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    1,3-(HET)ARYL-SUBSTITUTED PYRAZOLE COMPOUNDS
    32.
    发明申请
    1,3-(HET)ARYL-SUBSTITUTED PYRAZOLE COMPOUNDS 审中-公开
    1,3-（HET）芳基取代的吡唑化合物

    公开(公告)号：WO2015022293A2

    公开(公告)日：2015-02-19

    申请号：PCT/EP2014067165

    申请日：2014-08-11

    Applicant: BASF SE

    Inventor： KÖRBER KARSTEN ,  VON DEYN WOLFGANG ,  DIETZ JOCHEN ,  NARINE ARUN ,  WACH JEAN-YVES ,  KOLLER RAFFAEL ,  DICKHAUT JOACHIM

    IPC: C07D401/14

    CPC classification number: C07D401/06 ,  C07D401/14 ,  C07D403/06

    Abstract: The present invention relates to 1,3-aryl- or hetaryl-substituted pyrazole compounds of formula (I), wherein the variables are as defined in the claims and the description. The compounds are useful for combating or controlling invertebrate pests, in particular arthropod pests and nematodes. The invention also relates to a method for controlling invertebrate pests by using these compounds and to plant propagation material and to an agricultural and a veterinary composition comprising said compounds. The invention further relates to a method for preparing the pyrazole compounds of the invention.

    Abstract translation: 本发明涉及式（I）的1,3-芳基 - 或杂芳基 - 取代的吡唑化合物，其中变量如权利要求和说明书中所定义。 这些化合物可用于防治或控制无脊椎害虫，特别是节肢动物害虫和线虫。 本发明还涉及通过使用这些化合物防治无脊椎害虫的方法和植物繁殖材料以及包含所述化合物的农业和兽医学组合物。 本发明还涉及制备本发明吡唑化合物的方法。

    FUNGICIDAL MIXTURES II
    36.
    发明申请
    FUNGICIDAL MIXTURES II 审中-公开
    真菌混合物II

    公开(公告)号：WO2009063075A3

    公开(公告)日：2010-05-06

    申请号：PCT/EP2008065604

    申请日：2008-11-14

    Applicant: BASF SE ,  RENNER JENS ,  ULMSCHNEIDER SARAH ,  DIETZ JOCHEN ,  HADEN EGON

    Inventor： RENNER JENS ,  ULMSCHNEIDER SARAH ,  DIETZ JOCHEN ,  HADEN EGON

    IPC: A01P3/00 ,  A01N37/34 ,  A01N43/40 ,  A01N43/50 ,  A01N43/54 ,  A01N43/653 ,  A01N43/88 ,  A01N47/12 ,  A01N47/38

    CPC classification number: A01N43/40 ,  A01N37/34 ,  A01N43/50 ,  A01N43/54 ,  A01N43/653 ,  A01N43/88 ,  A01N47/12 ,  A01N47/18 ,  A01N47/38 ,  A01N2300/00

    Abstract: The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 3-hydroxyl-3-(3-pyridyl)propanoate compound of the formula (I) X1 and X2 are hydrogen or X1 together with X2 form a covalent bond; R1 is H, CN, C1-C6-alkyl, C2-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6- alkylthio-C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, aryl-C1-C4-alkyl, ary- loxy-C1-C4-alkyl, arylthio-C1-C4-alkyl, aryl, hetaryl-C1-C4-alkyl, hetaryloxy- C1-C4-alkyl, hetarylthioC1-C4-alkyl or heteroaryl, wherein the cyclic moieties of the last eight radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C2-C4-alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-alkylsulfinyl, C1-C4-alkylsulfonyl, C1-C4-haloalkoxy, C1-C4-haloalkylthio, cyano and nitro; A is a covalent bond or Ci-C4-alkylen, which is unsubstituted or which may carry a substitutent selected from Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and cyano; Ar is aryl or heteroaryl, wherein the cyclic moieties of the aromatic radicals are unsubstituted or substituted with 1, 2 or 3 radicals Ra, where the radicals Ra are identical or different and selected from halogen, C1-C4-alkyl, C2-C4- alkenyl, C2-C4-alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, C1-C4-haloalkylthio, cyano, nitro, aryl, hetaryl, aryloxy, hetaryloxy, aryloxy-C1-C4-alkyl and hetaryloxy-C1-C4-alkyl, wherein the cyclic moieties of the six last mentioned radicals are unsbsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, cyano and nitro; or a tautomer or a salt thereof. and at least one further fungicidally active compound II.

