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11. 发明申请

WO2008152138A3 METHOD FOR PRODUCING DIFLUOROMETHYL-SUBSTITUTED PYRAZOLE COMPOUNDS 审中-公开
标题翻译：用于生产二氟吡唑
公开(公告)号：WO2008152138A3
公开(公告)日：2009-05-28
申请号：PCT/EP2008057506
申请日：2008-06-13
申请人： BASF SE , NETT MARKUS , GROTE THOMAS , LOHMANN JAN KLAAS , DIETZ JOCHEN , SMIDT SEBASTIAN PEER , RACK MICHAEL , ZIERKE THOMAS
发明人： NETT MARKUS , GROTE THOMAS , LOHMANN JAN KLAAS , DIETZ JOCHEN , SMIDT SEBASTIAN PEER , RACK MICHAEL , ZIERKE THOMAS
IPC分类号： C07D231/12 , C07D231/14
CPC分类号： C07D231/12 , C07D231/14
摘要： The invention relates to a method for producing 3-difluoromethyl-substituted pyrazole compounds of formula (I), wherein R1 represents H, halogen, nitro, C1-C8 alkyl, C1-C8 haloalkyl, C3-C8 cycloalkyl, phenyl, naphthyl, hetaryl, cyano, -C(=O)-OR1a, -C(=O)-NR1bR1c, -C(=O)-SR1d or -C(=S)-SR1 e; R2 represents H, C1-C4 alkyl, benzyl or phenyl; R3 represents H, halogen, C1-C8 alkoxy, C1-C8 haloalkoxy, C3-C8 cycloalkoxy, C2-C8 alkenyloxy, C1-C8 alkylthio, C1-C8 haloalkylthio, C3-C8 cycloalkylthio or C2-C8 alkenylthio; to compounds of formula (II.a) or (II.b), wherein R1 and R3 have one of the above definitions; R4 represents halogen, -OR4a, -SR4a , -O-SO2-R4a or a group -NR4bR4c; R5 and R6 represent C1-C8 alkyl, C1-C8 haloalkyl, C3-C8 cycloalkyl, benzyl or phenyl or together with the nitrogen atom to which they are bound represent a 3- to 8-membered heterocycle; to Lewis acid adducts of compounds of formula (II.b); to the use of compounds of formula (II.a) or (II.b) and of the Lewis acid adducts thereof for producing compounds of formula (I) or (VI); and to a method for converting said compounds to the corresponding 3-difluoromethylpyrazole-4-yl carboxylic acids.
摘要翻译：本发明涉及一种用于制备式-3-二氟甲基吡唑（I）化合物其中R1是H，卤素，硝基，C1-C8烷基，C1-C8卤代烷基，C3-C8环烷基，苯基，萘基，杂芳基，氰基，-C（= O）-OR1a，-C（= O）-NR1bR1c，-C（= O）-SR1d或-C（= S）-SR1e基; R2是H，C1-C4烷基，苄基或苯基; R 3为H，卤素，C1-C8烷氧基，C1-C8卤代烷氧基，C3-C8环烷氧基，C2-C8链烯氧基，C1-C8烷硫基，C1-C8卤代烷硫基，C3-C8-环烷硫基或C 2 -C C8-烯硫基;式（二.a）或（二.b）的化合物，其中R 1和R 3具有以上给出的含义之一; R 4是卤素，-OR4a，-SR4a，-O-SO2-R4A或一组-NR4bR4c基; R5和R6是C1-C8烷基，C1-C8卤代烷基，C3-C8环烷基，苄基或苯基或一起与氮原子到它们所键合的，代表3-至8-元杂环; 式（二.b）化合物的路易斯酸加合物;使用（二.a）或（二.b）和路易斯酸加合物，式I化合物的对式（I）或（VI）的化合物的制备方法; 并且这些化合物转变成相应的3-二氟甲基吡唑-4-基甲磺酸的方法。

