 Quaternary nitrogen heterocycles, processes for their preparation and their use as pesticides
专利摘要:
Compound of Formula (I): Formula I In the above formula, A is CH and D is N + R, A is nitrogen and D is N + R, or A is N + R and D is nitrogen, R is -CR 4 R 5 -ER 6 and Q n- is Inorganic or organic anions, n is 1, 2, 3 or 4, and R 1 -R 6 , E, X, Y and Z are as described above. 公开号:KR20000053299A 申请号:KR1019990704285 申请日:1997-11-03 公开日:2000-08-25 发明作者:야코비하랄드；오르트오스왈드；샤퍼볼프강；브라운랄프；크라우트스트룬크게르하르트；매르클마르틴；스타르크헤르베르트；산프트울리흐；퇴네센마리-테레시아；케른만프레드；보닌베르너 申请人:슈미트；훽스트 쉐링 아그레보 게엠베하；루츠； IPC主号:
专利说明:
QUATERNARY NITROGEN HETEROCYCLES, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS PESTICIDES} Certain 4-amino- and 4-alkoxy-heterocycles are already known to have bactericidal, insecticidal (eg EP-A-57 440, EP-A-196 524, EP-A-264 217, EP -A-326 329, EP-A-323 757, EP-A-432 894, DE-A-4 116 089, WO 93/04 580). However, the biological action of these compounds, especially at low application rates and concentrations, is not satisfactory in all application examples. The novel, positively charged nitrogen heterocycles of formula (I) are as follows: Wherein the radicals and groups are as defined below and exhibit good resistance to plants and good toxicity to warm-blooded animals inhibits animal pests such as insects, arachnids, nematodes, parasites and mollusks, and in the veterinary field parasites And highly suitable for inhibiting in vitro parasites and inhibiting harmful bacteria. The present invention therefore relates to compounds of formula (I): (1) A is CH and D is N + R, or A is nitrogen and D is N + R, or A is N + R and D is nitrogen; R is ego; (2) Q n- is any inorganic or organic anion and n is 1, 2, 3 or 4; (3) R 1 is hydrogen, halogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl or (C 3 -C 5 ) -cycloalkyl; (4) R 2 and R 3 are the same or different and are each hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 2 -C 4 ) -alkenyl, ( C 2 -C 4) - haloalkenyl, (C 2 -C 4) - alkynyl, (C 2 -C 4) - haloalkynyl, (C 1 -C 8) - trialkyl silil alkynyl, preferably dimethyl - (C 1 -C 8) - alkyl silil alkynyl, (C 1 -C 4) - alkoxy, (C 1 -C 4) - haloalkoxy, (C 1 -C 4) - alkoxy - (C 1 - C 4 ) -alkyl, (C 1 -C 4 ) -haloalkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -haloalkoxy- (C 1 -C 4 ) -haloalkyl, halogen, hydroxyl, (C 1 -C 4 ) -hydroxyalkyl, (C 1 -C 4 ) -alkanoyl, (C 1 -C 4 ) -alkanoyl- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkanoyl, (C 3 -C 5 ) -cycloalkyl, (C 3 -C 5 )- Halocycloalkyl, cyano, (C 1 -C 4 ) -cyanoalkyl, nitro, (C 1 -C 4 ) -nitroalkyl, thiocano, (C 1 -C 4 ) -thiocyanoalkyl, ( C 1 -C 4 ) -alkoxycarbonyl, (C 1 -C 4 ) -alkoxycarbonyl- (C 1 -C 4 ) -alkyl , (C 1 -C 4 ) -haloalkoxycarbonyl, (C 1 -C 4 ) -alkylthio, (C 1 -C 4 ) -alkylthio- (C 1 -C 4 ) -alkyl, (C 1- C 4 ) -haloalkylthio, (C 1 -C 4 ) -alkylsulfinyl, (C 1 -C 4 ) -haloalkylsulfinyl, (C 1 -C 4 ) -alkylsulfonyl or (C 1 -C 4 ) -haloalkylsulfonyl; or R 2 and R 3 together with the attached carbon atoms may contain oxygen or sulfur atoms instead of CH 2 if they are five-membered rings, or one or two nitrogen atoms instead of one or two CH units if they are six-membered rings; 1, 2 or 3 same or different radicals (these radicals being (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, preferably trifluoromethyl, halogen, (C 1- To form an unsaturated 5 or 6 membered isocyclic ring which may be substituted by C 4 ) -alkoxy or (C 1 -C 4 ) -haloalkoxy) alkyl; or R 2 and R 3 together with the carbon atoms to which they are attached may contain oxygen and / or sulfur instead of one or two CH 2 groups and may be substituted by one, two or three (C 1 -C 4 ) -alkyl groups To form a saturated 5-, 6- or 7-membered isocyclic ring which may be substituted; (5) X is O or NH, Groups Y-Z can have the following meanings: a) Y is CHR 7 , R 7 is hydrogen, (C 1 -C 4 ) -alkyl or (C 3 -C 6 ) -cycloalkyl, Z is a branched or straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, wherein at least one, preferably up to three, non-adjacent carbon units are oxygen or S (O) x where x is 0 These hydrocarbon radicals, which may be substituted by heteroatoms or carbonyl groups, such as 1 or 2, and with or without the mentioned variables, are one or more, preferably up to three (in the case of up to fluorine) Which may be substituted by halogen, hydroxyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkenyl, deca-, tetra- or dihydronaphthyl, substituted or unsubstituted Benzyloxy, substituted or unsubstituted phenylthio, substituted or unsubstituted benzylthio, imidazol-1-yl, triazol-1-yl, pyrazol-1-yl, (C 1 -C 4 ) -alkoxy Same or different radicals or groups MGR 8 selected from the group consisting of carbonyl, wherein M is oxygen or NH may be, G may be carbonyl, thiocarbonyl or sulfonyl, and R 8 is (C 1 -C 8 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, (C 1 -C 8 ) -Haloalkyl, (C 1 -C 8 ) -alkoxy, substituted or unsubstituted phenyl group, substituted or unsubstituted phenoxy group, substituted or unsubstituted alinino group, imidazol-1-yl, triazole-1- yl, pyrazol-1-yl or mono- or di - (C 1 -C 4) - If either be alkylamino, it not included in the above definition, b) Y is a (C 1 -C 6 ) -alkylene unit, branched or straight chain, up to three halogen atoms, preferably fluorine or chlorine, or hydroxyl, (C 1 -C 4 ) -alkoxy, ( May be substituted by a C 3 -C 6 ) -cycloalkyl or cyano group, Z is an unsubstituted or substituted aryl, aryloxy, heterocyclyl or unsubstituted pyridinyloxy group, the aryloxy or pyridinyloxy group is separated from X by two or more carbon atoms, or c) when X is NH, Y is a carbonyl or thiocarbonyl group, Z is in each case substituted by a substituted or unsubstituted heterocyclic or benzo fused carbocyclic or heterocyclic ring system or by a substituted or unsubstituted (C 3 -C 8 ) -cycloalkyl or cycloalkenyl radical Substituted or unsubstituted aryl- (C 1 -C 4 ) -alkyl radicals, (C 1 -C 4 ) -alkyl radicals. In the formula, the term “(C 1 -C 4 ) -alkyl” in the radicals and substituents described under group YZ under a) refers to straight or branched hydrocarbon radicals having 1 to 4 carbon atoms (eg, methyl, ethyl, propyl, iso Propyl, 1-butyl, 2-butyl, 2-methylpropyl or tert-butyl radicals); The term “(C 3 -C 6 ) -cycloalkyl” is a cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl group; "A branched or straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, wherein at least one, preferably up to three, non-adjacent saturated carbon units are oxygen or S (O) x where x is 0 It may be substituted by a heteroatom or a carbonyl group such as ", 1 or 2", for example methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl or undecyl radical or branched Radicals (eg sec-butyl, tert-butyl, isobutyl, isopentyl, 7-methyloctyl or 10-methylundecyl radicals) or unsaturated radicals (eg allyl, 3,7-dimethyl-6-octene-1 Sulfur, sulfoxide or sulfonyl, such as -yl radical or, for example, 4- (propylthio) butyl, 7- (methylthio) -heptyl, 7- (methylsuloxy) heptyl or 7- (methylsulfonyl) heptyl radical Hexyloxymethyl, methoxyhexyl, butoxypropyl, 2- (ethoxyethoxy) ethyl or 3- (methoxyethoxy) prop containing groups Means a propargyl radical or a radical containing a carbonyl group such as 6-oxo-8-oxo-cyclopentyl or nonil radical or a radical containing one or more oxygen, such as a radical or radicals, and; The term "(C 3 -C 6 ) -cycloalkenyl" means, for example, a cyclopenten-4-yl group, a cyclohexen-3-yl group or a cyclohexen-4-yl group; "Substituted benzyloxy group" means, for example, 4-chloro, 4-fluoro, 4-methyl, 4-trifluoromethyl or 2,4-dimethylbenzyloxy group; Further, the group MGR 8 is for example N, N-dimethylcarbamoyloxy, N, N-dimethylthiocarbamoyloxy, imidazol-1-yl-carbonyloxy, benzoyloxy, pivaloyloxy, 4-methylphenyl Carbamoyloxy, methylsulfonyloxy or 4-methylphenylsulfonyloxy; Further at substituents and radicals described under group Y Z under b), Can be substituted by up to three halogen atoms, preferably fluorine or chlorine, or by hydroxyl, (C 1 -C 4 ) -alkoxy, (C 3 -C 6 ) -cycloalkyl or cyano group (C 1 -C 6 ) -alkylene units, branched or straight chain ”is, for example, methylene, ethylene, CH (CH 3 ), propylene, CH (C 2 H 5 ), butylene, CH (CH 3 ) (CH 2 ) 2 ,-(CH 2 ) 2 -CH (CH 3 ), CH 2 CH (CH 3 ) CH 2 , ; CH (CH 2 OH) CH 2 , CH (CH 2 OH) CH 2 CH 2 , CH (CH 2 CN) CH 2 or CH (CH 2 CN) CH 2 CH 2 ; "Aryl group" means naphthyl or preferably phenyl group; "Substituted aryl group" means naphthyl or, preferably, a phenyl group, even when all hydrogen atoms are fluorine as substituents, up to three hydrogen atoms are substituted by the same or different substituents, and possible substituents are halogen , (C 3 -C 8 ) -cycloalkyl, (C 3 -C 8 ) -cycloalkenyl, group UW (where U is a direct bond, oxygen, S (O) x (where x is 0, 1 or 2), (C 1 -C 4 ) -alkylene or (C 1 -C 4 ) -alkyleneoxy, W is substituted or unsubstituted aryl or heteroaryl, preferably pyridinyl, pyrimidinyl, thiene One or furyl; Nitro, cyano, hydroxyl, (C 1 -C 8 ) -alkanoyloxy, group R 9 is (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy, cycloalkyl, phenyl or substituted phenyl, group NR 10 R 11 , wherein R 10 and R 11 are each hydrogen, (C 1 -C 4 ) -alkyl or (C 1 -C 4 ) -aryl); Group LS (O) y R 12 , wherein L is a direct bond or oxygen, R 12 is (C 1 -C 8 ) -alkyl, aryl, substituted aryl, benzyl or substituted benzyl, y is 1 or 2 May be); SiR 13 R 14 R 15 or OSiR 13 R 14 R 15 wherein R 13 , R 14 and R 15 are each independently (C 1 -C 8 ) -alkyl, (C 3 -C 8 ) -cycloalkyl or substituted Unsubstituted phenyl); Saturated or unsaturated C 1 -C 12 -hydrocarbon radicals and one or two saturated carbon units, which may be branched or straight chain, are selected from oxygen, sulfur or groups SO, SO 2 , NR 10 ′ or SiR 13 ′ R 14 ′ . Wherein R 10 ' , R 13' and R 14 ' are as defined above for R 10 , R 13 and R 14 , and a hydroxyl group, (C 3 -C 8 ) -cycloalkyl, ( C 3 -C 8 ) -cycloalkenyl, (C 1 -C 4 ) -acyl, (C 1 -C 4 ) -alkoxycarbonyl, phenyl, substituted phenyl, phenoxy, substituted phenoxy, phenylthio, Substituted phenylthio or cyano; (C 1 -C 8 ) -alkoxy can be substituted with phenyl, substituted phenyl, phenoxy, substituted phenoxy, (C 3 -C 8 ) -cycloalkyl or (C 3 -C 8 ) -cycloalkenyl There is; (C 3 -C 8 ) -cycloalkoxy; (C 1 -C 8 ) -alkylthio can be substituted with phenyl, substituted phenyl, phenoxy, substituted phenoxy, (C 3 -C 8 ) -cycloalkyl; (C 1 -C 8 ) -alkenyloxy; (C 1 -C 8 ) -alkynyloxy or group or Wherein R 15 is hydrogen, (C 1 -C 4 ) -alkyl or (C 3 -C 6 ) -cycloalkyl, R 16 is (C 1 -C 10 ) -alkyl, (C 2 -C 12 ) -alkoxyalkyl, (C 3 -C 8 ) -alkenyloxy- (C 1 -C 4 ) -alkyl, (C 3- C 8 ) -alkynyloxy- (C 1 -C 4 ) -alkyl, (C 2 -C 12 ) -alkylthioalkyl, aryl, aryloxy- (C 1 -C 4 ) -alkyl, aryl- (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkyl, heteroaryloxy- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkoxy - (C 1 -C 4) - alkyl or aryl - (C 1 -C 4) - alkyl; In addition, two substituents of the aryl groups that are ortho to each other may be saturated or partially saturated carbocyclic or heterocyclic ring systems (e.g., tetrahydronaphthyl, tetrahydroquinoline, dihydrobenzopyran, dihydrobenzofuran, Benzodioxane, bezodioxol system) or cyclic to form a system of formula Z a or Z b and Wherein T is oxygen, sulfur, methylene or ethylene, R 17 is hydrogen, methyl, ethyl or cyanomethyl, R 18 is (C 1 -C 6 ) -alkyl or (C 1 -C 6 ) -alkylthio; The term “aryloxy” refers to a phenoxy or naphthoxy group; The term "substituted aryloxy group" means naphthoxy or preferably phenoxy group, even in the case of all fluorine, up to three hydrogen atoms can be substituted by the same or different substituents, and possible substituents are halogen, cyano, nitro, (C 1 -C 8) - alkyl, (C 1 -C 8) - alkenyl, (C 1 -C 8) - alkynyl, (C 1 -C 8) - alkoxy, (C 1 -C 8 ) -alkylthio, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkoxy- (C 1- C 4 ) -alkyl, a group of the formula M'-Ph, wherein M 'is oxygen, methylene or a direct bond, and Ph is a substituted or unsubstituted phenyl group; The term "unsubstituted heterocyclyl group" refers to a 5- or 6-membered monocyclic or 8-, 9- or 10-membered molten ring system in which an aromatic or all or part is hydrogenated, and 0 to 4 nitrogens, 0 It contains from 1 to 4 oxygen or 1 to 4 of the same or different hetero atoms selected from 0 or 2 sulfur, for example furan, thiophene, thiazole, isothiazole, oxazole, isoxazole, pyrrole, pyrazole , Imidazole, triazole, thiadiazole, oxadiazole, pyridine, pyrimidine, triazine, quinoline, quinazoline, benzothiazole, benzoxazole, benzimidazole, tetrahydrofuran, 