EP0973770A1 - Fungicidal methoximinomethyldioxazines - Google Patents

Abstract

The invention concerns novel methoximinomethyldioxazines of formula (I), a plurality of processes for their preparation, and their use as fungicides, as well as novel intermediate products and a process for their preparation.

Description

 FUNGICIDAL METHOXMINOMETHYLDIOXAZI.NE

The invention relates to new methoximinomethyldioxazines, several processes for their preparation and their use as fungicides, as well as new intermediates and a process for their production

It has already become known that certain methoximinomethyldioxazines, which are constitutionally similar to the ones described below, have fungicidal properties (compare, for example, WO-A 9504728). The fungicidal activity of these compounds, however, leaves much to be desired, especially when the application rates are low

The new compounds of the general formula (I) have now been found

in which

R represents optionally substituted alkyl, arylalkyl, arylalkenyl, alkenyl,

Is alkynyl or cycloalkyl,

Q for oxygen, sulfur, -NH- or where R ^{1 is} alkyl,

E ¹ , E ² , E ³ and E ^{4 are the} same or different and each independently represent hydrogen, alkyl, haloalkyl or hydroxyalkyl, or E and E ² or E ^ and E ³ or E ^ and E ⁴ together with the respective carbon atoms to which they are attached form a cycloahphatic ring and

L ¹ , L ² , L ³ and L ^{4 are the} same or different and each independently represent hydrogen, halogen, cyano, nitro, each optionally substituted by halogen substituted alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl

In the definitions, the saturated or unsaturated hydrocarbon chains, such as alkyl, alkanediyl, alkenyl or alkynyl, are in each case straight-chain or branched, also in combination with heteroatoms, such as in alkoxy, alkylthio or alkylamino

Halogen generally represents fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine, in particular fluorine or chlorine

Aryl stands for aromatic, mono- or polycychic hydrocarbon rings, such as phenyl, naphthyl, anthranyl, phenanthryl, preferably phenyl or naphthyl, especially phenyl

Heterocyclyl stands for saturated or unsaturated, as well as aromatic, ring-shaped compounds, in which at least one ring member contains a hetero atom, ie an atom other than carbon. If the ring contains several heteroatoms, these can be the same or different. Heteroatoms are preferably oxygen, nitrogen or sulfur the ring-shaped compounds together with further carbocyclic or heterocychic, fused or bridged rings together form a polycyclic ring system. Mono- or bicyclic ring systems are preferred, in particular mono- or bicyclic, aromatic ring systems

Cycloalkyl stands for saturated, carbocyclic, ring-shaped compounds which optionally form a polycyclic ring system with other carbocyclic, fused or bridged rings It was also found that the new methoximinomethyldioxazines of the general formula (I) are obtained if (process a) 4-halo-2-phenoxypyπmιdιne of the general formula (II)

in which

E, E ² , E ³ , E ⁴ , L *, L ² , ³ and L ^{4 have} the meanings given above and

X represents halogen, in particular chlorine,

with a nucleophilic compound of the general formula

in which

R and Q have the meanings given above,

if appropriate in the presence of a diluent and if appropriate in the presence of an acid acceptor,

or if (process b) alkylsulfonylpyπmidines of the general formula (IV)

~ <t -

in which

R and Q have the meanings given above and

R ^{1 represents} alkyl or arylalkyl,

with a 3- (l-hydroxyphenyl-l-methoxιmιnomethyl) dιoxazιn of the general formula

in which

E ¹ , E ² , E ³ , E ⁴ , Ll, L ² , L ³ and L ^{4 have} the meanings given above,

if appropriate in the presence of a diluent and if appropriate in the presence of an acid acceptor

Finally, it was found that the new methoximinomethyldioxazines of the general formula (I) show a very strong fungicidal activity

The compounds according to the invention can optionally be present as mixtures of various possible isomeric forms, in particular of stereoisomers, such as, for example, E and Z, or optical isomers. Both the E and the

Z isomers, the individual enantiomers, the racemates, as well as any mixtures of these isomers, are claimed - -

The present application preferably relates to compounds of the formula (I) in which

R for optionally single to triple by halogen and / or simply by

Cycloalkyl with 3 to 6 carbon atoms substituted methyl, the cycloalkyl groups in turn optionally being substituted by 1 to 4 halogen atoms and / or 1 to 3 alkyl groups having 1 to 3 carbon atoms, or

for optionally single to n-fold (where n is the number of hydrogen atoms of the respective unsubstituted hydrocarbon radical) by halogen and / or 1 to 2 alkoxy groups with 1 to 8 carbon atoms and / or 1 to 2 cycloalkyl groups with 3 to 6 carbon atoms (where the Cycloalkyl groups are in turn optionally substituted by 1 to 4 halogen atoms and / or 1 to 3 alkyl groups having 1 to 3 carbon atoms) substituted alkyl, alkenyl or alkynyl having 2 to 12 carbon atoms, or

for cycloalkyl optionally substituted up to five times by alkyl having 1 to 4 carbon atoms, halogen and / or alkoxy having 1 to 4 carbon atoms or having 3 to 8 carbon atoms or

represents arylalkyl or arylalkenyl with 1 to 5 carbon atoms in the alkyl part or 2 to 5 carbon atoms in the alkenyl part and 6 to 10 carbon atoms in the aryl part which is monosubstituted to pentasubstituted or substituted in the aryl part, the substituents of the aryl part preferably being selected from the following list

Halogen, cyano, nitro, amino, hydroxy, formyl, carboxy, carbamoyl, thiocarbamoyl, ~ b -

Alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl each having 1 to 6 carbon atoms,

Alkenyl or alkenyloxy each having 2 to 6 carbon atoms,

Haloalkyl, haloalkoxy, haloalkylthio, haloalkylsulfinyl or haloalkylsulfonyl each having 1 to 6 carbon atoms and 1 to 13 identical or different halogen atoms,

Haloalkenyl or haloalkenyloxy each having 2 to 6 carbon atoms and 1 to 1 1 identical or different halogen atoms,

Alkylammo, dialkylammo, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl or alkylsulfonyloxy, each having 1 to 6 carbon atoms in the individual alkyl parts,

each optionally mono- or polysubstituted, identically or differently, by halogen and / or straight-chain or branched alkyl having 1 to 4 carbon atoms and / or straight-chain or branched haloalkyl having 1 to 4 carbon atoms and 1 to 9 identical or different halogen atoms, in each case doubly linked alkylene or Dioxyalkylene with 1 to 6 carbon atoms each,

Cycloalkyl with 3 to 8 carbon atoms,

Heterocyclyl or heterocyclyl-methyl, each with 3 to 7 ring members, of which 1 to 3 are identical or different heteroatoms - in particular nitrogen, oxygen and / or sulfur -

A ¹ or a grouping ₂ ', wherein -? "AI represents alkyl having 1 to 4 carbon atoms or cycloalkyl having 1 to 6 carbon atoms and

A ^{2 represents} alkyl with 1 to 4 carbon atoms optionally substituted by cyano, alkoxy, alkylthio, alkylamino, dialkylamino or phenyl, alkenyl or alkynyl each with 2 to 4 carbon atoms,

R ¹

Q represents oxygen, sulfur, -NH- or, where R ^{1 represents} alkyl having 1 to 4 carbon atoms,

El, E ² , E ³ and E ^{4 are} identical or different and independently of one another represent hydrogen, alkyl or hydroxyalkyl each having 1 to 4 carbon atoms or haloalkyl having 1 to 4 carbon atoms and 1 to 5 identical or different halogen atoms, or

El and E ² or El and E ³ or E ³ and E ⁴ together with the respective carbon atoms to which they are attached form a cycloaliphatic

Form a ring with five, six or seven carbon atoms and

Ll, L ² , L ³ and L ^{4 are the} same or different and are each independently of the other hydrogen, halogen, cyano, nitro, each optionally substituted by 1 to 5 halogen atoms, alkyl, alkoxy, alkylthio,

Alkylsulfinyl or alkylsulfonyl each having 1 to 6 carbon atoms

The present application relates in particular to compounds of the formula (I) in which

