Title of Invention

"PROCESS FOR THE PREPARATION OF HALOGENOPYRIMIDINES"

Abstract

Process for the preparation of halogenopyrimidines compound of the formula (1) In which A represents optinally substituted alkanediyl, R represents in each case optionally substituted cycloalkyl, aryl or benzofused heterorcyclyl E represents -CH= or nitrogen, Q represents oxygen, sulphur, -CH2-0-, a single bond, or a nitrogen atom which is optionally substituted by alkyl, and X represents halogen. Characterized in that a) hydroxy compound of the general formula (II) in which A and E have the meanings as given above are reacted with a substituted halogenopyrimidine of the general formula (III) In which R,Q and X have the meanings as stated earlier and Y1 represents halogen, in the presence of a diluent and an acid acceptor.

Full Text

The present invention relates to a process for the preparation of halogenopyrimidines. The invention relates to new halogenopyrimidines and the use as pesticides. Certain pyrimidines which have a similar substitution pattern have already been disclosed (WO-A 95D4728). However, the activity of these prior-art compounds is not entirely satisfactory in all fields of application, in particular when low rates and concentrations are applied. According to the present invention, there is provided a process for the preparation of halogenopyrimidines of the formula (1) (Formula Removed) in which A represents optionally substituted alkanediyl, R represents in each case optionally substituted cycloalkyl, aryl or benzo- fused heterocyclyl, 1£ represents -CH= or nitrogen, Q represents oxygen, sulphur, -CH2-0-, a single, bond, or a nitrogen atom which is optionally substituted by alkyl, and X represents halogen, characterized in that a) hydroxy compounds of the general formula (II) (Formula Removed) in which A and E have the meanings as given ■above are reacted with a substituted halogenopyrimidine of the general formula III (Formula Removed) in which R, Q and X have the meanings as stated earlier and Y1 represents halogen, in the presence of a diluent and an acid acceptor, or when b) phenoxypyrimidines of the general formula (IV) (Formula Removed) in which A, E and X have the abovementioned meanings and Y2 represents halogen are reacted with a cyclic compound of the general formula (V) (Formula Removed) in which R and Q have the abovementioned meanings, if appropriate in the presence of a diluent, if appropriate in the presence of an acid acceptor and if appropriate in the presence of a catalyst. Finally, it has been found that the new halogenopyrimidines of the general formula (I) have a very powerful fungicidal activity. Where appropriate, the compounds according to the invention can exist in the form of mixtures of various isomeric forms which are possible, in particular of stereoisomers, such as, for example, E and Z isomers. Claimed are not only the E and the Z isomers, but also any mixtures of these isomers. The invention preferably relates to compounds of the formula (I) in which A represents alkanediyl having 1 to 5 carbon atoms which is optionally substituted by halogen, R represents cycloalkyl having 3 to 7 carbon atoms which is in each case optionally monosubstituted to disubstituted by halogen, alkyl or hydroxyl; or represents benzodioxanyl which is optionally substituted by alkyl having 1 to 4 carbon atoms; or represents phenyl or naphthyl, each of which is optionally monosub-stituted to tetrasubstituted by identical or different substituents, other sub-stituents which are possible preferably being selected from amongst the enumeration which follows: halogen, cyano, nitro, amino, hydroxyl, formyl, carboxyl, carbamoyl, thio-carbamoyl; in each case straight-chain or branched alkyl, hydroxyalkyl, oxoalkyl, alkoxy, alkoxyalkyl, alkylthioalkyl, dialkoxyalkyl, alkylthio, alkylsulphinyl or alkyl sulphonyl, each of which has 1 to 8 carbon atoms; in each case straight-chain or branched alkenyl or alkenyloxy, each of which has 2 to 6 carbon atoms; in each case straight-chain or branched halogenoalkyl, halogenoalkoxy, halogenoalkylthio, halogenoalkylsulphinyl or halogenoalkylsulphonyl, each of which has 1 to 6 carbon atoms and 1 to 13 identical or different halogen atoms; in each case straight-chain or branched halogenoalkenyl or halogeno-alkenyloxy, each of which has 2 to 6 carbon atoms and 1 to 11 identical or different halogen atoms; in each case straight-chain or branched alkylamino, dialkylamino, alkyl-carbonyl, alkylcarbonyloxy, alkoxycarbonyl, alkylaminocarbonyl, dialkyl-aminocarbonyl, arylalkylaminocarbonyl, dialkylaminocarbonyloxy, alkenyl-carbonyl or alkinylcarbonyl, each of which has 1 to 6 carbon atoms in the respective hydrocarbon chains; cycloalkyl or cycloalkyloxy, each of which has 3 to 6 carbon atoms; alkylene having 3 or 4 carbon atoms, oxyalkylene having 2 or 3 carbon atoms or dioxyalkylene having 1 or 2 carbon atoms, in each case optionally monosubstituted to tetrasubstituted by identical or different substituents from the series consisting of fluorine, chlorine, oyio, methyl, trifluoromethyl or ethyl; (Formula Removed) represents hydrogen, hydroxyl or alkyl having 1 to 4 carbon atoms or cycloalkyl having 1 to 6 carbon atoms and represents hydroxyl, amino, methylamino, phenyl, benzyl, or represents alkyl or alkoxy having 1 to 4 carbon atoms, each of which is optionally substituted by cyano, hydroxyl, alkoxy, alkylthio, alkylamino, dialkylamino or phenyl, or represents alkenyloxy or alkinyl-oxy, each of which has 2 to 4 carbon atoms, and also phenyl, phenoxy, phenylthio, benzoyl, benzoylethenyl, cinnamoyl, heterocyclyl, phenylalkyl, phenylalkyloxy, phenyl alkylthio or heterocyclyl-alkyl, each of which has 1 to 3 carbon atoms in the respective alkyl moieties and each of which is optionally monosubstituted to trisubstituted in the cyclic moiety by halogen and/or straight-chain or branched alkyl or alkoxy having 1 to 4 carbon atoms, E represents -CH= or nitrogen, Q represents oxygen, sulphur, a single bond or a nitrogen atom which is optionally substituted by methyl, ethyl or n- or i-propyl and X represents fluorine, chlorine, bromine or iodine. In the definitions, the saturated or unsaturated hydrocarbon chains, such as alkyl, alkanediyl, alkenyl or alldnyl, also together with hetero atoms, such as, for example, in alkoxy, alkylthio or alkylamino, are in each case straight-chain or branched. In particular, the invention relates to compounds of the formula (I) in which A represents methylene, ethane-1,1-diyl, ethane-1,2-diyl, propane-1,1-diyl, propane-1,2-diyl, propane-1,3-diyl, butane-1,1-diyl, butane-1,2-diyl, butane- 1,3-diyl or butane-2,2-diyl, each of which is optionally substituted by fluorine or chlorine, R represents cyclopentyl or cyclohexyl, each of which is optionally monosub-stituted to disubstituted by fluorine, chlorine, methyl, ethyl or hydroxyl; or represents benzodioxanyl which is optionally substituted by methyl or ethyl; or represents phenyl or naphthyl, each of which is optionally mono-substituted to tetrasubstituted by identical or different substituents, the substituents which are possible preferably being selected from amongst the enumeration which follows: fluorine, chlorine, bromine, iodine, cyano, nitro, amino, hydroxyl, formyl, carboxyl, carbamoyl, thiocarbamoyl, methyl, 