Abstract:
Die Erfindung betrifft bicyclische Verbindungen der allgemeinen Formel I, worin X, Y unabhängig voneinander für N oder C-R 4 stehen; n für 1, 2, 3, 4 oder 5 steht; R a für Halogen, Cyano, C 1 ,-C 6 -Alkyl, C 1 ,-C 6 -Alkoxy, C 1 ,-C 6 -Halogenalkyl, C 1 ,-C 6 -Halogenalkoxy, C 2 -C 6 -Alkenyl, C 2 -C 6 -Alkenyloxy oder C(O)R 5 steht; R 1 Halogen, Cyano, C 1 -C 6 -Alkyl, C 1 ,-C 6 -Halogenalkyl, C 2 -C 6 -Alkenyl, C 2 -C 6 -Alkinyl, C 3 -C 8 -Cycloalkyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, C 5 -C 8 Cycloalkenyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, OR 6 , SR 6 oder NR 7 R 8 bedeutet; R 2 Halogen, Cyano, C 1 ,-C 6 -Alkyl, C 1 ,-C 6 -Halogenalkyl, C 2 -C 6 -Alkenyl, C 2 -C 6 -Alkinyl, C 3 -C 8 -Cycloalkyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, C 5 -C 8 -Cycloalkenyl, das gegebenenfalls mit Alky und/oder Halogen ein- oder mehrfach substituiert ist, OR 6 , SR 6 oder NR 7 R 8 bedeutet; R 3 für Wasserstoff, C 1 ,-C 6 -Alkyl, C 1 -C 6 -Halogenalkyl oder C 3 -C 6 -Cycloalkyl, das gegebenenfalls mit Alkyl und/oder Halogen ein- oder mehrfach substituiert ist, steht; sowie die landwirtschaftlich verträglichen Salze von Verbindungen (I), Pflanzenschutzmittel, enthaltend wenigstens eine Verbindung der allgemeinen Formel (I) und/oder ein landwirtschaftlich verträgliches Salz von (I) und wenigstens einen flüssigen oder festen Trägerstoff sowie ein Verfahren zur Bekämpfung von pflanzenpathogenen Schadpilzen.
Abstract:
Die vorliegende Erfindung betrifft Trifluormethyl-thiophencarbonsäureanilide der allgemeinen Formeln I, II und III, in denen die Substituenten die folgende Bedeutung haben: R 1 ,R 4 unabhängig voneinander C 1 -C 4 -Alkyl, C 3 -C5-Cycloalkyl, C 2 -C 4 -Alkenyl, C 2 -C 4 Alkinyl, C 1 -C 4 -Alkoxy, wobei diese Gruppen durch Halogen substituiert sein können, H, Halogen, Nitro, CN; R 2 H, OH, C 1 -C 4 -Alkyl, C 3 -C 6 -Cycloalkyl, C 1 -C 4 -Alkoxy, wobei diese Gruppen durch Halogen substituiert sein können; R 3 C 1 -C 12 -Alkyl, C 3 -C 12 - Cycloalkyl, C 2 -C 12 -Alkenyl, C 5 -C 12 - Cycloalkenyl, C 2 -C 12 - Alkinyl, C 3 -C 12 - Cycloalkyl -C 1 -C 4 -alkyl, wobei diese Gruppen durch R 7 substituiert sein können; Phenyl, Phenyl-C 1 -C 6 -Alkyl, Phenyl-C 2 -C 6 -Alkenyl, Phenyl-C 2 -C 6 -Alkinyl, Pheny- loxy-C 1 -C 6 -Alkyl, Phenyloxy-C 2 -C 6 -Alkenyl, Phenyloxy-C 2 -C 6 -Alkinyl, wobei der Alkyl-, Alkenyl- und Alkinyl-Teil mit R 7 und der Phenylring mit R 5 substituiert sein kann; -C(R 8 )=NOR 6 ; O, S oder direkte Bindung; R 5 H, C 1 -C 4 -Alkyl, C 3 -C 6 - Cycloalkyl, C l -C 4 -Alkoxy, C 2 -C 4 -Alkenyl, C 2 -C 4 -Alkinyl, wobei diese Gruppen durch Halogen substituiert sein können, Halogen, Nitro, CN, Phenyl, das mit R 1 substituiert sein kann, Phenoxy, das mir R 1 substituiert sein kann, C l -C 6 -Alkyl-Phenyl, wobei der Alkylteil mit Halogen substituiert sein kann und der Phenylring mit R 1 substituiert sein kann; R 6 C 1 -C 4 -Alkyl, C 3 -C 6 -Cycloalkyl, C 2 -C 4 -Alkenyl, C 2 -C 4 -Alkinyl, wobei diese Gruppen durch Halogen substituiert sein können, Phenyl, das durch R 1 substituiert sein kann; R 7 C 1 -C 4 -Alkyl, C 1 -C 8 -Alkoxy, C 2 -C 8 -Alkenyloxy, C 2 -C 8 -Alkinyloxy, C l -C 4 -Alkoxy- C 1 -C 8 -alkoxy, wobei diese Gruppen durch Halogen substituiert sein können, Halogen; R 8 H , R 7 oder C 1 -C 12 -Alkyl, C 3 -C 12 -Cycloalkyl, C 2 -C 12 -Alkenyl, C 5 -C 12 -Cycloalkenyl, C 3 -C 12 -Cycloalkyl-C 1 -C 4 -alkyl, wobei diese Gruppen mit Halogen substituiert sein können; Phenyl, das mit R5 substituiert sein kann; n 0-4 m 0, 1sowie die Verwendung der Trifluormethyl-thiophencarbonsäureanilide als Fungizide und diese enthaltende Mittel.