R for optionally single, double or triple by fluorine, chlorine or

Bromine and / or simply by cyclopropyl, cyclobutyl, cyclopentyl or Cyclohexyl substituted methyl, the cycloalkyl groups in turn optionally being substituted by 1 to 4 fluorine, chlorine or bromine atoms and / or 1 to 3 methyl or ethyl groups,

or for optionally single to n-fold (where n represents the number of hydrogen atoms of the respective unsubstituted hydrocarbon radical), in particular single to triple, by fluorine, chlorine or bromine and / or simple to double by methoxy, ethoxy, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl (the cycloalkyl groups in turn being optionally substituted by 1 to 4 fluorine, chlorine or bromine atoms and / or 1 to 3 methyl or ethyl groups) substituted ethyl, n- or l-propyl, n-, l-, s- or t-butyl, 1-, 2-, 3-, neo-pentyl, 1-, 2-, 3-, 4- (2-methylbutyl), 1 -, 2-, 3-hexyl, 1-, 2- , 3-, 4-, 5- (2-methylpentyl), 1-, 2-, 3- (3-methylpentyl), 2-ethylbutyl, 1-, 3-, 4- (2,2-dimethylbutyl), 1st -, 2- (2,3-dimethylbutyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, allyl, but-2-en-1-yl, But-l-en-3-yl, hex-2-en-l-yl, hexa-2,4-dιen-l-yl, propargyl, but-2-en-l-yl, or

for cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl or optionally substituted up to five times by methyl, ethyl, n- or l-propyl, n-, l-, s- or t-butyl, fluorine, chlorine, bromine, methoxy or ethoxy

for benzyl, 1-phenylethyl, 2-phenylethyl, 1-phenylpropyl, 2-phenylpropyl, 3-phenylpropyl, l-phenylprop-2-yl, 2-phenylprop-2-yl, 3 optionally mono- to pentasubstituted in the phenyl or naphthyl part -Phenylbutyl, 4-phenylbutyl, 5-phenylpentyl, 3-phenylallyl, naphth-1-ylmethyl or naphth-2-ylmethyl, the substituents of the aryl part preferably being selected from the following list

Fluorine, chlorine, bromine, cyano, methyl, ethyl, n- or l-propyl, n-, I-, s- or t-butyl methoxy, ethoxy, n- or l-propoxy, methylthio, ethylthio, n- or I. -

Propylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl or ethylsulfonyl, trifluoromethyl, trifluoroethyl, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, difluoromethylthio, trifluoromethylthio, difluorochloro- -q - methylthio, trifluoromethylsulfinyl or trifluoromethylsulfonyl, methoxycarbonyl, ethoxycarbonyl,

each optionally monosubstituted to tetrasubstituted, identically or differently, by fluorine, chlorine, methyl, trifluoromethyl or ethyl and in each case doubly linked methylenedioxy, ethylenedioxy

A 'or a grouping _{2 ■} ! _■ ■ _> where

A 'represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, cyclopropyl or cyclobutyl and

A ² for methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, allyl,

Propargyl, but-2-en-l-yl, 2-methyl-prop-l-en-3-yl, cyanomethyl, methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, dimethylaminomethyl, Dimethylaminoethyl, methylaminomethyl, methylaminoethyl or benzyl,

CH ₃ C ₂ H ₅

Q represents oxygen, sulfur, -NH-, or ^,

E ¹ , E ² , E ³ and E ^{4 are the} same or different and are independently hydrogen, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, hydroxymethyl, trifluoromethyl or trifluoroethyl, or

E 'and E ² or E ^ and E ³ or E ³ and E ⁴ together with the respective carbon atoms to which they are attached form a cycloaliphatic ring with five, six or seven carbon atoms and Ll, L ² , L ³ and L ^{4 are the} same or different and are each independently hydrogen, fluorine, chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, 1-, s- or t-butyl, methoxy, ethoxy, n- or l-propoxy, methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl or ethylsulphonyl, trifluoromethyl, trifluoromethyl, difluoromethoxy, trifluoromethoxy, di-fluorochloromethoxy, difluoromethylthio, difluoromethylthiochloro Tπfluormethylthio, Tπfluormethylsulfinyl or Tπfluormethylsulfonyl stand

A particularly preferred group of compounds according to the invention are those compounds of the formula (I) in which

R for optionally single, double or triple by fluorine, chlorine or

Bromine and / or simply by cyclopropyl, cyclobutyl, cyclopentyl or

Cyclohexyl substituted methyl, where the cycloalkyl groups in turn, if appropriate, by 1 to 4 fluorine, chlorine or bromine atoms and / or 1 to 3

Methyl or ethyl groups are substituted,

or for optionally up to n times (where n stands for the number of hydrogen atoms of the respective unsubstituted hydrocarbon radical) ms - especially single to triple, by fluorine, chlorine or bromine and / or simply to twice by methoxy, ethoxy, cyclopropyl, cyclobutyl, Cyclopentyl or cyclohexyl (the cycloalkyl groups in turn optionally being substituted by 1 to 4 fluorine, chlorine or bromine atoms and / or 1 to 3 methyl or ethyl groups) substituted ethyl, n- or l-propyl, n-, l-, s- or t-butyl, 1-, 2-, 3-, neo-pentyl, 1-, 2-, 3-, 4- (2-methylbutyl), 1-, 2-,

3-hexyl, 1 -, 2-, 3-, 4-, 5- (2-methylpentyl), 1-, 2-, 3- (3-methylpentyl), 2-ethylbutyl, 1-, 3-, 4- (2,2-dimethylbutyl), 1-, 2- (2,3-dimethylbutyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, allyl, but -2-en-l-yl, but-l-en-3-yl, hex-2-en-l-yl, hexa-2,4-dιen-l-yl, propargyl, but-2-ιn-l -yl, or

for cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl or optionally substituted up to five times by methyl, ethyl, n- or l-propyl, n-, l-, s- or t-butyl, fluorine, chlorine, bromine, methoxy or ethoxy - left -

for benzyl, 1-phenylethyl, 2-phenylethyl, 1-phenylpropyl, 2-phenylpropyl, 3-phenylpropyl, 1-phenylprop-2-yl, 2-phenylprop-2-yl, optionally mono- to pentasubstituted in the phenyl or naphthyl part, 3-phenylbutyl, 4-phenylbutyl, 5-phenylpentyl, 3-phenylallyl, naphth-1-ylmethyl or naphth-2-ylmethyl, the substituents of the aryl part preferably being selected from the following list

Fluorine, chlorine, bromine, cyano, methyl, ethyl, n- or l-propyl, n-, l-, s- or t-butyl methoxy, ethoxy, n- or l-propoxy, methylthio, ethylthio, n- or I. -

Propylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl or ethylsulfonyl, trifluoromethyl, trifluoromethyl, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, difluoromethylthio, trifluoromethylthio, difluoromethylchloromethylchlorofluoromethylchlorofluoromethyl, methyl fluoroxymethyl

each optionally monosubstituted to tetrasubstituted, identically or differently, by fluorine, chlorine, methyl, trifluoromethyl or ethyl and in each case doubly linked methylenedioxy, ethylenedioxy

or a grouping _> where

A ^{1 represents} methyl, ethyl, n- or i-propyl, n-, 1-, s- or t-butyl, cyclopropyl or cyclobutyl and

A ² for methyl, ethyl, n- or i-propyl, n-, 1-, s- or t-butyl, allyl, propargyl, but-2-en-l-yl, 2-methyl-prop-l -en-3-yl, cyanomethyl, methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, dimethylaminoethyl, dimethylaminoethyl, methylammomethyl, methylammoethyl or benzyl, - -

, 3 _{| 2} 5

Q represents oxygen, sulfur, -NU-, or

E and E ^{2 are the} same or different and each independently represent hydrogen or methyl,

E ³ and E ^{4 represent} hydrogen,

L and L ^{3 are the} same or different and each independently represent hydrogen or methyl and