1,3-dioxolane, Tetrahydropyran, piperidine, piperazine, morpholine, 4,5-dihydro-5-isoxazole, benzofuran, benzothiophene, benzopyran, benzodioxane, dihydrobenzofuran, benzodioxol, 1 , 2,3,4-tetrahydroquinoline or 4,5,6,7-tetrahydrofuran Or a 4,5,6,7-thiophene system; The term "substituted heterocyclyl group" refers to, for example, one of the aforementioned heterocyclic groups, and up to three (even in the case of fluorine as all substituents) hydrogen atoms may be substituted by the same or different substituents and , Possible substituents are (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkylthio, (C 1 -C 4 ) -alkoxyalkyl, halogen, cyano , Nitro, substituted or unsubstituted phenyl, or substituted or unsubstituted phenoxy; The term “unsubstituted or substituted pyridyloxy” refers to a 2-, 3- or 4-pyridyloxy group, where up to two hydrogen atoms are halogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 2 -C 4 ) -alkenyl or (C 1 -C 4 ) -alkoxy; Furthermore, in alkyl, cycloalkyl, alkylene, alkenyl, cycloalkenyl, alkynyl, saturated or unsaturated hydrocarbon radicals or for example alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkoxycarbonyl or b) Unless otherwise specified in radicals derived from such as radical substituents of the ring system under the group YZ or CH 2 -groups of the component benzodioxol group, hydrogen atoms are even in the case of fluorine as a whole in halogen, preferably chlorine or fluorine May be partially substituted, furthermore, the CH 2 group may be substituted by O, S, SO or SO 2 ; The term “unsubstituted aryl- (C 1 -C 4 ) -alkyl radicals” in substituents and radicals described under group YZ under c) is for example benzyl, naphthylmethyl, 2-phenylethyl, 1-phenylethyl or 3 -Phenylpropyl group; The term “substituted aryl- (C 1 -C 4 ) -alkyl radicals” refers to, for example, one of the aforementioned aryl- (C 1 -C 4 ) -alkyl radicals, preferably benzyl radicals, even all fluorine in the case, the hydrogen atoms of the phenyl ring may be substituted by substituents, possible substituents are halogen, (C 3 -C 8) - cycloalkyl, (C 3 -C 8) - cycloalkenyl, UW group (wherein , U is a direct bond, oxygen, S (O) x (where x is 0, 1 or 2), (C 1 -C 4 ) -alkylene or (C 1 -C 4 ) -alkyleneoxy, W is substituted or unsubstituted phenyl or substituted or unsubstituted heteroaryl, preferably pyridinyl, pyrimidinyl, thienyl or furyl), nitrile, cyano, hydroxyl, acetoxy, group Wherein R 9 is (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy, cycloalkyl, phenyl or substituted phenyl, group NR 10 R 11 , wherein R 10 and R 11 are Each independently is hydrogen, (C 1 -C 4 ) -alkyl or (C 1 -C 4 ) -aryl), a group LS (O) y R 12 , wherein L is a direct bond or oxygen, and R 12 is ( C 1 -C 8 ) -alkyl, aryl, substituted aryl, benzyl or substituted benzyl, y may be 1 or 2), SiR 13 R 14 R 15 or OSiR 13 R 14 R 15 , wherein R 13 , R 14 and R 15 are each independently of each other (C 1 -C 8 ) -alkyl, (C 3 -C 8 ) -cycloalkyl or substituted or unsubstituted phenyl), saturated or unsaturated, which may be branched or straight-chained The C 1 -C 12 -hydrocarbon radical and one or two saturated carbon units can be substituted by oxygen, sulfur or group SO, SO 2 , NR 10 or SiR 13 ′ R 14 ′ , wherein R 10 ′ , R 13 'and R 14' has the meaning given above for R 10, R 13 and R 14 Have, a hydroxyl group, (C 3 -C 8) - cycloalkyl, (C 3 -C 8) - cycloalkenyl, (C 1 -C 4) - acyl, (C 1 -C 4) - alkoxycarbonyl , Phenyl, substituted phenyl, phenoxy, substituted phenoxy, phenylthio, substituted phenylthio or cyano; phenyl, substituted phenyl, phenoxy, substituted phenoxy, (C 3- C 8) - cycloalkyl, (C 3 -C 8) - cycloalkoxy or (C 3 -C 8) - cycloalkyl which may be substituted by an alkenyl group (C 1 -C 8) - alkoxy, phenyl, substituted phenyl , phenoxy, substituted phenoxy, (C 3 -C 8) - which may be substituted by cycloalkyl (C 1 -C 8) - alkylthio; (C 3 -C 8) - cycloalkoxy; (C 1 -C 8 ) -alkenyloxy; or (C 1 -C 8 ) -alkynyloxy; the term “substituted or unsubstituted heterocyclic or benzo fused carbocyclic or heterocyclic ring system” is, for example, furyl , Thienyl, thiazolo, oxazolyl, benzodioxolyl, indanyl, tetrahydrona Butyl, benzothienyl, benzofuryl, benzoxazolyl, quinolinyl, isoquinolinyl, benzodioxanyl, benzotetrahydropyranyl, 1,2,3,4-tetrahydroquinolinyl or 2,3 Refers to a -dihydrobenzofuranyl or -thienyl radical, wherein one or two hydrogen atoms in the aromatic moiety of the ring system are independently of each other halogen, (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -Alkoxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 6 ) -alkylthio, (C 1 -C 6 ) -alkylsulfinyl, (C 1- Can be substituted by C 6 ) -alkylsulfonyl, phenyl, benzyl, phenoxy, phenylthio, nitro, cyano, (C 1 -C 4 ) -alkanoyl or (C 1 -C 4 ) -alkoxycarbonyl There is; The term “substituted or unsubstituted (C 3 -C 8 ) -cycloalkyl or cycloalkenyl radicals” is for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclopenten-4-yl Refers to a cyclohexen-4-yl or cyclohexen-3-yl radical, wherein one or two hydrogen atoms are (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkyl, halogen or (C May be substituted by 1 -C 4 ) -alkanoyl; Furthermore, alkyl, cycloalkyl, alkylene, alkenyl, cycloalkenyl, alkynyl, saturated or unsaturated hydrocarbon radicals or radicals described as, for example, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkoxycarbonyl and Radicals derived from the same, substituents or components of the ring system under group YZ under c), unless otherwise specified, the hydrogen atoms may even be partially substituted by halogen, preferably chlorine or fluorine in the case of fluorine as a whole, Furthermore, the CH 2 group can be substituted by O, S, SO or SO 2 ; Moreover, substituted phenyl, heterocyclyl, heteroaryl, phenoxy, phenylthio, benzyl, benzyloxy, benzylthio or anilino groups described as substituents under group YZ refer to radicals and even three for all fluorine Among the phenyl groups of these radicals up to hydrogen atoms are halogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -Haloalkoxy, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkylthio, (C 1 -C 4 ) -haloalkylthio, (C 1 -C 4 ) -alkylsulfonyl, (C 1 -C 4 ) -haloalkylsulfonyl, (C 1 -C 4 ) -alkylsulfinyl, (C 1 -C 4 ) -haloalkylsulfinyl, trimethylsilyl , (C 1 -C 4 ) -alkoxycarbonyl, nitro, cyano, mono- (C 1 -C 4 ) -alkylamino, di- (C 1 -C 4 ) -alkylamino, and more a) R 4 and R 5 are the same or different and are each hydrogen, branched chain, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, halogen, aryl, substituted aryl or (C 3 -C 6 )- Cycloalkyl; E is oxygen, S (O) q (where q is 0,1 or 2) or NR 19 (where R 19 is hydrogen, (C 1 -C 4 ) -alkyl, (C 2 -C 4 )- Alkenyl or (C 1 -C 4 ) -acyl), R 6 is saturated or unsaturated, branched, straight chain (C 1 -C 20 ) -hydrocarbon radical, (C 3 -C 6 ) -cycloalkyl, aryl , Substituted aryl or Wherein V is oxygen or sulfur and R 20 is a branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, aryl, substituted aryl, heterocyclyl, substituted heterocyclyl, ( C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkenyl, and at least one, preferably up to three, non-adjacent CH of the (C 1 -C 20 ) -hydrocarbon radicals mentioned under R 6 Group 2 is O, S (O) y (where y is 0, 1 or 2), NR 10 " or SiR 13" R 14 " (where R 10 , R 13" and R 14 " are R 10 , Or a carbonyl group such as a heteroatom radical such as R 13 and R 14 , and in addition, three to six carbon atoms of these hydrocarbon radicals may form a ring, These hydrocarbon radicals, with or without hydroxyl, are (C 1 -C 4 ) -alkyl, halogen, (C 1 -C 4 ) -haloalkyl, (C 3 -C 6 ) -cycloalkyl, (C 1 -C 4 ) -acyl, phenoxy, chi Substituted phenoxy, phenyl, substituted phenyl, phenylthio, substituted phenylthio and NR 21 R 22 , wherein R 21 and R 22 are each independently of each other hydrogen, (C 1 -C 4 ) -alkyl, (C 2 -C 4 ) -alkenyl, (C 1 -C 4 ) -acyl, aryl, substituted aryl, heteroaryl or benzoyl); or E is NR 19 and R 6 is If, R 19 and R 20 together may also be (C 3 -C 6 ) -alkylene, the CH 2 group adjacent to nitrogen may be substituted by CO and / or the CH 2 CH 2 group is a group CH═CH or o— Phenylene, preferably (C 3 -C 6 ) -alkylene, -CO-CH 2 -CH 2- , -CO-CH = CH- or May be substituted by Or furthermore b) R 4 is hydrogen, halogen or (C 1 -C 4 ) -alkyl, R 5 is hydrogen, halogen, branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, ( C 3 -C 6 ) -cycloalkyl, aryl or substituted aryl, E is Wherein V ′ is oxygen, sulfur or NR 23 , and R 23 is aryl, substituted aryl, heteroaryl, substituted heteroaryl, hydroxyl, (C 1 -C 4 ) -alkoxy, aryloxy, substituted aryl Oxy, heteroaryloxy, substituted heteroaryloxy or monosubstituted or disubstituted amino, R 6 is branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon, individually substituted or unsubstituted aryl or heteroaryl or (C 3 -C 8 ) -cycloalkyl; The aryl and heteroaryl radicals mentioned above may be substituted by one or more, preferably up to three (in the case of up to fluorine) the same or different radicals QR q , Q is a direct bond, NR 24 , O, S (O) s (s is 0, 1 or 2), OSO 2 , SO 2 O, NR 25 SO 2 , SO 2 NR 26 , SiR 27 R 28 or R 27 and R 28 are (C 1 -C 4 ) -alkyl or phenyl, preferably methyl, and U ′ is a direct bond, NR 29 or O; V ″ is oxygen or sulfur, preferably oxygen; W ′ is a direct bond, NR 30 or oxygen, where R 24 , R 25 , R 26 , R 29 and R 30 are the same or different and are each hydrogen, (C 1 -C) 4 ) -alkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkanoyl or (C 3 -C 6 ) -cycloalkyl; R q are substituents that are independent of each other, and each represents a halogen, hydroxyl, cyano, nitro, branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, (C 3 -C 8 ) -cycloalkyl Or (C 4 -C 8 ) -cycloalkenyl, wherein at least one, preferably up to three, non-adjacent saturated carbon units of the last three radicals are oxygen, S (O) x (where x is 0, 1 Or 2), heteroatomic units such as NR 31 or SiR 32 R 33 or carbonyl groups, and these final three radicals with or without the mentioned variables may be at least one, preferably up to three ( In the case of fluorine up to the maximum number), may be substituted by the same or different radicals T 1 R 34 , or R q is aryl or heterocyclyl, wherein these two radicals may be unsubstituted or substituted by up to three (for the maximum number of fluorine) the same or different radicals T 2 R 35 , or are attached carbon Two adjacent radicals QR q together with the atom may form a molten ring having 4 to 6 ring atoms which are carbocyclic or at least one radical selected from the group consisting of halogen, (C 1 -C 4 ) -alkyl and oxo Contains a heterocyclic atom selected from the group consisting of O, S and N, which is unsubstituted or substituted by R 24 , R 26 and R 28 may be formed independently of each other with R q located in Q in a 4-8 membered ring system, one or two CH 2 groups, preferably one CH 2 group being oxygen, S (O ) t (where t is 0, 1 or 2) or a hetero atom unit such as NR 36, and R 31 is hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy or (C 1 -C 4 ) -alkanoyl; R 32 and R 33 are each independently of each other (C 1 -C 4 ) -alkyl, preferably methyl; T 1 and T 2 in each case are independent of each other and each is a direct bond, oxygen, S (O) k , SO 2 O, OSO 2 , CO, OCO, COO, NR 37 , SO 2 NR 37 , NR 37 SO 2 , ONR 37 , NR 37 O, NR 37 CO, CONR 37 or SiR 38 R 39 and k are 0,1 or 2, R 37 is independently of each other hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkanoyl or (C 3 -C 5 ) -cycloalkyl; R 38 and R 39 are each independently of each other (C 1 -C 4 ) -alkyl; R 34 and R 35 are each independently of each other hydrogen, cyano, nitro, halogen, (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkyl, (C 2 -C 8 ) -alkenyl , (C 2 -C 8) - haloalkenyl, (C 2 -C 8) - alkynyl, (C 2 -C 8) - haloalkynyl, (C 1 -C 8) - alkoxy - (C 1 - C 4 ) -alkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 8 ) -alkylthio- (C 1 -C 4 ) -alkyl, (C 1 -C 8 ) -haloalkylthio- (C 1 -C 4 ) -alkyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 3 -C 8 ) -Cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkyl, aryl, heterocyclyl, aryl- (C 1 -C 4 ) -Alkyl or heterocyclyl- (C 1 -C 4 ) -alkyl, of these final eight radicals the alicyclic, aromatic or heterocyclic system is up to three (for maximum number of fluorine) the same or different May be unsubstituted or substituted by substituent R 40 , or R 34 and R 35 together at the same carbon atom are oxo