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), hydroxymethyl, hydroxy ethyl, 3-oxobutyl, methoxy-methyl, dimethoxymethyl, methoxy, ethoxy, n- or i-propoxy, methylthio, ethylthio, n- or i-propylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl or ethylsulphonyl, vinyl, allyl, 2-methylallyl, propen-1-yl, crotonyl, propargyl, vinyloxy, allyloxy, 2-methylallyloxy, propen-1-yloxy, crotonyloxy, propargyloxy; trifluoromethyl, trifluoroethyl, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, difluoromethylthio, trifluoromethylthio, difluorochloromethylthio, trifluoro-methylsulphinyl or trifluoromethylsulphonyl, methylamino, ethylamino, n- or i-propylamino, dimethylamino, diethyl-amino, acetyl, propionyl, methoxycarbonyl, ethoxycarbonyl, methylaminocarbonyl, ethylaminocarbonyl, dimethylaminocarbonyl, diethylaminocarbonyl, dimethylaminocarbonyloxy, diethylaminocarbonyloxy, benzylamino-carbonyl, acryloyl, propioloyl, cyclopentyl, cyclohexyl, in each case divalent propanediyl, ethyleneoxy, methylenedioxy, ethylene-dioxy, each of which is optionally monosubstituted to tetrasubstituted by identical or different substituents from the series consisting of fluorine, chlorine, oxo, methyl or trifluoromethyl, or a group 11 where (Formula Removed) A1 represents hydrogen, methyl or hydroxyl and A2 represents hydroxyl, methoxy, ethoxy, amino, methylamino, phenyl, benzyl or hydroxyethyl, and phenyl, phenoxy, phenylthio, benzoyl, benzoylethenyl, cinnamoyl, benzyl, phenylethyl, phenylpropyl, benzyloxy, benzylthio, 5,6-di-hydro-l,4,2-dioxazin-3-ylmethyl, triazolylmethyl, benzoxazol-2-yl-methyl, l,3-dioxan-2-yl, benzimidazol-2-yl, dioxol-2-yl, oxadiazolyl, each of which is optionally monosubstituted to trisubstituted in the cyclic moiety by halogen and/or straight-chain or branched alkyl or alkoxy having 1 to 4 carbon atoms, represents -CH= or nitrogen, represents oxygen, sulphur, a single bond or a nitrogen atom which is optionally substituted by methyl, and X represents fluorine or chlorine. The definitions of radicals given above in general or in preferred ranges apply both to the end products of the formula (I) and, analogously, to the starting materials or intermediates required in each case for the preparation. Independently of the combination given in each case, the definitions of radicals given individually for these radicals in the respective combinations or preferred combinations of radicals are also replaced by definitions of radicals of other preferred ranges as required. Formula (II) provides a general definition of the hydroxy compounds required as starting materials for carrying out Process a) according to the invention. In this formula (II), A and E preferably, or in particular, have those meanings which have already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for A and E. Some of the starting materials of the formula (II) are known, and/or they can be prepared by processes known per se (cf. WO-A 9504728). New, and also the subject of the present application, are methoxyvinyl compounds of the general formula (Ha) (Formula Removed) in which has the abovementioned meaning. The methoxyvinyl compounds of the formula (Ha) are obtained when (Process a-1) tetrahydropyranylethers of the general formula (VI) (Formula Removed) in which A has the abovementioned meaning, are treated with an acid, preferably an inorganic or organic protonic or Lewis acid, such as, for example, hydrogen chloride, sulphuric acid, phosphoric acid, formic acid, acetic acid, trifluoroacetic acid, methanesulphonic acid, trifluoromethanesulphonic acid, toluenesulphonic acid, boron trifluoride (also as the etherate), boron tribromide, aluminium trichloride, zinc chloride, iron(III) chloride, antimony penta-chloride, or else with a polymeric acid such as, for example, an acidic ion exchanger, an acidic aluminum oxide or acidic silica gel, at temperatures from -20°C to 120°C, preferably at temperatures from -10°C to 80°C, if appropriate in the presence of a diluent, preferably an ether, such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetra-hydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole; a sulphoxide, such as dimethyl sulphoxide; a sulphone, such as sulpholane; an alcohol such as methanol, ethanol, n- or i-propanol, n-, i-, sec- or tert-butanol, ethanediol, propane-1,2-diol, ethoxy ethanol, methoxyethanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, their mixtures with water, or pure water. Formula (VI) provides a general definition of the tetrahydropyranyl ethers required as starting materials for carrying out Process a-1) according to the invention. In this formula (VI), A preferably, or in particular, has the meaning which has already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for A. The starting materials of the formula (VI) are new and also a subject of the present application. The tetrahydropyranol ethers of the formula (VI) are obtained when (Process a-2) keto compounds of the general formula (VII) (Formula Removed) in which A has the abovementioned meaning, are reacted with methoxymethyl-triphenyl-phosphonium chloride, bromide or iodide, if appropriate in the presence of a diluent, preferably an inert aprotic solvent such as, for example, an ether such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxy-ethane, 1,2-diethoxyethane or anisole; an amide such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylformanilide, N-methylpyrrolidone or hexamethyl-phosphoric triamide; a sulphoxide such as dimethyl sulphoxide, or of a sulphone such as sulpholane, and if appropriate in the presence of a base, preferably of an alkaline earth metal hydride, hydroxide, amide or alcoholate or of an alkali metal hydride, hydroxide, amide or alcoholate such as, for example, sodium hydride, sodium amide, sodium methoxide, sodium ethoxide, potassium tert-butoxide, sodium hydroxide or potassium hydroxide, at temperatures from 0°C to 100°C, preferably from 20°C to 80°C. Formula (VII) provides a general definition of the keto compounds required as starting materials for carrying out Process a-2) according to the invention. In this formula (VII), A preferably, or in particular, has the meaning which has already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for A. The starting materials of the formula (VII) are new and also a subject of the present application. The keto compounds of the formula (VII) are obtained when (Process a-3) halo-genophenyl compounds of the general formula (VIII) (Formula Removed) in which YJ represents halogen are reacted with amides of the formula (IX) (Formula Removed) in which A has the abovementioned meaning and R1 and R2 are identical or different and represent alkyl, or together with the nitrogen atom to which they are bonded represent a 3- to 8-membered saturated heterocyclic ring, at temperatures from -80 to 20°C, preferably -60 to -20°C, if appropriate in the presence of a diluent, preferably an aliphatic, alicyclic or aromatic hydrocarbon such as, for example, petroleum ether, hexane, heptane, cyclohexane, methylcyclohexane, benzene, toluene, xylene or decalin, or of an ether such as diethyl ether, diisopropyl ether, methyl t-butyl ether, methyl t-amyl ether, dioxane, tetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane or anisole and if appropriate