L ² and L ^{4 represent} hydrogen

The general definitions given above or those specified in the preferred ranges apply both to the end products of the formula (I) and correspondingly to the starting materials or intermediates required in each case for the preparation

The radical definitions given for these radicals in the respective combinations or preferred combinations of radicals are independently replaced by corresponding radical definitions of other preferred ranges, regardless of the combination specified in each case

Compounds of the formula (I) in which

Q represents oxygen or sulfur and in particular oxygen

Compounds of the formula (I) in which

R represents unsubstituted or substituted methyl, ethyl, propyl, pentyl, hexyl, heptyl, octyl, these radicals optionally being in straight-chain, branched or cyclic form - ι 2> ~

Suitable substituents for these radicals are preferably the substituents specified in the application and in particular fluorine, chlorine and / or unsubstituted or preferably substituted by fluorine, chlorine, bromine, methyl and / or ethyl phenyl

A very particularly preferred group of compounds according to the invention are those compounds of the formula (I) in which

E 1, E ² , E ³ , E ⁴ , L *, L ² , L ³ and L ^{4 represent} hydrogen

The 4-halo-2-phenoxypyπmιdιne required to carry out process a) according to the invention are generally defined by the formula (II). In this formula (II) E, E ² , E ³ , E ⁴ , L ^, L ² , L ³ and L ⁴ preferably or in particular those meanings which, in connection with the description of the compounds of the formula (I) according to the invention, are preferred or as particularly preferred for E ^, E ² , E ³ , E ⁴ , L, L ² , L ³ and L ^{4 were} specified X represents halogen, preferably chlorine

The 4-halogen-2-phenoxypyπmιdιne of formula (II) are not yet known, they are also the subject of the present application as new substances

They are obtained (process c) if 4-halo-2-alkylsulfonylpyπmιdιne of the general formula (VI)

in which

X has the meaning given above and R ^{2 represents} alkyl or arylalkyl,

with a 3- (l-hydroxyphenyl-l-methoxιmιnomethyl) dιoxazιn of the general formula (V), optionally in the presence of a diluent and optionally in the presence of an acid acceptor

Formula (VI) provides a general definition of the 4-halo-2-alkylsulfonylpyπmιdιne required as starting materials for carrying out process c) according to the invention. In this formula (VI), X preferably or in particular has the meaning already given in connection with the description the inventive

Intermediates of the formula (II) have been indicated as preferred or as particularly preferred for X. R ² represents alkyl or arylalkyl, preferably methyl or benzyl

The 4-halo-2-alkylsulfonylpyπmιdιne of the formula (VI) are known and can be prepared by known processes (see, for example, WO 95-24396)

The 3- (l-hydroxyphenyl-l-alkoxymomethyl) doxoxins required as starting materials for carrying out process c) according to the invention are generally defined by the formula (V). In this formula (V) E ¹ , E ² , E ³ , E ⁴ , L ¹ , L ² ,

L ^J and L ⁴ preferably or in particular those meanings which, in connection with the description of the compounds of the formula (I) according to the invention, are preferred or as particularly preferred for E ^, E ² , E ³ , E ⁴ , L ^, L ² , L ³ and L ^{4 were} specified

The 3- (l-hydroxyphenyl-l-alkoxιmιnomethyl) dιoxazιne of the formula (V) are known and can be prepared by known processes (compare, for example, WO 95-04728)

Formula (III) provides a general definition of the nucleophilic compounds which are further required as starting materials for carrying out process a) according to the invention. In this formula (III), R and Q preferably or in particular have those meanings which have already been described in connection with the description of the invention. Compounds of formula (I) according to the invention have been indicated as preferred or as particularly preferred for R and Q.

The nucleophilic compounds of the formula (III) are known synthetic chemicals. The alkylsulfonylpyrimidines required as starting materials for carrying out the process b) according to the invention are generally defined by the formula (IV). In this formula (IV) R and Q preferably or in particular have those meanings which Already in connection with the description of the compounds of the formula (I) according to the invention as being preferred or as being particularly preferred for R and Q, R is alkyl or arylalkyl, preferably methyl or benzyl

The alkylsulfonylpyrimidines of the formula (IV) are known and can be prepared by known processes (compare, for example, WO 95-24396)

The 3- (l-hydroxyphenyl-l-alkoximinomethyl) dioxazne, which are further required as starting materials for carrying out process b) according to the invention, have already been described above in the description of process c) according to the invention

Suitable diluents for carrying out processes a), b) and c) according to the invention are all inert organic solvents. These preferably include ethers, such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1 , 2-dimethoxyethane, 1,2-dιethoxyethane or anisole, nitriles, such as acetonitrile, propionite, n- or i-butyronitrile or benzonitrile,

Amides, such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone or hexamethylphosphoric acid amide, sulfoxides, such as dimethyl sulfoxide, or sulfones, such as sulfolane

The processes a), b) and c) according to the invention are, if appropriate, carried out in the presence of a suitable acid acceptor. All customary inorganic or organic bases are suitable as such. These preferably include alkaline earth metal or alkali metal hydrides, amides, hydroxides, alcoholates, carbonates, hydro- ~ lb - gene carbonates, and alkaline earth metal or alkali metal alkyl compounds such as sodium hydride, sodium amide, potassium tert-butoxide, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, potassium hydrogen carbonate, sodium hydrogen carbonate or butyllitium

The reaction temperatures can be varied within a substantial range when carrying out processes a), b) and c) according to the invention. In general, temperatures from -20 ° C. to 130 ° C., preferably at temperatures from -10 ° C. to 80 ° C. C.

To carry out the process a) according to the invention for the preparation of the compounds of the formula (I), generally 0.5 to 5 mol, preferably 0.8 to 2 mol, of a nucleophilic is employed per mole of 4-halo-2-phenoxypyπmιdιn of formula (II) Compound of formula (III)

To carry out the process b) according to the invention for the preparation of the compounds of the formula (I), 0.5 to 5 mol, preferably 0.8 to 2 mol, of a 3- (1-hydroxyphenyl-) is generally employed per mole of alkylsulfonylpyπmidine of the formula (IV). l-methoxιmιnomethyl) dιoxazιns of formula (V)

To carry out the process c) according to the invention for the preparation of the compounds of the formula (II), in general 0.5 to 5 mol, preferably 0.8 to 2 mol, of a 3rd is used per mole of 4-halo-2-alkylsulfonylpyπmιdιn of the formula (VI) - (l-Hydroxyphenyl-l-methoxιmιnomethyl) dιoxazιns of formula (V) a

The processes according to the invention are generally carried out under normal pressure. However, it is also possible to work under increased or reduced pressure - generally between 0.1 bar and 10 bar

The reaction is carried out, worked up and isolated by the generally customary processes (see also the preparation examples). The substances according to the invention have a strong microbicidal action and can be used to combat unwanted microorganisms, such as fungi and bacteria, in crop protection and in material protection

Fungicides can be used to control Plasmodiophoromycetes,

Use Oomycetes, Chytπdiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes

Bactericides can be used in crop protection to combat Pseudomonadaceae, Rhizobiaceae, Enterobacteπaceae, Corynebacteπaceae and Streptomycetaceae

Some pathogens of fungal and bacterial are exemplary but not limiting

Diseases that come under the generic names listed above, called Xanthomonas species, such as, for example, Xanthomonas campestπs pv oryzae,

Pseudomonas species, such as, for example, Pseudomonas syπngae pv lachrymans,

Erwinia species, such as, for example, Erwinia amylovora,

Pythium species, such as Pythium ultimum,

Phytophthora species, such as, for example, Phytophthora infestans, Pseudoperonospora species, such as, for example, Pseudoperonospora humuli or

Pseudoperonospora cubensis,

Plasmopara species, such as, for example, Plasmopara viticola,

Bremia species, such as, for example, Bremia lactucae,

Peronospora species, such as, for example, Peronospora pisi or P brassicae, Erysiphe species, such as, for example, Erysiphe graminis,

Sphaerotheca species, such as, for example, Sphaerotheca füligmea,

Podosphaera species, such as, for example, Podosphaera leucotπcha,

Ventuπa species, such as, for example, Ventuπa inaequalis,

Pyrenophora species, such as, for example, Pyrenophora teres or P graminea (conidial form Drechslera, Syn Helminthospoπum),

