concentration of the use forms can be from 0.0000001 to 95% by weight of active substance, preferably between 0.0001 and 1% by weight.

The application takes place in a customary manner adapted to the application forms

Wise.

When used against hygiene pests and pests of stored products, the active substance is distinguished by an excellent residual action on wood and clay and by a good stability to alkali on limed substrates. As already mentioned above, according to the invention, all plants and their parts can be treated. In a preferred embodiment, wild plant species or plant species and their parts obtained by conventional biological breeding methods, such as crossing or protoplast fusion, are treated. In a further preferred embodiment, transgenic plants and plant cultivars which have been obtained by genetic engineering methods, if appropriate in combination with conventional methods (genetic modified organisms) and their parts are treated. The term "parts" or "parts of plants" or "plant parts" was explained above.

Plants of the plant varieties which are in each case commercially available or in use are particularly preferably treated according to the invention. Plant cultivars are understood to mean plants with new properties (“traits”) which have been grown both by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, bio and genotypes.

Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, growing season, nutrition), the treatment according to the invention can also cause superadditive ("synergistic") effects. For example, reduced application rates and / or extensions of the

Spectrum of activity and / or an intensification of the action of the substances and agents which can be used according to the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, acceleration of ripening, higher crop yields , higher quality and / or higher

Nutritional value of the harvested products, higher shelf life and / or workability of the harvested products possible, which go beyond the expected effects.

The preferred transgenic (genetically engineered) plants or plant cultivars to be treated according to the invention include all plants which are Technological modification received genetic material, which gives these plants special advantageous valuable properties ("traits"). Examples of such properties are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated ripening, higher harvest yields, higher quality and / or higher nutritional value the harvest products, higher shelf life and / or workability of the harvest products. Further and particularly highlighted examples of such properties are an increased defense of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and or

Viruses and an increased tolerance of the plants to certain herbicidal agents. Examples of transgenic plants are the important cult plants, such as cereals (wheat, rice), corn, soybeans, potatoes, cotton, rapeseed and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with corn, soybeans, potatoes and cotton and rapeseed are highlighted. The traits are particularly emphasized as the increased defense of the plants against insects by toxins arising in the plants, in particular those which are caused by the genetic material from Bacillus thuringiensis (for example by the genes CryΙA (a), CryIA (b), CryΙA (c), CrylTA, CryHIA, CryIJIB2, Cry9c Cry2Ab, Cry3Bb and CrylF and their combinations) in the

Plants are produced (hereinafter "Bt plants"). The properties ("traits") also emphasize the increased defense of plants against fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins. The properties (“traits”) which are particularly emphasized are the increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (for example ^M PAT “gene). The desired properties (“ traits ”) in each case. Genes conferring genes can also be found in combinations with one another in the transgenic plants, examples of "Bt plants" being maize varieties, cotton varieties, soy varieties and potato varieties which are among the Commercial names YTELD GARD® (e.g. corn, cotton, soy), KnockOut® (e.g. corn), StarLink® (e.g. corn), Bollgard® (cotton), Nucotn® (cotton) and NewLeaf® (potato) are sold. Examples of herbicide-tolerant plants are corn varieties, cotton varieties and soy varieties which are sold under the trade names Roundup Ready® (tolerance to glyphosate, for example corn,

Cotton, soy), Liberty Link® (tolerance to phosphinotricin, e.g. rapeseed), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulfonylureas e.g. maize). The herbicide-resistant plants (conventionally bred to herbicide tolerance) include the varieties sold under the name Clearfield® (e.g. maize). Of course, these apply

Statements also for plant varieties developed in the future or coming onto the market in the future with these or future-developed genetic properties ("traits").

The plants listed can be particularly advantageous according to the invention with the

Compounds of the general formula I or the active compound mixtures according to the invention are treated. The preferred ranges given above for the active substances or mixtures also apply to the treatment of these plants. Plant treatment with the compounds or mixtures specifically listed in the present text should be particularly emphasized.

The active compounds according to the invention act not only against pests from plants, hygiene and stored products, but also in the veterinary medicine sector against animal parasites (ectoparasites) such as tick ticks, leather ticks, mites, running mites, flies (stinging and licking), parasitic fly larvae, lice,

Hair lice, featherlings and fleas. These parasites include:

From the order of the Anoplurida, for example Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp .. From the order of the Mallophagida and the subordinates Amblycerina and Ischnocerina, for example Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp .. From the Order Diptera and the subordinates Nematocerina and Brachycerina eg Aedes spp., Anopheles spp., Culex spp., Simulium spp.,

Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Täbanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp ., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp., Sarcophaga spp., Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus spp ..

From the order of the Siphonapterida e.g. Pulex spp., CtenocephaHdes spp., Xenopsylla spp., Ceratophyllus spp ..

From the order of the Heteropterida e.g. Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp ..

From the order of the Blattarida e.g. Blatta orientalis, Periplaneta americana, Blattela germanica, Supella spp ..

From the subclass of Acaria (Acarida) and the orders of the Meta and Mesostigmata e.g. Argas spp., Ornithodorus spp., Otobius spp., Ixodes spp., Amblyomma spp., Boophilus spp., Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp., Dermanyssus spp., Raillietia spp.,

Pneumonyssus spp., Sternostoma spp., Varroa spp ..

From the order of the Actinedida (Prostigmata) and Acaridida (Astigmata) e.g.

Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., HypodteroHpp., ., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp ..

The active compounds of the formula (I) according to the invention are also suitable for controlling arthropods which are used in agricultural animals, e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffalo, rabbits, chickens, turkeys, ducks, geese,

Bees, other pets such as Dogs, cats, house birds, aquarium fish and so-called experimental animals, such as Infest hamsters, guinea pigs, rats and mice. By fighting these arthropods, deaths and reduced performance (in meat, milk, wool, skins, eggs, honey, etc.) are to be reduced, so that the use of the active compounds according to the invention enables more economical and simple animal husbandry.