in the presence of a base, preferably an alkaline earth metal hydride or amide or alkali metal hydride or amide, such as, for example, sodium hydride or sodium amide, or of an alkali metal hydrocarbon compound or alkaline earth metal hydrocarbon compound, such as butyllithium. Formula (VIII) provides a general definition of the halogenophenyl compounds required as starting materials for carrying out Process a-3) according to the invention. In this formula (VIII), Y3 represents halogen, preferably bromine. The starting materials of the formula (VIII) are known, and/or they can be prepared by known methods (compare, for example, Synthesis 1987, 951). Formula (IX) provides a general definition of the amides furthermore required as starting materials for carrying out Process a-3) according to the invention. In this formula (IX), A preferably, or in particular, has the meaning which has already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for A. R and R2 are identical or different and represent alkyl, preferably methyl, ethyl, n- or i-propyl or n-, i-, s- or t-butyl, or together with the nitrogen atom to which they are bonded represent a 3- to 8-membered saturated heterocyclic ring, preferably azetidinyl, pyrrolidinyl, morpholinyl, piperidinyl, hexahydroazepinyl. The starting materials of the formula (IX) are new and also an object of the present application. The amides of the formula (IX) are obtained when (Process a-4) oxamates of the general formula (X) (Formula Removed) in which R1 and R2 have the abovementioned meanings and R3 represents alkyl, are first reacted with hydroxylamine or with an acid addition salt thereof, if appropriate in the presence of a diluent, preferably of an alcohol such as methanol, ethanol, n- or i-propanol, n-, i-, sec- or tert-butanol, ethanediol, propane- 1,2-diol, ethoxyethanol, methoxyethanol, diethylene glycol monomethyl ether, diethylene glycol monethyl ether, and if appropriate in the presence of a base, preferably of an alkaline earth metal hydroxide, alcoholate, acetate, carbonate or hydrogen carbonate, such as, for example, sodium amide, sodium methoxide, sodium ethoxide, potassium tert-butoxide, sodium hydroxide, potassium hydroxide, sodium acetate, potassium acetate, calcium acetate, sodium carbonate, potassium carbonate, potassium hydrogen carbonate or sodium hydrogen carbonate, at temperatures from -20 to 50°C, preferably 0 to 40° C, and the resulting hydroxamic acid of the formula (XI) (Formula Removed) without working up, is reacted with an alkylene derivative of the general formula (XII) (Formula Removed) in which A has the abovementioned meaning and Y4 and Y5 are identical or different and represent halogen, alky 1 sulphonyl or aryl-sulphonyl, if appropriate in the presence of a diluent, preferably of an alcohol, and if appropriate in the presence of a base, preferably of an alkaline earth metal hydroxide, alcoholate, acetate, carbonate or hydrogen carbonate, such as, for example, sodium amide, sodium methoxide, sodium ethoxide, potassium tert-butoxide, sodium hydroxide, potassium hydroxide, sodium acetate, potassium acetate, calcium acetate, sodium carbonate, potassium carbonate, potassium hydrogen carbonate or sodium hydrogen carbonate. Formula (X) provides a general definition of the oxalamidates required as starting materials for carrying out the first step of Process a-4) according to the invention. In this formula (X), R1 and R2 preferably, or in particular, have those meanings which have already been given in connection with the description of the compounds of the formula (IX) according to the invention as being preferred, or particularly preferred, for R1 and R2. R3 represents alkyl, preferably methyl or ethyl. The starting materials of the formula (X) are known, and/or they can be prepared by known methods (compare, for example, EP-A 469889). Hydroxylamine or salts thereof, which are furthermore required for carrying out the first step of Process a-4) according to the invention, are generally customary chemicals for synthesis. Formula (XII) provides a general definition of the alkylene derivatives required as starting materials for carrying out the second step of Process a-4) according to the invention. In this formula (XII), A preferably, or in particular, has the meaning which has already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for A. Y4 and Y5 are identical or different and represent halogen, prefer- ably chlorine or bromine; alkylsulphonyl, preferably methanesulphonyl; or arylsul-phonyl, preferably toluenesulphonyl. Formula (III) provides a general definition of the halogenopyrimidines furthermore required as starting materials for carrying out Process a) according to the invention. In this formula (III), R, Q and X preferably, or in particular, have the meanings which have already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for R, Q and X. Y1 represents halogen, preferably fluorine or chlorine. The starting materials of the formula (III) are known, and/or they can be prepared by known methods (compare, for example, DE-A 4340181; Chem.Ber., 90 942, 951). Formula (IV) provides a general definition of the phenoxypyrimidines required as starting materials for carrying out Process b) according to the invention. In this formula (IV), A, E and X preferably, or in particular, have the meanings which have already been given in connection with the description of the compounds of the formula (I) according to the invention as being preferred, or particularly preferred, for A, E and X. Y2 represents halogen, preferably fluorine or chlorine. The starting materials of the formula (IV) are new and also the subject of the present invention. The phenoxypyrimidines of the general formula (IV) are obtained (Process b-1) when hydroxy compounds of the general formula (II) are reacted with a trihalo-genopyrimidine of the general formula (XIII) (Formula Removed) in which X, Y1 and Y2 are identical or different and represent in each case halogen, if appropriate in the presence of a diluent, if appropriate in the presence of an acid acceptor and if appropriate in the presence of a catalyst. The hydroxy compounds of the formula (II) required as starting materials for carrying out Process b-1) according to the invention have already been described in connection with the description of Process a) according to the invention. Formula (XIII) provides a general definition of the trihalogenopyrimidines furthermore required as starting materials for carrying out Process b-1) according to the invention. In this formula (XIII), X, Y1 and Y2 represent halogen, preferably fluorine or chlorine. The trihalogenopyrimidines are known, and/or they can be prepared by known methods (compare, for example, Chesterfield et al., J. Chem. Soc, 1955; 3478, 3480). Formula (V) provides a general definition of the cyclic compounds furthermore required as starting materials for carrying out Process b) according to the invention. In this formula (V), R and Q preferably, or in particular, have the meanings which have already been given in connection with the description of the compounds of the formula (I) as being preferred, or particularly preferred, for R and Q. The cyclic compounds of the formula (V) are known chemicals for synthesis or can be prepared by simple