Coch obolus species, such as, for example, Cochhobolus sativus

(Conidia form Drechslera, Syn Helminthospoπum), Uromyces species, such as, for example, Uromyces appendiculatus, Puccinia species, such as, for example, Puccinia recondita, Sclerotinia species, such as, for example, Sclerotinia sclerotiorum, Tilletia species, such as, for example, Tilletia caπes,

Ustilago species, such as, for example, Ustilago nuda or Ustilago avenae, Pelliculaπa species, such as, for example, Pel culaπa sasakn,

Pyπculaπa species, such as, for example, Pyπculaπa oryzae, Fusaπum species, such as, for example, Fusanum culmorum, Botrytis species, such as, for example, Botrytis cinerea, Septoπa species, such as, for example, Septoπa nodorum, Leptosphaeπa species, such as, for example, Leptosphaeπa nodorum,

Cercospora species, such as, for example, Cercospora canescens, Alternaπa species, such as, for example, Alternaria brassicae, Pseudocercosporella species, such as, for example, Pseudocercosporella herpotπchoides

The good plant tolerance of the active ingredients in the concentrations necessary to combat plant diseases allows treatment of above-ground parts of plants, of propagation stock and seeds, and of the soil

The active compounds according to the invention can be used with particularly good results in combating cereal diseases, for example against Erysiphe species

Diseases in wine, fruit and vegetable cultivation, such as against Sphaerotheca and Plasmopara species, or rice diseases, such as against Pyπculaπa species, use

The active compounds according to the invention are also suitable for increasing the crop yield

They are also less toxic and have good plant tolerance

In material protection, the substances according to the invention can be used to protect technical materials against attack and destruction by undesired microorganisms

In the present context, technical materials are to be understood as non-living materials that have been prepared for use in technology ~ / 9- are, for example, technical materials that are to be protected against microbial change or destruction by active substances according to the invention, adhesives, glues, paper and cardboard, textiles, leather, wood, paints and plastic articles, cooling lubricants and other materials that are from Mikroor - organisms can be attacked or decomposed. In the context of the materials to be protected, parts of production plants, for example cooling water circuits, which can be impaired by the multiplication of microorganisms may also be mentioned. Within the scope of the present invention, technical materials are preferably adhesives, glues, papers and cartons, Leather, wood, paints, cooling lubricants and heat transfer liquids called, particularly preferably wood

Bacteria, fungi, yeasts, algae and slime organisms may be mentioned as microorganisms which can bring about a degradation or a change in the technical materials. The active compounds according to the invention preferably act against fungi, in particular mold, wood-staining and wood-destroying fungi (Basidiomycetes) and against slime organisms and algae

For example, microorganisms of the following genera may be named Alternaπa, such as Alternaria tenuis,

Aspergillus, such as Aspergillus niger,

Chaetomium, like Chaetomium globosum,

Coniophora, such as Coniophora puetana,

Lentinus, such as Lentinus tigπnus, Penicillium, such as Penicil um glaucum,

Polyporus, such as Polyporus versicolor,

Aureobasidium, such as Aureobasidium pullulans,

Sclerophoma, such as Sclerophoma pityophila,

Tπchoderma, such as Tnchoderma viπde, Escheπchia, such as Escheπchia coh,

Pseudomonas, such as Pseudomonas aeruginosa,

Staphylococcus, such as Staphylococcus aureus Depending on their respective physical and / or chemical properties, the active ingredients can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine encapsulations in polymeric substances and in coating compositions for seeds, and ULV -Cold and warm mist shapes

These formulations are prepared in a known manner, for example by mixing the active ingredients with extenders, that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, ie emulsifiers and / or dispersants and / or Foam-producing agents If water is used as an extender, organic solvents can, for example, also be used as auxiliary solvents. Liquid solvents are essentially aromatics, such as xylene, toluene or alkylnaphtha ne, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes. Chlorethylene or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, alcohols, such as butanol or glycol, and their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methylsobutyl ketone or cyclohexanone, strongly polar solvents, such as dime thylformamide and dimethyl sulfoxide, as well as water Liquefied gaseous extenders or carriers are those liquids which are gaseous at normal temperature and under normal pressure, eg aerosol propellants, such as halogenated hydrocarbons as well as butane, propane, nitrogen and carbon dioxide. Solid carriers come in as solid For example, natural stone powder, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmoleonite or diatomaceous earth, and synthetic rock powders, such as highly disperse silica,

Aluminum oxide and silicates Possible solid carrier materials for granules are, for example, 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 stalks Suitable emulsifiers and / or foaming 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. Suitable dispersants are, for example, lignin sulfite waste liquors 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 also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids, and synthetic phospholipids can be used in the formulations. Additional additives can be mineral and vegetable oils

Dyes such as inorganic pigments, for example iron oxide, titanium oxide, ferrocyan blue and organic dyes, such as alizine, azo and metal phthalocyanine dyes and trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc, can be used become

The formulations generally contain between 0.1 and 95 percent by weight

Active ingredient, 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, acacids, nematicides or insecticides, in order to broaden the spectrum of action, for example, or to prevent the development of resistance. In many cases, synergistic effects, ie the effectiveness, are obtained the mixture is greater than the effectiveness of the individual components

The following compounds can be considered as mixing partners, for example

Fungicides:

Aldimorph, Ampropylfos, Ampropylfos-Ka um, Andopπm, Anilazin, Azaconazol, Azoxystrobm, Benalaxyl, Benodanil, Benomyl, Benzamacπl, Benzamacryl-Isobutyl, Bialaphos,

Binapacryl, biphenyl, bitertanol, blasticidin-S, bromuconazole, bupiπmat, buthiobate, calcium polysulfide, capsimycin, captafol, captan, carbendazim, carboxin, carvone, quinomethionate (quinomethionate), chlobenthiazon, chlorfenazol, chloroneb, chloroneb - λX- ropicrin, chlorothalonil, chlozolinate, clozylacon, cufraneb, cymoxanil, cyproconazole, cyprodinil, cyprofüram,

Debacarb, dichlorophene, diclobutrazole, diclofluanide, diclomezin, dicloran, diethofencarb, difenoconazole, dimethirimol, dimethomorph, diniconazole, diniconazole-M, dinocap, diphenylamine, dipyrithione, ditalimfos, dorphianon, dithianon, dithianon,

Drazoxolon,

Ediphenphos, Epoxiconazole, Etaconazole, Ethirimol, Etridiazole,

Famoxadone, fenapanil, fenarimol, fenbuconazole, fenfüram, fenitropan, fenpiclonil, fenpropidin, fenpropimorph, fentin acetate, fentin hydroxide, ferbam, ferimzon, fluazinam, flumetover, fluoromid, fluquinconazole, flurprimidol, flusilazol

Flusulfamide, flutolanil, flutriafol, folpet, fosetyl-aluminum, fosetyl sodium, falidid, fuberidazole, furalaxyl, furametpyr, furcarbonil, furconazole, furconazole-cis, furmecyclox, guazatin, hexachlorobenzole, hexaconazole, hexaconazole, hexaconazole,

Imazalil, Imibenconazol, Iminoctadin, Iminoctadinealbesilat, Iminoctadinetriacetat, Iodocarb, Ipconazol, Iprobefos (IBP), Iprodione, Irumamycin, Isoprothiolan, Isovaledione,

Kasugamycin, Kresoxim-methyl, copper preparations such as: copper hydroxide, copper naphthenate, copper oxychloride, copper sulfate, copper oxide, oxy-copper and

Bordeaux mix,

Mancopper, Mancozeb, Maneb, Meferimzone, Mepanipyrim, Mepronil, Metalaxyl, Metconazol, Methasulfocarb, Methfüroxam, Metiram, Metomeclam, Metsulfovax, Mildiomycin, Myclobutanil, Myclozolin, Nickel-dimethyldithiochalamopropyl, Nitrile