The active compounds according to the invention are used in the neterinary sector in a known manner by enteral administration in the form of, for example, tablets, capsules, drinkers, drenches, granules, pastes, boluses, the feed-through method, suppositories, by parenteral administration, for example by Injections (intramuscular, subcutaneous, intravenous, intraperitonal, etc.), implants, by nasal application, by dermal application in the form of, for example, diving or bathing (dipping), spraying (spray), pouring on (pour-on and spot-on), washing , powdering and with the help of active ingredient-containing moldings, such as

Collars, ear tags, tail tags, G-hedraen straps, holsters, marking devices, etc.

When used for cattle, poultry, pets, etc., the active ingredients of the formula (!) Can be used as formulations (for example powders, emulsions, flowables)

Agents), which contain the active ingredients in an amount of 1 to 80% by weight, directly or after 100 to 10,000-fold dilution or use them as a chemical bath.

It was also found that the compounds of the invention have a high

Show insecticidal activity against insects that destroy technical materials. The following insects may be mentioned by way of example and preferably, but without limitation:

Beetle like

Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinus pecticomis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus Hnescis, speculum, Lyctus Hnescis, speculum Tryptodendron spec. Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec. Dinoderus minutus. Skin wing like

Sirex juvencus, Urocerus gigas, Urocerus gigas taignus, Urocerus augur. Termites such as Kalotermes flavicolHs, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, ReticuHtermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis, Coptotermes formosanus. Bristle tails such as Lepisma saccharina.

In the present context, technical materials include non-living ones

Understand materials, such as preferably plastics, adhesives, glues, papers and cartons, leather, wood, wood processing products and paints.

The material to be protected from insect infestation is very particularly preferably wood and wood processing products.

Wood and wood processing products that can be protected by the agent according to the invention or mixtures containing it are to be understood as examples: Lumber, wooden beams, railway sleepers, bridge parts, jetties, wooden vehicles, boxes, pallets, containers, telephone poles, wooden cladding, wooden windows and doors, plywood, chipboard, carpentry or wooden products that are generally used in house construction or joinery.

The active compounds can be used as such, in the form of concentrates or generally customary formulations, such as powders, granules, solutions, suspensions, emulsions or pastes.

The formulations mentioned can be prepared in a manner known per se, e.g. by mixing the active ingredients with at least one solvent or diluent, emulsifier, dispersant and / or binder or fixative, water repellant, optionally siccatives and UN stabilizers and optionally dyes and pigments and further processing aids.

The insecticidal compositions or concentrates used to protect wood and wood-based materials contain the active compound according to the invention in a concentration of 0.0001 to 95% by weight, in particular 0.001 to 60% by weight.

The amount of the agents or concentrates used depends on the type and occurrence of the insects and on the medium. The optimum amount of use can be determined in each case by test series. In general, however, it is sufficient to use 0.0001 to 20% by weight, preferably 0.001 to 10% by weight, of the active compound, based on the material to be protected.

An organic chemical solvent or solvent mixture and / or an oily or oily or low-volatile organic chemical solvent or solvent mixture and / or a polar organic chemical solvent or solvent mixture and / or water and optionally an emulsifier and / or wetting agents. The organic chemical solvents used are preferably oily or oily solvents with an evaporation number above 35 and a flash point above 30 ° C., preferably above 45 ° C. Corresponding mineral oils or their aromatic fractions or mineral oil-containing solvent mixtures, preferably white spirit, petroleum and / or alkylbenzene, are used as such low-volatility, water-insoluble, oil and oil-like solvents.

Mineral oils with a boiling range of 170 to 220 ° C, white spirit with a boiling range of 170 to 220 ° C, spindle oil with a boiling range of 250 to 350 ° C, petroleum or aromatics with a boiling range of 160 to 280 ° C are advantageous.

Turpentine oil and the like.

In a preferred embodiment, liquid aliphatic hydrocarbons with a boiling range of 180 to 210 ° C or high-boiling mixtures of aromatic and aliphatic hydrocarbons with a boiling range of

180 to 220 ° C and / or locker oil and / or monochloronaphthalene, preferably α-monochloronaphthalene used.

The organic low-volatility oily or oily solvents with an evaporation number above 35 and a flash point above 30 ° C, preferably above 45 ° C, can be partially replaced by slightly or medium-volatile organic chemical solvents, with the proviso that the solvent mixture also has an evaporation number above 35 and has a flash point above 30 ° C, preferably above 45 ° C, and that the insecticide-fungicide mixture is soluble or emulsifiable in this solvent mixture.

According to a preferred embodiment, part of the organic chemical solvent or solvent mixture or an aliphatic polar organic chemical solvent or solvent mixture is replaced. Aliphatic hydroxyl and / or ester and / or ether groups are preferably used organic chemical solvents such as glycol ether, ester or the like for use.

In the context of the present invention, the known organic-chemical binders are synthetic resins which are known per se and which are water-thinnable and / or soluble or dispersible or emulsifiable in the organic-chemical solvents used and / or binding drying oils, in particular binders consisting of or containing Acrylate resin, a vinyl resin, e.g. Polyvinyl acetate, polyester resin, polycondensation or polyaddition resin, polyurethane resin, alkyd resin or modified alkyd resin, phenolic resin, hydrocarbon resin such as

Coumarone resin, silicone resin, drying vegetable and or drying oils and / or physically drying binders based on a natural and / or synthetic resin are used.

The synthetic resin used as a binder can be used in the form of an emulsion, dispersion or solution. Bitumen or bituminous substances up to 10% by weight can also be used as binders. In addition, known dyes, pigments, water-repellants, odor correctors and inhibitors or anticorrosive agents and the like can be used.