methods. Diluents which are suitable for carrying out Processes a), b) and bl), 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-diethoxyethane or anisole; nitriles, such as acetonitrile, propionitrile, n- or i-butyronitrile or benzonitrile; amides such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylformanilide, N-methyl-pyrrolidone or hexamethylphosphoric triamide; sulphoxides, such as dimethyl sulphoxide; or sulphones such as sulpholane. If appropriate, Processes a), b) and b-1) according to the invention are carried out in the presence of a suitable acid acceptor. Suitable acid acceptors are all custom- ary inorganic or organic bases. These preferably include alkaline earth metal hydrides, hydroxides, alcoholates, carbonates or hydrogen carbonates or alkali metal hydrides, hydroxides, alcoholates, carbonates or hydrogen carbonates such as, for example, sodium hydride, sodium amide, potassium tert-butoxide, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, potassium hydrogen carbonate or sodium hydrogen carbonate. Suitable catalysts for Processes a), b) and b-1) according to the invention are all copper(I) salts, such as, for example, copper(I) chloride, copper(I) bromide or copper(I) iodide. When carrying out Processes a), b) and b-1) according to the invention, the reaction temperatures can be varied within a substantial range. In general, the processes are carried out at temperatures from -20°C to 100°C, preferably at temperatures from -10°C to 80°C. All the processes according to the invention are generally carried out under atmospheric pressure. However, it is also possible to carry out the processes under elevated or reduced pressure, in general between 0.1 bar and 10 bar. The reaction is carried out and the reaction products are worked up and isolated by generally customary methods (compare also the preparation examples). The active compounds according to the invention have a powerful microbicidal activity and can be employed in practice for controlling undesirable microorganisms. The active compounds are suitable for use as crop protection agents, in particular as fungicides. Fungicidal agents are employed in crop protection for controlling Plasmodio-phoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basi-diomycetes and Deuteromycetes. Bactericidal agents are employed in crop protection for controlling Pseudo-monadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Strepto-mycetaceae. Some pathogens causing fungal and bacterial diseases which come under the generic names listed above may be mentioned as examples, but not by way of limitation: Xanthomonas species, such as, for example, Xanthomonas campestris pv. oryzae; Pseudomonas species, such as, for example, Pseudomonas syringae pv. lachrymans; Erwinia species, such as, for example, Erwinia amylovora; Pythium species, such as, for example, 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 fuliginea; Podosphaera species, such as, for example, Podosphaera leucotricha; Venturia species, such as, for example, Venturia inaequalis; Pyrenophora species, such as, for example, Pyrenophora teres or P. graminea (conidia form: Drechslera, syn: Helminthosporium); Cochliobolus species, such as, for example, Cochliobolus sativus (conidia form: Drechslera, syn: Helminthosporium); 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 caries; Ustilago species, such as, for example, Ustilago nuda or Ustilago avenae; Pellicularia species, such as, for example, Pellicularia sasakii; Pyricularia species, such as, for example, Pyricularia oryzae; Fusarium species, such as, for example, Fusarium culmorum; Botrytis species, such as, for example, Botrytis cinerea; Septoria species, such as, for example, Septoria nodorum; Leptosphaeria species, such as, for example, Leptosphaeria nodorum; Cercospora species, such as, for example, Cercospora canescens; Alternaria species, such as, for example, Alternaria brassicae and Pseudocercosporella species, such as, for example, Pseudocercosporella herpotri-choides. The fact that the active compounds are well tolerated by plants at the concentrations required for controlling plant diseases permits the treatment of aerial parts of plants, of propagation stock and seeds, and of the soil. The active compounds are employed particularly successfully for controlling cereal diseases, such as, for example, against Erysiphe, Fusarium, Pseudocercosporella and Puccinia species, or for controlling diseases in viticulture or fruit and vegetable production, such as, for example, against Venturia, Sphaerotheca, Phyto-phthora and Plasmopara species, or else for controlling rice diseases, such as, for example, Pyricularia species. Furthermore, the active compounds according to the invention have a very powerful and broad in-vitro activity. Depending on their particular physical and/or chemical properties, the active compounds can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, microencapsulations in polymeric substances and in coating compositions for seed, or else ULV cold- and hot-fogging formulations. These formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is, liquid solvents, liquefied gases under pressure, and/or solid carriers, optionally with the use of surface-active agents, that is, emulsifiers and/or dispersants, and/or foam formers. In the case of the use of water as an extender, organic solvents can, for example, also be used as auxiliary solvents. The following are mainly suitable as liquid solvents: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example mineral oil fractions, 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 sulphoxide, or else water. Liquefied gaseous extenders or carriers are to be understood as meaning liquids which are gaseous at ambient temperature and under atmospheric pressure, for example aerosol propellants such as halogenohydrocarbons, or else butane, propane, nitrogen and carbon dioxide. Suitable solid carriers are: for example ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals such as highly-disperse silica, alumina and silicates. Suitable solid carriers for granules are: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, or else synthetic granules of inorganic and organic meals, and granules of organic material such as sawdust, coconut shells, maize cobs and tobacco stalks. Suitable emulsifiers and/or foam formers are: for example nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates, or else protein hydrolysates. Suitable dispersants are: for example lignin-sulphite waste liquors and methylcellulose. Adhesives such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, or else natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations. Other additives can be mineral and vegetable oils. It is possible to use colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian blue, and organic dyestuffs such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc. The formulations generally comprise between 0.1 and 95 per cent 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 as a mixture with known fungicides, bactericides, acaricides, nematicides or insecticides, for example to widen the spectrum of action or to prevent the build-up of resistance. In many cases, synergistic effects are obtained, i.e. the activity of the mixture is greater than the