12. 发明专利

JP2010215642A Intermediate of isoxazolin-3-ylacyl benzene and method for producing the same 有权
标题翻译： ISOXAZOLIN-3- YLACYL BENZENE的中间体及其生产方法
公开(公告)号：JP2010215642A
公开(公告)日：2010-09-30
申请号：JP2010112839
申请日：2010-05-17
申请人： Basf Se , ビーエーエスエフソシエタス・ヨーロピアBasf Se
发明人： RHEINHEIMER JOACHIM , VON DEYN WOLFGANG , GEBHARDT JOACHIM , RACK MICHAEL , LOCHTMAN RENE , GOETZ NORBERT , KEIL MICHAEL , WITSCHEL MATTHIAS , HAGEN HELMUT , MISSLITZ ULF , BAUMANN ERNST
IPC分类号： C07C251/48 , C07B61/00 , C07C20060101 , C07C201/12 , C07C205/44 , C07C249/06 , C07C251/52 , C07C253/00 , C07C255/50 , C07C315/04 , C07C317/32 , C07C317/44 , C07C319/14 , C07C321/28 , C07C323/09 , C07D20060101 , C07D261/02 , C07D261/04 , C07D261/08 , C07D413/02 , C07D413/10
CPC分类号： C07C249/06 , C07C201/10 , C07C201/12 , C07C205/44 , C07C209/62 , C07C251/48 , C07C253/00 , C07C255/50 , C07C315/04 , C07C319/14 , C07D261/04 , C07D413/10 , C07C323/09 , C07C317/24 , C07C317/32 , C07C205/06 , C07C211/52
摘要： PROBLEM TO BE SOLVED: To provide an intermediate of an isoxazolin-3-ylacyl benzene useful as an agricultural chemical, and a new method for producing the intermediate. SOLUTION: A benzaldoxime derivative represented by formula III (wherein R 1 is a 1-6C alkyl group) can be obtained by reacting a corresponding methylbenzene derivative with an organic nitrite in an aprotic polar solvent in the presence of a base at lower temperature than -20°C. COPYRIGHT: (C)2010,JPO&INPIT
摘要翻译：待解决的问题：提供可用作农业化学品的异恶唑啉-3-基酰基苯的中间体，以及用于制备中间体的新方法。解决方案：通过使相应的甲基苯衍生物与有机亚硝酸盐在非质子传递极性溶剂中反应，可以得到由式III（其中R 1 为1-6C烷基）表示的苯甲醛肟衍生物在比-20℃低的温度下存在碱。版权所有（C）2010，JPO＆INPIT

13. 发明申请

WO2007063028A3 METHOD FOR PRODUCING SULFONAMIDES 审中-公开
标题翻译：用于生产磺胺
公开(公告)号：WO2007063028A3
公开(公告)日：2007-08-23
申请号：PCT/EP2006068832
申请日：2006-11-23
申请人： BASF AG , SCHMIDT THOMAS , GEBHARDT JOACHIM , LOEHR SANDRA , KEIL MICHAEL , WEVERS JAN HENDRIK , RACK MICHAEL , MAYER GUIDO , PLESCHKE AXEL
发明人： SCHMIDT THOMAS , GEBHARDT JOACHIM , LOEHR SANDRA , KEIL MICHAEL , WEVERS JAN HENDRIK , RACK MICHAEL , MAYER GUIDO , PLESCHKE AXEL
IPC分类号： C07C303/38 , C07C201/12 , C07C205/58 , C07C303/40 , C07C311/51
CPC分类号： C07C303/38 , C07C201/12 , C07C303/40 , C07C311/51 , C07C205/58
摘要： The invention relates to methods for producing sulfonamides of formula I, wherein the variables have the designations cited in the description, by reacting m-nitro-benzoic acid chlorides of formula II with aminosulfons of formula III, under the influence of B equivalents of base IV. Said method is characterised in that, during step a) the aminosulfon of formula III is reacted with B1 equivalents of base IV, and during step b), the reaction mixture resulting from step a) is reacted with m-nitro-benzoic acid chlorides of formula II and B2 equivalents of base IV; B, B1 and B2 having the designations cited in the description.
摘要翻译：一种用于磺酰胺的制备（I）其中各变量具有说明书中给出的含义，由间硝基 - 苯甲酰氯II与aminosulfones III的反应中，碱IV的乙等同物的影响下，其特征在于在步骤a工艺）包括一氨基砜III用碱IV的B1当量反应，和在步骤b），其从步骤a）的反应混合物结果与间 - 硝基 - 苯甲酰氯Ⅱ和的碱IV发生反应B2当量; 其中B，B1和B2具有说明书中给出的含义。