Ofürace, Oxadixyl, Oxamocarb, Oxolinicacid, Oxycarboxim, Oxyfenthiin, Paclobutrazol, Pefürazoat, Penconazol, Pencycuron, Phosdiphen, Pimaricin, Piperalin, Polyoxin, Polyoxorim, probenazole, Prochloraz, Procymarbosol, Propylazol, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazolone, Propylazole Pyrimethanil, pyroquilon, pyroxy for,

Quinconazole, quintozen (PCNB), sulfur and sulfur preparations, -21- Tebuconazole, tecloftalam, tecnazen, tetcyclacis, tetraconazole, thiabendazole, thicyofen, thifluzamide, thiophanate-methyl, thiram, tioxymid, tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triazoxidylzolifl, triazoxidiflizoll, triazbutiflzumlol, triazoxidiflizoll, triazoxidiflizoll , Triforin, triticonazole, uniconazole,

Validamycin A, vinclozolin, viniconazole, zarilamide, zineb, ziram and Dagger G, OK-8705, OK-8801, α- (1, 1-dimethylethyl) -ß- (2-phenoxyethyl) - 1 H-1, 2.4 -triazole-1-ethanol, α- (2,4-dichlorophenyl) -ß-fluoro-b-propyl-1H-1, 2,4-triazole-1-ethanol, α- (2,4-dichlorophenyl) -ß -methoxy-a-methyl- 1 H- 1, 2,4-triazol-1-ethanol, α- (5-methyl-1, 3-dioxan-5-yl) -ß - [[4- (trifluoromethyl) - phenyl] methylene] - 1 H-1, 2,4-tri-azole-1-ethanol,

(5RS, 6RS) -6-hydroxy-2,2,7,7-tetramethyl-5- (1H-l, 2,4-triazol-l-yl) -3-octanone, (E) -a- (methoxyimino ) -N-methyl-2-phenoxy-phenylacetamide, {2-methyl-l - [[[l- (4-methylphenyl) ethyl] amino] carbonyl] propyl} carbamic acid 1-isopropyl ester 1 - ( 2,4-dichlorophenyl) -2- (1 H-1, 2,4-triazol-1-yl) -ethanone-O- (phenylmethyl) oxime,

1 - (2-methyl-1-naphthalenyl) - 1 H-pyrrole-2, 5-dione, l- (3,5-dichlorophenyl) -3- (2-propenyl) -2,5-pyrrolidinedione, l- [ (Diiodomethyl) sulfonyl] -4-methyl-benzene, 1 - [[2- (2,4-dichlorophenyl) - 1, 3-dioxolan-2-yl] methyl] - 1 H-imidazole, 1 - [[ 2- (4-chlorophenyl) -3 -phenyloxiranylj-methyl] - 1 H-1, 2,4-triazole, l- [l- [2 - [(2,4-dichlorophenyl) methoxy] phenyl] ethenyl ] -l H-imidazole, l-methyl-5-nonyl-2- (phenylmethyl) -3-pyrrolidinol,

2 ', 6'-dibromo-2-methyl-4'-trifluoromethoxy-4'-trifluoromethyl-l, 3-thiazole-5-carboxanilide, 2,2-dichloro-N- [l- (4- chlorphenyl) ethyl] -l-ethyl-3-methyl-cyclopropanecarboxamide,

2,6-dichloro-5- (methylthio) -4-pyrimidinyl-thiocyanate, 2,6-dichloro-N- (4-trifluoromethylbenzyl) benzamide, -2 <? ~

2,6-dichloro-N - [[4- (trifluoromethyl) phenyl] methyl] benzamide, 2- (2, 3, 3-triiodo-2-propenyl) -2H-tetrazole, 2 - [(1 - Methylethyl) sulfonyl] -5- (trichloromethyl) - 1, 3, 4-thiadiazole, 2 - [[6-deoxy-4-O- (4-O-methyl-ß-D-glycopyranosyl) -aD-glucopyranosyl] -amino] -4- methoxy-1 H-pyrrolo [2,3-d] pyrimidine-5-carbonitrile,

2-aminobutane,

2-bromo-2- (bromomethyl) pentandinitrile,

2-chloro-N- (2,3-dihydro-l, l, 3-trimethyl-lH-inden-4-yl) -3-pyridinecarboxamide, 2-chloro-N- (2,6-dimethylphenyl) -N- (isothiocyanatomethyl) acetamide, 2-phenylphenol (OPP),

3,4-dichloro-l- [4- (difluoromethoxy) phenyl] -IH-pyrrole-2,5-dione, 3,5-dichloro-N- [cyan [(l-methyl-2-propynyl) -oxy ] -methyl] -benzamide, 3- (1,1-dimethylpropyl-1-oxo-1 H-indene-2-carbonitrile, 3- [2- (4-chlorophenyl) -5-ethoxy-3-isoxazolidinyl] pyridine , 4-chloro-2-cyan-N, N-dimethyl-5- (4-methylphenyl) -1 H-imidazole-1-sulfonamide,

4-methyl-tetrazolo [1,5-a] quinazolin-5 (4H) -one,

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

9H-xanthene-9-carboxylic acid 2 - [(phenylamino) carbonyl] hydrazide, bis- (l-methylethyl) -3-methyl-4 - [(3-methylbenzoyl) -oxy] -2,5-thiophene dicarboxylate, ice-1 - (4-chlorophenyl) -2- (1 H-1, 2,4-triazole-1-yl) cycloheptanol, cis-4- [3- [4- (l, l-dimethylpropyl) phenyl -2-methylpropyl] -2,6-dimethyl-morpholine hydrochloride,

Ethyl - [(4-chlorophenyl) azo] cyanoacetate, potassium hydrogen carbonate,

Methane tetrathiol sodium salt,

Methyl 1 - (2,3-dihydro-2,2-dimethyl-1 H-inden-1-yl) - 1 H-imidazole-5-carboxylate, methyl-N- (2,6-dimethylphenyl) -N- (5-isoxazolylcarbonyl) -DL-alaninate, methyl-N- (chloroacetyl) -N- (2,6-dimethylphenyl) -DL-alaninate, N- (2,3-dichloro-4-hydroxyphenyl) -l-methyl- cyclohexane carboxamide

N- (2,6-dimethylphenyl) -2-methoxy-N- (tetrahydro-2-oxo-3-furanyl) acetamide, N- (2,6-dimethylphenyl) -2-methoxy-N- (tetrahydro-2 -oxo-3-thienyl) -acetamide, N- (2-chloro-4-nitrophenyl) -4-methyl-3-nitro-benzenesulfonamide, N- (4-Cyclohexylphenyl) - 1, 4,5,6-tetrahydro-2-pyrimidinamine, N- (4-hexylphenyl) -l, 4,5,6-tetrahydro-2-pyrimidinamine, N- (5-chloro -2-methylphenyl) -2-methoxy-N- (2-oxo-3-oxazolidinyl) acetamide, N- (6-methoxy) -3-pyridinyl) cyclopropanecarboxamide, N- [2,2,2-trichloro- 1 - [(chloroacetyl) amino] ethyl] benzamide,

N- [3-chloro-4,5-bis (2-propynyloxy) phenyl] -N'-methoxymanimidamide, N-formyl-N-hydroxy-DL-alanine sodium salt,

O, O-Diethyl- [2- (dipropylamino) -2-oxoethyl] ethylphosphoramidothioate, O-Methyl-S-phenyl-phenylpropylphosphoramidothioate, S-Methyl-l, 2,3-benzothiadiazole-7-carbothioate, spiro [2H] -l-benzopyran-2, l '(3Η) -isobenzofüran] -3'-one,

Bactericides:

Bromopol, dichlorophene, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furan carboxylic acid, oxytetracycline, probenazole, streptomycin, tecloftalam, copper sulfate and other copper preparations

Insecticides / acaricides / nematicides:

Abamectin, Acephat, Acrinathrin, Alanycarb, Aldicarb, Alphamethrin, Amitraz, Avermectin, AZ 60541, Azadirachtin, Azinphos A, Azinphos M, Azocyclotin,