activity of the individual components. Examples of particularly advantageous mixtures are the following compounds. Fungicides: 2-aminobutane; 2-anilino-4-methyl-6-cyclopropyl-pyrimidine; 2',6'-dibromo-2- methyl-4l-trifluoromethoxy-4'-trifluoro-methyl-l,3-thizole-5-carboxanilide; 2,6- dichloro-N-(4-trifluoromethylbenzyl)benzamide; (E)-2-methoxyimino-N-methyl-2- (2-phenoxyphenyl)acetamide; 8-hydroxyquinoline sulphate; methyl (E)-2-{2-[6-(2- cyanophenoxy)-pyrimidin-4-yloxy]-phenyl}-3-methoxyacrylate; methyl (E)- methoximino[alpha-(o-tolyloxy)-o-tolyl]acetate; 2-phenylphenol (OPP), aldimorph, ampropylfos, anilazine, azaconazole, benalaxyl, benodanil, benomyl, binapacryl, biphenyl, bitertanol, blasticidin-S, bromuconazole, bupirimate, buthiobate, calcium polysulphide, captafol, captan, carbendazim, carboxin, quinomethionate, chloroneb, chloropicrin, chlorothalonil, chlozolinate, cufraneb, cymoxanil, cypro- conazole, cyprofuram, dichlorophen, diclobutrazol, diclofluanid, diclomezin, dicloran, diethofencarb, difenoconazole, dimethirimol, dimethomorph, diniconazole, dinocap, diphenylamine, dipyrithion, ditalimfos, dithianon, dodine, drazoxolon, edifenphos, epoxyconazole, ethirimol, etridiazole, fenarimol, fenbuconazole, fenfuram, fenitropan, fenpiclonil, fenpropidin, fenpropimorph, fentin acetate, fentin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, fluoromide, fluquinconazole, flusilazole, flusulfamide, flutolanil, flutriafol, folpet, fosetyl-aluminium, fthalide, fuberidazole, furalaxyl, furmecyclox, guazatine, hexachlorobenzene, hexaconazole, hymexazol, imazalil, imibenconazole, iminoctadine, iprobenfos (IBP), iprodione, isoprothiolane, kasugamycin, copper preparations such as: copper hydroxide, copper naphthenate, copper oxychloride, copper sulphate, copper oxide, oxine- copper and Bordeaux mixture, mancopper, mancozeb, maneb, mepanipyrim, mepronil, metalaxyl, metconazole, methasulfocarb, methfuroxam, metiram, metsulfovax, myclobutanil, nickel dimethyldithiocarbamate, nitrothal-isopropyl, nuarimol, ofurace, oxadixyl, oxamocarb, oxycarboxin, pefurazoate, penconazole, pencycuron, phosdiphen, pimaricin, piperalin, polyoxin, probenazole, prochloraz, procymidone, propamocarb, propiconazole, propineb, pyrazophos, pyrifenox, pyrimethanil, pyroquilon, quintozene (PCNB), sulphur and sulphur preparations, tebuconazole, tecloftalam, tecnazene, tetraconazole, thiabendazole, thicyofen, thiophanate-methyl, thiram, tolclophos-methyl, tolylfluanid, triadimefon, triadimenpl, triazoxide, trichlamide, tricyclazole, tridemorph, triflumizole, triforine, triticonazole, validamycin A, vinclozolin, zineb, ziram. Bactericides: bronopol, dichlorophen, nitrapyrin, nickel dimethyldithiocarbamate, kasugamycin, octhilinone, furanecarboxylic acid, oxytetracyclin, probenazole, streptomycin, tecloftalam, copper sulphate and other copper preparations. Insecticides/Acaricides/Nematicides: abamectin, acephate, acrinathrin, alanycarb, aldicarb, alphamethrin, amitraz, aver- mectin, AZ 60541, azadirachtin, azinphos A, azinphos M, azocyclotin, Bacillus thuringiensis, 4-bromo-2-(4-chlorophenyl)-1 -(emoxymethyl)-5-(trifluoro- methyl)-lH-pyrrole~3-carbonitrile, bendiocarb, benfuracarb, bensultap, betacyfluthr- in, bifenthrin, BPMC, brofenprox, bromophos A, bufencarb, buprofezin, buto- carboxin, butylpyridaben, cadusafos, carbaryl, carbofuran, carbophenothion, carbosulfan, cartap, chloethocarb, chloroethoxyfos, chlorofenvinphos, chlorofluazuron, chloromephos, N-[(6-chloro-3-pyridinyl)-methyl]-N'-cyano-N-methyl-ethanimidamide, chloro- pyrifos, chloropyrifos M, cis-resmethrin, clocythrin, clofentezine, cyanophos, cycloprothrin, cyfluthrin, cyhalothrin, cyhexatin, cypermethrin, cyromazine, deltamethrin, demeton-M, demeton-S, demeton-S-methyl, diafenthiuron, diazinon, dichlofenthion, dichlorvos, dicliphos, dicrotophos, diethion, diflubenzuron, dimethoate, dimethylvinphos, dioxathion, disulfoton, edifenphos, emamectin, esfenvalerate, ethiofencarb, ethion, ethofenprox, ethoprophos, etrimphos, fenamiphos, fenazaquin, fenbutatin oxide, fenitrothion, fenobucarb, fenothiocarb, fenoxycarb, fenpropathrin, fenpyrad, fenpyroximate, fenthion, fenvalerate, fipronil, fluazinam, fluazuron, flucycloxuron, flucythrinate, flufenoxuron, flufenprox, flu- valinate, fonophos, formothion, fosthiazate, fubfenprox, furathiocarb, HCH, heptenophos, hexaflumuron, hexythiazox, imidacloprid, iprobenfos, isazophos, isofenphos, isoprocarb, isoxathion, ivermectin, lambda-cyhalothrin, lufenuron, malathion, mecarbam, mevinphos, mesulfenphos, metaldehyde, methacrifos, methamidophos, methidathion, methiocarb, methomyl, metolcarb, milbemectin, monocrotophos, moxidectin, naled, NC 184, nitenpyram, omethoate, oxamyl, oxydemethon M, oxydeprofos, parathion A, parathion M, permethrin, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimicarb, pirimiphos M, pirimiphos A, profenofos, promecarb, propaphos, propoxur, prothiofos, prothoate, pymetrozin, pyrachlophos, pyridaphenthion, pyresmethrin, pyrethrum, pyridaben, pyrimidifen, pyriproxifen, quinalphos, salithion, sebufos, silafluofen, sulfotep, sulprofos, tebufenozid, tebufenpyrad, tebupirimiphos, teflubenzuron, tefluthrin, temephos, terbam, terbufos, tetrachlorvinphos, thiafenox, thiodicarb, thiofanox, thiomethon, thionazin, thuringiensin, tralomethrin, triarathen, triazophos, triazuron, trichlorfon, triflumuron, trimethacarb, vamidothion, XMC, xylylcarb, zetamethrin. A mixture with other known active compounds, such as herbicides or with fertilizers or growth regulators is also possible. The active compounds can be used as such, in the form of their commercially available formulations or the use forms prepared therefrom, such as ready-to-use solutions, suspensions, wettable powders, pastes, soluble powders, dusts and granules. They are used in the customary manner, for example by pouring, spraying, atomizing, scattering, foaming, brushing on and the like. It is also possible to apply the active compounds by the ultra-low volume method, or to inject the active compound formulation or the active compound itself into the soil. The seed of the plants can also be treated. In the treatment of parts of plants, the active compound concentrations in the use forms can be varied within a substantial range: They are, in general, between 1 and 0.0001 % by weight, preferably between 0.5 and 0.001 % by weight. In the treatment of seed, amounts of active compound of 0.001 to 50 g per kilogram of seed, preferably 0.01 to 10 g, are generally required. For the .treatment of soil; aoti^ cb^ % by weight, § preferably CCKOOOl tbfs0^02 %byf weight, {are requif|et!|ai|the site of action, Preparation Examples: Example 1 (Formula Removed) Process a) 136.8 g (0.56 mol) of 4-(2-chlorophenoxy)-5,6-difluoropyrimidine are added all at once to a mixture of 135.3 g (0.56 mol) of 3-[l-(2-hydroxyphenyl)-l-(methox-imino)-methyl]-5,6-dihydro-l,4,2-dioxazine and 197.6 g of ground potassium carbonate in 460 ml of acetonitrile at 20°C, during which process the temperature rises to 31°C. The mixture is stirred for a further 6 hours at 50°C and then without further heating overnight, during which process the mixture cools. The reaction mixture is added to 2.3 1 of ice-water and stirred for 5 hours, the product crystallizing out. This product is filtered off with suction and washed with 0.57 1 of water in portions. 