According to the invention, at least one alkyd resin or modified alkyd resin and / or a drying vegetable oil is preferably contained in the agent or in the concentrate as the organic chemical binder. Alkyd resins with an oil content of more than 45% by weight, preferably 50 to 68% by weight, are preferably used according to the invention.

All or part of the binder mentioned can be replaced by a fixative (mixture) or a plasticizer (mixed). These additives are intended to prevent volatilization of the active ingredients and crystallization or precipitation. They preferably replace 0.01 to 30% of the binder (based on

100% of the binder used). The plasticizers come from the chemical classes of phthalic acid esters such as dibutyl, dioctyl or benzyl butyl phthalate, phosphoric acid esters such as tributyl phosphate, adipic acid esters such as di- (2-ethylhexyl) adipate, stearates such as butyl stearate or amyl stearate, oleates such as butyl oleate, higher glycerol glycerol or glycerol - Kolether, glycerol ester and p-toluenesulfonic acid ester.

Fixing agents are chemically based on polyvinyl alkyl ethers such as e.g. Polyvinyl methyl ether or ketones such as benzophenone, ethylene benzophenone.

Water is also particularly suitable as a solvent or diluent, optionally in a mixture with one or more of the above-mentioned organic chemical solvents or diluents, emulsifiers and dispersants.

Particularly effective wood protection is achieved through large-scale impregnation processes, e.g. Vacuum, double vacuum or pressure process.

The ready-to-use compositions may optionally contain further insecticides and, if appropriate, one or more fungicides.

The insecticides and fungicides mentioned in WO 94/29268 are preferably suitable as additional admixing partners. The compounds mentioned in this document are an integral part of the present application.

Insecticides, such as chlorpyriphos, phoxime, silafluofin, alphamethrin, cyfluthrin, cypermethrin, deltamethrin, permethrin, imidacloprid, NI-25, flufenoxuron, hexaflumuron, transfluthrin, trifluoridophenidone, as well as methoxyphenophenidone, as well as fungloxidonoprid, as well as fungloxidononoprid, as well as fungloxidonoprid, as well as thifuridifuronoprid, such as Epoxyconazole, Hexaconazole, Azaconazole, Propiconazole, Tebuconazole, Cyproconazole, Metconazole, ImazaHl, Dichlorfluanid, Tolylfluanid, 3-iodo-2-propynyl butyl carbamate, N-octyl-isothiazoHn-3-one and 4,5-dichloro-N-octyl isothiazoHn-3-one.

At the same time, the compounds according to the invention can be used to protect objects, in particular hulls, sieves, nets, structures,

Quays and signaling systems that come into contact with sea or brackish water are used.

Overgrowth by sessile oligochaetes, such as lime tube worms, and by mussels and species of the group Ledamorpha (barnacles), such as various Lepas and

ScalpeUum species, or by species from the group Balanomorpha (barnacles), such as Baianus or pollicipes species, increases the frictional resistance of ships and consequently leads to a significant increase in operating costs due to increased energy consumption and, in addition, frequent dry dock stays.

In addition to the growth by algae, for example Ectocarpus sp. and Ceramium sp., vegetation by sessile Entomostraken groups, which are grouped under the name Cirripedia (tendril crayfish), is particularly important.

It has now surprisingly been found that the compounds according to the invention, alone or in combination with other active ingredients, have an excellent antifouling effect.

By using compounds according to the invention alone or in combination with other active ingredients, heavy metals such as bis (trialkyltin) sulfides, tri-w-butyltin laurate, tri - butyltin chloride, copper (I) oxide, triethyltin chloride can be used , Tri-n-butyl (2-phenyl-4-chlorophenoxy) tin, tributyltin oxide, molybdenum disulfide, antimony oxide, polymeric butyl titanate, phenylispyridine) - bismuth chloride, tri - «- butyltin fluoride, manganese ethylene bisbiocarbamate, zinc di-methyldithamido carbamate, zinc di-methyldithamocarbamate and copper salts of 2- Pyridinthiol-1-oxide, bisdimethyldit ocarbamoylzmkethylenbisthiocarbamat, zinc oxide, copper (I) ethylene bisdithiocarbamate, copper thiocyanate, copper phthalate and tributyltin halides are omitted or the concentration of these compounds can be significantly reduced.

The ready-to-use antifouling paints may also contain other active ingredients, preferably algicides, fungicides, herbicides, molluscicides or other antifouling active ingredients.

Suitable combination partners for the antifouling agents according to the invention are preferably:

Algicides like

2-tert-butylanHno-4-cyclopropylannho-6-methyltMo-l, 3,5-triazine, dichlorophene,

Diuron, ehdothal, fentin acetate, isoproturon, methabenzthiazuron, oxyfluorfen, qumoclamine and terbutryn;

Fungicides like

Benzo [b] 1Mophencarbonsäurecyclohexylamid-S, S-Dioxid, dichlofluanid, fluorofolpet, 3-iodo-2-propynyl butyl carbamate, tolylfluanid and azoles such as

Azaconazole, cyproconazole, epoxyconazole, hexaconazole, metconazole, propiconazole and tebuconazole;

Molluscicides like

Fentin acetate, metaldehyde, methiocarb, niclosamide, thiodicarb and trimethacarb; or conventional antifouling agents such as

4,5-dicrdor-2-octyl-4-isothiazolin-3-one, diiodomethylparatrylsulfone, 2- (N, N-di- me1hyl1lιiocarbamoyltbio) -5-nitrothiazyl, potassium, copper, sodium and zinc salts of 2-pyridinthiol-l-oxide, pyridine triphenylborane, tetrabutyldistannoxane, 2,3,5,6-tetrachloro-4- (methylsulfonyl) pyridine, 2,4,5,6-tetrachloroisophthalonitrile, tetramethylthiuram disulfide and 2,4,6-trichlorophenylmaleimide.

The antifouling agents used contain the active compound according to the invention of the compounds according to the invention in a concentration of 0.001 to 50% by weight, in particular of 0.01 to 20% by weight.