Abstract:
Beschrieben wird ein Verfahren zur Herstellung von 3-Trifluormethylphenyl-4-cyanobenzylketon durch Umsetzung eines 3-Trifluormethylbenzoesäure-C 1 -C 2 -alkylesters mit 4-Tolunitril in einem aprotischen polaren Lösungsmittel oder einem aprotisch polaren Lösungsmittelgemisch in Gegenwart wenigstens einer äquimolaren Menge einer Base, wobei die Base ausgewählt ist unter Kaliumalkoholaten primärer C 1 -C 4 -Alkanole.
Abstract:
The invention relates to heteroaroyl-substituted serine amides of formula (I), wherein the variables A and R1 to R6 have the meanings indicated in the description, the agriculturally useful salts thereof, methods and intermediate products for the production thereof, and the use of said compounds or agents that contain said compounds and are used for controlling undesired plants.
Abstract:
The invention relates to the use of triazolopyrimidines of formula (I), wherein R1, R2 represent hydrogen, alkyl, alkyl halide, cycloalkyl, cycloalkyl halide, alkenyl, alkadienyl, alkenyl halide, cycloalkenyl, cycloalkenyl halide, alkinyl, alkinyl halide, C3-C6 cycloalkinyl, phenyl, naphthyl, or a five-membered or ten-membered saturated, partially unsaturated, or aromatic heterocycle containing one, two, three, or four heteroatoms from the group comprising O, N, or S. R1, R2 can be substituted as described in the description, or R1 and R2 form five-membered to eight-membered heterocyclyl or heteroaryl along with the nitrogen atom to which the same are bound, said heterocyclyl or heteroaryl being bound via N. Furthermore, R1, R2 contain one, two, or three additional heteroatoms from the group comprising O, N, and S as a ring member and/or can be substituted as defined in the description. Additionally, in formula (I), L independently represents halogen, alkyl, alkyl halide, alkoxy, alkoxy halide, alkenyloxy, cyano, C(=O)A1, S(=O)mA2, NRcRd, or NRc-(C=O)-Rd, A1, A2, Rc, Rd, and m being defined as indicated in the description; L1 represents halogen, alkyl, alkyl halide; L2 represents nitro, a -C(S)NR3R4 group, a -C(=N-OR5)(NR6R7) group, or a -C(=N-NR8R9)(NR10R11) group; X represents halogen, cyano, alkyl, alkoxy, alkyl halide, or alkoxy halide; R3, R4, R5, R6, R7, R8, R9, R10, and R11 are independently selected among hydrogen, alkyl, cycloalkyl, alkenyl, or alkinyl, the last four radicals mentioned being optionally substituted as defined in the description; R3 and R4, R6 and R7, R8 and R9, and/or R10 and R11 form a four-membered, five-membered, or six-membered saturated or partially unsaturated ring along with the nitrogen atom, said ring being optionally substituted as defined in the description; and n represents 0, 1, 2, or 3. Also disclosed are the agriculturally acceptable salts thereof, novel triazolopyrimidines, crop protection agents containing at least one compound of general formula (I) and at least one liquid or solid carrier substance, and a method for controlling plant-pathogenic harmful fungi.