260 g (97.8 % of theory) of 3-{l-[2-(4--5-fiuoropyrimid-6-yloxy)-phenyl]-l-(methoximino)-methyl}-5,6-dihydro-l,4,2-di-oxazine of melting point 75°C are obtained. Example 2 (Formula Removed) 0.119 g of potassium hydride (60% suspension in mineral oil) is added to a solution of 0.7 g (0.00298 mol) of 3-[l-(2-hydroxyphenyl)-2-methoxyethen-l-yl]-5,6-dihydro-l,4,2-dioxazine and 0.6 g (0.00288 mol) of 4-phenoxy-5,6-difiuoro-pyrimidine in 10 ml of dimethylformamide at 0°C, and the mixture is then stirred for 12 hours at 20°C. The reaction mixture is poured into water and extracted using ethyl acetate. The combined organic phases are dried over sodium sulphate and concentrated under reduced pressure. The residue is chromatographed on silica gel using cyclohexane/ethyl acetate (1:1). 0.4 g (82 % of theory) of 3-{l-[2-(4-phenoxy-5-fluoropyrimid-6-yloxy)-phenyl]-2-methoxyethen-l-yl}-5,6-dihydro-1,4,2-dioxazine is obtained. ;H NMR spectrum (CDC13/TMS): 5 - 3.678 (3H); 4.056/4.069/4.083 (2H); 4.300/4.314/4.328 (2H); 6.891 (1H); 7.199 - 7.475 (9H); 8.063 (1H) ppm. Example 3 (Formula Removed) Process b) A mixture of 124.1 g (0.333 mol) of 3-{l-[2-(4,5-difluoropyrimid-6-yloxy)-phenyl]-l-(methoximino)-methyl}-5,6-dihydro-l,4,2-dioxazine, 31.3 g (0.333 mol) of phenol, 46 g (0.333 mol) of potassium carbonate and 3.3 g of copper(I) chloride in 1 1 of dimethylformamide is stirred overnight at 100°C. After the mixture has cooled to 20°C, the solvent is distilled off under reduced pressure. The residue is taken up in ethyl acetate and washed repeatedly using water. The organic phase is dried over sodium sulphate and reconcentrated under reduced pressure. The residue is chromatographed on silica gel using hexane/acetone (7:3). 112.4 g (97 % of theory) of 3-{l-[2-(4-phenoxy-5-fluoropyrimid-6-yloxy)-phenyl]-l-(methoximino)-methyl}-5,6~dihydro-l,4,2-dioxazine of melting point 110°C are obtained. The compounds of the formula (I) mentioned in Table 1 below are obtained analogously to Examples 1 to 3 and following the information given in the general description of the process. Table 1: (Table Removed) The TH NMR spectra were recorded in deuterochloroform (CDC13) or hexa-deuterodimethyl sulphoxide (DMSO-d6) using tetramethylsilane (TMS) as the internal standard. The data given is the chemical shift as 5 value in ppm. Preparation of the starting compounds of Formula (Ha): (Formula Removed) Example (IIa-1): Process a-1) 7.5 g (0.0235 mol) of 3-{l-[2-(tetrahydropyran-2-yloxy)-phenyl]-2-methoxyethen-l-yl}-5,6-dihydro-l,4,2-dioxazine are stirred for 16 hours at 20°C in 20 ml of methanol together with 0.15 g of acidic ion-exchanger resin. The ion-exchanger resin is filtered off and the filtrate is concentrated under reduced pressure. The residue is chromatographed on silica gel using cyclohexane/ethyl acetate (1:1). 1 g (18 % of theory) of 3~[l-(2-hydroxyphenyl)-2-methoxyethen-l-yl]-5,6-dihydro-1,4,2-dioxazine. 1H NMR spectrum (CDCl/TMS): 5 - 3.794 (3H); 4.102-4.130 (2H); 4.383-4.411 (1H); 6.846 1H); 6.885-6.994 (2H); 7.157-7.260 (2H) ppm. Preparation of starting materials of Formula (HP Example (III-1) (Formula Removed) A solution of 42.4 g (0.45 mol) of phenol and 50.4 g (0.45 mol) of potassium tert-butoxide in 400 ml of tetrahydrofuran is added dropwise at 0°C to a solution of 80 g (0.6 mol) of 4,5,6-trifluoropyrimidine in 1 1 of tetrahydrofuran. When the addition was complete, the reaction mixture was stirred for 30 minutes at 0°C and then poured into water and extracted using ethyl acetate. The organic phase is dried over sodium sulphate and concentrated in vacuo, and the residue is stirred with low-boiling petroleum ether. 63.8 g (68.1 % of theory) of 4-phenoxy-5,6-difluoropyrimidine of melting point 65-66°C are obtained. The compounds of the formula are obtained analogously to Example (III-l). (Table Removed) Preparation of the starting materials of Formula (IV): Example (IV-1): Process b-1) (Formula Removed) A solution of 47.2 g (0.2 mol) of 3-[l-(2-hydroxyphenyl)-l-(methoximino)-methyl]-5,6-dihydro-l,4,2-dioxazine (WO-A 9504728) in 1 1 of tetrahydrofuran is treated, at 0°C, first with 29.3 g (0.22 mol) of 4,5,6-trifluoropyrimidine and subsequently with 6.0 g (0.2 mol) of sodium hydride (80 % suspension in mineral oil), a little at a time. The mixture is stirred for 3 hours at 0°C and subsequently overnight without further cooling. The residue is taken up in ethyl acetate and washed repeatedly with water. The organic phase is dried over sodium sulphate and reconcentrated under reduced pressure, after which a viscous oil remains which crystallizes slowly. 68.7 g (98 % of theory) of 3-{l-[2-(4,5-difluoropyrimid-6-yloxy)-phenyl]-l-(methoximino)-methyl}-5,6-dihydro-l,4,2-dioxazine of melting point 98°C are obtained. 3-{l-[2-(5-chloro-4-fluoropyrimid-6-yloxy)-phenyl]-l-(methoximino)-methyl}-5,6-dihydro-l,4,2-dioxazine, Example (IV-2), was obtained analogously to Example (IV-1) in the form of a highly viscous oil. ]H NMR spectrum (CDC13/TMS): 5-3.80 (s, 3H) ppm. Preparation of the precursors of Formula (VI): Example (VI-1): Process a-2) (Formula Removed) A mixture of 31.2 g (0.091 mol) of methoxymethylene-triphenyl-phosphonium chloride and 10.2 g (0.091 mol) of potassium tert-butoxide in 100 ml of tetrahydrofuran is stirred for 20 minutes at 20°C. A solution of 13.3 g (0.0457 mol) of 3-[2-(tetrahydropyran-2-yloxy)-benzoyl]-5,6-dihydn>l,4,2-dioxazine in 100 ml of tetrahydrofuran is then added, and the mixture is refiuxed at the boil for 12 hours. The mixture is concentrated under reduced pressure and the residue is partitioned between water and ethyl acetate. The organic phase is separated off and dried over sodium sulphate. The residue is chromatographed on silica gel using cyclohexane/ethyl acetate (1:1). 9.2 g (63% of theory) of 3-{l-[2-(tetrahydropyran-2-yloxy)-phenyl]-2-methoxyethen-l-yl}-5,6-dihydro-l,4,2-dioxa-zine are obtained. 1H NMR spectrum (CDC13/TMS): 5 = 1.5 - 1.92 (6H); 3.5 - 4.0 (2H); 3.730 (3H); 4.056 - 4.111 (2H); 4.295 - 4.325 (2H); 5.410/5.420 (1H); 6.963 (1H); 6.950 -7.461 (4H) ppm. Preparation of the precursors of Formula (VED Example (VII-1)- Process a-3) (Formula Removed) 5 g (0.0193 mol) of l-(tetrahydropyran-2-yloxy)-2-bromobenzene (Synthesis 1987, page 951) are dissolved in 20 ml of tetrahydrofuran, and the solution is cooled to -40°C. First, 10.8 g (0.0388 mol) of N-butyllithium (23 % strength solution in hexane) and then a 50 % strength solution of 7.2 g (0.0195 mol) of l-(5,6-dihydro-l,4,2-dioxazin-3-yl)-l-(pyrrolidin-l-yl)-methanone in tetrahydrofuran are added dropwise at this temperature, and the mixture is stirred for 10 minutes at -40°C. A solution of 4.2 g (0.0785 mol) of ammonium chloride in 25 ml of water is then added dropwise, diethyl ether is added, the organic phase is separated off, and the aqueous phase is extracted repeatedly using diethyl ether. The combined organic phases are dried over sodium sulphate and concentrated under reduced pressure. The residue crystallizes upon trituration with pentane. The crystals are filtered off and washed twice using 5 ml of diisopropyl ether. 