BENZYL AMIDOXIME DERIVATIVES, INTERMEDIATE PRODUCTS AND METHOD FOR THEIR PRODUCTION AND USE AS FUNGICIDES
    11.
    发明申请
    BENZYL AMIDOXIME DERIVATIVES, INTERMEDIATE PRODUCTS AND METHOD FOR THEIR PRODUCTION AND USE AS FUNGICIDES 审中-公开
    BENZYLAMIDOXIM衍生物,中间产品和工艺及其及其作为杀菌剂

    公开(公告)号:WO0125187A3

    公开(公告)日:2001-11-01

    申请号:PCT/EP0009744

    申请日:2000-10-05

    CPC classification number: C07C259/14 A01N37/52 C07C2601/02

    Abstract: The invention relates to benzyl amidoxime derivatives of formula (I) as fungicides wherein: A represents an aryl or heteraryl radical; Y represents a straight-chained or branched C1-C4 alkylene group, whereby a carbon atom can be substituted by an oxygen, nitrogen or sulphur atom or by a cyclopropyl group; Rn represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy; R represents optionally substituted phenyl C1-C6 alkyl, thienyl C1-C4 alkyl, or pyrazolyl C1-C4 alkyl, Rp represents one to five similar or different radicals from the group consisting of hydrogen, halogen, C1-C6 alkyl, C1-C6 alkoxy, C1-C4 halogen alkyl, C1-C4 halogen alkoxy, C1-C4 alkylthio, C1-C4 alkoxyalkoxy, C1-C6 alkyl carbonyl; n represents 0-5; and p represents 0-4, according to the number of free valences.

    Abstract translation: 本申请涉及式(I)作为杀真菌剂的Benzylamidoxim衍生物。 其中A为芳基或杂芳基; Y线性或支链的C1-C4亚烷基,其中一个碳原子可以被氧,氮或硫原子或由环丙基取代; RN <1>一至选自五个相同或不同的基团:氢,卤素,C1-C6烷基,C1-C6-烷氧基,C1-C4卤代烷基,C1-C4卤代烷氧基,C1-C4烷硫基,C1 -C4烷氧烷; [R <2>任选取代的苯基-C 1 -C 6 - 烷基,噻吩基-C 1 -C 4 - 烷基,或吡唑基-C 1 -C 4 - 烷基,卢比<3>一个从组五个相同或不同的基团:氢,卤素 ,C1-C6烷基,C1-C6-烷氧基,C1-C4卤代烷基,C1-C4卤代烷氧基,C1-C4烷硫基,C1-C4烷氧基烷氧基,C1-C6烷基羰基; n为0-5; p取决于自由价的0-4的数量。

    SUBSTITUTED 5-HETARYLPYRIMIDINES
    12.
    发明申请
    SUBSTITUTED 5-HETARYLPYRIMIDINES 审中-公开
    取代的5 HETARYLPYRIMIDINE

    公开(公告)号:WO2007113322A2

    公开(公告)日:2007-10-11

    申请号:PCT/EP2007053332

    申请日:2007-04-04

    CPC classification number: C07D401/04 A01N43/54

    Abstract: The invention relates to 5-hetaryl-4-pyrimidines of formula (I) and to their salts and plant protection agents which contain at least one compound of said type as an active component, wherein W represents oxygen, sulphur, a group S=O or S(=O) 2 ; R 1 represents optionally substituted C 1 -C 8 -alkyl, C 3 -C 8 -cycloalkyl, C 5 -C 10 -bicycloalkyl, C 2 -C 8 -alkenyl, C 4 -C 10 -alkadienyl, C 3 -C 6 -cycloalkenyl, C 2 -C 8 -alkynyl, phenyl, naphthyl, or a C-bound five- or six-membered saturated, partially unsaturated or aromatic heterocycle containing one, two, three or four heteroatoms from the groups O, N or S as ring members; R 2 represents halogen, cyano, hydroxy, mercapto, N 3 , C 1 -C 6 -alkyl, C 2 -C 8 -alkenyl, C 2 -C 8 -alkynyl, C 1 C 6 -halogenalkyl, C 1 C 6 -alkoxy, C 3 -C 8 -alkenyloxy, C 3 -C 8 -alkynyloxy, C 1 C 6 -halogenalkoxy, C 1 -C 6 -alkylthio, C 3 -C 8 -alkenylthio, C 3 -C 8 -alkynylthio, C 1 -C 6 -halogenalkylthio, or a radical of formulae C(=Z)OR 21 , C(=Z)NR 22 R 23 , C(=Z)NR 24 -NR 22 R 23 , C(=Z)R 25 , CR 26 R 27 -OR 28 , CR 26 R 27 -NR 22 R 23 , ON(=CR 29 R 30 ), O-C(=Z)R 25 , NR 22 R 23a , NR 31 (C(=Z)R 25 ), NR 31 (C(=Z)OR 21 ), NR 31 (C(=Z)-NR 22 R 23 ), NR 32a (N=CR 29 R 30 ), NR 32 NR 22 R 23 , NR 32 OR 21 , or C(=N-Z'-R 25 )SR 21 ; or a cyclic radical; R3 represents hydrogen, OH, halogen, cyano, NR 37 R 38 , C 1 -C--alkyl, C 1 -C 8 -alkoxy, C 1 -C 8 -alkylthio, C 1 -C 8 -alkylsulfinyl, C 1 -C--alkylsulfonyl, C 2 -C 8 -alkenyl or C 2 -C 8 -alkinyl, whereby the seven latter radicals can be partially or totally halogenated and/or optionally can support one, two or three substitutes, selected among nitro, cyano, OH, C 1 -C 2 -alkoxy, C 1 -C 4 -alkoxycarbonyl, amino, C 1 -C 4 -alkylamino and Di-C 1 -C 4 -alkylamino, Het represents a substituted C- or N-bound, 5-or 6-membered aromatic heterocycle which comprises 1, 2, 3 or 4 heteroatoms as ring members selected among nitrogen, oxygen and sulphur. The invention also relates to the use of 5-hetaryl-4-pyrimidines of formula (I) and there salts for combating plant pathogenic fungi.