14. 发明申请

WO2006097279A8 AMIDRAZONE COMPOUNDS FOR COMBATING ANIMAL PESTS 审中-公开
标题翻译：用于组合动物疫苗的咪唑啉酮化合物
公开(公告)号：WO2006097279A8
公开(公告)日：2007-05-18
申请号：PCT/EP2006002331
申请日：2006-03-14
申请人： BASF AG , KORADIN CHRISTOPHER , DEYN WOLFGANG VON , RACK MICHAEL , KUHN DAVID G , CULBERTSON DEBORAH L , ANSPAUGH DOUGLAS , OLOUMI-SADEGHI HASSAN
发明人： KORADIN CHRISTOPHER , VON DEYN WOLFGANG , RACK MICHAEL , KUHN DAVID G , CULBERTSON DEBORAH L , ANSPAUGH DOUGLAS , OLOUMI-SADEGHI HASSAN
IPC分类号： A01N37/52 , A01P5/00 , A01P7/00 , A01P7/04 , C07C259/20
CPC分类号： C07C259/20 , A01N37/52 , C07C2601/02
摘要： The present invention relates to new amidrazone compounds which are useful for combating animal pests, in particular insects, arachnids and nematodes. The invention also relates to a method for combating insects, nematodes and arachnids. The amidrazone compounds are of the general formula (I) including the tautomers of I and the salts thereof; wherein X and Y are hydrogen or together form a chemical bond; Ar is an aromatic radical selected from phenyl and a 5- or 6-membered heteroaryl having 1 , 2, 3 or 4 heteroatoms as ring members, which are selected, independently of one another, from O, N and S, and where the aromatic radical may have 1 , 2, 3, 4 or 5 substituents R a ; R 1 is selected from the group consisiting of C 1 -C 1O -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, cyano-C 1 -C 4 -alkyl, hydroxy-C 1- C 4 -alkyl, C 1 -C 10 -haloalkyl, tri-(C 1 -C 4 -alkyl)-silyl-C 1 - C 4 -alkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 2 -C 10 -haloalkynyl, C 3 -C 10 -cycloalkyl, phenyl, heteroaryl, C 3 -C 10 -cycloalkyl-C 1 C 4 -alkyl, phenyl-C 1 -C 4 - alkyl and heteroaryl-C 1 C 4 alkyl, wherein C 3 -C 10 -cycloalkyl, heteroaryl and phenyl in the last six mentioned radicals may be unsubstituted or carry 1 , 2, 3, 4 or 5 substituents R b as defined above; R 2 is selected from the group consisiting of C 1- C 1 0-alkyl, c 1- c 4 -alkoxy- C 1- C 4 -alkyl, C 1- C 10 -haloalkyl, C 2 -C 10 -alkenyl, C 2 -C 10 -haloalkenyl, C 2 -C 10 -alkynyl, C 2 -C 10 - haloalkynyl,c 3 -C 10 -cycloalkyl, phenyl, heteroaryl, C 3 -C 10 -cycloalkyl-C 1- C 4 -alkyl, phenyl-C 1 -C 4 -alkyl and heteroaryI-C 1- C 4 -alkyl, wherein C 3 -C 10 -cycloalkyl, heteroaryl and phenyl in the last six mentioned radicals may be unsubstituted or carry 1 , 2, 3, 4 or 5 substituents R b as defined above.
摘要翻译：本发明涉及可用于对抗动物害虫，特别是昆虫，蜘蛛和线虫的新的氨基腙化合物。本发明还涉及一种防治昆虫，线虫和蜘蛛的方法。氨基腙化合物具有通式（I），其包括I的互变异构体及其盐; 其中X和Y是氢或一起形成化学键; Ar是选自苯基和具有1,2,3或4个杂原子作为环成员的5-或6-元杂芳基的芳族基团，其彼此独立地选自O，N和S，并且其中芳族基团可以具有1,2,3,4或5个取代基R a， R 1选自C 1 -C 10 - 烷基，C 1 -C 1 - 烷基， C 1 -C 4烷基，C 1 -C 4烷基，C 1 -C 4烷基，氰基-C 1 -C 4烷基， C 1 -C 6烷基，羟基-C 1 -C 4 - 亚烷基，C 1 -C 10 - 烷基，卤代烷基，三 - （C 1 -C 4 - 烷基） - 甲硅烷基-C 1 -C 4 - 烷基，C 2 -C 10 - 烯基，C 2 -C 10 - 卤代烯基，C 1 -C 10 - C 2 -C 10 - 炔基，C 2 -C 10 - 卤代炔基，C 3 - C 10 - 环烷基，苯基，杂芳基，C 3 -C 10 - 环烷基-C 1 -C C 1-4烷基，苯基-C 1 -C 4 - 烷基和杂芳基-C 1 -C 4烷基，其中C 3 -C 10 - 环烷基，杂芳基和苯基在后面六个提及的基团中可以是未取代的或携带1,2,3,4或4个 5个取代基R b如上所定义; R 2选自C 1 -C 1-4烷基，C 1 -C 4烷基， C 1-4烷基，C 1 -C 10烷基，C 1 -C 4烷基，C 1〜亚烷基，C 2 -C 10 - 烯基，C 2 -C 10 - 卤代烯基，C C 2 -C 10 - 炔基，C 2 -C 10 - 卤代炔基，C 3 - C 1 -C 10 - 环烷基，苯基，杂芳基，C 3 -C 10 - 环烷基-C 1 - C 1 -C 4 - 烷基，苯基-C 1 -C 4 - 烷基和杂芳基C 1 -C 其中C 3 -C 10 - 环烷基，最后六个所述基团中的杂芳基和苯基可以是未取代的或携带1， 2,3,4或5个如上定义的取代基R b。