The antifouling agents according to the invention furthermore contain the usual ones

Components such as in Ungerer, Chem. Ind. 1985, 37, 730-732 and Williams, Antifouling Marine Coatings, Noyes, ParkRidge, 1973.

Antifouling paints contain, in addition to the algicidal, fungicidal, molluscicidal and insecticidal active compounds according to the invention, in particular binders.

Examples of recognized binders are polyvinyl chloride in a solvent system, chlorinated rubber in a solvent system, acrylic resins in a solvent system, especially in an aqueous system, vinyl chloride / vinyl acetate copolymer systems in the form of aqueous dispersions or in the form of organic solvent systems, butadiene / styrene acrylonitrile rubbers , drying oils, such as linseed oil, resin esters or modified hard resins in combination with tar or bitumen, asphalt and epoxy compounds, small amounts of chlorinated rubber, chlorinated polypropylene and ninyl resins.

Paints may also contain inorganic pigments, organic pigments or dyes, which are preferably insoluble in seawater. Paints may also contain materials, such as rosin, to enable controlled release of the active ingredients. The paints can also contain plasticizers, modifiers that influence the theological properties and other conventional components. Also in self-poshing antifouling Systems, the Nerbindungen invention or the above-mentioned mixtures can be incorporated.

The active ingredients are also suitable for controlling animal pests, in particular insects, arachnids and mites, which live in closed spaces such as, for example, apartments, factories, offices, vehicle cabins, etc. occurrence. To combat these pests, they can be used alone or in combination with other active ingredients and auxiliaries in household insecticide products. They are effective against sensitive and resistant species and against all stages of development. These pests include:

From the order of the Scorpionidea e.g. Buthus occitanus.

From the order of the Acarina e.g. Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat,

Rhipicephalus sangurneus, Trombicula alfreddugesi, Νeutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae.

From the order of the Araneae e.g. Aviculariidae, Araneidae.

From the order of the Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.

From the order of the Isopoda e.g. Oniscus asellus, Porcellio scäber.

From the order of the Diplopodaz.B. Blaniulus guttulatus, Polydesmus spp ..

From the order of the Chilopoda e.g. Geophilus spp ..

From the order of the Zygentoma e.g. Ctenolepisma spp., Lepisma. saccharina,

Lepismodes inquilinus. From the order of the Blattaria e.g. Blatta orientalies, Blattella germanica, Blattella asahinai, Leucophaea maderae, Panchlora spp., Parcoblatta spp., Periplaneta austtalasiae, Periplaneta americana, Periplaneta brunnea, Periplaneta fuliginosa, Supella longipalpa.

From the order of the Saltatoria e.g. Acheta domesticus.

From the order of the Dermaptera e.g. Forficula auricularia.

From the order of the Isoptera e.g. Kalotermes spp., Reticulitermes spp.

From the order of the Psocoptera e.g. Lepinatus spp., Liposcelis spp.

From the order of the Coleptera e.g. Anthrenus spp., Attagenus spp., Dermestes spp.,

Latheticus oryzae, Necrobia spp., Ptinus spp., Rhizopertha dominica, Sitophilus granarius, Sitophilus oryzae, Sitophilus zeamais, Stegobium paniceum.

From the order of the Diptera e.g. Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., CalHphora erythrocephala, Chrysozona pluvialis,

Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaga carnaria, Simulium spp., Stomoxys calcitrans, Tipula paludosa.

From the order of the Lepidoptera e.g. Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tineapellionella, Tineola bisselliella.

From the order of the Siphonaptera, for example Ctenocephahdes canis, Ctenocephahdes feHs, Pulex irritans, Tunga penetrans, Xenopsylla cheopis. From the order of the Hymenoptera, for example Camponotus herculeanus, Lasius fuliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitum.

From the order of the anoplura e.g. Pediculus humanus capitis, Pediculus humanus corporis, Phthirus pubis.

From the order of the Heteroptera e.g. Cimex hemipterus, Cimex lectularius, Rhodinus prolixus, Triatoma infestans.

The application in the field of household insecticides is carried out alone or in combination with other suitable active compounds such as phosphoric acid esters, carbamates, pyrethroids, growth regulators or active compounds from other known classes of insecticides.

They are used in aerosols, non-pressurized sprays, e.g. Pump and atomizer sprays, fog machines, foggers, foams, gels, vaporizer products with ner vaporizer platelets made of cellulose or plastic, liquid vaporizers, gel and membrane vaporizers, propeller-driven vaporizers, energy-free or passive evaporation systems, moth papers, moth bags and

Moth angels, as granules or dusts, in lures or bait stations.

The preparation and use of the active compounds according to the invention can be seen from the examples below. Herstelliingsbeispiele

Example (I-a-1)

Procedure A:

A solution of 53.3 g (0.16 mol) of the compound according to Preparation Example (Tf-1) (99%, cis / trans 97: 3) in 160 ml of dimethylformamide (DMF) becomes a solution of 30% at room temperature methanolic NaOMe solution (72 g, 0.4 mol) in 240 ml of DMF (with the methanol being completely distilled off beforehand).

The reaction mixture is heated to 60 ° C. and stirred at 60 ° C. for 4 h.

The methanol formed in the reaction is distilled off in a weak vacuum. A mixture of 32% hydrochloric acid (96 ml) and 960 ml of water is then added dropwise at 50-60 ° C. The solution is stirred for 1 h at room temperature, the solid is filtered off with suction, washed twice with 200 ml of water and dried.

Yield: 44.16 g (91.6% of theory), mp 224-228 ° C Example (Ia-2

Procedure E:

1.75 g of the compound according to Example (I-c-2) are placed in 5 ml of ethanol and 0.5 g of NaOH in 4 ml of water are added dropwise at room temperature. The mixture is stirred at 40-50 ° C. and the reaction is followed by thin layer chromatography.