groups, R 40 is (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -haloalkoxy, cyano, nitro or Halogen; R 36 is hydrogen, (C 1 -C 8 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkylthio, (C 3 -C 5 ) -cycloalkyl, (C 2 -C 4 ) -alkenyl, (C 2 -C 4 ) -alkynyl, (C 1 -C 4 ) -alkanoyl, (C 2 -C 4 ) -halo Alkanoyl, (C 2 -C 4 ) -alkoxyalkyl, phenyl- (C 1 -C 4 ) -alkyl or phenyl, with up to three phenyl groups (for up to fluorine) the same or different substituents R 41 Substituted or unsubstituted by R41Silver (COne-C4) -Alkyl, (COne-C4) -Haloalkyl, (COne-C4) -Alkoxy, (COne-C4) -Alkylthio, halogen or cyano; R4, R5And R6(C) mentioned under a) and b)One-C20At least one, preferably up to three non-adjacent CHs, unless otherwise defined in the) -hydrocarbon radicals2Group is S (O)y(Where y is 0, 1 or 2), NR10 '"Or SiR13 '"R14 '"Where R10 "', R13 '"And R14 '"Silver r10, R13And R14Which may be substituted by a hetero atom radical or a carbonyl group, and additionally 3 to 6 carbon atoms of these hydrocarbon radicals may form a ring and those with or without the aforementioned variables Hydrocarbon radicals are halogen, (C3-C8) -Cycloalkyl, phenoxy, substituted phenoxy, phenyl, substituted phenyl can be substituted by one or more, preferably up to three (for the maximum number of fluorine) the same or different radicals selected from the group consisting of , Moreover R under a) and b)4, R5, R6And "aryl", "substituted aryl", "aryloxy", "substituted aryloxy", "heterocyclyl", "substituted heterocyclyl", "phenyl", "substituted phenyl" described for E "," Phenoxy "," substituted phenoxy "," phenylthio "," substituted phenylthio "," branched, straight chain, saturated or unsaturated (COne-C20Radicals of the "4, R5, R6And unless otherwise specified in the components of radicals, substituents or ring systems derived from such as the alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl or alkoxycarbonyls described for E, the hydrogen atoms as a whole are in the case of fluorine. It may be partially substituted by halogen, preferably chlorine or fluorine. Preferred among the radicals R are given among the radicals mentioned under a), R 4 is hydrogen, halogen or methyl; R 5 is hydrogen, halogen, (C 1 -C 8 ) -alkyl, (C 2 -C 8 ) -alkenyl, (C 2 -C 8 ) -alkynyl, phenyl, substituted phenyl or (C 3 -C 6 ) -cycloalkyl; E is oxygen, NR 19 , S (O) q , where q is 0,1 or 2 and R 19 is hydrogen, methyl or acetyl; R 6 is (C 1 -C 4 ) -alkyl, (C 2 -C 4 ) -alkenyl, (C 1 -C 4 ) -haloalkyl, (C 3 -C 6 ) -cycloalkyl, phenyl or Wherein V is oxygen or sulfur, and R 20 is (C 1 -C 8 ) -alkyl, (C 2 -C 8 ) -alkenyl, (C 2 -C 8 ) -alkynyl, aryl, substituted aryl , Heterocyclyl, substituted heterocyclyl, (C 1 -C 8 ) -haloalkyl, (C 2 -C 8 ) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3- C 6) - cycloalkyl, (C 3 -C 6) - halocycloalkyl, (C 5 -C 6) - cycloalkenyl, (C 5 -C 6) - alkenyl is halocycloalkyl), mentioned hydrocarbon radical Silver alkyl, haloalkyl, cycloalkyl, phenoxy, substituted phenoxy, phenyl, substituted phenyl and NR 21 R 22 (R 21 and R 22 are independently of each other hydrogen, (C 1 -C 8 ) -alkyl, ( C 2 -C 8 ) -alkenyl, (C 1 -C 8 ) -acyl, aryl, heteroaryl or benzoyl), and may be substituted by one or more, preferably up to three, identical or different radicals selected from the group consisting of: There is; or E is NR 19 and R 6 is If, R 19 and R 20 together may also be (C 3 -C 6 ) -alkylene, the CH 2 group adjacent to nitrogen may be substituted by CO and / or the CH 2 —CH 2 group is a group CH═CH or o -Phenylene, preferably (C 3 -C 6 ) -alkylene, -CO-CH 2 -CH 2- , -CO-CH = CH- or It may be substituted by. Most preferred of these are the compounds of formula (I): R 4 is hydrogen; R 5 is hydrogen or (C 1 -C 8 ) -alkyl; E is oxygen and NH; And R 6 is Where V is oxygen, Furthermore, preference among the radicals R is given for the radicals mentioned under b): R 4 is hydrogen; R 5 is hydrogen, halogen, (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkyl, (C 2 -C 8 ) -alkenyl, (C 2 -C 8 ) -alkynyl ; E is or ego; R 6 is aryl or heteroaryl, and the aryl and heteroaryl radicals may be substituted by one or more, preferably up to three (for maximum number of halogens) the same or different radicals QR q , Q is a direct bond, O, OSO 2 or , U 'is a direct bond or O; V ″ is oxygen; W 'is a direct bond, NR 30 or oxygen; R 30 is hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkanoyl or (C 3 -C 5 ) -cycloalkyl; R q are independent of each other and each is (C 1 -C 20 ) -alkyl or (C 2 -C 20 ) -alkenyl and is one or more, preferably up to three (for up to fluorine) the same or different Is a substituent which may be substituted by a radical T 1 R 34 , or R q is halogen, hydroxyl, nitro or cyano or R q is aryl or heterocyclyl, wherein these two radicals may be unsubstituted or substituted by up to three (for the maximum number of fluorine) the same or different radicals T 2 R 35 ; T 1 and T 2 are independent of each other and each is a direct bond, -O-, -S (O) k- , -SO 2 O-, -OSO 2- , -CO-, -OCO-, -COO-,- a and k is 0, 1 or 2, - NR 37 -, -SO 2 NR 37 -, -NR 37 SO 2 -, -ONR 37 -, -NR 37 O-, -NR 37 CO-, -CONR 37 R 37 is independently of each other hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkanoyl or (C 3 -C 5 ) -cycloalkyl; R 34 and R 35 are each independently of each other hydrogen, halogen, preferably fluorine, (C 1 -C 8 ) -alkyl, (C 3 -C 8 ) -cycloalkyl, aryl or heterocyclyl, wherein the last three In a radical, an alicyclic, aromatic or heterocycle ring system may be unsubstituted or substituted by up to three (up to the maximum number of fluorine) with the same or different substituents R 40 , R 40 independently of one another is (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -haloalkoxy, cyano , Nitro, halogen. Of these, most preferred are those given by compounds of formula (I): R 4 is hydrogen, R 5 is hydrogen or methyl, E is ego, R 6 is aryl or heteroaryl, and the aryl and heteroaryl radicals may be substituted by one or more, preferably up to three (for maximum number of halogens) the same or different radicals QR q , Q is a direct bond, O or ego, U 'is a direct bond or O; V ″ is oxygen; W 'is a direct bond, NR 30 or oxygen; R 30 is hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkanoyl or (C 3 -C 5 ) -cycloalkyl, R q are independent of each other and each is (C 1 -C 12 ) -alkyl or (C 2 -C 12 ) -alkenyl and is one or more, preferably up to three (for up to fluorine) the same or different Is a substituent which may be substituted by radical R 34 , or R q is halogen, nitro or cyano, or R q is aryl or heterocyclyl, these two radicals may be unsubstituted or substituted by up to three (for the maximum number of fluorine) the same or different radicals T 2 R 35 , T 2 in each case is independent of each other and is a direct bond, -O-, -S (O) k- , -SO 2 O-, -OSO 2- , -CO-, -OCO-, -COO-, a and k is 0, 1 or 2, - -NR 37 -, -SO 2 NR 37 -, -NR 37 SO 2 -, -ONR 37 -, -NR 37 O-, -NR 37 CO-, -CONR 37 R 37 is independently of each other hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkanoyl or (C 3 -C 5 ) -cycloalkyl; R 34 and R 35 are each independently of each other hydrogen, halogen, preferably fluorine, (C 1 -C 8 ) -alkyl, (C 3 -C 8 ) -cycloalkyl, aryl or heterocyclyl, wherein the last three In a radical, an alicyclic, aromatic or heterocycle ring system may be unsubstituted or substituted by up to three (up to the maximum number of fluorine) with the same or different substituents R 40 , R 40 independently of one another is (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -haloalkoxy, cyano , Nitro, halogen. Preferred anions are Q n- is Hal -, NO 3 -, BF 4 -, BPh 4 - or PF 6 - is. Preferred radicals YZ are derived from the radicals described under a). R 7 is hydrogen, (C 1 -C 4 ) -alkyl or cyclopropyl, in particular R 7 is hydrogen, methyl, ethyl or cyclopropyl, Z is branched or is preferably a straight chain (C 5 -C 12 ) -alkyl radical; from radicals described under b) ba) Y is a group CH (CH 3 ), CH (C 2 H 5 ) or ego, Z is a substituted phenyl group at position 4, or bb) Y is a (C 2 -C 4 ) -alkylene group, Z is a phenoxy group which is monosubstituted or disubstituted by an alkyl radical or a radical derived from being separated from X by at least 2 carbon atoms, or bc) Y is a (C 2 -C 4 ) -alkylene group, Z is a substituted phenyl group at position 4 and Z is separated from X by at least 2 carbon atoms; from radicals described under c) Y is a carbonyl group, Z is a benzyl radical substituted at position 4 of the phenyl nucleus and further in this case A is CH. More preferred from the radicals described under ba) are given as radicals for: Y is CHCH 3 and CH (C 2 H 5 ), Z is substituted or unsubstituted phenyl, phenoxy, pyridyloxy, pyrimidinyloxy or (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -haloalkoxy or (C 1 -C 4 )- Phenyl group in each case substituted by haloalkyl. More preferred from the radicals described under bb) are given as radicals for: Y is (C 2 -C 4 ) -alkylene, The Z moves a hydrogen or methyl in position 2, and 3, position 4 (C 1 -C 4) - alkyl, (C 1 -C 4) - alkoxy or (C 1 -C 4) - alkoxy - (C 1 A phenoxy group which transfers a -C 4 ) -alkyl radical and is separated from X by at least 2 carbon atoms, More preferred from the radicals described under bc) are given by the following radicals: Y is a (C 2 -C 3 ) -alkylene group, Z is substituted at position 4 by (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -alkoxy, (C 1 -C 8 ) -haloalkoxy Phenyl group or substituted or unsubstituted phenyl or phenoxy group, which is separated from X by two or more carbon atoms. More preferred from the radicals described under c) are given by the following radicals: Y is a carbonyl group, Z is substituted at position 4 by (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -alkoxy, (C 1 -C 8 ) -haloalkoxy Benzyl radical or substituted or unsubstituted phenyl or phenoxy group, and further in this case A is CH. With respect to radicals and groups R 1 , R 2 , R 3 , A and D, preference is given to compounds of the formula (I): R 1 is hydrogen, methyl, chlorine or fluorine; R 2 and R 3 are each hydrogen, (C 1 -C 4 ) -alkyl, (C 2 -C 4 ) -alkenyl, (C 2 -C 4 ) -alkynyl, trimethylsilylethynyl, methoxycarbonyl , (C 1 -C 4 ) -haloalkyl, halogen, (C 1 -C 4 ) -alkoxy, methoxymethyl or cyano; or R 2 and R 3 together with the carbon atom to which they are attached form a five-membered ring optionally substituted unsaturated five- or six-membered ring which may contain a sulfur atom instead of a CH 2 unit; or R 2 and R 3 together with the carbon atom to which they are attached form a saturated five or six membered ring which may contain sulfur or oxygen atoms instead of CH 2 units; X is NH; Especially in these compounds R 1 is hydrogen; R 2 and R 3 are each hydrogen, methyl, ethyl, propyl, (C 2 -C 3 ) -alkenyl, (C 2 -C 3 ) -chloro or (C 2 -C 3 ) -fluoroalkenyl, (C 2 -C 3 ) -alkynyl, trimethylsilylethynyl, (C 1 -C 3 ) -chloroalkyl, (C 1 -C 3 ) -fluoroalkyl, methoxy, methoxymethyl, halogen or cyano; R 2 and R 3 together with the ring system to which they are attached form a quinazoline or quinoline system which may be substituted in the carbocyclic moiety by fluorine; or R 2 and R 3 together with the carbon atom to which they are attached form a saturated six-membered ring which may contain oxygen or sulfur atoms instead of CH 2 groups. Especially preferred are given by compounds of formula I: R 1 is hydrogen; R 2 is methyl, ethyl, propyl, isopropyl, (C 1 -C 2 ) -fluoroalkyl or methoxymethyl; R 3 is fluorine, chlorine, bromine, cyano, vinyl, ethynyl or methoxy; or R 2 and R 3 together with the ring system to which they are attached form a quinazoline system which may be substituted by a fluorine atom; A and D describe pyrimidine systems when YZ has the meanings given under a) and b), and pyridine systems when YZ has the meanings given under c); X is NH; Especially in compounds of formula (I) R 1 is hydrogen; R 2 is ethyl or methoxymethyl; R 3 is chlorine, bromine or methoxy, R 2 is ethyl, R 3 is bromine or chlorine or R 2 is methoxymethyl and R 3 is methoxy; X is NH. Some compounds of formula (I) have one or more asymmetric carbon atoms or stereoisomers on the double bond. Thus enantiomers or diastereomers may occur. The present invention includes pure isomers and mixtures thereof. The mixture of diastereomers can be separated into components by conventional methods such as selective crystallization or chromatography from a suitable solvent. The rasem may be decomposed into enantiomers by