2.4 g (35.8 % of theory) of 3-[2-(tetrahydropyran-2-yioxy)-benzoyl]-5,6-dihydro-l,4,2-dioxazine (content according to HPLC analysis: 84 %) are obtained. lH NMR spectrum (CDC13/TMS): 5 - 1.565-1.954 (6H); 3.54-3.68 (1H); 3.78-4.0 (1H); 4.154-4.354 (2H); 4.448-4.510 (2H); 5.512 (1H); 7.004-7.056 (1H); 7.199/-7.227 (1H); 7.408-7.463 (2H) ppm. Preparation of the precursors of Formula (IX) Example (IX-1): Process a-4) (Formula Removed) 44.9 g (0.8 mol) of potassium hydroxide are dissolved in 107 ml of methanol, 27.8 g (0.4 mol) of hydroxylammonium chloride are dissolved in 180 ml of methanol, and the two solutions are combined at 35°C to 40°C. Then, 34.2 g (0.2 mol) of ethyl oxopyrrolidin- 1-ylacetate (EP-A 469889) are added at 10 to 20°C, and the mixture is stirred for 30 minutes at 20°C. 27.6 g (0.2 mol) of potassium carbonate and 169.1 g (0.9 mol) of dibromoethane are subsequently added, and the mixture is boiled for 4 hours under reflux. The salts are removed by filtration, the filtrate is concentrated under reduced pressure, the residue is taken up in 600 ml of ethyl acetate, and the organic phase is washed in succession with 50 ml of saturated aqueous sodium chloride solution and with 50 ml of semi-saturated aqueous sodium chloride solution. The organic phase is dried over sodium sulphate, and the solvent is distilled off in vacuo, finally under a high vacuum at 2 Torr and 60°C. 20.9 g (52.2 % of theory) of l-(5,6-dihydro-l,4,2-dioxazin-3-yl)-l-(pyrrolidin-l-yl)-methanone (content according to HPLC analysis: 92 %). 1H NMR spectrum (CDC13/TMS): 5 = 1,841-1,978 (4H); 3.491-3.547 (2H); 3.709-3.793 (2H); 4.166-4.194 (2H); 4.460-4.487 (2H) ppm. Preparation of a precursor of Formula (XHD Example (XIII-1) A mixture of 60^ * in 2.3 I of suiphoiane is dried by distilling off 500 ml of liquid at 145°C and 20 mbar. 1054 g of 5-chloro-4,6-di-fluoropyrimidine (DE-A 3843558) and 25 g of tetraphenylphosphonium bromide are subsequently added, 5 bar of nitrogen is injected and the mixture is stirred for 24 hours at 240°C, during which process the pressure rises to 11 bar. The reaction mixture is cooled to 80°C and the pressure is released. The mixture is now reheated slowly under atmospheric pressure, during which process the product distils off. When the bottom temperature has reached 200°C, the pressure is reduced to 150 mbar to accelerate the distillation and to obtain further product. In total, 664 g (70.7 % of theory) of 4,5,6-trifluoropyrimidine of boiling point 86 to 87°C are obtained. Use Examples Example A Phytophthora Test (tomato)/protective Solvent: 4.7 parts by weight of actone Emulsifier: 0.3 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 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. After the spray coating has dried on, the plants are inoculated with an aqueous spore suspension of Phytophthora infestans. The plants are placed in an incubation cabin at about 20°C and 100 % relative atmospheric humidity. The test is evaluated 3 days after inoculation. In this test, an efficacy of over 90 % is shown, for example, by the compounds of Preparation Examples (1), (2), (3), (6), (8), (10), (17), (40), (41), (43), (47), (49), (55), (63), (76), (77) and (78) at an active compound concentration of 100 ppm. Example B Plasmopara test (vines)/protective Solvent: 4.7 parts by weight of acetone Emulsifier: 0.3 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 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. After the spray coating has dried on, the plants are inoculated with an aqueous spore suspension of Plasmopara viticola and then remain in a humidity chamber at 20 to 22°C and 100 % relative atmospheric humidity for 1 day. The plants are then placed in a greenhouse at 21°C and about 90 % atmospheric humidity for 5 days. The plants are then moistened and placed in a humidity chamber for 1 day. The test is evaluated 6 days after inoculation. In this test, an efficacy of up to 100 % is shown, for example, by the compounds of Preparation Examples (1), (2), (3), (4), (5), (6), (8), (10), (11), (14), (15), (16), (17), (18), (22), (23), (26), (28), (32), (33), (38), (39), (40), (41), (43), (45), (47), (48), (49), (53), (55), (63), (76), (77) and (78) at an exemplary active compound concentration of 100 ppm. Example C Sphaerotheca test (cucumber) / protective Solvent: 4.7 parts by weight of acetone Emulsifier: 0.3 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 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. After the spray coating has dried on, the plants are dusted with conidia of the fungus Sphaerotheca fuliginea. The plants are then placed in a greenhouse at 23 to 24°C and at a relative atmospheric humidity of about 75 %. The test is evaluated 10 days after inoculation. In this test, an efficacy of up to 100 % is shown, for example, by the compounds of Preparation Examples (1), (2), (3), (8), (10), (13), (15), (17), (22), (23), (26), (28), (32), (37), (41), (47), (48) and (49) at an active compound concentration of 100 ppm. Example D Venturia test (apple) / protective Solvent: 4.7 parts by weight of acetone Emulsifier: 0.3 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 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. After the spray coating has dried on, the plants are inoculated with an aqueous conidia suspension of the pathogen causing apple scab (Venturia inaequalis) and then remain in an incubation cabin at 20°C and 100 % relative atmospheric humidity for 1 day. The plants are then placed in a greenhouse at 20°C and a relative atmospheric humidity of about 70 %. The test is evaluated 12 days after inoculation. In this test, an efficacy of up to 100 % is shown, for example, by the compounds of Preparation Examples (1), (2), (3), (4), (5), (6), (8), (10), (11), (13), (14), (15), (16), (17), (18), (22), (26), (28), (32), (33), (37), (38), (39), (41), (43), (45), (47), (48), (49), (53), (55), (63), (77) and (78) at an active compound concentration of 10 ppm. Example E Erysiphe test (barley) / protective Solvent: 10 parts by weight of N-methylpyrrolidone Emulsifier: 0.6 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 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 at the application rate indicated. After the spray coating 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 about 20°C and a relative atmospheric humidity of about 80 %, in order to promote the development of powdery mildew pustules. The test is evaluated 7 days after the inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by compound (59) at an application rate of active compound of 250 g/ha. Example F Erysiphe test (barley) / curative Solvent: 10 parts by weight of N-methylpyrrolidone Emulsifier: 0.6 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 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 inoculation, the plants are sprayed with the preparation of active compound at the application rate indicated. The plants are placed in a greenhouse at a temperature of about 20°C and a relative atmospheric humidity of about 80 %, in order to promote the development of powdery mildew pustules. The test is evaluated 7 days after the inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compounds of Preparation Examples (1) and (6) at an application rate of active compound of 250 g/ha. Example G Fusarium nivale (var. majus) test (wheat)/protective Solvent: 10 parts by weight of N-methylpyrrolidone Emulsifier: 0.6 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 