15. 发明申请

WO2006125745A3 1-(1,2-DIPHENYL-ETHYL)-3-(2-HYDROXYETHYL)-THIOUREA COMPOUNDS FOR COMBATING ANIMAL PESTS 审中-公开
标题翻译： 1-（1,2-二苯基乙基）-3-（2-羟基乙基） - 硫脲化合物，用于组合动物饲料
公开(公告)号：WO2006125745A3
公开(公告)日：2007-05-10
申请号：PCT/EP2006062413
申请日：2006-05-18
申请人： BASF AG , KORDES MARKUS , HOFMANN MICHAEL , PUHL MICHAEL , GOETZ NORBERT , RACK MICHAEL , TEDESCHI LIVIO , TREACY MICHAEL F , CULBERTSON DEBORAH L , BUCCI TONI , KUHN DAVID G , OLOUMI-SADEGHI HASSAN , BRAUN FRANZ-JOSEF , ANSPAUGH DOUGLAS D
发明人： KORDES MARKUS , HOFMANN MICHAEL , PUHL MICHAEL , GOETZ NORBERT , RACK MICHAEL , TEDESCHI LIVIO , TREACY MICHAEL F , CULBERTSON DEBORAH L , BUCCI TONI , KUHN DAVID G , OLOUMI-SADEGHI HASSAN , BRAUN FRANZ-JOSEF , ANSPAUGH DOUGLAS D
IPC分类号： A01N47/28 , A01P7/04 , C07C335/12
CPC分类号： C07C335/12 , A01N47/28
摘要： The present invention relates to a method of combating animal pests which comprises contacting the animal pest, their habit, breeding ground, food supply, plant, seed, soil, area, material or environment in which the animal pests are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from animal at- tack or infestation, with a pesticidally effective amount of at least one 1-(1 ,2-diphenyl- ethyl)-3-(2-hydroxyethyl)-thiourea compound I or an agriculturally acceptable salt thereof, wherein m is 0 to 5, n is 0 to 5, R 3 and R 4 are H or optionally substituted alkyl, haloalkyl, cycloalkyl, phenyl or benzyl, R 7 , R 8 , R 9 and R 10 are H or optionally substituted C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 - alkylamino, C 1 -C 6 -alkoxy, C 3 -C 6 -cycloalkyl, phenyl or benzyl and the variables R 1 , R 2 , R 5 and R 6 are as defined in the claims. The invention relates also to a method for protecting crops from attack or infestation by animal pests, a method for protecting non-living materials from attack or infestation by animal pests, novel 1-(1 ,2-diphenyl-ethyl)-3-(2-hydroxyethyl)-thiourea compounds I and their agriculturally acceptable salts as well as to an agricultural composition comprising a 1-(1 ,2-diphenyl-ethyl)-3-(2-hydroxyethyl)-thiourea compound I or a salt thereof.
摘要翻译：本发明涉及一种防治动物害虫的方法，包括使动物害虫，其习惯，繁殖地，食物供应，植物，种子，土壤，区域，动物害虫生长或可能生长的物质或环境接触;或防止动物死亡或侵染的材料，植物，种子，土壤，表面或空间，具有杀虫有效量的至少一种1-（1,2-二苯基 - 乙基）-3-（2-羟乙基） - 硫脲化合物I或其农业上可接受的盐，其中m为0至5，n为0至5，R 3和R 4为H或任选取代的烷基，卤代烷基，环烷基，苯基或苄基，R 7，R 8，R 9和R 10是H 或任选取代的C 1 -C 6 - 烷基，C 1 -C 6 - 卤代烷基，C _{1，R 2，R 5和R 6如权利要求中所定义。本发明还涉及一种保护作物免受动物害虫侵袭或侵袭的方法，一种保护非生物材料免受动物害虫侵袭或侵染的方法，新的1-（1,2-二苯基 - 乙基）-3-（ 2-羟乙基） - 硫脲化合物I及其农业上可接受的盐，以及包含1-（1,2-二苯基 - 乙基）-3-（2-羟乙基） - 硫脲化合物I或其盐的农业组合物。}