Abstract translation:本发明涉及式(I)三唑并嘧啶的用途,其中R 1,R 2表示氢,烷基,烷基卤,环烷基,环烷基卤,链烯基,链二烯基,链烯基卤化物,环烯基,环烯基卤化物,炔基, C6环烷基,苯基,萘基或含有1,2,3或4个选自O,N或S的杂原子的五元或十元饱和,部分不饱和或芳族杂环。R1,R2可以是 如说明书中所述被取代,或者R 1和R 2与其所连接的氮原子一起形成五元至八元杂环基或杂芳基,所述杂环基或杂芳基通过N连接。此外,R 1,R 2含有一个 ,两个或三个另外的选自O,N和S的杂原子作为环成员和/或可以如说明书中所定义的那样被取代。 此外,在式(I)中,L独立地表示卤素,烷基,卤代烷基,烷氧基,烷氧基卤化物,烯氧基,氰基,C(= O)A1,S(= O)mA2,NRcRd或NRc-(C = O )-Rd,A1,A2,Rc,Rd和m如说明书中所示定义; L1代表卤素,烷基,烷基卤; L 2表示硝基,-C(S)NR 3 R 4基,-C(= N-OR 5)(NR 6 R 7)基或-C(= N-NR 8 R 9)(NR 10 R 11) X代表卤素,氰基,烷基,烷氧基,烷基卤或烷氧基卤; R3,R4,R5,R6,R7,R8,R9,R10和R11独立地选自氢,烷基,环烷基,烯基或炔基,所述最后四个基团任选如说明书中所定义的那样被取代; R 3和R 4,R 6和R 7,R 8和R 9和/或R 10和R 11与氮原子一起形成四元,五元或六元饱和或部分不饱和的环,所述环任选如定义 在描述中; 并且n代表0,1,2或3.还公开了其农业上可接受的盐,新的三唑并嘧啶,含有至少一种通式(I)的化合物和至少一种液体或固体载体物质的作物保护剂和 控制植物病原性有害真菌的方法。
Abstract:
The invention relates to 6-(2,6-dichlorophenyl)-triazolopyrimidines of formula (I) wherein the substituents have the following designations: R1 and R2 represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group containing O, N or S; R1 and R2 can also form, together with the nitrogen atom to which they are bound, a five-membered or six-membered heterocycle or heteroaryl which is bound by N and contains between one and three other heteroatoms from the group containing O, N and S as a cyclic member and is substituted according to the description; and X represents alkyl, cyano, alkoxy, halogenalkoxy, alkenyloxy or halogenalkenyloxy, but does not represent C1-C4 alkyl when R1 and R2 together represent piperidin-1-yl or 4-methylpiperidin-1-yl. The invention also relates to a method for producing said compounds, agents containing the same, and the use thereof for controlling plant pathogenic fungi.
Abstract:
The present invention relates to 1 -(azolin-2-yl)amino-1,2-diphenylethane compounds of the general formula (I) wherein A is a radical of the formulae A' or A2: N R A' A2 and wherein m is 0, 1, 2, 3, 4 or 5, n is 0, 1, 2, 3, 4 or 5, X is sulfur or oxygen, and wherein the variables R1, R2, R3, R4, R5a, R5b, R5c, R5d are as defined in the claims, and to the agriculturally acceptable salts thereof. The invention relates also to a method of combating animal pests, selected from insects, arachnids and nematodes and to a method for protecting crops from attack or infestation by insects, arachnids or nematodes, which comprises contacting a crop with a pesticidally effective amount of a 1 -(azolin-2-yl)amino-1,2-diphenylethane compounds of the general formula I and/or at least one salt thereof.
Title translation:FUNGIZIDE TRIAZOLOPYRIMIDINE,VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ZURBEKÄMPFUNGVON SCHADPILZEN SOWIE SIE ENTHALTENDE MITTEL
Abstract:
Triazolopyrimidines of formula (I), wherein the index and substituents have the following meaning: n = 0 or a whole number of 1 - 5; R = halogen, cyano, hydroxy, cyanate, alkyl, alkenyl, alkinyl, halogenalkyl, halogenalkenyl, alkoxy, alkenyloxy, alkinyloxy, halogenalkoxy, cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkinyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkinylcarbonyl, cycloalkylcarbonyl or a five to ten membered saturated, partially unsaturated or aromatic heterocycle, containing one to four heteroatoms from the group O, N or S; R1 = alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, phenyl, naphthyl or a five to ten membered saturated, partially unsaturated or aromatic heterocycle, containing one to four heteroatoms from the group O, N or S, R and/or R1 being able to be substituted according to the description; R2 = alkyl, alkenyl or alkinyl which can be substituted by halogen, cyano, nitro, alkoxy or alkoxycarbonyl. The invention also relates to a method for the production of said compounds, agents containing same, and the use thereof in controlling noxious fungi.