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 at the application rate indicated. After the spray coating has dried on, the plants are sprayed with a conidia suspension of Fusarium nivale var. majus. The plants are placed in a greenhouse at a temperature of about 15°C and a relative atmospheric humidity of about 100 % under translucent incubation hoods. The test is evaluated 4 days after inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compounds of Preparation Examples (8), (11), (14), (15), (24), (33), (41), (42) and (55) at an exemplary application rate of active compound of 250 g/ha. Example H Fusarium nivale (var. majus) test (wheat)/curative Solvent: 10 parts by weight of N-methylpyrrolidone Emulsifier: 0.6 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 amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration. To test for curative activity, young plants are sprayed with a conidia suspension of Fusarium nivale var. majus. The plants remain in an incubation cabin at 15°C and a relative atmospheric humidity of 100 % for 24 hours. The plants are subsequently sprayed with the preparation of the active compound at the application rate indicated. After the spray coating has dried on, the plants remain in a greenhouse under translucent incubation hoods at a temperature of about 15°C and a relative atmospheric humidity of about 100 %. The test is evaluated 4 days after inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compound of Preparation Example (43) at an exemplary application rate of active compound of 250 g/ha. Example I Fusarium nivale (var. nivale) test (wheat)/protective Solvent: 10 parts by weight of N-methylpyrrolidone Emulsifier: 0.6 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 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 at the application rate indicated. After the spray coating has dried on, the plants are sprayed with a conidia suspension of Fusarium nivale var. nivale. The plants are placed in a greenhouse at a temperature of about 15°C and a relative atmospheric humidity of about 100 % under translucent incubation hoods. The test is evaluated 4 days after inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compounds of Preparation Examples (10), (11), (15), (24), (32), (34), (43) and (55) at an exemplary application rate of active compound of 250 g/ha. Example K Fusarium nivale (var. nivale) test (wheat)/curative Solvent: 100 parts by weight of dimethylformamide Emulsifier: 0.25 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 amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration. To test for curative activity, young plants are sprayed with a conidia suspension of Fusarium nivale var. nivale. The plants remain in an incubation cabin at 15°C and a relative atmospheric humidity of 100 % for 24 hours. The plants are subsequently sprayed with the preparation of the active compound until dew-moist. After the spray coating has dried on, the plants remain in a greenhouse under translucent incubation hoods at a temperature of about 15°C and a relative atmospheric humidity of about 100 %. The test is evaluated 4 days after inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compounds of Preparation Examples (24), (30), (31), (34) and (43) at an exemplary application rate of active compound of 250 g/ha. Example L Pseudocercosporella herpotrichoides test (wheat)/protective Solvent: 10 parts by weight of N-methylpyrrolidone Emulsifier: 0.6 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 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 at the application rate indicated. After the spray coating has dried on, the plants are inoculated on the stem base with spores of Pseudocercosporella herpotrichoides. The plants are placed in a greenhouse at a temperature of about 10°C and a relative atmospheric humidity of about 80 %. The test is evaluated 21 days after inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compounds of Preparation Examples (15), (69) and (71) at an application rate of active compound of 250 g/ha. Example M Puccinia test (wheat) / protective Solvent: 10 parts by weight of N-methylpyrrolidone 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 activity, young plants are inoculated with a spore suspension of Puccinia recondita in a 0.1 % strength aqueous agar solution. After the spore suspension has dried on, the plants are sprayed with the preparation of active compound at the application rate indicated. The plants remain in an incubation cabin at 20°C and 100 % relative atmospheric humidity for 24 hours. The plants are placed in a greenhouse at a temperature of about 20°C and a relative atmospheric humidity of about 80 % to promote the development of rust pustules. The test is evaluated 10 days after the inoculation. In this test, an efficacy of 100 % in comparison with the untreated control is shown, for example, by the compounds of Preparation Examples (6) and (17) at an application rate of active compound of 250 g/ha. Example N Pyricularia test (rice) / protective Solvent: 12.5 parts by weight of acetone Emulsifier: 0.3 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 amounts of solvent, and the concentrate is diluted with water and the stated amount of emulsifier to the desired concentration. To test for protective activity, young rice plants are sprayed with the preparation of active compound until dew-moist. 1 day after the spray coating has dried on, the plants are inoculated with an aqueous spore suspension of Pyricularia oryzae. The plants are then placed in a greenhouse at 25°C and a relative atmospheric humidity of 100 %. The disease level is evaluated 4 days after inoculation. An efficacy of up to 100 % in comparison with the untreated control is shown, in this test, for example by the compound of Preparation Examples (2), (16), (17), (18), (19), (23), (24), (30), (32), (35), (41) and (48) at a concentration of active compound of 0.05 %. WE CLAIM-: 1. Process for the preparaton of halogenopyrimidines of the formula (1) (Formula Removed) in which A represents optionally substituted alkanediyl, R represents in each case optionally psubstituted cycloalkyl, aryl or benzo- fused heterocyclyl, E represents -CH= or nitrogen, Q represents oxygen, sulphur, -CH2-0-, a single bond, or a nitrogen atom which is optionally substituted by alkyl, and X represents halogen, characterized in that a) hydroxy compounds of the general formula (II) (Formula Removed) in which A and E have the meanings as given above are reacted with a substituted halqgenopyrirnidine of the general formula III in which R, Q and X have the meanings as stated earlier and Y1 represents halogen, in the presence of a diluent and an acid acceptor. 2. Process for the preparation of halogenopyrimidines substantially as herein described with reference to the foregoing examples!, 2, IIa-1, III-1. VI-1, VIM and IX-1.

Documents:

113-del-1997-abstract.pdf

113-del-1997-claims.pdf

113-del-1997-complete-spacition(granted).pdf

113-del-1997-correspondence-others.pdf

113-del-1997-correspondence-po.pdf

113-del-1997-description (complete).pdf

113-del-1997-form-1.pdf

113-del-1997-form-2.pdf

113-del-1997-form-3.pdf

113-del-1997-form-4.pdf

113-del-1997-form-6.pdf

113-del-1997-pa.pdf

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