conventional methods such as forming salts with optically active acids, separating diastereomeric salts and dissociating pure enantiomers with bases. The invention further relates to a process for the preparation of a compound of formula (I) comprising reacting a compound of formula (II) with an electrophile of formula (III): In the above formulas, B is CH or N, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , X, Y, Z and E are each as defined in formula (I), and Lg is a leaving group, such as Halogen, alkylthio, alkanesulfonyloxy or arylsulfonyloxy, alkylsulfonyl or arylsulfonyl, preferably halogen, suitably add salts such as eg AgBF 4 , AgNO 3 or Nal and suitably The anions of the compounds obtained in the method are replaced with other anions similar to known methods (see, eg, Liebigs Ann. Chem. 1978, 1937; Methoden der Org. Chemie / Houben-Weyl (D. Klamann, Ed), 4th). edition, Vol. E16a, Part 2, p. 1008ff, Thieme, Stuttgart 1990]. The theory of the aforementioned substitution reactions is known (see, eg, Method der Org. Chemie / Houben-Weyl (D. Klamann, Ed.), 4th edition, Vol. E16a, Part 2, p. 997 ff., Thieme, Stuttgart, 1990, Liebigs Ann. Chem., 621 (1959) 106, Arch. Pharm. (Weinheim), 328 (1995) 531). The structures of formulas (II) and (III) may vary within wide limits. The reaction is carried out in the temperature range of 20 to 150 ° C., optionally with acetonitrile, acetone, 2-butanone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, N-methylpyrroli In an inert organic solvent such as din-2-one, dioxane, tetrahydrofuran, 4-methyl-2-pentanone, methanol, ethanol, butanol, ethylene glycol, ethylene glycol dimethyl ether, toluene, crawlobenzene or xylene Is done. Most of the compounds of formula II which are required starting materials are described in, for example, EP-A-57 440, EP-A-196 524, EP-A-264 217, EP-A-326 329, EP-A-323 757, EP-A-432 894, DE-A-116 089, WO 93/04 580, or may be similarly prepared by known methods. Compounds of formula III are commercially available or can be obtained by methods known in theory (see, eg, The Chemistry of Functional Groups, Supplement D (Patai, Rappopart) by Verne, De Kimpe). , Eds.), Part 1, p. 813 ff., Wiley, New York, 1983; Acta Chem. Scand. 20 (1966) 1273; Chem. Ber. 92 (1959) 1599; J. Am. Chem. Soc. 95 (1973) 7813; Zh. Obshch. Khim, 28 (1958) 1930; J. Am. Chem. Soc. 43 (1921) 660). The active substances of the present invention exhibit good resistance in plants and desirable toxicity in warm-blooded animals, while in the areas of agriculture, animal breeding, forestry, storage and protection of substances and hygiene, particularly insects, ticks, worms and It is suitable for insect repellents of molluscs, more preferably insects and ticks. The material is generally active against susceptible and resistant species and active against all or certain stages of development of these species. The pests are as follows: Examples of mite are Acarus siro, Argas species, Ornithodoros species, Dermanyssus gallinae, Eriophyes ribis, and phycocotulu from Eriopi. Phyllocoptruta oleivora, Boophilus species, Rhipicephalus species, Amblyomma species, Hyalomma species, Ixodes species, Psorophthes Psoroptes species, Chorioptes species, Sarcoptes species, Tarsonemus species, Briobia praetiosa, Panonychus species, and tetranicus Tetranychus species, Eotetranychous species, Oligonychus species and Eutetranychus species; Examples of throbbing necks include Oniscus asselus, Armadillidium vulgar and Porcellio scaber; Examples of millipede throats include: Blaniulus guttulatus; Examples of centipede necks include Geophilus carpophagus and Scutigera species; Examples of stalk necks include Scutigerella immaculata; Examples of the moth, Lepisma saccharina; Examples of fungi include Onychiurus armatus; Examples of the order Orthoptera are: Blata orientalis, Periplaneta americana, Leucophaea madeirae, Blatella germanica ), Acheta domesticus, Gryllotalpa species, Locusta migratoria migratorioides, Melanoplus differentialis and Skistosica Gregaria (Schistocerca gregaria); Examples of termite include, but are not limited to, Reticulitermes species; Examples of this species include Phylloera vastatrix, Pemphigus species, Pediculus humanus corporis, Haematopinus species, and Linognathus species; Examples of hairy necks include Trichodecte species and Damalalinea species; Examples of the herbaceous shrub include Hercinothrips femoralis, Tripps tabaci, and Frankliniella species; Examples of stinkwood are Eurygaster species, Dysdercus intermedius, Piesma quadrata, Cimex lectularius, Rodnius prolixus ) And Triatoma species; Examples of the Homoptera order include: Aleuurodes brassicae, Béricia tabaci, Trialourodes vaporariorum, Apis species, Brevi Brevicoryme brassicae, Cryptomyzus ribis, Doralis fabae, Doralis pomi, Eriosoma lanigerum, Hyrallotherus arandidi Niceopterus arandinis, Macrosisph avenae, Nusus species, Phorodon humuli, Rhopalosiphum padi, Empoasca species, Eucelus bill Ebatusus bilobatus, Nephotettix cincticeps, Lecanium corni, Saissetia oleae, Laodelphax striatellus, Nila Nilaparvata lugen s), Aonidiella aurantii, Aspidiotus hederae, Pseudococcus species and Psylla species; Examples of Lepidoptera include: Pectinophora gossypiella, Bupalus piniarius, Cheimatobia brumata, Lithocolletis blancardella, Hyphonomuta padella (Huponomeuta padella), Plutella maculipennis, Malacosoma neustria, Euprotis chrysorrhoea, Lymantria species, Buculattrix turberella Bucculatrix thurberiella, Phyllocnistis citrella, Agrotis spp., Euxoa spp., Feltia spp., Earias insulana, Heliotis spp. , Laphygma exigua, Mamestra brassicae, Panolis flammea, Prodenia litura, Spodoptera species, tr Trichoplusia ni, Carpocapsa pomonella, Pieris species, Chilo species, Pyrausta nubilalis, Ephestia kuehniella , Galleria mellonella, Cacoacia podana, Capua reticulana, Choristoneura fumiferana, Clysia ambiguella Homona magnanima, Tortrix viridana, Cuapalolocrocis species and Manduca species; Examples of coleoptera include Anobium punctatum, Rhizopertha dominica, Bruchidius obtectus, Acanthoscelides obtectus, and Hylotrupes Hyruprupes bajulus, Agelastica alni, Leptinotarsa decemlineata, Phaedon cochleariae, Diabrotica species, Psyloides chrysepalla (Psylloides chrysocephala), Antonumus spp., Sitophilus spp., Otiorrhynchuys sulcatus, Cosmopolites sordidus, Strynx sassicichus ceu assimilis Hypera postica, Dermestes species, Trorogma species, Antrenus species, Atengeus species, Lycusus species, Mel Getethes aeneus, Ptinus species, Niptus hololeucus, Gibbium psylloides, Tribolium species, Tenebrio molito molitor, Agriotes species, Conorus species, Melonta melolontha, Amphimallon solstitialis, Costelytra zealandica and Lysolop Lissorhoptes species; Examples of fellings include Diprion species, Hoplocampa species, Lasius species, Monomorium pharaonis and Vespa species; Examples of the fly tree include Aedes species, Anopheles species, Culex species, Drosophila melanogaster, Musca species, Fania species, and Cali Calliphora erythrocephala, Lucilia species, Chrysomyia species, Cuterebra species, Gastrophilus species, Hypobosca species, Stomp Sithoxys species, Oestrus species, Hyporma species, Tabanus species, Tannis species, Bibio hortulanus, Oscinella frit Phobia spp., Pegomia hyoscyami, Ceratitis capitata, Dacus oleae and Tipula paludosa; Examples of fleas include Xenopsylla cheopsis and Ceratophyllus species; Examples of arachnoid necks include Scorpio maurus and Latrodectus mactans; Examples of helminthic rivers are Haemonchs, Trichostrongulus, Ostertagia, Copereria, Chabertia, Strongyloides, and Oesopagosto Oesophagostomum, Hyostrongulus, Ancylostoma, Ascaris and Heterakis and also Fasciola; Examples of gastropods include Deroceras species, Arion species, Lymnaea species, Galba species, Succinea species, Biomphalaria species, and Bulinus. ) Species and Oncomelania species; An example of a shellfish river, the Dreissena species. Nematodes, which are parasitic on plants that can be parasitic according to the present invention, for example, Meloidogyne genus (root hog nematodes, for example Meloidogyne incognita, Meloidogye halpa) And Meloidogyne javanica, Heterodera genus, Globoderra genus (cyst nematodes, for example Globodera rostochiensis, Globodera salida) (Globodera pallida and Heterodera trifolii), the genus Radopholus (e.g. Radopholus similis), the genus Pretilenecus (e.g. Pretyllenus neglectus, Pretyllenus penetrans and Pratyllencus curvitatus, Tylenchulus genus (e.g. Net Tylenchulus semipenetrans), Genus Tylenchorhynchus (e.g. Tylenchorhynchys dubius and Tylenchorhynchus claytoni), Rotylenchus genus For example, Rotylenchus Robustus), Helicotylenechus genus (e.g., Helicotylenechus multicinctus), Belonoaimus genus (e.g. For example, Belonoaimus longicaudatus, Longidorus genus (eg, Longidorus elongatus), Trichodorus genus (eg, Soil nematodes parasitic to roots such as Trichodorus primitivus) and the genus Xiphinema (eg, the Xiphinema index). Compounds of the invention are also useful in the genus Ditylenchus (stem parasites such as Ditylenchus dipsaci and Ditylenchus destructor), the genus Apelencoides (leaf nematodes) For example, it can be used for nematode insects belonging to the genus Aphelenchoides ritzemabosi) and the genus Anguina (leaf wound nematodes, for example Anguina tritici). The present invention also relates to compositions comprising compounds of formula (I), in particular insecticide compositions and tick repellent compositions, in addition to suitable blending aids. Compositions according to the invention generally comprise an active substance of formula (I) in a ratio of 1 to 95% by weight. The compositions of the present invention can be formulated in a variety of ways depending on the prevailing biological and / or physicochemical parameters. Thus a suitable combination possible is as follows: Wettable Powder (WP) Emulsifiable Concentrate (EC), Aqueous Solution (SL), Emulsion, Spray, Oil-Based or Aqueous Dispersion (SC), Suspoemulsion (SE), Powder (DP), Seed-dressing ) Feeds for products, granules (eg in the form of particulates, spray granules, coated granules and adsorptive granules), water dispersible granules (WG), ULV blends, microcapsule, wax or bait. The theory of each of these types of combinations is known and is described, for example, in Winnecker-Kuchler, Chemises Technologie, Volume 7, C. Hauser Verlag Munich, 4th ed. 1986, van Falkenberg, Pesticides Formulations, Marcel Dekker N. Y., 2nd ed. 1972-73 and K. Martens, Spray Drying Handbook, 3rd ed., G. Goodwin Ltd., London, 1979. Necessary compounding aids such as inert materials, surfactants, solvents and other additives are also known and are described, for example, in the following literature: Watkins, Handbook of Insecticide Dust Diluents and Carriers, 2nd ed., Darland Books, Caldwell NJ, H. v. Olphen, Introduction to Clay Colloid Chemistry, 2nd ed., J. Wiley & Sons, NY, Marsden, Solvents Guide, 2nd ed., Interscience, NY, 1950, McCutcheon's, Detergents and Emulsifiers Annual, MC Publ. Corp., Ridgewood N.J., Sisley and Wood, Encyclopedia of Surgace Active Agents, Chem. Publ. Co. Inc., N.Y., 1964, Schonfeldt, Glenzflachenaktive Athylenoxidaddukte [Surface-active ethylene oxide adducts], Wiss. Verlagsgesell., Stuttgart, 1967 and Winnecker-Kucler (Chemische Technologie, Volume 7, C. Hauser Verlag Munich, 4th ed., 1986). Based on these formulations, it is also possible to prepare combinations with other pesticidal active substances, fertilizers and / or growth regulators, for example in the form of readymixes or tank mixtures. Wettable powders include wetting agents (e.g., polyoxyethylated alkylphenols, polyoxyethylated fatty alcohols, alkylsulfonates or alkylphenolsulfonates) and dispersants (e.g., in addition to the active and diluent or inert materials). , Sodium ligninsulfonate or sodium 2,2'-dinaphthylmethane-6,6'-disulfonate). Emulsifiable concentrates can be prepared by dissolving the active substance in an organic solvent (eg, butanol, cyclohexanone, dimethylformamide, xylene, high boiling aromatic or high boiling hydrocarbon) by adding one or more emulsifiers. As emulsifiers, the following materials can be used: calcium salts of alkylarylsulfonates (eg calcium dodecylbenzenesulfonate) or nonionic emulsifiers (eg fatty acid polyglycol esters, alkylaryl polyglycol ethers) Fatty alcohol polyglycol ethers, propylene oxide / ethylene oxide, condensation products, alkyl polyethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters or polyoxyethylene sorbitol esters. Powders can be obtained by grinding the actives with