    Abstract translation: 本发明涉及杀真菌活性化合物的混合物，其包含至少一种式（I）的取代的3-羟基-3-（3-吡啶基）丙酸酯化合物，X 1和X 2是氢或X 1与X 2一起形成共价键; R 1是H，CN，C 1 -C 6烷基，C 2 -C 6炔基，C 1 -C 6烷氧基-C 1 -C 6烷基，C 1 -C 6烷基硫代-C 1 -C 6烷基，C 1 -C 6卤代烷基， C 1 -C 4 - 烷氧基，芳基-C 1 -C 4 - 烷基，芳氧基-C 1 -C 4 - 烷基，芳硫基-C 1 -C 4 - 烷基，芳基，杂芳基-C 1 -C 4烷基，苯氧基-C 1 -C 4烷基， C4-烷基或杂芳基，其中最后八个基团的环状部分是未取代的或被1,2或3个选自卤素，C 1 -C 4 - 烷基，C 2 -C 4 - 炔基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - C 1 -C 4 - 烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4烷基亚磺酰基，C 1 -C 4烷基磺酰基，C 1 -C 4卤代烷氧基，C 1 -C 4卤代烷硫基，氰基和硝基; A是共价键或C 1 -C 4亚烷基，其是未取代的或可以携带选自C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和氰基的取代基; Ar是芳基或杂芳基，其中芳族基团的环状部分是未取代的或被1,2或3个基团R a取代，其中基团R a相同或不同并且选自卤素，C 1 -C 4烷基，C 2 -C 4 - 烯基，C 2 -C 4 - 炔基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4卤代烷氧基，C 1 -C 4卤代烷硫基，氰基，硝基，芳基，杂芳基，芳氧基， 芳氧基-C 1 -C 4 - 烷基和芳基氧基-C 1 -C 4 - 烷基，其中六个最后提到的基团的环状部分是未取代的或被1,2或3个选自卤素，C 1 -C 4 - 烷基，C 1 -C 4 卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4卤代烷氧基，氰基和硝基; 或其互变异构体或其盐。 和至少一种其它杀真菌活性化合物II。

    FUNGICIDAL MIXTURES III
    39.
    发明申请
    FUNGICIDAL MIXTURES III 审中-公开
    真菌混合物III

    公开(公告)号：WO2009063076A2

    公开(公告)日：2009-05-22

    申请号：PCT/EP2008065606

    申请日：2008-11-14

    Applicant: BASF SE ,  RENNER JENS ,  ULMSCHNEIDER SARAH ,  DIETZ JOCHEN ,  HADEN EGON

    Inventor： RENNER JENS ,  ULMSCHNEIDER SARAH ,  DIETZ JOCHEN ,  HADEN EGON

    IPC: A01P3/00 ,  A01N37/34 ,  A01N37/50 ,  A01N43/40 ,  A01N43/50 ,  A01N43/54 ,  A01N43/653 ,  A01N43/88 ,  A01N47/04 ,  A01N47/12 ,  A01N47/14 ,  A01N47/24

    CPC classification number: A01N43/40 ,  A01N37/34 ,  A01N37/50 ,  A01N43/50 ,  A01N43/54 ,  A01N43/653 ,  A01N47/04 ,  A01N47/12 ,  A01N47/14 ,  A01N47/24 ,  A01N61/00 ,  A01N2300/00

    Abstract: The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 2-[hydroxyl(pyridine-3-yl)methyl]acrylate compound of the formula (I) wherein: R1 is H, C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkyl,C1-C6-haloalkyl, aryl or het- eroaryl, wherein the cyclic moieties of the last two radicals are unsubsti- tuted or substituted with 1, 2 or 3 radicals selected from halogen, C1-C4 alkyl, C2-C4-alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4- haloalkoxy, cyano and nitro; A is a covalent bond or C1-C4-alkylen, which is unsubstituted or which may carry a substitutent selected from C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy and cyano; Ar is aryl or heteroaryl, wherein the cyclic moieties of the aromatic radicals are unsubstituted or substituted with 1, 2 or 3 radicals Ra, where the radicals Ra are identical or different and selected from halogen, C1-C4-alkyl, C2-C4- alkenyl, C2-C4-alkynyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1- C4-haloalkoxy, C1-C4-haloalkylthio, cyano, nitro, aryl, hetaryl, aryloxy, hetaryloxy, aryloxy-C1-C4-alkyl and hetaryloxy-C1-C4-alkyl, wherein the cyclic moieties of the six last mentioned radicals are unsubstituted or substi- tuted with 1, 2 or 3 radicals selected from halogen, C1-C4-alkyl, C1-C4- haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-haloalkoxy, cyano and nitro; or a salt thereof; and at least one further fungicidally active compound II.