Bacillus thuringiensis, 4-bromo-2- (4-chlorophenyl) -1 - (ethoxymethyl) -5- (trifluoromethyl) -lH-pyrrole-3-carbonitrile, bendiocarb, benufracarb, bensultap, betacyfluthrin, bifenthrin, BPMC , Brofenprox, Bromophos N Bufencarb, Buprofezin, Butocarboxim, Butylpyridaben, Cadusafos, Carbaryl, Carbofüran, Carbophenothion, Carbosulfan, Cartap, Chloethocarb, Chlorethoxyfos, Chlorfenapyr, Chlorfenvinphos, Chlorfluazuron - Chlormephos 6-(((Mephos 6-Ν -pyridinyl) -methyl] -Ν'-cyano-Ν-methyl-ethanimidamide. Chlorpyrifos, Chlorpyrifos M, Cis-Resmethrin, Clocythrin, Clofentezm, Cyanophos, Cycloprothrin, Cyfluthrin, Cyhalothrin, Cyhexatin, Cypermethrin, Cyromazin, Deltamethrin, Demeton M, Demeton S, Demeton-S-methyl, Diazenton

Dichlofenthion, dichlorvos, dicliphos, dicrotophos, diethion, diflubenzuron, dimethoate, dimethylvinphos, dioxathione, disulfoton, Edifenphos, Emamectin, Esfenvalerat, Ethiofencarb, Ethion, Ethofenprox, Ethoprophos, Etrimphos,

Fenamiphos, fenazaquin, fenbutatin oxide, fenitrothion, fenobucarb, fenothiocarb,

Fenoxycarb, Fenpropathrin, Fenpyrad, Fenpyroximat, Fenthion, Fenvaierate, Fipronil, Fluazinam, Fluazuron, Flucycloxuron, Flucythrinat, Flufenoxuron, Flufenprox,

Fluvalinate, Fonophos, Formothion, Fosthiazat, Fubfenprox, Furathiocarb,

HCH, heptenophos, hexaflumuron, hexythiazox,

Imidacloprid, Iprobefos, Isazophos, Isofenphos, Isoprocarb, Isoxathion, Ivermectin,

Lamda-cyhalothrin, Lufenuron, Malathion, Mecarbam, Mevinphos, Mesulfenphos, Metaldehyde, Methacrifos, Methamidophos, Methidathion, Methiocarb, Methomyl, Metolcarb, Milbemectin, Mono-crotophos, Moxidectin,

Naled, NC 184, Nitenpyram

Omethoat, Oxamyl, Oxydemethon M, Oxydeprofos, Parathion N Parathion M, Permethrin, Phenthoat, Phorat, Phosalon, Phosmet, Phosphamidon, Phoxim, Pirimicarb, Pirimiphos M, Pirimiphos N Profenophos, Promececarb, Propaphothat, Propoxuros, Propoxuros , Pymetrozine, pyrachlophos,

Pyridaphenthion, Pyresmethrin, Pyrethrum, Pyridaben, Pyrimidifen, Pyπproxifen,

Quinalphos, Salithion, Sebufos, Silafluofen, Sulfotep, Sulprofos,

Tebufenozide, Tebufenpyrad, Tebupirimiphos, Teflubenzuron, Tefluthπn, Temephos,

Terbam, Terbufos, Tetrachlorvinphos, Thiafenox, Thiodicarb, Thiofanox, Thiomethon, Thionazin, Thuringiensin, Tralomethrin, Triarathen, Triazophos, Triazuron, Trichlorofon, Triflumuron, Trimethacarb, VamidothyamlinCarb

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

The active ingredients can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, suspensions, wettable powders, pastes, soluble powders, dusting agents and granules. The application is carried out in the customary manner, for example by pouring, spraying, spraying, - 2 - Scattering, dusting, foaming, brushing, etc. It is also possible to apply the active ingredients using the ultra-low-volume process or to inject the active ingredient preparation or the active ingredient into the soil. The seeds of the plants can also be treated

When using the active compounds according to the invention as fungicides, the application rates can be varied within a relatively wide range, depending on the type of application. When treating parts of plants, the application rates of active compound are generally between 0.1 and 10 000 g / ha, preferably between 10 and 1000 g / ha In the case of seed treatment, the active compound application rates are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 10 g per kilogram of seed. When treating the soil, the active compound application rates are generally between 0.1 and 10 000 g / ha, preferably between 1 and 5 000 g / ha

The agents used to protect industrial materials generally contain the active ingredients in an amount of 1 to 95%, preferably 10 to 75%

The application concentrations of the active compounds according to the invention depend on the type and the occurrence of the microorganisms to be controlled and on

Composition of the material to be protected The optimum amount to be used can be determined by test series. In general, the application concentrations are in the range from 0.001 to 5% by weight, preferably from 0.05 to 1.0% by weight, based on the material to be protected

The effectiveness and the spectrum of activity of the active substances to be used according to the invention in the protection of materials, or of the agents, concentrates or very general formulations which can be prepared therefrom, can be increased if further antimicrobial compounds, fungicides, bactericides, herbicides, insecticides or other active substances are used to enlarge the spectrum of activity or to achieve them special effects such as additional protection against insects are added. These mixtures can have a broader spectrum of activity than the compounds according to the invention -IS ¹ -

Preparation Examples:

Example 1)

Procedure a)

A mixture of 1.5 g (0.0028 mol) of [2- (4-chloro-pyπmιdιn-2-yloxy) phenyl] - (5,6- dιhydro- [l, 4,2] dιoxazιn-3-yl ) -methanone-O-methyloxιm, 0.3 g (0.0034 mol) 1,3-Dι-fluoropropan-2-ol and 0.5 g potassium carbonate in 20 ml dry Acetonitπl is over

Stirred overnight at 50 ° C. After cooling to room temperature, the mixture is concentrated under reduced pressure and the residue is taken up in ethyl acetate. The solution is washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue is washed with hexane / acetone (8 2 ) Chromatographed on silica gel. 0.8 g (70% of theory) is obtained (5,6-dιhydro- [l, 4,2] dιoxazιn-3-yl) - {2- [4- (2-fluoro-l- fluoromethyl-ethoxy) -pyπmι- dιn-2-yloxy] -phenyl} -methanone-O-methyloxime

HPLC logP = 2.2

Production of the starting material:

Example (11-11

A mixture of 1.9 g (0.01 mol) of 4-chloro-2-methylsulfonylpyπmιdιn, 2.4 g (0.01 mol) (5,6-Dιhydro- [l, 4,2] dιoxazιn-3-yl ) - (2-hydroxy-phenyl) -methanone-O-methyl-oxime and 1.7 g of potassium carbonate in 30 ml of dry acetonitrile is stirred overnight at 50 ° C. After cooling to room temperature, the mixture is concentrated under reduced pressure and the residue was taken up in ethyl acetate

The solution is washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue is chromatographed on silica gel using hexane / acetone (8 2). 1.5 g (43% of theory) are obtained [2- (4-chloro pyπmι- dιn-2-yloxy) -phenyl] - (5,6-dιhydro- [l, 4,2] dιoxazm-3-yl) -methanon-O-methyloxιm HPLC logP = 2,0

Example (2)

Procedure b)

To 0.3 g (0.009 mol) of sodium hydride (80% in mineral oil) in 30 ml of dry dimethylformamide, 2.0 g (0 009 mol) (5,6-dihydro- [1,4, 2] dιoxazιn-3-yl) - (2-hydroxy-phenyl) -methanone-O-methyl-oxιm given After the end of the water 2.6 g (0.009 mol) of 4- (2,2,2-trichloroethoxy) -2-methylsulfonylpyπmidine are added in portions. The mixture is stirred overnight and then concentrated under reduced pressure. The residue is taken up in ethyl acetate , the solution is washed twice with water, dried over sodium sulfate and concentrated under reduced pressure. The residue is chromatographed on silica gel using hexane / acetone (7 3). 1.45 g (34% of theory) (5,6-dihydro- [l, 4,2] dιoxazιn-3-yl) - {2- [4- (2,2,2-tπchlorethoxy) -pyπmιdιn-2-yloxy] -phenyl} -methanone-O-methyloxιm HPLC logP = 3, l