    Abstract translation: 本发明涉及式(I)的包含至少一种这样的化合物作为有效成分的5-杂芳基-4-嘧啶和它们的盐和杀虫剂。 其中W = O或S(= O) 2 表示氧,硫,基团S; [R 1 表示任选subsitituiert.esç 1 -C 8 烷基,C 3 -C 8 环烷基,C 5 -C 10 双环,C 2 -C 8 - 烯基,C 4 -C 10 链二烯基,C 3 -C 6 环烯基,C 2 -C 8 是炔基,苯基,萘基或C-连接的五元或六元饱和,部分不饱和或芳族的含有一个,两个,三个或四个杂原子的从杂环 包含基团的O,N或S作为环成员; [R 2 表示卤素,氰基,羟基,巯基,N 3 ,C 1 -C 6 烷基, ç 2 -C 8 烯基,C 2 -C 8 - 炔基,C 1 < / SUB> C 6 卤代烷基,C 1 C 6 烷氧基,C 3 -C 8 烯,C 3 -C 8 炔氧基,C 1 C 6 卤代烷氧基 ,C 1 -C 6 烷硫基,C 3 -C 8 烯,C 3 -C 8 炔硫基,C 1 -C 6 卤代烷硫基,或一个基团,式C(= Z) OR 21 ,C(= Z)NR 22 - [R 23 ,C(= Z)NR 24 -NR 22 - [R 23 ,C(= Z)R 25 ,CR 26 - [R 27 -OR 28 ,CR 26 - [R 27 -NR 22 - [R 23 , ON(= CR 29 - [R 30 ),OC(= Z)R 25 ,NR 22 - [R 图23A ,NR 31 (C(= Z)R 25 ),NR 31 (C(= Z)OR < SUP> 21 )NR 31 ( C(= Z)-NR 22 - [R 23 ),NR 32A (N = CR 29 - [R 30 ),NR 32 NR 22 - [R 23 ,NR 32 OR 21 ,或C(= N-Z'-R 25 )SR 21 ; 或环状基团; R 3是氢,OH,卤素,氰基,NR 37 - [R 38 ,C 1 -C - 烷基,C 1 -C 8 烷氧基,C 1 -C 8 烷硫基,C 1 -C 8 烷基亚磺酰基,C 1 -C - 烷基磺酰基,C 2 -C 8 链烯基或C 2 -C 8 炔基,其中所述7最后提到的基团可以部分或完全卤化和/或选自硝基一个,两个或三个取代基,氰基,OH,C 1 -C 2 烷氧基,C 1 -C 4 烷氧基羰基,氨基,C 1 -C 4 烷基氨基和二C 1 -C 4可携带>烷基氨基,

    FUNGICIDAL AGENTS CONTAINING PYRROLIDONES AS THEIR ACTIVE AGENTS AND USE THEREOF FOR TREATING PLANTS
    15.
    发明申请
    FUNGICIDAL AGENTS CONTAINING PYRROLIDONES AS THEIR ACTIVE AGENTS AND USE THEREOF FOR TREATING PLANTS 审中-公开
    杀真菌剂含有作为活性吡咯烷酮和它们在植物的处理