At the end of the reaction, the ethanol is distilled off and the residue is dissolved in water

10 ml volume filled. The mixture is acidified at 0-10 ° C. with concentrated hydrochloric acid, the precipitate is filtered off with suction and dried.

Yield: 1.35 g (92% of theory), mp. 274 ° C.

In analogy to example (I-a-2), method E gives example (1-a-1) with a melting point of 226 ° C.

Example I-c-1)

Procedure C

3.02 g (10 mmol) of the compound according to Example (I-a-1) and 1.21 g (12 mmol) of triemylamine are placed in 20 ml of chlorobenzene. A solution of 1.14 g (10.5 mmol) of ethyl chloroformate in 8 ml of chlorobenzene is then added dropwise at 60-65 ° C. The mixture is stirred at 60-65 ° C. for 4 h. At room temperature, the reaction solution is diluted with 20 ml of chlorobenzene, shaken with 20 ml of water, 20 ml of 5% sodium hydroxide solution and finally with 10 ml of saturated aqueous NaCl solution, the organic phase is dried and the solvent is distilled off. 3.88 g of crude product are obtained. 1.523 g of this was recrystallized from 15 ml of methylcyclohexane. 1.437 g of product were obtained, which gives a total yield of 3.72 g for the total amount of I-c-1. Based on a purity of 99.6%, the yield is 3.68 g (4 98.6% of theory), mp. 142-143 ° C.

Example fll-l)

107 g (0.43 mol) of cis-4-methoxy-cyclohexane-l-aπιmo-carboxylic acid methyl ester hydrochloride (WO 02/02532, Ex. 15) and 221 g (1.6 mol) of potassium carbonate are in

370 ml of acetone iril submitted.

A solution of 75.1 g (0.4 mol) of 2,5-dimethylphenylacetic acid chloride in 140 ml of acetonitrile is added at 5-10 ° C. The mixture is then stirred for 3 hours at room temperature. The reaction mixture is then added to 2 l of ice water. The mixture is stirred for about 1 h and the precipitate is filtered off, which is washed 3 times with 150 ml of water each time and then dried.

Yield: 131 g (98.2% of theory), mp. 101-102 ° C

Example (I-c-2)

Procedure D

24.68 g of the compound according to Example (Ila-28) (WO 98/05638) in 560 ml of anhydrous dichloromethane are mixed with 9.4 ml (67 mmol) of triethylamine and at 0-10 ° C 6.7 ml ( 67 mmol) ethyl chloroformate in 56 ml of anhydrous CH ₂ Cl2 were added dropwise.

The mixture is stirred at room temperature under thin-layer chromatography.

After the end of the reaction, the solvent is distilled off and washed twice with 500 ml of 0.5 N NaOH solution. The organic phase is dried

The solvent is distilled off and the residue is purified by column chromatography (silica gel, DicMormethan 3: 1 ethyl acetate)

Yield: 9.82 g (33% of theory), mp. 159 ° C. The cis isomer (Ic-2) (9.82 g) obtained by process D is again purified by column chromatography on silica gel with dichloromethane / acetone 5: 1.

Yield: 4.24 g (14% of theory), mp. 164 ° C.

Analogously to example (Tc-2), chromatography on silica gel with CH ₂ Cl2 / acetone gives 5: 1 example (Ic-1) with a melting point of 144 ° C.

Example q-c-4)

Procedure D

0.8 g of a cis / trans isomer mixture (approx. 81:18) of the compound according to Example I-1-c-32 from WO98 / 05638 were mixed with silica gel

Chromatographed methylene chloride ethyl acetate, 2: 1 as eluent.

Yield: 0.51 g mp 160 ° C

Purity HPLC (area percent)> 99%. Analogously to Examples (Ic-1) and (Ic-2) and in accordance with the general information on the preparation and isolation, the following compounds of the formula (Ic) are obtained

Ex. Νr X Y A M R2 Mp ° C

Ic-3 Br CH ₃ CH ₃ 0 C5H5-CH2-171

Analogously to Examples (I-c-1) and (I-c-2) and in accordance with the general information on the preparation and isolation, the following compounds of the formula (I-b) are obtained

Bsp.-Νr. X Y A Rl mp ° C

Ib-1 Br CH ₃ CH ₃ 205

Ib-2 Cl CHo C ₂ H ₅ i-> C ₃ H- ₇ 159

Example A

Aphis gossypii test

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted to the desired concentration with water containing emulsifier.

Cotton leaves (Gossypium hhsutum), which are heavily infested with the cotton aphid (Aphis gossypü), are treated by dipping into the active ingredient preparation of the desired concentration.

After the desired time, the failure is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.

In this test, for example, the following compound of the production examples shows superior effectiveness compared to the prior art:

Table A plant-damaging insects

Aphis gossipii test

Drug concentration concentration in ppm in% after 6 ^d

Example I-l-c-4

40 70 known from WO98 / 05638

Example I-c-1

20 90 according to the invention

Example B

Heliothis virescens test

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of the active substance, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired concentration with water containing emulsifier.

Soybean shoots (Glycine max) are treated by dipping into the active ingredient preparation of the desired concentration and are populated with Heliothis virescens caterpillars while the leaves are still moist.

After the desired time, the kill is determined in%. 100% means that all caterpillars have been killed; 0% means that no caterpillars have been killed.

In this test, for example, the following compound of the production examples shows superior effectiveness compared to the prior art:

Table B plant-damaging insect Heliothis virescens test

Drug concentration concentration in ppm in% after 6 ^d

Example I-l-c-22

500 65 known from WO98 / 05638

Example I-c-2

500 100 according to the invention

Example C

Phaedon larvae test

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable active substance preparation, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired concentration with water containing emulsifier.

Cabbage leaves (Brassica oleracea) are treated by dipping into the preparation of the desired concentration and populated with larvae of the horseradish leaf beetle (Phaedon cochleariae) while the leaves are still moist.