Analogously to Examples (1) and (2), and in accordance with the general description of the production process a) and b) according to the invention, the compounds of the formula (I-a) according to the invention listed in Table 1 below are also obtained

Table 1

- '

-2> 2-

-J3-

~ IH ~

~ 3

-3 «? -

Examples of use:

Example A

Erysiphe test (barley) / protective

Solvent 10 parts by weight of N-methyl-pyrrohdon emulsifier, 0.6 part by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weight is mixed

Active ingredient with the specified amounts of solvent and emulsifier and dilute the concentrate with water to the desired concentration

To test for protective effectiveness, young plants are sprayed with the active compound preparation in the stated application rate

After the stain covering has dried on, the plants are dusted with spores of Erysiphe graminis fsp hordei

The plants are placed in a greenhouse at a temperature of approx. 20 ° C and a relative air humidity of approx. 80% in order to promote the development of mildew pustules

Evaluation is carried out 7 days after the inoculation. 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infection is observed

In this test, for example, the compound of preparation example (3) shows an efficiency of 100% in comparison with the untreated control at an exemplary active compound application rate of 250 g / ha - 18-

Table A

Erysiphe test (barley) / protective

Example B

Erysiphe test (barley) / curative

Solvent 10 parts by weight of N-methyl-pyrro don

Emulsifier 0.6 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 with water to the desired concentration

To test for curative activity, young plants are dusted with spores of Erysiphe graminis f sp hordei 48 hours after the inoculation, the plants are sprayed with the preparation of active compound in the stated application rate

The plants are placed in a greenhouse at a temperature of approx. 20 ° C and a relative air humidity of approx. 80% in order to promote the development of mildew pustules

Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of 100% means that no infection is observed

In this test, for example, the compounds of preparation examples (3) and (6) show an efficacy of 100% compared to the untreated control at an exemplary active compound application rate of 250 g / ha - ho-

Table B

Erysiphe test (barley) / curative

-hι-

Example C

Erysiphe test (barley) / protective

Solvent 25 parts by weight of N, N-dimethylacetamid

Emulsifier 0.6 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 with water to the desired concentration

To test for protective effectiveness, young plants are sprayed with the active compound preparation in the stated application rate

After the stain covering has dried on, the plants are dusted with spores of Erysiphe graminis fsp hordei

The plants are placed in a greenhouse at a temperature of approx. 20 ° C and a relative air humidity of approx. 80% in order to promote the development of mildew pustules

Evaluation is carried out 7 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of 100% means that no infection is observed

In this test, for example, the compound of preparation example (13) shows an efficiency of 100% in comparison to the untreated control with an exemplary active compound application rate of 250 g / ha ^ 1-

Table C.

Erysiphe test (barley) / protective

Example D

Plasmopara test (vine) / protective

Solvent 47 parts by weight of acetone

Emulsifier 3 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 with water to the desired concentration

To test for protective activity, young plants are sprayed with the preparation of active compound in the stated application rate. After the sponge coating has dried on, the plants are inoculated with an aqueous spore suspension of Plasmopara viticola and then remain in an incubation cabin at about 20 ° C. for 1 day

100%. Relative humidity The plants are then placed in the greenhouse at about 21 ° C. and about 90% relative humidity for 5 days. The plants are then moistened and placed in an incubation cabin for 1 day

Evaluation is carried out 6 days after the inoculation. 0% means on

Efficiency that corresponds to that of the control, while an efficiency of 100% means that no infection is observed

In this test, the compounds of preparation examples (1), (2), (3), (7), (8), (9), (10), (11), (12), (13) and ( 14) with an exemplary active ingredient application rate of 100 g / ha, an efficiency of up to 100% compared to the untreated control -7 * ^~

Table D

Plasmopara test (vine) / protective

- -

-H-

Example E

Sphaerotheca test (cucumber) / protective

Solvent 47 Weight point acetone

Emulsifier 3 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 mixture is diluted

Concentrate with water to the desired concentration

To test for protective activity, young plants are sprayed with the preparation of active compound in the stated application rate. After the sponge covering has dried on, the plants are sprayed with a water spore suspension of

Sphaerotheca fuliginea inoculated The plants are then placed in a greenhouse at around 23 ° C and a relative humidity of around 70%

Evaluation is carried out 10 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of

100% means that no infection is observed

In this test, for example, the compounds of preparation examples (2), (6) and (8) show an efficacy of more than 90% compared to the untreated control with an exemplary active compound application rate of 100 g / ha - <, <? -

Table E

Sphaerotheca test (cucumber) / protective

Example F

Pynculaπa test (rice) / protective

Solvent 2.5 parts by weight of acetone

Emulsifier 0.06 weight 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 and the concentrate is diluted to the desired concentration with water and the stated amount of emulsifier

To test for protective efficacy, young rice plants are sprayed with the preparation of active compound in the stated application rate. After the sponge coating has dried on, the plants are inoculated with a water spore suspension of Pynculaπa oryzae. The plants are then placed in a greenhouse at 100% relative atmospheric humidity and 25 ° C.

Evaluation is carried out 4 days after the inoculation. 0% means an efficacy which corresponds to that of the control, while an efficacy of 100% means that no infection is observed

In this test, for example, the compounds of preparation examples (3), (5) and (6) show an efficiency of at least 70% compared to the untreated control with an exemplary active compound application rate of 750 g / ha

-SJ-

Table F

Pyricularia test (rice) / protective

Claims

 -S2 -

claims

Compounds of formula (I)

in which

R represents optionally substituted alkyl, arylalkyl, arylalkenyl,

Is alkenyl, alkynyl or cycloalkyl,

R ¹

I stands for oxygen, sulfur, -NH- or, where Rl stands for alkyl,

El, E ² , E ³ and E ^{4 are the} same or different and each independently represent hydrogen, alkyl, haloalkyl or hydroxyalkyl, or

El and E ² or El and E ³ or E ³ and E ⁴ together with the respective carbon atoms to which they are attached form a cycloaliphatic

Form ring and

Ll, L ² , L ³ and L ^{4 are the} same or different and each independently represents hydrogen, halogen, cyano, nitro, each optionally substituted by halogen substituted alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl Compounds of formula (I) according to claim 1, in which

R represents methyl which is optionally monosubstituted to trisubstituted by halogen and / or monosubstituted by cycloalkyl having 3 to 6 carbon atoms, the cycloalkyl groups in turn optionally being substituted by 1 to 4 halogen atoms and / or 1 to 3 alkyl groups having 1 to 3 carbon atoms, or

for optionally single to n-fold (where n is the number of hydrogen atoms of the respective unsubstituted hydrocarbon radical) by halogen and / or 1 to 2 alkoxy groups with 1 to 8 carbon atoms and / or 1 to 2 cycloalkyl groups with 3 to 6 carbon atoms, (where the cycloalkyl groups in turn optionally with 1 to 4 halogen atoms and / or 1 to 3 alkyl groups

1 to 3 carbon atoms are substituted) substituted alkyl, alkenyl or alkynyl having 2 to 12 carbon atoms, or

for cycloalkyl optionally substituted up to five times by alkyl having 1 to 4 carbon atoms, halogen and / or alkoxy having 1 to 4 carbon atoms or having 3 to 8 carbon atoms or

represents arylalkyl or arylalkenyl with 1 to 5 carbon atoms in the alkyl part or 2 to 5 carbon atoms in the alkenyl part and 6 to 10 carbon atoms in the aryl part which is monosubstituted to pentasubstituted or substituted in the aryl part, the substituents of the aryl part preferably being selected from the following list

Halogen, cyano, nitro, amino, hydroxy, formyl, carboxy, carbamoyl, thiocarbamoyl,

Alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl each having 1 to 6 carbon atoms, Alkenyl or alkenyloxy each having 2 to 6 carbon atoms;

Haloalkyl, haloalkoxy, haloalkylthio, haloalkylsulfinyl or haloalkylsulfonyl each having 1 to 6 carbon atoms and 1 to 13 identical or different halogen atoms,