finely ground solid materials (eg talc, natural clay (eg kaolin), bentonite, pyrophyllite or diatomaceous earth). Granules may be sprayed with an active material on an adsorbent, granulated inert material, or an active material concentrate may be applied to a carrier material (e.g. sand or kaolinite) or an adhesive (e.g., polyvinyl) on the surface of the granulated inert material. Alcohol or sodium polyacrylate) or optionally mineral oil. Suitable active substances may also be granulated, optionally in a form customary for the preparation of fertilizer granules, in admixture with fertilizers. The concentrate of the active substance in the wettable powder is, for example, about 10 to 90% by weight and is adjusted to 100% by weight with the remaining components consisting of conventional blending components. In the case of emulsifiable concentrates, the concentration of active substance may be about 5 to 80% by weight. The powder formulation is in most cases 5-20% by weight of the active substance and the spray solution is about 2-20% by weight. In the case of granules, the content of the active substance depends in part on whether the active compound is in liquid or solid form and whether granulation aids, fillers or the like are used. In addition, the aforementioned combinations of the active substances optionally include adhesives, wetting agents, dispersants, emulsifiers, penetrants, solvents, fillers or carriers commonly used in each case. Concentrates in commercially customary form are optionally diluted in a conventional manner, depending on their use, for example wettable powders, emulsifiable concentrates, dispersions and some fines using water. Powder preparations, granule preparations and spray solutions are generally not diluted further with other inert materials until used. The application rate required varies among external conditions, such as temperature and humidity. The rate of application can vary within wide limits, for example 0.0005 to 10.0 kg / ha, but for most active materials it is preferably 0.001 to 5 kg / ha. The active substances according to the invention may exist in commercially customary combinations and with other active substances (e.g. insecticides, attractants, fungicides, mite repellents, nematicides, fungicides, growth regulators or preparations). It may also be present in the form of an application made from these combinations as a mixture. Pesticides include, for example, phosphoric acid, carbamic acid, carboxylic acids, formamidine, tin compounds and substances produced by microorganisms in particular. Preferred mixture components are those of 1 to 6 below: 1. As an example of a group of phosphoric acid compounds, Acetate, Azametifoss, Ajinfoss-ethyl, Ajinfoss-methyl, Bromophos, Bromophos-ethyl, Chlorfenbinfos, Chlormephos, Chlorpyriphos, Chlorpyrifos-methyl, Dimethone, Dimethone -S-methyl, dimethone-5-methylsulfone, dialilifos, diazinone, diclobos, dicrotophos, O, O-1,2,2,2-tetrachloroethyl phosphorothioate (SD 208 304), dimethoate, disulfotone, EPN, ethion, etoprofos, etrimforce, pamper, phenamifos, phentrithiothone, pensulfothione, pention, phonophos, formothione, hepteno Force, isozofos, isothioate, isoxation, malathion, methacryphos, metamidophos, metidathione, salityon, mevinfoss, monochromophos, naled, ometoate, oxydimethone -Methyl, parathion, parathion-methyl, pentoate, forate, posalon, phospholane, phosphmet, phosphamidone, fr Shim, pyrimifos, pyrimifos-ethyl, pyrimifos-methyl, propenophos, propaphos, proetamphos, prothiophos, pyraclophos, pyridapention, quinalfoss, sulfrofoss , Temefos, terbufoss, tetrachlorbinfoss, thiopetones, triazofoss, triclofone, bamidothione; 2. Examples of groups of carbamic acid, Aldicarb, 2-tert-butylphenyl methylcarbamate (BPMC), carbaryl, carbofuran, carbosulphan, floretocarb, benfuracarb, ethiophencarb, furathiocarb, isoprocarb, metholyl, 5 -Methyl-m-cumenylbutyryl (methyl) carbamate, oxamyl, pyricarb, propoxa, thiodicarb, thiophanox, ethyl 4,6,9-tria-4-benzyl-6,10 -Dimethyl-8-oxa-7-5,11-dithia-9-dodecenoate (OK 135), 1-methylthio (ethylideneamino) -N-methyl-N- (morpholinothio) carbamate (UC 51717); 3. Examples of the group consisting of carboxylic acids, Alletrin, alphamethrin, 5-benzyl-3-furylmethyl (E)-(1R) -cis-2,2-dimethyl-3- (2-oxothiolane-3-ylidenemethyl) cyclopropanecarboxylic acid, bio Alletrin, BioAllerrin ((S) cyclopentyl isomer), Bioresmethrin, Biphenate, (RS) -1-Cyano-1- (6-phenoxy-2-pyridyl) methyl (1RS)- Trans-3- (4-tert-butylphenyl) -2,2-dimethylcyclopropanecarboxylate (NCI 85139), cycloprotrin, sihalothrin, citrine, cypermethrin, cifenotrine, deltamethrin , Empentrin, espenvalrate, fenfluthrin, phenpropatrine, penvalrate, flucitrinate, flumethrin, fluvalinate (D-isomer), permethrin, phenotrine ((R) Isomers), d-pratrethrin, pyrethrin (natural product), resmethrin, tefluthrin, tetramethrin, tralomethrin; 4. Examples of amidine groups include Amitrak, chlordimeform; 5. Examples of tin compound groups include Cyhexa tin, fenbuta tin oxide; 6. Other examples include: Abamect tin, Bacillus thuringiensis, benzaltar, vinapacryl, meramopropylate, buprofezin, campechlor, cartaf, chlorobenzylate, chlorfluazuron, 2- (4-chloro Phenyl) -4,5-diphenylthiophene (UBI-T 930), clopentazine, 2-naphthylmethyl cyclopropanecarboxylic acid (Ro 12-0470), cyromazine, ethyl N- (3,5-dichloro- 4- (1,1,2,3,3,3-hexafluoro-1-propyloxy) phenyl) carbamoyl) -2-chlorobenzocarboximidate, DDT, dicopol, N- (N- ( 3,5-dichloro-4- (1,1,2,2-tetrafluoroethoxy) phenylamino) carbonyl) -2,6-difluorobenzamide (XRD 473), diflubenzuron, N- (2,3-dihydro-3-methyl-1,3-thiazole-2-ylidene) -2,4-xyldine, dinobutone, dinocap, endosulfan, etofenprox, (4-ethoxy Phenyl) (dimethyl) (3- (3-phenoxyphenyl) propyl) silane, (4-ethoxyphenyl) (3- (4-fluoro-3-phenoxyphenyl) propyl) dimethylsilane, phenoxy Carb, 2-fluoro-5- (4- (4-ethoxyphenyl) -4-methyl-1-pentyl) diphenyl ether (MTI 800), granulosis virus, nucleus polyhedrosis virus, pentiocarb , Flubenzimine, flucycloxlon, flufenoxuron, gamma-HCH, hexthiaxose, hydratmethylnon (AC 217300), ivermec tin, 2-nitromethyl-4,5-dihydro-6H -Thiazine (DSA 52618), 2-nitro-methyl-3,4-dihydrothiazole (SD 35651), 2-nithromethylene-1,2-thiazinan-3-ylcarbamaldehyde (WL 108477), Propargite, teflubenzuron, tetradipon, tetrasul, thiocyclam, tripufuron and imidacloprid. The active substance content in the use form prepared from commercially common formulations can be from 0.00000001 to 95% by weight of active substance, preferably from 0.00001 to 1% by weight. Application takes place in a customary form to suit the application form. The active substances according to the invention are also suitable for extermination of external parasites and internal parasites in the veterinary or livestock industry. In this case, the active substances according to the invention may be administered orally in the form of tablets, capsules, pig liquids or granules; Transdermal administration such as dipping, spraying, surface pouring, surface spotting and powder spraying; And known forms such as parenteral administration in the form of injections. Thus, the novel compounds of formula (I) according to the invention can also be applied in particular to the livestock industry (eg cattle, sheep, pigs and poultry (eg chickens, geese, etc.). In a preferred embodiment of the invention, the novel compounds of the invention are optionally administered orally to animals in appropriate combinations (see above) and optionally in combination with drinking water or feed. Since the compounds of the present invention are excreted in the active form in animals, insects in the developmental stage in animal excretion can also be very simply inhibited in this manner. Suitable dosages and combinations in each case depend in particular on the type and stage of development of the animal being produced, or on the extent of infection, and can be readily determined and adjusted by conventional methods. In cattle, the novel compounds of the invention can be used, for example, in dosages of 0.01 to 1 mg / kg of body weight. The compounds of formula I according to the invention also exhibit excellent fungicidal action. Fungal pathogens that have already penetrated plant tissues can also be successfully cured. This fact is particularly important and advantageous in the case of fungal diseases which can be effectively killed by other conventional fungicides when already infected. The spectrum of action of the compounds claimed in the present invention is environmentally important, including various plant pathogen fungi, for example Plasmopara viticola, Phytophthora infestans, erythrope graminis. (Erysiphe graminis), Piricularia oryzae, Pyrenophora teres, Leptosphaeria nodorum, Pellicularia sasakii and Fuchsia reconditta (Puccinia recondita). The compounds of the invention are also suitable for use in the technical field, for example as wood preservatives and as preservatives in paints, cooling lubricants in metal working, drilling oils or cutting oils. In commercially customary combinations the active substances according to the invention can be used alone or in combination with other fungicides known in the literature. Examples of fungicides which are known in the literature and which can be combined with the compounds of formula (I) according to the invention include the following products: Aldimorph, Andofrim, Anilazin, BAS 480F, BAS 450F, BAS 490F, Benal Laxyl, Benodanil, Benomyl, Binapacryl, Bittertanol, Bromuconazole, Butyl Obate, Captapol, Captan, Carbendazim, Carboxin, CGA 173506, Ciprodinyl, Ciprophoram, Diclofluanide, Diclomezine, Diclobutrazole, Dietofencarb, Difenconazole (CGA 169374), Difluconazole, Dimethymolol, Dimethomorph, Diniconazole, Dinocap, Dithianon, Dodephorf, Dodine, Eddy Fenforce, ethirimol, ethriazole, epoxyconazole, fenbuconazole, phenarimol, fenfuram, fenpiclonil, fenpropidine, phenpropimorph, fentin acetate, fentin hydroxide, perimzone ( TF164), fluazinam, fluorbenzimine, fludioxynyl, fluquinconazole, fluorine Imide, flusilazole, flutolanyl, flutriafol, follpet, pocetylaluminum, fuberidazole, fulsulfamid (MT-F 651), forolaxyl, poconazole, pomecyclox, guaztine, hexa Conazole, ICI A5504, Imazalyl, Imibenconazole, Iprobenfos, Iprodione, Isoprothiolane, KNF 317, Copper Compounds (e.g. Cu oxychloride, Auxin-Cu, Cu Oxide), Mancozeb, Manet Bromine, mepanipyrim (KIF 3535), metconazole, mepronil, metallaxyl, metasulfocarb, metforoxam, MON 24000, myclobutanyl, nabam, nitrotalidopropyl, noarimol, opu Lace, oxadixyl, oxycarboxine, fenconazole, kensicuron, pp 969, probenazole, propyneb, prochloraz, procmidone, propamocarb, propiconazole, prothiocarb, piracaboll Reed, pyrazophos, pyrifenox, pyrimethanyl, pyroquilon, pavenzazole, RH7592, sulfur, tebuconazole, TF 167, thia Dozol, Tsiofene, Thiorenatemethyl, Thiram, Tollclofos-methyl, Tolylufluoride, Preadimethone, Triadimenol, Triazoxide, Tricyclazole, Tridemorph, Tripleluminazole, Tri Porin, tripionazole, validamycin, vinclozoline, XRD 563, geneb, sodium dodecylsulfonate, sodium dodecyl sulfate, sodium C13 / C15 alcohol ether sulfonate, sodium cetostearyl phosphate ester, sodium dioctylsulfosuccinate Cyanate, sodium isopropylnaphthalenesulfonate, sodium methylenebisnaphthalenesulfonate, cetyltrimethylammonium chloride, salts of long chain primary, secondary or tertiary amines, alkylpropyleneamines, laurylpyrimidinium bromide, ethoxylated quaternized Fatty amines, alkyldimethylbenzylammonium chloride and 1-hydroxyethyl-2-alkylimidazoline. The above-mentioned ingredients in the composition are mostly known active substances, described in Worthing, Ch. R. and Walker, SB, The Pesticide Manual, 7th edition, British Crop Protection Council, 1983. to be. The active ingredient content of the use form prepared from a commercially available combination can vary within wide limits, and the concentration of the active substance in the use form is from 0.0001 to 95% by weight, preferably 0.0001 to 1% by weight of the active substance. Can be. The blend is used in a conventional manner suitable for the use form. The present invention will be explained without restricting the invention with reference to the following examples. The present invention relates to novel substituted pyridine, substituted pyrimidine and condensation systems derived therefrom, methods for their preparation and their use as insecticides and fungicides. A. Formulation Examples a) 10 parts by weight of the active substance and 90 parts by weight of talc as the unactive substance are mixed and ground in a hammer mill to obtain a powder. b) mix 25 parts by weight of active