Process for the preparation of thiazole derivatives
    31.
    发明授权
    Process for the preparation of thiazole derivatives 失效
    噻唑衍生物的制备方法

    公开(公告)号:US06677457B2

    公开(公告)日:2004-01-13

    申请号:US10047807

    申请日:2002-01-15

    IPC分类号: C07D27716

    摘要: The invention relates to a process for the preparation of a compound of the formula wherein Q, Y, Z, R1, R2, R3, R4 and R5 are as defined in the specification, which comprises a) reacting a compound of the formula  with a halogenating agent to form a compound of the formula or b) converting a compound of formula (II) by means of a halogenating agent into a compound of the formula optionally c) converting the compound of formula (IV) into a compound of formula (III); d) converting a compound of formula (III) by means of a compound of the formula into a compound of the formula or e) converting a compound (IV) by means of a compound (V) into a compound (VI); and f) converting a compound (VI) by means of a chlorinating agent into a compound (I); a compound (IV); to a process for the preparation of a compound (III) and to a process for the preparation of a compound (IV).

    摘要翻译: 本发明涉及制备糠醛的化合物的方法,其中Q,Y,Z,R 1,R 2,R 3,R 4和R 5如本说明书中所定义,其包括:a)将卤化剂的化合物与 将式(II)化合物通过卤化剂转化成式(Ⅲ)的化合物,将式(Ⅳ)化合物转化为式(Ⅳ)化合物; d)将化合物 通过化学式(Ⅳ)将化合物(Ⅳ)转化为化合物(Ⅵ);将式(Ⅳ)化合物与式 和(f)通过氯化剂将化合物(VI)转化为化合物(I);化合物(IV); 涉及制备化合物(III)的方法和制备化合物(IV)的方法。

    Thiazole compounds
    32.
    发明授权
    Thiazole compounds 失效
    噻唑化合物

    公开(公告)号:US06211381B1

    公开(公告)日:2001-04-03

    申请号:US09077569

    申请日:1998-06-01

    IPC分类号: C07D27732

    摘要: The invention relates to a process for preparing a compound of formula (I), in which X is CH or N, Y is NO2 or CN, Z is CHR3, O, NR3 or S, R1 and R2 are either each, independently of the other, hydrogen or unsubstituted or R4-substituted alkyl or together a two- or three-membered alkylene bridge or a two- or three-membered alkylene bridge in which one member is replaced by a hetero member selected from the group, consisting of NR5, O and S, R3 is H or unsubstituted or R4-substituted alkyl, R4 is an unsubstituted or substituted aryl or heteroaryl group, and R5 is H or alkyl, which comprises a) reacting a compound of formula (II) with a chlorinating agent or b1) initially reacting a compound of formula (IV) with a compound of formula (V) and b2) further reacting the compound of formula (II) obtainable thereby, with or without intermediate isolation, with a chlorinating agent, to intermediates used in this process, to the use of these intermediates and to a process for the preparation of these intermediates.

    摘要翻译: 本发明涉及制备式(I)化合物的方法,其中X是CH或N,Y是NO 2或CN,Z是CHR 3,O,NR 3或S,R 1和R 2各自独立地是 另一个,氢或未取代的或R4取代的烷基或二元或三元亚烷基桥或二元或三元亚烷基桥,其中一个成员被选自NR5, O和S,R 3是H或未取代的或R 4取代的烷基,R 4是未取代或取代的芳基或杂芳基,R 5是H或烷基,其包括a)使式(II)化合物与氯化剂或 b1)最初使式(Ⅳ)化合物与式(Ⅴ)化合物反应,和b2)使可得到的式(Ⅱ)化合物进一步与中间体分离与氯化剂反应,得到本发明的中间体 过程,使用这些中间体和制备过程 这些中间体。