After the desired time, the kill is determined in%. 100% means that all beetle larvae have been killed; 0% means that none of the beetle larvae have been killed.

In this test, for example, the following compound of the production examples shows superior effectiveness compared to the prior art:

TabeUe C insect pests

Phaedon larvae test

Drug concentration concentration in ppm in% after 7 ^d

Example I-l-c-4

100 90 10 0 known from WO98 / 05638

Example I-c-1

100 100 20 80 according to the invention

Example D

Plutella test (resistant strain)

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable active substance preparation, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired concentration with water containing emulsifier.

Cabbage leaves (Brassica oleracea) are treated by dipping into the preparation of the desired concentration and populated with caterpillars of the cockroach (Plutella xylostella / resistant stem) while the leaves are still moist.

After the desired time, the kill is determined in%. 100% means that all caterpillars have been killed; 0% means that no caterpillars have been killed.

In this test, for example, the following compound of the production examples shows superior effectiveness compared to the prior art:

Table D insect pests

Plutella test (resistant strain)

Drug concentration concentration in ppm in% after 6 ^d

Example I-l-c-22

75 known from WO98 / 05638

Example I-c-2

100 according to the invention

Example E

Tetranychus test (OP-resistant / immersion treatment)

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted to the desired concentration with water containing emulsifier.

Bean plants (Phaseolus vulgaris), which are heavily infested with all stages of the common spider mite (Tetranychus urticae), are immersed in an active ingredient preparation of the desired concentration.

After the desired time, the effect is determined in%. 100% means that all spider mites have been killed; 0% means that no spider mites have been killed.

In this test, for example, the following compound of the production examples shows superior effectiveness compared to the prior art:

Table E mites harmful to plants

Tetranychus test (OP-resistant / immersion treatment)

Drug concentration concentration in ppm in% after 7 ^d

Example I-l-a-28

1 0 known from WO98 / 05638

Example I-a-2

0.8 80 according to the invention

Example F

Myzus Test

Solvent: 7 parts by weight of dimethylformamide emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier and the concentrate is diluted to the desired concentration with water containing emulsifier.

Cabbage leaves (Brassica oleracea), which are heavily infested with peach aphids (Myzus persicae), are treated by immersing them in the preparation of the desired concentration.

After the desired time, the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.

In this test, e.g. B. The following compounds of the preparation examples have superior activity over the prior art:

Table F insect pests

Myzus Test

Drug concentration concentration in ppm in% after 6 ^d

Example I-l-c-32 10 20 known from WO 98/05638

Example I-c-4 4 50 according to the invention

Example I-l-b-47 100 60 known from WO 98/05638

Example Ib-1 100 80 according to the invention

Example G

Phaedon larvae test

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable active substance preparation, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired amount with water containing emulsifier

Concentration.

Cabbage leaves (Brassica oleracea) are treated by being dipped into the preparation of active compound of the desired concentration and populated with larvae of the horseradish leaf beetle (Phaedon cochleariae) while the leaves are still moist.

After the desired time, the kill is determined in%. 100% means that all beetle larvae have been killed; 0% means that none of the beetle larvae have been killed.

In this test, e.g. B. The following compounds of the preparation examples have superior activity over the prior art:

Table G insect pests

Phaedon larvae test

Drug concentration concentration in ppm in% after 7 ^d

Example I-l-a-4 100 0 known from WO 98/05638

Example I-a-1 100 100 according to the invention

Example I-l-c-32 100 0 known from WO 98/05638

Example Ic-4 100 25 according to the invention

Example H

Spodoptera frugiperda test

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired amount with water containing emulsifier

Concentration.

Cabbage leaves (Brassica oleracea) are treated by dipping into the preparation of the desired concentration and populated with caterpillars of the army worm (Spodoptera frugiperda) while the leaves are still moist.

After the desired time, the kill is determined in%. 100% means that all caterpillars have been killed; 0% means that no caterpillars have been killed.

In this test, e.g. B. The following compounds of the preparation examples have superior activity over the prior art:

Table H plant-damaging insect Spodoptera frugiperda test

Drug concentration concentration in ppm in% after 7 ^d

Example I-l-a-4 100 35 known from WO 98/05638

Example I-a-1 100 50 according to the invention

Example I-l-c-32 100 0 known from WO 98/05638

Example I-c-4 100 20 according to the invention

Example I-l-c-39 1000 80 known from WO 98/05638

Example I-c-3 500 100 according to the invention

Example I-l-b-47 100 0 known from WO 98/05638

Example Ib-1 100 60 according to the invention Example I

Tetranychus test (OP-resistant / spray treatment)

Solvent: 78 parts by weight of acetone, 1.5 parts by weight of dimethylformamide

Emulsifier: 0.5 part by weight of alkylaryl polyglycol ether

To produce a suitable preparation of the substance, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired concentration with water containing emulsifier.

Bean leaf slices (Phaseolus vulgaris), which are affected by all stages of the common spider mite (Tetranychus urticae), are sprayed with an active ingredient preparation of the desired concentration.

After the desired time, the effect is determined in%. 100% means that all spider mites have been killed; 0% means that no spider mites have been killed.

In this test, e.g. B. the following compound of the manufacturing examples superior effectiveness over the prior art: Table l mites harmful to plants

Tetranychus test (OP-resistant / spray treatment)

Drug concentration concentration in pp in% after 4 ^d

Example Ilb-2 100 100 according to the invention

Example J

Tetranychus test (OP-resistant / immersion treatment)

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: 2 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted to the desired amount with water containing emulsifier

Concentration.

Bean plants (Phaseolus vulgaris), which are heavily infested with all stages of the common spider mite (Tetranychus urticae), are immersed in a drug preparation of the desired concentration

After the desired time, the effect is determined in%. 100% means that all spider mites have been killed; 0% means that no spider mites have been killed.