material, 65 parts by weight of kaolin-containing quartz as inert material, 10 parts by weight of potassium ligninsulfonate, and 1 part by weight of sodium oleoylmethyltautinate as wetting agent and dispersant, Grinding into a disk mill yields a wettable powder that can be easily dispersed in water. c) 40 parts by weight of active substance is mixed with 7 parts by weight of sulfosuccinic acid monoester, 2 parts by weight of sodium ligninsulfonate, and 51 parts by weight of water and ground in a ball mill to a powder degree of 5 microns or less. To produce a dispersible concentrate that can be readily dispersed in water. d) Emulsifiable concentrates can be prepared from 15 parts by weight of active substance, 75 parts by weight of cyclohexane as solvent and 10 parts by weight of ethoxylated nonylphenol (10 EO) as emulsifier. e) Granules can be prepared from 2 to 15 parts by weight of active material and inert granular carrier material (eg, attapulgite, granulated pumice and / or silica sand). It is advantageous to spray on the surface of the attapulgite granules using the wettable powder dispersion of formulation b) having a solids content of 30%, and then dry and mix immediately. In this case the weight ratio of the wettable powder is about 5% of the final granules and the weight ratio of the inert carrier material is about 95% of the final granules. B. Manufacturing Example Example I 4- (2-decylamino) -5-methoxy-6-methoxymethyl-1-phenacylpyrimidinium bromide 1.5 g (4.84 mmol) of 2-decylamino-5-methoxy-6-methoxy-methylpyrimidine (DE-A-4 116 089) and 0.96 g (4.84 mmol) of phenacyl bromide in 50 ml of ethanol. The mixture was heated under reflux for 8 hours. After cooling, the solvent was removed under reduced pressure and the oil residue was stirred with petroleum ether. The resulting crystal slurry was aspirated and filtered, and the product was stirred in hot petroleum ether for an additional 5 minutes. Aspiration filtration gave 1.15 g (61% of theory) of yellow solid. Melting point. 118 ° C. Example II 1-benzoyloxymethyl-5-bromo-6-ethyl-4 [2- (2,4-dimethylphenoxy) -propylamino] pyrimidinium iodide 0.3 g (8.2 mmol) of 5-bromo-6-ethyl-4- [2- (2,4-dimethylphenoxy) -propylamino] pyrimidine (EP-A-57 440), 0.17 in 25 ml of acetone g (9.8 mmol) chloromethyl benzoate and 0.12 g (8.2 mmol) sodium iodide were heated under reflux for 8 hours. After cooling, the precipitated sodium chloride was filtered off and the filtrate was concentrated. The residue was taken up in dichloromethane and washed by stirring with water. The organic phase was dried and concentrated. The residue was immersed in ethyl acetate. Aspiration filtration gave 0.97 g (53.3% of theory) of bright yellow crystals. Melting point: 159-161 degreeC. The following examples can be prepared similarly to the above-described preparation examples (a definition of "Het n " is shown in Table 1 below). A high likelihood of heterocycle radicals is the configuration defined for pyrimidine. However, the radical -CHR 5 -ER 6 cannot exclude the absolute certainty that is bonded to N + at position 3 of the pyrimidine system instead of N + at position 1 of the ring system. C. Biological Examples Use as insecticide / insecticide / anti-nematode Example 1 In each case, 1 ml of the preparation to be tested emulsified with acetone was applied uniformly inside the lid and bottom of the Petri dish. After the coating had dried, 10 adult German cockroaches (Blattella germanica) were placed in a Petri dish. The dish was sealed and left at room temperature and the mortality of the test species was examined after 3 hours. At concentrations of 300 ppm (based on the content of active compound), the preparations of Examples 24 and 25 exhibit a mortality of 90 to 100% in the test animals used. Example 2 1 ml of the combined preparation aqueous solution to be tested was pipetted into the filter paper disc. After the solution was leaked, the filter paper was placed in a Petri dish and incubated with ten Southern corn rootworms (Diabrotia undecimpunctata) L2 larvae. After holding for 2 days in a constant temperature room at 26 ℃, mortality was examined. At concentrations of 300 ppm (based on the content of active compound), mortality activity of 90-100% was shown in the test species using the preparation of Example 25. Example 3 The cut stems of one leaf bean plants (Phaseolus vulgaris) were transferred to brown bottles filled with tap water, followed by propagation of about 100 spider mites (Tetranychus urticae). Plant leaves and spider mites were sprayed to the outflow point with a blended aqueous solution to be tested.After the solution was drained, the plants and animals were kept in a constant temperature room (16 hours of illumination per day, 25 ° C., 40-60% relative humidity). After 6 days, the effect of the preparation on spider mites was investigated The preparations of Examples 24 and 25 exhibited a mortality of 90 to 100% at a concentration of 300 ppm (based on the content of active compound). Example 4 The culture medium (freeze dried cube) is immersed in an aqueous solution of the formulation to be tested and then placed in a petri dish. Ten L2 larvae of the Egyptian cotton leaf beetle (Spodoptera litoralis) are placed in a small beaker and sealed with a lid. After 4 days storage at about 23 ° C., the effect of the preparation on the worms is measured. At a concentration of 300 ppm (based on the content of active compound), the preparation of Example 24 exhibits a mortality of 90 to 100% relative to the larvae. Example 5 (Contact activity): In a glass container containing a combined aqueous solution of the root wound nematode (Meloidogyne incognita) about 5000 recently hatched active (mobile) larvae (second developmental stage) to be tested. Put in. After continuing to expose the nematode larvae for 2 days, the percentage of the sample larva that stopped moving (fixed) due to the effect of the preparation (% nematode contact activity) was measured compared to the untreated control. At concentrations of 3 ppm (based on the content of the active compound in each case), the formulations of Examples 24 and 25 have 90-100% activity against bulb bile nematode meloidogincognita. Example 6 The bottom was covered with filter paper and a Petri dish containing about 5 ml of culture medium was prepared. Ten L2 larvae of the Egyptian cotton leaf beetle (Spodoptera litoralis) were placed in a small beaker. 200 μl of the combined preparation aqueous solution to be tested was pipetted into the beaker. The treated larvae were then placed in a Petri dish and an additional 200 μl aqueous solution was sprayed onto the culture medium. The Petri dishes were sealed and incubated in a thermostat at about 25 ° C. After storage for 6 days the effect of the preparation on the larvae was measured. At concentrations of 300 ppm (based on the content of active compound), the preparations of Examples 526 and 25 exhibit a mortality of 90 to 100% relative to the larvae. Example 7 The bottom was covered with filter paper and a Petri dish containing about 5 ml of culture medium was prepared. A filter paper with about 30 24-hour eggs of tobacco buttwarm (Heliothis virescens) was immersed in an aqueous solution of formulated preparation to be tested for about 5 seconds and then placed in a Petri dish. Further 200 μl of aqueous solution was sprayed onto the culture medium. The Petri dishes were sealed and incubated in a thermostat at about 25 ° C. After 6 days, the effect of the preparation on eggs and larvae that could be hatched from eggs was investigated. At concentrations of 300 ppm (based on the amount of active compound), the preparations of Examples 219, 526 and 528 exhibit 90% to 100% mortality. Example 8 The leaves of 12 rice plants with a stem length of 8 cm were immersed for 5 seconds in the formulated aqueous solution to be tested. After the solution was drained, rice plants treated in this way were placed in a Petri dish to breed about 20 larvae (L3 stages) of the rice cicada species Nilaparvata Rugens. The Petri dishes were sealed and then kept in a thermostat (16 hours of illumination per day, 25 ° C., 40-60% relative humidity). After 6 days, the mortality of the larva larvae was examined. At concentrations of 300 ppm (based on the content of active compound), the preparations of Examples 526, 528, and 780 exhibit mortality of 90 to 100%. Example 9 Half of the bottom was covered with filter paper and a Petri dish containing germinated maize corn placed on a soaked pad was prepared. Eggs of about 50 4 or 5 day Southern Corn Root Beetles (Diabrotica Unsimsimuntata) were transferred to filter paper. Three drops of 200 μl of formulated aqueous solution were pipetted into eggs and the remaining solution was pipetted into maize corn. The Petri dish was sealed and placed in a thermostat at about 25 ° C. After 6 days, the effect of the preparation on eggs and larvae that could hatch in eggs was investigated. At concentrations of 300 ppm (based on the amount of active compound), the preparations of Examples 179, 219 and 526 exhibit a mortality of 90 to 100%. Example 10 The cut stems of the one leaf bean plant (Paseolus vulgaris) were transferred to a brown bottle filled with tap water, followed by propagation of about 100 spider mites (Tetranicus urtica). The plant leaves and spider mites were then immersed for 5 seconds in the formulated aqueous solution to be tested. After the solution was drained, the plants and animals were placed in a constant temperature room (16 hours of illumination per day, 25 ° C., 40-60% relative humidity). After 6 days, the effect of the preparation on spider mites of all developmental stages was investigated. At concentrations of 300 ppm (based on the content of active compound), the formulations of Examples 179, 219, 486, 528 and 780 exhibit a mortality of 90 to 100%. Example 11 (Contact activity): glass containing a combined aqueous solution (final volume 20 ml) of about 5000 recently hatched active (mobile) larvae (second developmental stage) of root wound nematodes (melaidocin incogita) Put in a container. After continuing to expose the nematode larvae for 6 days, the percentage of the sample larva that has stopped moving (fixed) due to the effect of the preparation (% nematode contact activity) is measured compared to the untreated control. At a concentration of 3 ppm, the preparations of Examples 219, 526, 528, and 780 have 90-100% activity against bulb bile nematode melidocin incognita. Use as a fungicide Compounds for activity were tested for one or more of the following organisms: Plasmopara viticola, phytophthora infestans, pyricularia orissa, leptosperia nodorum. An aqueous solution or dispersion of the compound at the desired concentration is applied to the leaves or stems of the test crop after the wetting agent is added. Crops or parts of crops were incubated with individual test pathogens and maintained under controlled environmental conditions suitable for crop growth and disease progression. After a suitable time, the extent of infection of the disease crop was visually recorded. Compounds are evaluated on a scale of 1 to 3, 1 means not compared for a suitable comparison, 2 means average comparison and 3 means good for a complete comparison. At concentrations below 500 ppm, the following compounds were obtained in a ratio of at least 2 for the sterilization described. Example 12 Activity against Plasmopara viticola (downy mildew) The following compounds were obtained in proportions of at least two: Examples 25, 179, 187. Example 13 Activity against phytophthora infestspan The following compounds were obtained in a ratio of at least two: Examples 24, 25. Example 14 Activity against Pycurulari Orissa The following compounds were obtained in proportions of at least 2: Example 25, 179. Example 15 Activity against Leptosperia nodorum The following compounds were obtained in a ratio of at least two: Example 179. Toxicological Examples Example 16 The test substance was dissolved in dimethylformamide to obtain 20% of the strong solution, soya oil was added to obtain 1% of the strong solution, for example 20 mg of the test substance was tested to test the material at a dose of 50 mg / kg. Dissolve in ml of DMF and add soya oil to give 2 ml of solution. As test animals, fast male Wistar rats with a weight of 80-100 g are provided. Test substance is administered orally by gastric tube. The volume of the solution to be treated is 0.5 ml per rat. The following period is 7 days after dosing and the toxic effects or mortality of the test animals is recorded.