Abstract:
The invention concerns 2-benzoyl-cyclohexan-1,3-diones of formula (I), in which R1, R2 stand for hydrogen, nitro, halogen, cyano, rhodano, alkyl, halogen alkyl, alkoxyalkyl, alkenyl, alkinyl, -OR?5, -OCOR6¿, -OSO¿2R?6, -SH, -S(O)¿n?R?7, -SO¿2OR5, -SO2NR?5R8, -NR8SO¿2R?6 or -NR8COR6; R3¿ stands for hydrogen, alkyl, halogen alkyl or alkinyl; R4 stands for hydrogen, optionally substituted alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkinyl, -COR9, -CO2R?9, -COSR9¿ or -CONR8R9; X stands for oxygen or sulphur; m equals 0 or 1; n equals 0, 1 or 2; R5 stands for hydrogen, alkyl, halogen alkyl, alkoxyalkyl, alkenyl or alkinyl; R6 stands for alkyl or halogen alkyl; R7 stands for alkyl, halogen alkyl, alkoxyalkyl, alkenyl or alkinyl; R8 stands for hydrogen or alkyl; R9 stands for alkyl, alkenyl, alkinyl, phenyl or benzyl; R10 stands for alkyl, halogen alkyl, alkenyl or alkinyl; Q stands for optionally substituted cyclohexan-1,3-dione ring linked in position 2, whereas m equals 1 when R3 stands for hydrogen. Also disclosed are the salts of these compounds useful in agriculture; processes and intermediate products for preparing the compounds of formula (I), agents containing the same and the use of these derivatives or agents containing the same for controlling undesirable plants.
Abstract translation:本发明涉及式I的2-苯甲酰基环己烷-1,3-二酮,其中R 1,R 2为氢,硝基,卤素,氰基,氰硫基,烷基,卤代烷基,烷氧基烷基,烯基,炔基,-OR 5,-OCOR 6,-OSO 2 R 6 - SH,-S(O)nR7,-SO2OR5,-SO2NR5R8,-NR8SO2R6或-NR8COR6; R3是氢,烷基,卤代烷基,烯基或炔基; R4是氢,未取代或取代的烷基,环烷基,烯基,环烯基,炔基, -COR 9,-CO 2 R 9,-COSR 9或-CONR 8 R 9; X为氧或硫; Z为氧或NR 8; m为0或1; n为0,1或2; R 5为氢,烷基,卤代烷基,烷氧基烷基, 炔基; R 6是烷基,卤代烷基,烯基或炔基; R 8是氢或烷基; R 9是烷基,烯基,炔基,苯基或苄基; 在2-位连接的未取代或取代的环己烷-1,3-二酮环;如果R3是氢,其中m为1;其农业上有用的盐;制备的方法和中间体o f式I化合物; 包含它们的组合物; 以及包含它们的这些衍生物或组合物用于防治不需要的植物的用途。
Abstract:
The invention concerns diphenylethers of formula (I) and their salts and N-oxides, the substituents and indices in the formula having the following meanings: Q is C(CO2CH3)=CHCH3, C(CO2CH3)=CHOCH3, C(CONH2)=CHOCH3, C(CO2CH3)=NOCH3, C(CONHCH3)=NOCH3 or N(OCH3)-CO2CH3; n is 0 or 1; R is hydrogen or an organic group bonded via a carbon atom; R is hydrogen, cyano, halogen or an organic group bonded via a carbon, oxygen, sulphur or nitrogen atom; or, if n stands for 1, an organic group bonded via a carbon atom; x is 0, 1 or 2; R is cyano, nitro, halogen, or an organic group bonded via a carbon, oxygen, sulphur or nitrogen atom; y is 0, 1, 2 or 3; and R is cyano, halogen, C1-C4 alkyl, C1-C4 alkyl halide or C1-C4 alkoxy. The invention further concerns a process and intermediate products for preparing these substance, and their use.