Haloalkenyl or haloalkenyloxy each having 2 to 6 carbon atoms and 1 to 11 identical or different halogen atoms;

Alkylamino, dialkylamino, alkylcarbonyl, alkylcarbonyloxy, alkoxycarbonyl or alkylsulfonyloxy, each having 1 to 6 carbon atoms in the individual alkyl parts;

each optionally mono- or polysubstituted, identically or differently, by halogen and / or straight-chain or branched alkyl having 1 to 4 carbon atoms and / or straight-chain or branched haloalkyl having 1 to 4 carbon atoms and 1 to 9 identical or different halogen atoms, in each case doubly linked alkylene or Dioxyalkylene with 1 to 6 carbon atoms each,

Cycloalkyl of 3 to 8 carbon atoms;

Heterocyclyl or heterocyclyl-methyl, each with 3 to 7 ring members, of which 1 to 3 are identical or different heteroatoms - in particular nitrogen, oxygen and / or sulfur -

or a group in which

for alkyl with 1 to 4 carbon atoms or cycloalkyl with 1 to 6

Carbon atoms stands and -5T-

A ^{2 represents} optionally substituted by cyano, alkoxy, alkylthio, alkylamino, dialkylamino or phenyl alkyl having 1 to 4 carbon atoms, alkenyl or alkmyl each having 2 to 4 carbon atoms,

R ¹ I

Q stands for oxygen, sulfur, -NH- or, where Rl stands for

Alkyl having 1 to 4 carbon atoms,

El, E ² , E ³ and E ^{4 are} identical or different and independently of one another represent hydrogen, alkyl or hydroxyalkyl each having 1 to 4 carbon atoms or haloalkyl having 1 to 4 carbon atoms and 1 to 5 identical or different halogen atoms, or

El and E ² or El and E ³ or E ³ and E ⁴ together with the respective

Carbon atoms to which they are attached form a cyclophatic ring with five, six or seven carbon atoms and

Ll, L ² , L ³ and L ^{4 are the} same or different and are independently hydrogen, halogen, cyano, nitro, each optionally substituted by 1 to 5 halogen atoms, alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl each having 1 to 6 carbon atoms stand

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

R is methyl, optionally substituted once, twice or three times by fluorine, chlorine or bromine and / or simply by cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, the cycloalkyl groups in turn being optionally substituted by 1 to 4 fluorine, chlorine or Bromine atoms and / or 1 to 3 methyl or ethyl groups are substituted,

or for optionally single to n-fold (where n represents the number of hydrogen atoms of the respective unsubstituted hydrocarbon radical), in particular single to triple, by fluorine, chlorine or bromine and / or simple to double by methoxy, ethoxy, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl (the cycloalkyl groups in turn optionally being substituted by 1 to 4 fluorine, chlorine or bromine atoms and / or 1 to 3 methyl or ethyl groups) substituted ethyl, n- or i-propyl, n-, i-, s- or t-butyl, 1-, 2-, 3-, neo-pentyl, 1-, 2-, 3-, 4- (2-methylbutyl), 1-, 2-, 3-hexyl, 1-, 2- , 3-, 4-, 5- (2-methylpentyl), 1-, 2-, 3- (3-methylpentyl), 2-ethylbutyl, 1-, 3-, 4- (2,2-dimethylbutyl), 1 -, 2- (2,3-dimethylbutyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, allyl, but-2-en-l-yl,

But-l-en-3-yl, hex-2-en-1-yl, hexa-2,4-dien-1-yl, propargyl, but-2-in-1-yl, or

for optionally up to five times by methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, fluorine, chlorine, bromine, methoxy or

Ethoxy substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl or

for benzyl, 1-phenylethyl, 2-phenylethyl, 1-phenylpropyl, 2- in the phenyl or naphthyl moiety which is mono- to pentasubstituted

Phenylpropyl, 3-phenylpropyl, 1-phenylprop-2-yl, 2-phenylprop-2-yl, 3-phenylbutyl, 4-phenylbutyl, 5-phenylpentyl, 3-phenylallyl, naphth-1-ylmethyl or naphth-2-ylmethyl , wherein the substituents of the aryl part are preferably selected from the following list

Fluorine, chlorine, bromine, cyano, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl methoxy, ethoxy, n- or l-propoxy, methylthio, ethyl thio, n- or i-propylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl or ethylsulfonyl, trifluoromethyl, trifluoromethyl, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluorethoxy, difluoromethylthio, trifluoromethylfluoromethyl, trifluoromethylluoxy, trifluoromethylluoxy, trifluoromethylluoxy, trifluoromethylluoxy, trifluoromethylluoxy, trifluoromethyl fluoroyl, trifluoromethyl fluoroyl, trifluoromethyl fluoroyl, trifluoromethyl fluoroyl, trifluoromethyl fluoroyl, trifluoromethyl fluoroyl, trifluoromethyloxy, trifluoromethyl, methoxy, trifluoromethyl, methoxy, trifluoromethyl, methyl, trifluoromethyl

each optionally monosubstituted to tetrasubstituted, identically or differently, by fluorine, chlorine, methyl, trifluoromethyl or ethyl and in each case doubly linked methylenedioxy, ethylenedioxy

A ¹ or a grouping ₂ ″, where

Al represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, cyclopropyl or cyclobutyl and

A ² for methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, allyl,

Propargyl, but-2-en-l-yl, 2-methyl-prop-l-en-3-yl, cyanomethyl,

Methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, dimethylaminomethyl, dimethylaminoethyl, methylaminomethyl, methylaminoethyl or benzyl,

for oxygen, sulfur, -NH-, stands,

El, E ² , E ³ and E ^{4 are the} same or different and are independently hydrogen, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, hydroxymethyl, trifluoromethyl or trifluoroethyl , or - εv-

El and E ² or El and E ³ or E ³ and E ⁴ together with the respective carbon atoms to which they are attached form a cycloaliphatic ring with five, six or seven carbon atoms and

Ll, L ² , L ³ and L ^{4 are the} same or different and are each independently hydrogen, fluorine, chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, 1-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, methylsulfonyl or ethylsulfonyl, trifluoromethyl, trifluoroethyl, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy,

Difluoromethylthio, difluorochloromethylthio, trifluoromethylthio, trifluoromethylsulfinyl or trifluoromethylsulfonyl

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

E _h E ² , E ³ , E ⁴ , L ¹ , L ² , L ³ and L ^{4 represent} hydrogen

Pesticides, characterized in that they contain at least one compound of the formula (I) according to Claim 1

Process for combating pests, characterized in that compounds of the formula (I) according to Claim 1 are allowed to act on pests and / or their rife in life

Use of compounds of formula (I) or agents according to claims 1 to 5 for controlling pests

Process for the preparation of pesticides, characterized in that compounds of the formula (I) according to Claims 1 to 4 are mixed with extenders and / or surface-active agents Process for the preparation of compounds of the formula (I) as defined in claim 1, characterized in that (process a) 4-halo-2-phenoxypyrimidines of the general formula (II)

in which

El, E ² , E ³ , E ⁴ , Ll, L ² , L ³ and L ^{4 have} the meanings given in claim 1 and

X represents halogen, in particular chlorine,

with a nucleophilic compound of the general formula

in which

R and Q have the meanings given in claim 1,

if appropriate in the presence of a diluent and if appropriate in the presence of an acid acceptor,

or that (process b) alkylsulfonylpyrimidines of the general formula (IV)

in which

R and Q have the meanings given in claim 1 and

Rl represents alkyl or arylalkyl,

with a 3- (l-hydroxyphenyl-l-methoximinomethyl) dioxazine of the general formula

in which

El, E ² , E ³ , E ⁴ , Ll, L ² , L ³ and L ^{4 have} the meanings given in Claim 1,

if appropriate in the presence of a diluent and if appropriate in the presence of an acid acceptor.

10. Compounds of the formula (II)

in which

χl L ² L ³ L ⁴ El E ² E ³ and E ⁴ ^ ^em claim 1 have meanings and

stands for halogen.