权利要求:
Claims (19) [1" claim-type="Currently amended] Compound of Formula (I): Formula I (1) A is CH and D is N + R, or A is nitrogen and D is N + R, or A is N + R and D is nitrogen; R is ego; (2) Q n- is any inorganic or organic anion and n is 1, 2, 3 or 4; (3) R 1 is hydrogen, halogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl or (C 3 -C 5 ) -cycloalkyl; (4) R 2 and R 3 are the same or different and are each hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 2 -C 4 ) -alkenyl, ( C 2 -C 4) - haloalkenyl, (C 2 -C 4) - alkynyl, (C 2 -C 4) - haloalkynyl, (C 1 -C 8) - trialkyl silil alkynyl, preferably dimethyl - (C 1 -C 8) - alkyl silil alkynyl, (C 1 -C 4) - alkoxy, (C 1 -C 4) - haloalkoxy, (C 1 -C 4) - alkoxy - (C 1 - C 4 ) -alkyl, (C 1 -C 4 ) -haloalkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -haloalkoxy- (C 1 -C 4 ) -haloalkyl, halogen, hydroxyl, (C 1 -C 4 ) -hydroxyalkyl, (C 1 -C 4 ) -alkanoyl, (C 1 -C 4 ) -alkanoyl- (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkanoyl, (C 3 -C 5 ) -cycloalkyl, (C 3 -C 5 )- Halocycloalkyl, cyano, (C 1 -C 4 ) -cyanoalkyl, nitro, (C 1 -C 4 ) -nitroalkyl, thiocano, (C 1 -C 4 ) -thiocyanoalkyl, ( C 1 -C 4 ) -alkoxycarbonyl, (C 1 -C 4 ) -alkoxycarbonyl- (C 1 -C 4 ) -alkyl , (C 1 -C 4 ) -haloalkoxycarbonyl, (C 1 -C 4 ) -alkylthio, (C 1 -C 4 ) -alkylthio- (C 1 -C 4 ) -alkyl, (C 1- C 4 ) -haloalkylthio, (C 1 -C 4 ) -alkylsulfinyl, (C 1 -C 4 ) -haloalkylsulfinyl, (C 1 -C 4 ) -alkylsulfonyl or (C 1 -C 4 ) -haloalkylsulfonyl; or R 2 and R 3 together with the attached carbon atoms may contain oxygen or sulfur atoms instead of CH 2 if they are five-membered rings, or one or two nitrogen atoms instead of one or two CH units if they are six-membered rings; 1, 2 or 3 same or different radicals (these radicals being (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, preferably trifluoromethyl, halogen, (C 1- To form an unsaturated 5 or 6 membered isocyclic ring which may be substituted by C 4 ) -alkoxy or (C 1 -C 4 ) -haloalkoxy) alkyl; or R 2 and R 3 together with the carbon atoms to which they are attached may contain oxygen and / or sulfur instead of one or two CH 2 groups and may be substituted by one, two or three (C 1 -C 4 ) -alkyl groups To form a saturated 5-, 6- or 7-membered isocyclic ring which may be substituted; (5) X is O or NH, Groups Y-Z can have the following meanings: a) Y is CHR 7 , R 7 is hydrogen, (C 1 -C 4 ) -alkyl or (C 3 -C 6 ) -cycloalkyl, Z is a branched or straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, wherein at least one, preferably up to three, nonadjacent tan th unit is oxygen or S (O) x (where x is These hydrocarbon radicals, which may be substituted by heteroatoms or carbonyl groups, such as 0, 1 or 2, and with or without the variables mentioned, are one or more, preferably up to three (in the case of up to a maximum number of fluorine) Can be substituted by halogen, hydroxyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkenyl, deca-, tetra- or dihydronaphthyl, substituted or unsubstituted Substituted benzyloxy, substituted or unsubstituted phenylthio, substituted or unsubstituted benzylthio, imidazol-1-yl, triazol-1-yl, pyrazol-1-yl, (C 1 -C 4 )- Same or different radical or group MGR 8 selected from the group consisting of alkoxycarbonyl, wherein M is oxygen or NH And G may be carbonyl, thiocarbonyl or sulfonyl, and R 8 is (C 1 -C 8 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, (C 1 -C 8 )- Haloalkyl, (C 1 -C 8 ) -alkoxy, substituted or unsubstituted phenyl group, substituted or unsubstituted phenoxy group, substituted or unsubstituted alinino group, imidazol-1-yl, triazol-1-yl , Pyrazol-1-yl or mono- or di- (C 1 -C 4 ) -alkylamino, or if not included in the above definition, b) Y is a (C 1 -C 6 ) -alkylene unit, branched or straight chain, up to three halogen atoms, preferably fluorine or chlorine, or hydroxyl, (C 1 -C 4 ) -alkoxy, ( May be substituted by a C 3 -C 6 ) -cycloalkyl or cyano group, Z is an unsubstituted or substituted aryl, aryloxy, heterocyclyl or pyridinyloxy group, with or without substitution, and the aryloxy or pyridinyloxy group is separated from two or more carbon atoms, or c) when X is NH, Y is a carbonyl or thiocarbonyl group, Z is in each case substituted by a substituted or unsubstituted heterocyclic or benzo fused carbocyclic or heterocyclic ring system or by a substituted or unsubstituted (C 3 -C 8 ) -cycloalkyl or cycloalkenyl radical Substituted or unsubstituted aryl- (C 1 -C 4 ) -alkyl radicals, (C 1 -C 4 ) -alkyl radicals, (6) a) R 4 and R 5 are the same or different and are each hydrogen, branched chain, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, halogen, aryl, substituted aryl or (C 3 -C 6 ) -cycloalkyl; E is oxygen, S (O) q (where q is 0,1 or 2) or NR 19 (where R 19 is hydrogen, (C 1 -C 4 ) -alkyl, (C 2 -C 4 )- Alkenyl or (C 1 -C 4 ) -acyl), R 6 is saturated or unsaturated, branched, straight chain (C 1 -C 20 ) -hydrocarbon radical, (C 3 -C 6 ) -cycloalkyl, aryl , Substituted aryl or Wherein V is oxygen or sulfur and R 20 is a branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, aryl, substituted aryl, heterocyclyl, substituted heterocyclyl, ( C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkenyl, and at least one, preferably up to three, non-adjacent CH of the (C 1 -C 20 ) -hydrocarbon radicals mentioned under R 6 Two groups are O, S (O) y (where y is 0, 1 or 2), NR 10 " or SiR 13" R 14 " , where R 10" , R 13 " and R 14" are R 10 , R 13 and have the meaning of R 14) and may be substituted by such a heteroatom radical or a carbonyl group, may form a ring added to a 3 to 6 carbon atoms of these hydrocarbon radicals, the above-mentioned variables These hydrocarbon radicals with or without are hydroxyl, (C 1 -C 4 ) -alkyl, halogen, (C 1 -C 4 ) -haloalkyl, (C 3 -C 6 ) -cycloalkyl, (C 1- C 4) - acyl, phenoxy, Hwandoen phenoxy, phenyl, substituted phenyl, phenylthio, substituted phenylthio, and NR 21 R 22 (wherein, R 21 and R 22 are each independently hydrogen, with each other (C 1 -C 4) - alkyl, (C 2 -C 4 ) -alkenyl, (C 1 -C 4 ) -acyl, aryl, substituted aryl, heteroaryl or benzoyl); or E is NR 19 and R 6 is If, R 19 and R 20 together may also be (C 3 -C 6 ) -alkylene, the CH 2 group adjacent to nitrogen may be substituted by CO and / or the CH 2 CH 2 group is a group CH═CH or o— Phenylene, preferably (C 3 -C 6 ) -alkylene, -CO-CH 2 -CH 2- , -CO-CH = CH- or May be substituted by Or furthermore b) R 4 is hydrogen, halogen or (C 1 -C 4 ) -alkyl, R 5 is hydrogen, halogen, branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, ( C 3 -C 6 ) -cycloalkyl, aryl or substituted aryl, E is Wherein V ′ is oxygen, sulfur or NR 23 , and R 23 is aryl, substituted aryl, heteroaryl, substituted heteroaryl, hydroxyl, (C 1 -C 4 ) -alkoxy, aryloxy, substituted aryl Oxy, heteroaryloxy, substituted heteroaryloxy or monosubstituted or disubstituted amino, R 6 is branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon, individually substituted or unsubstituted aryl or heteroaryl or (C 3 -C 8 ) -cycloalkyl; The aryl and heteroaryl radicals mentioned above may be substituted by one or more, preferably up to three (in the case of up to fluorine) the same or different radicals QR q , Q is a direct bond, NR 24 , O, S (O) s (s is 0, 1 or 2), OSO 2 , SO 2 O, NR 25 SO 2 , SO 2 NR 26 , SiR 27 R 28 or R 27 and R 28 are (C 1 -C 4 ) -alkyl or phenyl, preferably methyl, and U ′ is a direct bond, NR 29 or O; V ″ is oxygen or sulfur, preferably oxygen; W ′ is a direct bond, NR 30 or oxygen, where R 24 , R 25 , R 26 , R 29 and R 30 are the same or different and are each hydrogen, (C 1 -C) 4 ) -alkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkanoyl or (C 3 -C 6 ) -cycloalkyl; R q are substituents that are independent of each other, and each represents a halogen, hydroxyl, cyano, nitro, branched, straight chain, saturated or unsaturated (C 1 -C 20 ) -hydrocarbon radical, (C 3 -C 8 ) -cycloalkyl Or (C 4 -C 8 ) -cycloalkenyl, wherein at least one, preferably up to three, non-adjacent saturated carbon units of the last three radicals are oxygen, S (O) x (where x is 0, 1 Or 2), heteroatomic units such as NR 31 or SiR 32 R 33 or carbonyl groups, and these final three radicals with or without the mentioned variables may be at least one, preferably up to three ( In the case of fluorine up to the maximum number), may be substituted by the same or different radicals T 1 R 34 , or R q is aryl or heterocyclyl, wherein these two radicals may be unsubstituted or substituted by up to three (for the maximum number of fluorine) the same or different radicals T 2 R 35 , or are attached carbon Two adjacent radicals QR q together with the atom may form a molten ring having 4 to 6 ring atoms which are carbocyclic or at least one radical selected from the group consisting of halogen, (C 1 -C 4 ) -alkyl and oxo Contains a heterocyclic atom selected from the group consisting of O, S and N, which is unsubstituted or substituted by R 24 , R 26 and R 28 may be formed independently of each other with R q located in Q in a 4-8 membered ring system, one or two CH 2 groups, preferably one CH 2 group being oxygen, S (O ) t (where t is 0, 1 or 2) or a hetero atom unit such as NR 36, and R 31 is hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkoxy or (C 1 -C 4 ) -alkanoyl; R 32 and R 33 are each independently of each other (C 1 -C 4 ) -alkyl, preferably methyl; T 1 and T 2 in each case are independent of each other and each is a direct bond, oxygen, S (O) k , SO 2 O, OSO 2 , CO, OCO, COO, NR 37 , SO 2 NR 37 , NR 37 SO 2 , ONR 37 , NR 37 O, NR 37 CO, CONR 37 or SiR 38 R 39 and k is 0,1 or 2, R 37 is independently of each other hydrogen, (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -alkanoyl or (C 3 -C 5 ) -cycloalkyl; R 38 and R 39 are each independently of each other (C 1 -C 4 ) -alkyl; R 34 and R 35 are each independently of each other hydrogen, cyano, nitro, halogen, (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkyl, (C 2 -C 8 ) -alkenyl , (C 2 -C 8) - haloalkenyl, (C 2 -C 8) - alkynyl, (C 