    公开(公告)号:WO0162087A3

    公开(公告)日:2002-02-14

    申请号:PCT/EP0102059

    申请日:2001-02-23

    Abstract: The invention relates to agrochemical compositions with a fungicidal action, containing compounds of formula (I) as their active agents. The radicals of said formula have the following meanings: R means hydrogen, C1-C6-alkyl, C1-C6-alkylcarbonyl, formyl or C1-C6-halogenalkylcarbonyl; R means halogen, C1-C6-alkylthio, C1-C6-alkoxy, C3-C6-cycloalkyl-C1-C6-alkoxy, C1-C6-alkoxy-C1-C6-alkyl, halogen-C1-C6-alkoxy, C1-C6-alkylsulfonyl, C1-C6-alkylsulfinyl, halogen-C1-C6-alkylsulfonyl, cyano or a radical NR R ; R -R mean hydrogen, halogen, C1-C8-cycloalkyl, C1-C6-alkyl, halogen-C1-C6-alkyl, C1-C6-alkoxy, halogen-C1-C6-alkoxy, C1-C6-alkylsulfonyl, halogen-C1-C6-alkylsulfonyl, formyl, C1-C6-alkylcarbonyl, cyano, C1-C6-alkylthio or phenyl, which can optionally be substituted by halogen atoms, C1-C6-alkyl or halogen-C1-C6-alkyl groups; R means hydrogen, C1-C6-alkyl; and R means C1-C6-alkyl, C1-C8-cycloalkyl or together with R and the nitrogen atom to which they are bonded, a saturated or unsaturated heterocyclic five or six-membered ring which has one or two heteroatoms selected from a group consisting of nitrogen atoms and oxygen atoms. The invention also relates to salts of said compositions which are suitable for agricultural use.

    Abstract translation: 本发明的目的是具有包含(I),其中各基团具有以下含义的式作为活性成分的化合物的杀真菌作用的农药组合物,R <1>是氢,C1-C6烷基,C1-C6烷基羰基,甲酰基或C1-C6 卤代; [R <2>为卤素,C1-C6-烷硫基,C1-C6烷氧基,C3-C6环烷基-C1-C6-烷氧基,C1-C6烷氧基C1-C6烷基,卤代C1-C6烷氧基, C1-C6烷基磺酰基,C1-C6-烷基亚磺酰基,卤代C1-C6烷基磺酰基,氰基或基团NR <13> - [R <14>; [R <3> -R <12>为氢,卤素,C1-C8环烷基,C1-C6-烷基,卤代C1-C6烷基,C1-C6-烷氧基,卤代C1-C6烷氧基,C1-C6 烷基磺酰基,卤代C1-C6烷基磺酰基,甲酰基,C1-C6烷基羰基,氰基,C1-C6烷硫基或苯基,其是任选地被卤素原子,C1-C6烷基或烷基 - 卤素-C 1 -C 6 - 取代的 基团可被取代,R <13>为氢,C1-C6烷基,R <14> C1-C6-烷基,C1-C8环烷基,或一起为R <13>和的氮原子它们所连接形成其 意味着饱和或ungesätttigten杂环五元或含有从包含氮原子或氧原子,和它们的可农用可用的盐的组中选择的一个或两个杂原子的六元环。

    2-SUBSTITUTED 7-AMINO-AZOLOPYRIMIDINE, A METHOD FOR THE PRODUCTION AND USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI AND AGENTS CONTAINING SAID COMPOUND
    18.
    发明申请
    2-SUBSTITUTED 7-AMINO-AZOLOPYRIMIDINE, A METHOD FOR THE PRODUCTION AND USE THEREOF FOR CONTROLLING PATHOGENIC FUNGI AND AGENTS CONTAINING SAID COMPOUND 审中-公开
    2-取代的7- aminoazolopyrimidines,METHOD用于生产和它们用于防治有害真菌和代理含

    公开(公告)号:WO2006092428A2

    公开(公告)日:2006-09-08

    申请号:PCT/EP2006060399

    申请日:2006-03-02

    CPC classification number: C07D487/04

    Abstract: The invention relates to 2-substituted 7-amino-azolopyrimidine of formula (I), wherein substituents have the following meanings: R 1 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, Cycloalkyl, alkoxy, alkoxyalkyl, benzyloxyalkyl, alkoxyalkenyl or akoxyalkinyl; R 2 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkoxyalkyl and alkylthioalkyl, wherein a carbon chain in R 1 and/or R 2 are substitutable according to a description; R 3 is halogen, Cyano, NR A R B , hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phe- nylthio, benzyloxy, benzylthio, alkyl-S(O) m- ; A N and CR x ; R x is hydrogen or one of above groups for R 3 . A method and intermediate products for producing said compounds, agents containing said compounds and the use thereof for combating plant-pathogen fungi are also disclosed.

    Abstract translation: 2-取代的式(I)其中取代基具有以下含义的7-氨基azolopyrimidines:R t 1 为氢,卤素,氰基,烷基,卤代烷基,烯基,炔基,环烷基,烷氧基,烷氧基烷基, benzyloxyalkyl,烷氧基烯基或alkoxyalkynyl; [R 2 为氢,卤素,氰基,烷基,卤代烷基,烯基,炔基,环烷基,烷氧基,烷氧基烷基和烷硫基烷基,其中在R中的碳链 1 和/或R 2 可以根据描述被取代; [R 3 为卤素,氰基,NR - [R ,羟基,巯基,烷基,卤代烷基,环烷基,烷氧基,烷硫基,环烷氧基,环烷硫基, 羧基,甲酰基,烷基羰基,烷氧基羰基,烯氧基羰基,炔氧基羰基,苯基,苯氧基,苯丙氨酸nylthio,苄氧基,苄硫基,烷基-S(O)米 - ; A N和CR X ; ,R 3 X 是氢或其中R 称作; 的方法和中间体制备这些化合物,含有它们和它们在防治植物病原性有害真菌的组合物。

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