Abstract:
The invention relates to 2-(2-pyridyl)-5-phenyl-6-aminopyrimidines of formula I, wherein the substitutes and the index have the following meaning: R1 represents halogen, hydroxy, hyano, hxo, nitro, amino, mercapto, alkyl, halogenalkyl, alkenyl, alkinyl, cycloalkyl, alkoxy, halogenalkoxy, carboxyl, alkoxycarbonyl, carbamoyl, alkylaminocarbonyl, dialkylamincarbonyl, morpholinocarbonyl, pyrrolidinocarbonyl, alkylcarbonylamino, alkylamino. dialkylamino, alkylthio, alkylsulfinyl, alkylsulfonyl, hydroxysulfonyl, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl; m=0 or 1-4; R2 represents hydrogen, halogen, cyano, alkyl, halogenalkyl or alkoxy; R3, R4 represents hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl or cycloalkinyl, R3 and R4 together with the nitrogen atom to which they are connected, form a five or six-membered ring which is interrupted by an atom from the group O, N or S and/or can be substituted according to the description; R5 represents halogen, alkyl or halogenalkyl; R6 represents hydrogen or one of the known groups in R5; R7, R8 represent hydrogen, halogen, alkyl or halogenalkyl; R9 represents hydrogen, halogen, hydroxy, cyano, alkyl, alkoxy, cycloalkoxy, halogenalkoxy, alkoxycarbonyl or alkylaminocarbonyl. The invention also relates to a method and intermediate product for the production of said compound in addition to the use thereof for combating undesirable plants
Abstract translation:本发明涉及式I的2-(2-吡啶基)-5-苯基-6-氨基嘧啶,其中取代基和指数具有以下含义:R 1表示卤素,羟基,杂环基, 烷氧基,烷氧基羰基,氨基甲酰基,烷基氨基羰基,二烷基氨基羰基,吗啉代羰基,吡咯烷基羰基,烷基羰基氨基,烷基氨基。 二烷基氨基,烷硫基,烷基亚磺酰基,烷基磺酰基,羟基磺酰基,氨基磺酰基,烷基氨基磺酰基,二烷基氨基磺酰基; m = 0或1-4; R 2表示氢,卤素,氰基,烷基,卤代烷基或烷氧基; R 3,R 4表示氢,烷基,卤代烷基,环烷基,卤代烷基,烯基,卤代烯基,环烯基,炔基,卤代炔基或环炔基,R 3 O 和R 4与它们连接的氮原子一起形成5或6元环,其被来自基团O,N或S的原子和/或可被取代 根据说明; R 5表示卤素,烷基或卤代烷基; R 6表示氢或R 5中的已知基团之一; R 7,R 8表示氢,卤素,烷基或卤代烷基; R 9表示氢,卤素,羟基,氰基,烷基,烷氧基,环烷氧基,卤代烷氧基,烷氧基羰基或烷基氨基羰基。 本发明还涉及用于生产所述化合物的方法和中间产物,除了其用于对抗不期望的植物之外
Abstract:
6-Phenyl-7-aminotriazolopyrimidines of the formula I in which the substituents are as defined below: R1 is hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle, which comprises one to four heteroatoms from the group consisting of O, N and S, R2 is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S, R3,R4,R5,R6,R7 are hydrogen or one of the groups mentioned under R2, R4, together with R3 or R6, may also form a five- or six-membered saturated or unsaturated ring which, in addition to carbon atoms, may comprise one to three further heteroatoms from the group consisting of O, N and S as ring members; R2 with R3, R4 with R5, R6 with R7 may in each case together, with formation of spiro groups, also form a C2-C5-alkylene, or alkenylene or alkynylene chain which may be interrupted by one to three heteroatoms from the group consisting of O, N and S; p is zero or 1; L is halogen, alkyl, haloalkyl, alkoxy, cyano, nitro, amino, alkylamino, dialkylamino, alkylcarbonylamino, C(O)—R, S(O)n—R; where n is zero, 1 or 2; R is hydrogen, alkyl, haloalkyl, alkoxy, alkenyloxy, alkynyloxy, amino, alkylamino, dialkylamino; m is 1, 2, 3, 4 or 5; X is halogen, cyano, alkyl, alkoxy, alkenyloxy, alkynyloxy or haloalkoxy; Y is oxygen or sulfur; Z is hydrogen, alkyl, haloalkyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, alkenyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl, phenyl, naphthyl, a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which comprises one to four heteroatoms from the group consisting of O, N and S; or Z together with R4 or R6 may also form a five- or six-membered saturated or unsaturated ring which, in addition to carbon atoms and Y, may comprise one or two further heteroatoms from the group consisting of O, N and S as ring members the groups R1 to R7, Z and R may be substituted according to the description; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
Abstract:
Fungicidal mixtures comprising, as active components, 1) the triazolopyrimidine derivative of the formula I and 2) procymidone of the formula II in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compound I with the compound II and the use of the compound I with the compound II for preparing such mixtures, and also compositions comprising these mixtures.