2 -C 8) - haloalkynyl, (C 1 -C 8) - alkoxy - (C 1 - C 4 ) -alkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 4 ) -alkyl, (C 1 -C 8 ) -alkylthio- (C 1 -C 4 ) -alkyl, (C 1 -C 8 ) -haloalkylthio- (C 1 -C 4 ) -alkyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 ) -cycloalkenyl, (C 3 -C 8 ) -Cycloalkyl- (C 1 -C 4 ) -alkyl, (C 4 -C 8 ) -cycloalkenyl- (C 1 -C 4 ) -alkyl, aryl, heterocyclyl, aryl- (C 1 -C 4 ) -Alkyl or heterocyclyl- (C 1 -C 4 ) -alkyl wherein of these final eight radicals the alicyclic, aromatic or heterocyclic ring system is equal to or equal to three (up to the maximum number of fluorine) May be unsubstituted or substituted by other substituents R 40 , or R 34 and R 35 together at the same carbon atom are oxo groups, R 40 is (C 1 -C 4 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -haloalkoxy, cyano, nitro or Halogen; R 36 is hydrogen, (C 1 -C 8 ) -alkyl, (C 1 -C 4 ) -haloalkyl, (C 1 -C 4 ) -alkoxy, (C 1 -C 4 ) -alkylthio, (C 3 -C 5 ) -cycloalkyl, (C 2 -C 4 ) -alkenyl, (C 2 -C 4 ) -alkynyl, (C 1 -C 4 ) -alkanoyl, (C 2 -C 4 ) -halo Alkanoyl, (C 2 -C 4 ) -alkoxyalkyl, phenyl- (C 1 -C 4 ) -alkyl or phenyl, with up to three phenyl groups (for up to fluorine) the same or different substituents R 41 Substituted or unsubstituted by R41Silver (COne-C4) -Alkyl, (COne-C4) -Haloalkyl, (COne-C4) -Alkoxy, (COne-C4) -Alkylthio, halogen or cyano; R4, R5And R6(C) mentioned under a) and b)One-C20At least one, preferably up to three non-adjacent CHs, unless otherwise defined in the) -hydrocarbon radicals2Group is S (O)y(Where y is 0, 1 or 2), NR10 '"Or SiR13 '"R14 '"Where R10 ''', R13 '''And R14 ''Silver r10, R13And R14Which may be substituted by a hetero atom radical or a carbonyl group, and additionally 3 to 6 carbon atoms of these hydrocarbon radicals may form a ring and those with or without the aforementioned variables Hydrocarbon radicals are halogen, (C3-C8Substituted by one or more, preferably up to three (for up to fluorine) identical or different radicals selected from the group consisting of) -cycloalkyl, phenoxy, substituted phenoxy, phenyl, substituted phenyl And furthermore R under a) and b)4, R5, R6And "aryl", "substituted aryl", "aryloxy", "substituted aryloxy", "heterocyclyl", "substituted heterocyclyl", "phenyl", "substituted phenyl" described for E "," Phenoxy "," substituted phenoxy "," phenylthio "," substituted phenylthio "," branched, straight chain, saturated or unsaturated (COne-C20Radicals of the "4, R5, R6And unless otherwise specified in the components of radicals, substituents or ring systems derived from such as the alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl or alkoxycarbonyls described for E, the hydrogen atoms as a whole are in the case of fluorine. It may be partially substituted in the case of halogen, preferably chlorine or fluorine. [2" claim-type="Currently amended] The method of claim 1, Compound of Formula (I): R 1 is hydrogen, methyl, chlorine or fluorine; R 2 and R 3 are each hydrogen, (C 1 -C 4 ) -alkyl, (C 2 -C 4 ) -alkenyl, (C 2 -C 4 ) -alkynyl, trimethylsilylethynyl, methoxycarbonyl , (C 1 -C 4 ) -haloalkyl, halogen, (C 1 -C 4 ) -alkoxy, methoxymethyl or cyano; or R 2 and R 3 together with the attached carbon atom form an unsaturated five or six membered ring with or without substituents which may contain a sulfur atom instead of a CH 2 unit when it is a five membered ring; or R 2 and R 3 together with the carbon atom to which they are attached form a saturated five or six membered ring which may contain sulfur or oxygen atoms instead of CH 2 units; X is NH. [3" claim-type="Currently amended] The method according to claim 1 or 2, Compound of Formula (I): R 1 is hydrogen; R 2 and R 3 are each hydrogen, methyl, ethyl, propyl, (C 2 -C 3 ) -alkenyl, (C 2 -C 3 ) -chloroalkenyl, (C 2 -C 3 ) -fluoroalkenyl, (C 2 -C 3 ) -alkynyl, trimethylsilylethynyl, (C 1 -C 3 ) -chloroalkyl, (C 1 -C 3 ) -fluoroalkyl, methoxy, methoxymethyl, halogen or cyano ego; R 2 and R 3 together with the ring system to which they are attached form a quinazoline or chinoline system which may be substituted in the carbocyclic moiety by fluorine; or R 2 and R 3 together with the carbon atom to which they are attached form a saturated six-membered ring which may contain oxygen or sulfur in place of the CH 2 group. [4" claim-type="Currently amended] The method according to any one of claims 1 to 3, Compound of Formula (I): R 1 is hydrogen; R 2 is methyl, ethyl, propyl, isopropyl, (C 1 -C 2 ) -fluoroalkyl or methoxymethyl; R 3 is fluorine, chlorine, bromine, cyano, vinyl, ethynyl or methoxy; or R 2 and R 3 together with the ring system to which they are attached form a quinazoline system which may be substituted by a fluorine atom; A and D describe pyrimidine systems when YZ has the meanings given under a) and b), and pyridine systems when YZ has the meanings given under c); X is NH. [5" claim-type="Currently amended] The method according to any one of claims 1 to 4, Compound of Formula (I): R 1 is hydrogen; R 2 is ethyl or methoxymethyl; R 3 is chlorine, bromine or methoxy, preferably R 2 is ethyl, R 3 is bromine or chlorine, or R 2 is methoxymethyl and R 3 is methoxy; X is NH. [6" claim-type="Currently amended] The method according to any one of claims 1 to 5, A process for preparing a compound of formula (I) comprising reacting a compound of formula (V) with an electrophile of anion formula (VI), suitably by adding a salt and suitably replacing the compound obtained in this way by another anion : G is CH or N, R 1 , R 2 , R 3 , X, Y and Z are as defined in formula (I), R 4 , R 5 , R 6 and E are as defined in formula (I) and L is a leaving group such as halogen, alkylthio, alkanesulfonyloxy or arylsulfonyloxy. [7" claim-type="Currently amended] A composition comprising at least one compound according to any one of claims 1 to 5 and at least one combination agent. [8" claim-type="Currently amended] The method of claim 7, wherein A bactericidal composition comprising a bactericidal effective amount of at least one compound according to any one of claims 1 to 5 together with conventional additives or auxiliaries for treatment. [9" claim-type="Currently amended] The method of claim 7, wherein A pesticidal, parasitic or anti-neutral composition comprising an effective amount of at least one compound according to any one of claims 1 to 5 together with conventional additives or auxiliaries for treatment. [10" claim-type="Currently amended] One or more further active substances selected from the group consisting of fungicides, insecticides, attractants, sterilizers, insect repellents, anti nematodes and herbicides, together with conventional auxiliaries and additives for treatment and any of claims 1 to 5 A crop protection composition comprising an effective amount of bactericidal, insecticidal, antiparasitic or anti-neutral of at least one compound according to claim. [11" claim-type="Currently amended] As a preservative in sealing compounds, paints, cooling lubricating oils or abrasives for metals, cutting oils and cutting oils comprising an effective amount of at least one compound according to any one of claims 1 to 5 together with conventional auxiliaries and additives for processing or Composition for use for wood protection. [12" claim-type="Currently amended] A compound according to any one of claims 1 to 5 or a composition according to claim 7 for use in animal pharmaceutics, preferably in the inhibition of an internal or external parasite. [13" claim-type="Currently amended] Process for the preparation of a composition according to any one of claims 7 to 11, which comprises mixing the active substance and other additives and using the mixture in a suitable treatment form. [14" claim-type="Currently amended] Use of a compound according to any one of claims 1 to 5 or a composition according to any one of claims 7, 8, 10 and 11 as a fungicide. [15" claim-type="Currently amended] As a preservative or wood preservative in sealing compounds, paints, cooling lubricants for metals or abrasive and cutting oils, the compound according to any one of claims 1 to 5 or according to any one of claims 7, 8 and 11. Use of the composition. [16" claim-type="Currently amended] A fungus or crop, a region or substance or seed infected with a fungus, is a bactericidal agent comprising a compound according to any one of claims 1 to 5 or a composition according to any one of claims 7, 8, 10 and 14. A method for inhibiting plant pathogenic fungi comprising treating with an effective amount. [17" claim-type="Currently amended] Effects of a compound according to any one of claims 1 to 5 and a composition according to any of claims 7 to 9 and 10 on harmful pests, pests and anti nematodes or crops, areas or substances infected therewith. A method of inhibiting harmful pests, hookworms and anti nematodes, comprising treating a dose. [18" claim-type="Currently amended] Use of a compound according to any one of claims 1 to 5 or a composition according to any of claims 7, 9 and 10 to inhibit harmful pests, hookworms and anti nematodes. [19" claim-type="Currently amended] A seed for treating or coating an effective amount of a compound according to any one of claims 1 to 5 or a composition according to any one of claims 7, 8, 10 and 11.
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同族专利:
公开号 | 公开日 JP2001504473A|2001-04-03| DE19647317A1|1998-05-20| TR199901075T2|1999-08-23| EP0944605A1|1999-09-29| US5925644A|1999-07-20| ZA9710187B|1998-05-15| AU7300798A|1998-06-10| WO1998022446A1|1998-05-28|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
法律状态:
1996-11-15|Priority to DE1996147317 1996-11-15|Priority to DE19647317.9 1997-11-03|Application filed by 슈미트, 훽스트 쉐링 아그레보 게엠베하, 루츠 2000-08-25|Publication of KR20000053299A
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申请号 | 申请日 | 专利标题 DE1996147317|DE19647317A1|1996-11-15|1996-11-15|Substituted nitrogen heterocycles, processes for their preparation and their use as pesticides| DE19647317.9|1996-11-15| 相关专利
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