16. 发明申请

WO2006125641A3 PYRIDINE COMPOUNDS FOR COMBATING ARTHROPOD PESTS AND NEMATODES 审中-公开
标题翻译：用于混合阿尔法糖和氰化物的吡啶化合物
公开(公告)号：WO2006125641A3
公开(公告)日：2007-02-15
申请号：PCT/EP2006004992
申请日：2006-05-24
申请人： BASF AG , PUHL MICHAEL , RACK MICHAEL , SCHMIDT THOMAS , HOFMANN MICHAEL , BAUMANN ERNST , KORDES MARKUS , DEYN WOLFGANG VON , KUHN DAVID G , CULBERTSON DEBORAH L , ANSPAUGH DOUGLAS , COTTER HENRY VAN TUYL , OLOUMI-SADEGHI HASSAN , BUCCI TONI , BASTIAANS HENRICUS M M
发明人： PUHL MICHAEL , RACK MICHAEL , SCHMIDT THOMAS , HOFMANN MICHAEL , BAUMANN ERNST , KORDES MARKUS , VON DEYN WOLFGANG , KUHN DAVID G , CULBERTSON DEBORAH L , ANSPAUGH DOUGLAS , COTTER HENRY VAN TUYL , OLOUMI-SADEGHI HASSAN , BUCCI TONI , BASTIAANS HENRICUS M M
IPC分类号： C07D401/12 , A01N43/40
CPC分类号： A01N43/40 , C07D401/12
摘要： The present invention relates to new pyridine compounds which are useful for combating animal pests, in particular insects, arachnids and nematodes. The invention also relates to a method for combating insects, nematodes and arachnids. The pyridine compounds have the formula I as defined below. Likewise, compounds of the formula Il are suitable for combating pests. In formulae I and Il n is 1 or 2, and R1, R2, R3, R4 and R5 are as defined in the claims and in the specification.
摘要翻译：本发明涉及可用于对抗动物害虫，特别是昆虫，蜘蛛和线虫的新的吡啶化合物。本发明还涉及一种防治昆虫，线虫和蜘蛛的方法。吡啶化合物具有如下定义的式I。同样地，式II化合物适用于防治害虫。在式I和II中，n为1或2，R1，R2，R3，R4和R5如权利要求书和说明书中所定义。