Abstract:
Fungicidal mixtures comprising, as active components, 1) the triazolopyrimidine derivative of the formula I and 2) spiroxamine of the formula II in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compound I with the compound II and the use of the compound I with the compound II for preparing such mixtures, and also compositions comprising these mixtures.
Abstract:
Fungicidal mixtures, comprising, as active components, 1) the triazolopyrimidine derivative of the formula I and 2) at least one biphenylamide of the formula II in which the variables are as defined below: A is oxathiinyl or 5-membered heteroaryl which contains one to four nitrogen atoms or one to three nitrogen atoms and/or one sulfur or oxygen atom, where A may be substituted according to the description; R1 is hydrogen, alkyl, alkylcarbonyl or a group A which is attached via carbonyl; Ra, Rb are halogen, cyano, alkyl, haloalkyl, alkoxycarbonyl, alkoxy, haloalkoxy, alkylthio, alkylcarbonyl, formyl, alkylene or alkenylene which links two adjacent carbon atoms; m is 0, 1, 2, 3, 4 or 5; n is 0, 1 or 2; in a synergistically effective amount, methods for controlling harmful fungi using mixtures of the compound I with compound II and the use of the compound I with compounds II for preparing such mixtures, and also compositions comprising these mixtures.
Abstract translation:包含作为活性成分的杀真菌混合物,1)式I的三唑并嘧啶衍生物和2)至少一种式II的联苯酰胺,其中变量如下所定义:A是氧亚硫代基或5元杂芳基,其含有1至 四个氮原子或一至三个氮原子和/或一个硫或氧原子,其中A可以根据描述被取代; R 1是氢,烷基,烷基羰基或通过羰基连接的基团A; R 2是卤素,氰基,烷基,卤代烷基,烷氧基羰基,烷氧基,卤代烷氧基,烷硫基,烷基羰基,甲酰基,亚烷基或亚链烯基,其连接两个相邻的碳原子; m为0,1,2,3,4或5; n为0,1或2; 在协同有效量的情况下,使用化合物I与化合物II的混合物控制有害真菌的方法以及化合物I与化合物II用于制备此类混合物的用途,以及包含这些混合物的组合物。
Abstract:
The invention relates to fungicidal mixtures containing: A) triazolopyrimidine of formula (I) and B) oxime derivatives of formula (II), wherein the index and substitutents have the following meaning: X=C1-halogen alkyl or C1-halogen alkoxy; R=halogen, alkyl, halogen alkyl, alkoxy or halogen alkoxy; n=0, 1, 2 or 3 in a synergistically effective amount. The invention also relates to a method for controlling harmful fungi with mixtures of compounds (I) and (II), to the agents containing said mixtures and to the utilization of compounds (I) and (II) for the production of said mixtures.