In this test, e.g. B. the following compound of the manufacturing examples superior effectiveness over the prior art:

Table J mites harmful to plants

Tetranychus test (OP-resistant / immersion treatment)

Drug concentration concentration in ppm in% after 7 ^d

Example I-l-c-32 ΪÖ 30 known from WO 98/05638

Example Ic-4 4 40 according to the invention

Example K

Limit concentration test / soil insects - treatment of transgenic plants

Test insect: Diabrotica balteata - larvae in the soil

Solvent: 7 parts by weight of acetone

Emulsifier: 1 part by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.

The active ingredient preparation is poured onto the floor. The plays

Concentration of the active ingredient in the preparation is practically irrelevant, the only decisive factor is the amount of active ingredient per unit volume of soil, which is given in ppm (mg / 1). You fill the bottom in 0.25 1 pots and let them stand at 20 ° C.

Immediately after the preparation, 5 pre-germinated maize kernels of the YIELD GUARD variety (trademark of Monsanto Comp., USA) are placed in each pot. After 2 days, the appropriate test insects are placed in the treated soil. After a further 7 days, the efficiency of the active ingredient is determined by counting the maize plants that have accumulated (1 plant = 20% activity). Example L

Heliothis virescens - test - treatment of transgenic plants

Solvent: 7 parts by weight of acetone

Emulsifier: 1 part by weight of alkylaryl polyglycol ether

To produce a suitable plastic preparation, 1 part by weight of active compound is mixed with the stated amount of solvent and the stated amount of emulsifier, and the concentrate is diluted with water to the desired level

Concentration.

Soybean shoots (Glycine max) of the Roundup Ready variety (trademark of Monsanto Comp. USA) are treated by dipping into the preparation of active compound of the desired concentration and populated with the tobacco bud caterpillar Heliothis virescens while the leaves are still moist.

The killing of the insects is determined after the desired time.

Claims

claims

1. Compounds of formula (T)

in which

X represents alkyl, halogen, alkoxy, haloalkyl or haloalkoxy,

Y represents hydrogen, alkyl, alkoxy, halogen, haloalkyl or haloalkoxy,

where only one of the radicals X or Y may be haloalkyl or haloalkoxy,

A represents C _r C ₆ alkyl,

G for hydrogen (a) or for one of the groups

stands,

where M represents oxygen or sulfur, R ^{1 is} in each case optionally substituted by halogen C ₁ -C ₂ o-alkyl,

C ₂ -C ₂₀ alkenyl, CrCs-alkoxy-Cr-alkyl, Cj-Cs-alkylthio-Cr - alkyl or poly-C Cg-alkoxy-Ci-Cg-alkyl or for optionally by halogen, CrCβ-alkyl or - C ₃ -C ₈ substituted C ₃ -C ₈ cycloalkyl, in which one or two non-directly adjacent methylene groups may be replaced by oxygen and or sulfur,

is alkoxy, C Ce-haloalkyl, Ci-Ce-haloalkoxy, CrC _{ö ö} -C alkylthio or alkylsulfonyl substituted phenyl or thienyl, - optionally substituted by halogen, cyano, nitro, C Ce-alkyl, Ci-C ₆

R ² for each optionally substituted by halogen -CC ₂ o-alkyl, C ₂ -C ₂ o-alkenyl, CrC ₈ -alkoxy-C ₂ -C8-alkyl or poly-C ₁ -C ₈ -alkoxy-C ₂ - Cs-alkyl,

for C ₃ -C ₈ -cycloalkyl optionally substituted by halogen, -Ce-alkyl or CrC ₆ -alkoxy or

for each optionally by halogen, cyano, nitro, -Ce-alkyl,

-C-C ₆ alkoxy, CrCe haloalkyl or CrC _ό haloalkoxy substituted phenyl or benzyl.

2. Compounds of formula (I) according to claim 1, in which

X represents chlorine, bromine, methyl, ethyl, propyl, trifluoromethyl, methoxy, difluoromethoxy or trifluoromethoxy,

Y represents hydrogen, chlorine, bromine, methoxy, methyl, ethyl, propyl, trifluoromethyl or trifluoromethoxy, where only one of the radicals X or Y may represent trifluoromethyl, difluoromethoxy or trifluoromethoxy,

A represents C _r C ₆ alkyl,

G for hydrogen (a) or for one of the groups

(b) or (c) stands

in which

M represents oxygen or sulfur,

R ^{1 is} in each case optionally mono- to trisubstituted by fluorine or chlorine-substituted CrC ^ alkyl, C ₂ -C ₁₆ alkenyl, CrCe alkoxy-Ci-Cö-alkyl,

CrCe-alkylthio-CrC _ö -alkyl or poly-Cι-C ₆ -alkoxy-Cι-C ₆ -alkyl or for optionally monosubstituted or disubstituted by fluorine, chlorine, C ₁ -C5-alkyl or C ₁ -C ₅ -alkoxy C ₃ -C cycloalkyl, in which one or two non-directly adjacent methylene groups are optionally replaced by oxygen and / or sulfur,

for phenyl which is optionally monosubstituted to trisubstituted by fluorine, chlorine, bromine, cyano, nitro, Ci- -alkyl, -C-C ₄ -alkoxy ₅ Cι-C ₃ -haloalkyl, QC ₃ - haloalkoxy, - -alkylthio or Cr -alkylsulfonyl or stands for thienyl,

R ^{2 is} in each case optionally mono- to trisubstituted by fluorine or chlorine-substituted CrC ^ alkyl, C ₂ -Ci6 alkenyl, CC ₆ alkoxy-C ₂ -C ₆ alkyl or poly -CC ₆ alkoxy-C ₂ - C ₆ alkyl, if necessary, C ₃ -C cycloalkyl which is monosubstituted or disubstituted by fluorine, chlorine, CC alkyl or C ₁ -C alkoxy

represents phenyl or benzyl which is optionally mono- to disubstituted by fluorine, chlorine, bromine, cyano, nitro, CrG _t -alkyl, Ci-Qj-alkoxy, CrCr-haloalkyl or CrC haloalkoxy.