    Abstract translation: 本发明涉及包含至少一种式（I）的取代的2- [羟基（吡啶-3-基）甲基]丙烯酸酯化合物的杀真菌活性化合物的混合物，其中：R1是H，C1-C6-烷基，C1- C 1 -C 6 - 烷氧基-C 1 -C 6烷基，C 1 -C 6卤代烷基，芳基或芳基，其中最后两个基团的环状部分未被取代或被1,2或3个选自卤素，C1- C4烷基，C2-C4-炔基，C1-C4-卤代烷基，C1-C4-烷氧基，C1-C4-烷硫基，C1-C4-卤代烷氧基，氰基和硝基; A是共价键或C1-C4-亚烷基，其是未取代的或可以携带选自C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基和氰基的取代基; Ar是芳基或杂芳基，其中芳族基团的环状部分是未取代的或被1,2或3个基团R a取代，其中基团R a相同或不同并且选自卤素，C 1 -C 4烷基，C 2 -C 4 - 烯基，C 2 -C 4 - 炔基，C 1 -C 4卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4卤代烷氧基，C 1 -C 4卤代烷硫基，氰基，硝基，芳基，杂芳基，芳氧基， 芳氧基-C 1 -C 4烷基和芳基氧基-C 1 -C 4 - 烷基，其中六个最后提到的基团的环状部分是未取代的或被1,2或3个选自卤素，C 1 -C 4 - 烷基，C 1 -C 4烷基的基团取代 C 1-4卤代烷基，C 1 -C 4 - 烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4卤代烷氧基，氰基和硝基; 或其盐; 和至少一种其它杀真菌活性化合物II。

    METHOD FOR PROTECTING SOYBEANS FROM BEING INFECTED BY FUNGI
    40.
    发明申请
    METHOD FOR PROTECTING SOYBEANS FROM BEING INFECTED BY FUNGI 审中-公开
    防治真菌感染大豆的方法

    公开(公告)号：WO2008113654A3

    公开(公告)日：2008-11-20

    申请号：PCT/EP2008051955

    申请日：2008-02-19

    Applicant: BASF SE ,  DIETZ JOCHEN ,  STRATHMANN SIEGFRIED ,  STIERL REINHARD

    Inventor： DIETZ JOCHEN ,  STRATHMANN SIEGFRIED ,  STIERL REINHARD

    IPC: A01N43/56 ,  A01N43/653 ,  A01P3/00

    CPC classification number: A01N43/56 ,  A01N2300/00

    Abstract: Method for protecting soybean plants from being infected by harmful fungi, wherein the soybean plants, their seed or the soil is treated with a fungicidal effective amount of a synergistically active combination comprising a) N-(2-bicycloprop-2-ylphenyl)-3-difluoromethyl-1-methyl-1H-pyrazole-4- carboxamide (I) or 3-(difluoromethyl)-1-methyl-N-[1,2,3,4-tetrahydro-9-(1- methylethyl)-1,4-methanonaphthalen-5-yl]-1H-pyrazole-4-carboxamide(II) and b) epoxiconazole or metconazole; a fungicidal agent and seed comprising said combination.

    Abstract translation: 保护大豆植物免受有害真菌感染的方法，其中用杀真菌有效量的协同活性组合处理大豆植物，其种子或土壤，其包含a）N-（2-双环丙-2-基苯基）-3 - 二氟甲基-1-甲基-1H-吡唑-4-甲酰胺（I）或3-（二氟甲基）-1-甲基-N- [1,2,3,4-四氢-9-（1-甲基乙基）-1 ，4-甲基萘-5-基] -1H-吡唑-4-甲酰胺（II）和b）环氧唑或甲康唑; 杀真菌剂和包含所述组合的种子。

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