Abstract translation:本发明涉及杀真菌混合物,其包含:A)式(I)的三氮代嘧啶和B)式(II)的肟衍生物,其中指数和取代基具有以下含义:X = C 1 - 卤素 烷基或C 1 - 卤代烷氧基; R =卤素,烷基,卤素烷基,烷氧基或卤素烷氧基; n = 0,1,2或3,具有协同有效量。 本发明还涉及一种利用化合物(I)和(II)的混合物将有害真菌控制在含有所述混合物的试剂中,以及利用化合物(I)和(II)来生产所述混合物的方法。
Abstract:
6-Pentafluorophenyltriazolopyrimidines of the formula I in which the substituents are as defined below: R1 is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkinyl, haloalkinyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R2 is hydrogen or one of the groups mentioned under R1, R1 and R2 together with the nitrogen atom to which they are attached may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and may contain one to three further heteroatoms from the group consisting of O, N and S as ring members; R1 and/or R2 may be substituted as defined in the description; X is cyano, alkyl, alkoxy, alkenyloxy, haloalkoxy or haloalkenyloxy, processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
Abstract translation:式I的6-五氟苯基三唑并嘧啶,其中取代基如下:R 1是烷基,卤代烷基,环烷基,卤代环烷基,烯基,卤代烯基,环烯基,卤代环烯基,炔基,卤代炔基或苯基,萘基, 或五元或六元饱和,部分不饱和或芳族杂环,其含有一至四个由O,N和S组成的组的杂原子,R 2是氢或下述基团之一 R 1,R 1和R 2与它们所连接的氮原子一起也可以形成五元或六元杂环基 或杂芳基,其通过N连接并且可以含有一个至三个由O,N和S组成的组的另外的杂原子作为环成员; R 1和/或R 2可以如说明书中所定义的取代; X是氰基,烷基,烷氧基,烯氧基,卤代烷氧基或卤代烯氧基,制备这些化合物的方法,包含它们的组合物及其用于控制植物病原性有害真菌的用途。
Abstract:
5-Phenylpyrimidines of the formula I, in which the substituents have the following meanings: R1 is a five- to ten-membered saturated, partially unsaturated or aromatic mono- or bicyclic heterocycle comprising one to four hetero atoms selected from the group consisting of O, N or S, which heterocycle can be substituted as defined in the description, R2 is hydrogen, halogen, cyano, alkyl, haloalkyl or alkoxy; R3, R4 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl or cycloalkynyl, R3 and R4 together with the nitrogen atom to which they are bonded may also form a five- or six-membered ring which can be interrupted by a hetero atom and have attached to it one or more substituents; R5, R6 are hydrogen, halogen, alkyl, haloalkyl or alkoxy; R7, R8 are hydrogen, halogen, alkyl or haloalkyl; R9 is hydrogen, halogen, alkyl, alkoxy, cycloalkoxy, haloalkoxy or alkoxycarbonyl, Processes and intermediates for the preparation of these compounds, and their use for controlling harmful fungi.
Abstract translation:式I的5-苯基嘧啶,其中取代基具有以下含义:R 1是5至10元饱和的,部分不饱和的或芳族的单环或双环杂环,其包含一至四个杂 选自O,N或S的原子,该杂环可以如描述中所定义而被取代,R 2是氢,卤素,氰基,烷基,卤代烷基或烷氧基; R 3,R 4是氢,烷基,卤代烷基,环烷基,卤代环烷基,烯基,卤代烯基,环烯基,炔基,卤代炔基或环炔基,R 3 O 和R 4与它们所键合的氮原子一起也可以形成五元或六元环,其可被杂原子间隔并且与其连接一个或多个取代基; R 5,R 6是氢,卤素,烷基,卤代烷基或烷氧基; R 7,R 8是氢,卤素,烷基或卤代烷基; R 9是氢,卤素,烷基,烷氧基,环烷氧基,卤代烷氧基或烷氧羰基。用于制备这些化合物的方法和中间体及其用于控制有害真菌的用途。
Abstract:
Triazolopyrimidines of the formula I in which the substituents are as defined below: R1, R2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S, R1 and R2 together with the nitrogen atom to which they are attached may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and may contain a further heteroatom from the group consisting of O, N and S as ring member and may be substituted as defined in the description; L1, L2 are hydrogen, cyano, haloalkyl, alkoxy, alkenyloxy or C(═O)A, where at least one group L1 or L2 is not hydrogen; A is hydrogen, hydroxyl, alkyl, alkoxy, haloalkoxy, C1-C8-alkylamino or dialkylamino; L3 is hydrogen, halogen, cyano, nitro, haloalkyl, alkoxy or alkoxycarbonyl; X is halogen, cyano, alkyl, haloalkyl, alkoxy or haloalkoxy; processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
Abstract:
The present invention relates to pyrimidines of the formula I in which the index n and the substituents L, R1-R3 are as defined in the description and R4 corresponds to one of the formulae and to processes and intermediates for preparing these compounds, to compositions comprising them and to their use for controlling phytopathogenic harmful fungi.