3. Compounds of formula (I) according to claim 1, in which

X for chlorine, bromine, methyl, ethyl, methoxy, trifluoromethyl,

Trifluoromethoxy or difluoromethoxy,

Y represents chlorine, bromine, methyl, ethyl, propyl, methoxy, trifluoromethyl or trifluoromethoxy, only one of the radicals X or Y representing trifluoromethyl,

May be trifluoromethoxy or difluoromethoxy,

A represents C _j -C ^ alkyl,

G for hydrogen (a) or for one of the groups

(c) stands

in which

M represents oxygen or sulfur,

R ¹ alkyl in each case optionally mono- to trisubstituted by fluorine or chlorine CRCS alkyl, _C2-C8 alkenyl, C ₁ -C ₂ alkoxy-C ₁ -C _2, C ₁ -C ₂ -Alkylthio -CC-C ₂ -alkyl or C ₃ -C ₆ -cycloalkyl, substituted by fluorine, chlorine, methyl or methoxy, in which case one or two methylene groups are optionally replaced by oxygen and / or sulfur is

represents phenyl which is optionally mono- to disubstituted by fluorine, chlorine, bromine, cyano, nitro, methyl, methoxy, trifluoromethyl or trifluoromethoxy or represents thienyl,

R ² stands for CC ₈ alkyl, C ₂ -C ₈ alkenyl or C ₁ -C ₄ alkoxy-C ₂ -C ₃ alkyl, for C ₅ -C ₆ cycloalkyl,

represents phenyl or benzyl which is in each case simply substituted by fluorine, chlorine, cyano, nitro, methyl, methoxy, trifluoromethyl or trifluoromethoxy.

4. Compounds of formula (I) according to claim 1, in which

X represents chlorine, bromine, methyl or trifluoromethyl,

Y represents chlorine, bromine or methyl,

A represents methyl, ethyl, propyl, butyl or isobutyl,

G for hydrogen (a) or for one of the groups

^stands > in which

M represents oxygen or sulfur, R ¹ for CrC ₆ alkyl, C ₂ -C ₆ alkenyl, C Cz-alkoxy-d-Ca alkyl, Cir alkylthio-CrC ₂ alkyl, each optionally optionally substituted by fluorine, chlorine, methyl or methoxy Cyclopropyl, cyclopentyl or cyclohexyl,

represents phenyl optionally substituted by fluorine, chlorine, bromine, cyano, nitro, methyl, methoxy, trifluoromethyl or trifluoromethoxy, or represents thienyl,

^~ R? represents -Cs-alkyl, C ₂ -C ₆ -alkenyl or -C-C ₃ -alkoxy-C ₂ -C ₃ -alkyl,

for cyclopentyl or cyclohexyl

or represents phenyl or benzyl which is optionally optionally substituted by fluorine, chlorine, cyano, nitro, methyl, methoxy, trifluoromethyl or trifluoromethoxy.

Compounds of formula (I) according to claim 1, in which the substituents have the meanings given in the table.

A process for the preparation of compounds of formula (T) according to claim 1, characterized in that to obtain

(A) compounds of the formula (I-1 -a)

in which

A, X and Y have the meanings given above,

Compounds of formula (TL). in which

A, X and Y have the meanings given above,

and

R ^{8 represents} alkyl,

intramolecularly condensed in the presence of a diluent and in the presence of a base,

(B) Compounds of formula (Ib) shown above, in which A, R ¹ , X and

Y has the meanings given above, compounds of the formula (I-a) shown above, in which A, X and Y have the meanings given above

Have meanings

α) with acid halides of the formula (HI)

Haim

O in what

R ^{1 has} the meaning given above and

Shark stands for halogen or

β) with carboxylic arihydrides of the formula (TV)

R ^ CO-O-CO-R ¹ ON)

in which

R ^{1 has} the meaning given above,

optionally in the presence of a diluent and optionally in the presence of an acid binder;

(C) compounds of the formula (Ic) shown above, in which A, R ² , M, X and Y have the meanings indicated above, compounds of formula (Ia) shown above, in which A, X and Y have the meanings indicated above have each

with chloroformate or chloroformate thioester

Formula (V)

R ² -M-CO-Cl (V)

in which

R and M have the meanings given above,

if appropriate in the presence of a diluent and, if appropriate, in the presence of an acid binder; (D) compounds of the formulas (Ia) to (Ic) cis / trans isomer mixtures of the formulas (Ia ¹ ) to (I-c ') shown above

in which

A, X, Y, M, R ¹ and R ^{2 have} the meaning given above using physical separation processes such as, for example, column chromatography or fractional crystallization,

(E) Compounds of the formula (Ia), compounds of the formulas (Ib) or (Ic) in which A, M, X, Y, R ¹ and R ^{2 have} the meaning given above, for example hydrolysed with aqueous bases and then acidified ,

7. Compounds of the formula (IT)

in which

A, X, Y and R ^{8 have} the meanings given above.

8. Connections of the formula (Nlfl)

in which

A, X and Y have the meanings given above.

9. pesticide, characterized by a content of at least one compound of the formula (I) according to claim 1.

10. A method for controlling animal pests, characterized in that compounds of the formula (I) according to Claim 1 are allowed to act on pests and / or their habitat.

11. Use of compounds of formula (I) according to claim 1 for combating animal pests.

12. A process for the preparation of pesticides, characterized in that compounds of the formula (I) according to Claim 1 are mixed with extenders and / or surface-active substances.

13. Use of compounds of formula (I) according to claim 1 for the preparation of pesticides.