    Chemical compounds
    34.
    发明授权
    Chemical compounds 失效
    化合物

    公开(公告)号:US08524896B2

    公开(公告)日:2013-09-03

    申请号:US12921000

    申请日:2009-03-02

    摘要: A compound of the formula (I) where, for example, W, X and Y are each CH; R1 and R6 together with the adjacent nitrogen forms a 3 to 10-membered saturated ring, wherein the ring may contain, in addition to the nitrogen and carbon ring members, 1, 2 or 3 heteroatoms and/or heteroatom groups as ring members, independently of one another, selected from the group consisting of sulfur, CO, SO, SO2 and N—R7 and/or the ring may carry 1, 2 or 3 radicals, independently of one another, each selected, for example, from the group consisting of halogen, cyano, nitro, amino, and C1-C6-alkyl. R2 is, for example, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy or C1-C6-alkoxy-C1-C6-alkoxy, and R7 is for example, R10C(═O), C1-C6 alkyl or C1-C6-haloalkyl; and/or salts thereof; and their use as pesticidal agents.

    摘要翻译: 式(I)的化合物,其中例如W,X和Y各自为CH; R1和R6与相邻的氮一起形成3至10元饱和环,其中除了氮和碳环成员之外,环可以独立地包含1,2或3个杂原子和/或杂原子基团作为环成员 彼此相互选择,选自硫,CO,SO,SO 2和N-R 7和/或环可以彼此独立地携带1,2或3个基团,每个选自例如 的卤素,氰基,硝基,氨基和C 1 -C 6 - 烷基。 R 2是例如卤素,C 1 -C 6烷基,C 1 -C 6卤代烷基,C 1 -C 6 - 烷氧基,C 1 -C 6 - 卤代烷氧基或C 1 -C 6 - 烷氧基-C 1 -C 6 - 烷氧基, R 10 C(= O),C 1 -C 6烷基或C 1 -C 6 - 卤代烷基; 和/或其盐; 并将其用作杀虫剂。

    Avermectins and avermectin monosacharides substituted in the 4′-and 4″ position having pesticidal properties
    39.
    发明授权
    Avermectins and avermectin monosacharides substituted in the 4′-and 4″ position having pesticidal properties 有权
    在具有杀虫性的4'和4“位置取代的阿维菌素和阿维菌素单糖苷

    公开(公告)号:US07704961B2

    公开(公告)日:2010-04-27

    申请号:US10568715

    申请日:2004-08-27

    CPC分类号: A01N43/90 C07H19/01

    摘要: Described is a compound of the formula (I) wherein the bond between carbon atoms 22 and 23 is a single or double bond; m is 0 or 1; R1, is C1-C12alkyl, C3-C8cycloalkyl or C2-C12alkenyl; and either (A) R2 is —N(R3)R4, and (1) X is 0, wherein R3 is, for instance, hydrogen, unsubstituted or mono- to pentasubstituted C1-C12alkyl, and R4 is, for instance, mono- to pentasubstituted C1-C12alkyl, unsubstituted or mono- to pentasubstituted C3-C12cycloalkyl; or (2) X is S, wherein R3 is, for instance, hydrogen, unsubstituted or mono- to pentasubstituted C1-C12alkyl, and R4 is, for instance, hydrogen, unsubstituted or mono- to pentasubstituted C1-C12alkyl; or (3) X is 0 or S, wherein R3 and R4 together are, for instance, a three- to seven membered alkylene or a four- to seven-membered alkenylene bridge; or (B) R2 is OR5, X is 0 or S, wherein R5 is, for instance, C1-C12alkyl, mono- to pentasubstituted C1-C12alkyl; or, if appropriate, an E/Z isomer, E/Z isomer mixture and/or tautomer thereof, in each case in free form or in salt form; such a compound demonstrates pesticidal activity.

    摘要翻译: 描述了式(I)的化合物,其中碳原子22和23之间的键是单键或双键; m为0或1; R1是C1-C12烷基,C3-C8环烷基或C2-C12链烯基; (A)R 2是-N(R 3)R 4,和(1)X是0,其中R 3是例如氢,未被取代的或单取代到五取代的C 1 -C 12烷基,R 4是例如, 至五取代的C 1 -C 12烷基,未取代的或一至五取代的C 3 -C 12环烷基; 或(2)X为S,其中R 3为例如氢,未取代或单价至五价取代的C 1 -C 12烷基,R 4为例如氢,未取代或单价至五价取代的C 1 -C 12烷基; 或(3)X为0或S,其中R3和R4一起为例如三至七元亚烷基或四至七元亚烯基桥; 或(B)R 2是OR 5,X是0或S,其中R 5是例如C 1 -C 12烷基,一至五取代的C 1 -C 12烷基; 或者如果合适的话,E / Z异构体,E / Z异构体混合物和/或其互变异构体在每种情况下都是游离形式或盐形式; 这种化合物显示出杀虫活性。

    Avermectin and avermectin monosaccharide derivatives substituted in the 4″-or 4′-position having pesticidal properties
    40.
    发明授权
    Avermectin and avermectin monosaccharide derivatives substituted in the 4″-or 4′-position having pesticidal properties 有权
    在4“ - 或4”位取代的具有杀虫性的阿维菌素和阿维菌素单糖衍生物

    公开(公告)号:US07678740B2

    公开(公告)日:2010-03-16

    申请号:US10543637

    申请日:2004-01-30

    CPC分类号: A01N43/90 C07H17/08

    摘要: What is described are a compound of the formula (I) Wherein U is —N(R2)OR3 or —N+(O−)═C(RE)RZ); n is 0 or 1; X—Y is —CH═CH— or —CH2—CH2—; R1 is C1-C12alkyl, C3-C8cycloalkyl or C2-C12alkenyl; R2 and R3 are, for example; independently from each other, —Q, —C(═O)—Z—Q or —CN; RZ and RE are, independently from each other, —Q, —C(═O)—Z—Q or —CN; or RZ and RE together are a three- to seven membered alkylene or alkenylene bridge, which is unsubstituted or mono- to tri-substituted; Z is a bond, O or —NR4—; Q is H, C1-C12alkyl, C2-C12alkenyl, C2-C12alkynyl, C3-C12-Cycloalkyl, C5-C12-cycloalkenyl, aryl, or heterocyclyl, which are unsubstituted or mono- to pentasubstituted; R4 is for example H, C1-C8alkyl, hydroxy-C1-C8alkyl, C3-C8cycloalkyl or C2-C8alkenyl; or, if appropriate, an E/Z isomer, E/Z isomer mixture and/or tautomer thereof; a process for preparing these compounds, their isomers and tautomers and the use of these compounds, their isomers and tautomers; pesticidal compositions whose active compound is selected from these compounds and their tautomers; intermediates for the preparation of the said compounds of the formula (I), methods for the preparation of the compounds of the formula (I), and a method for controlling pests using these compositions.

    摘要翻译: 描述的是式(I)的化合物,其中U是-N(R 2)OR 3或-N +(O-)= C(RE)R Z); n为0或1; X-Y是-CH = CH-或-CH 2 -CH 2 - ; R1是C1-C12烷基,C3-C8环烷基或C2-C12链烯基; R2和R3例如是: 独立地为-Q,-C(= O)-Z-Q或-CN; RZ和RE彼此独立地为-Q,-C(= O)-Z-Q或-CN; 或RZ和RE一起是三至七元的亚烷基或亚烯基桥,其是未取代的或一至三取代的; Z是O或-NR4-键; Q是未被取代或被一取代或五取代的H,C 1 -C 12烷基,C 2 -C 12烯基,C 2 -C 12炔基,C 3 -C 12环烷基,C 5 -C 12 - 环烯基,芳基或杂环基, R4是例如H,C1-C8烷基,羟基-C1-C8烷基,C3-C8环烷基或C2-C8链烯基; 或者,如果合适的话,E / Z异构体,E / Z异构体混合物和/或其互变异构体; 制备这些化合物,其异构体和互变异构体的方法以及这些化合物,其异构体和互变异构体的用途; 活性化合物选自这些化合物及其互变异构体的杀虫组合物; 用于制备所述式(I)化合物的中间体,式(I)化合物的制备方法和使用这些组合物来控制害虫的方法。