17. 发明申请

WO2007054558A2 RESORCINE DERIVATIVES AND THEIR USE AS PESTICIDES 审中-公开
标题翻译： RESORCINE衍生物及其作为杀虫剂的用途
公开(公告)号：WO2007054558A2
公开(公告)日：2007-05-18
申请号：PCT/EP2006068329
申请日：2006-11-10
申请人： BASF AG , PUHL MICHAEL , KORDES MARKUS , POHLMAN MATTHIAS , GOETZ NORBERT , RACK MICHAEL , LANGEWALD JUERGEN , SCHNEIDER FELIX , ANSPAUGH DOUGLAS D , CULBERTSON DEBORAH L , OLOUMI-SADEGHI HASSAN , KUHN DAVID G
发明人： PUHL MICHAEL , KORDES MARKUS , POHLMAN MATTHIAS , GOETZ NORBERT , RACK MICHAEL , LANGEWALD JUERGEN , SCHNEIDER FELIX , ANSPAUGH DOUGLAS D , CULBERTSON DEBORAH L , OLOUMI-SADEGHI HASSAN , KUHN DAVID G
CPC分类号： C07D213/64 , C07D277/34 , C07D307/80
摘要： This invention relates to resorcine derivatives of formula (I) wherein R 1 is phenyl or a 5- to 6-membered heteroaromatic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the heteroaromatic ring may be fused to a ring selected from phenyl and a 5- to 6-membered saturated, partially unsaturated or aromatic heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, nitrogen and sulfur, wherein phenyl or the 5- to 6-membered heteroaromatic ring or the respective fused ring systems may be unsubstituted or substituted by any combination of 1 to 6 optionally substituted groups R 3 , wherein R 3 is halogen, cyano, nitro, hydroxy, mercapto, amino, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, haloalkyl, haloalkenyl, haloalkynyl, halocycloalkyl, halocycloalkenyl, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, haloalkenyloxy, haloalkynyloxy, alkylthio, alkenylthio, alkynylthio, haloalkylthio, haloalkenylthio, haloalkynylthio, alkylamino, alkenylamino, alkynylamino, dialkylamino, dialkenylamino, dialkynylamino, alkyl-alkenylamino, alkyl-alkynylamino, alkenyl- alkynylamino, trialkylsilyl, or phenyl or a 5-to 7-membered saturated or partially unsaturated heterocyclic ring which may contain 1 to 3 heteroatoms selected from oxygen, sulfur and nitrogen or a 5- to 6-membered heteraromatic ring system which may contain 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur, which phenyl and which heteroaromatic ring may be bonded via an oxygen or a sulfur atom, or -C(=G)Ra, -C(=G)ORa, -C(=G)NRa2, -C(=G)[N=SRa2], -C(=NORa)Ra, -C(=NORa)NRa2, -C(=NNRa2)Ra , -OC(=G)-OC(=G)ORa, N=SRa2, -NRaC(=G)Ra, -N[C(=G)Ra]2, - NRaC(=G)ORa, -C(=G)NRa-NRa2, -C(=G)NRa-NRa [C(=G)Ra], -NRa-C(=G)NRa2, -NRa-NRaC(=G)Ra, -NRa-N[C(=G)Ra]2, -N[(C=G)Ra]-NRa2, -NRa-NRa[(C=G)GRa], -NRa[(C=G)NRa2, -NRa[C=NRa]Ra, -NRa(C=NRa)NRa2, -O-NRa2, -O-NRa(C=G)Ra, - SO2NRa2, -NRaSO2Ra, -S(=O)Ra, -S(=O)2Ra, -SO2ORa, or -OSO2Ra, wherein G is oxygen or sulfur and Ra is as defined in the description, R 2 is hydrogen, halogen, cyano, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkoxy, or haloalkoxy, x is 2, 3, 4, 5, 6, or 7, or the diastereomers, enantiomers, salts or N-oxides thereof, with the proviso that R 1 is not 5-chloro-2,2,-dimethyl-2,3-dihydrobenzo[b]furan-7-yl when R 2 is hydrogen and x is 3 or 4, processes and intermediates for the preparation of compounds I, use of compounds I for combating insects, acarids, or nematodes, and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using compounds I.
摘要翻译：本发明涉及其中R 1为苯基或可含有1-3个选自氧，氮和硫的杂原子的5至6元杂芳环的式（I）的间苯二酚衍生物，其中苯基或杂芳环可以与选自苯基和5-至6-元饱和，部分不饱和或芳族杂环的环稠合，所述杂环可以含有1-3个选自氧，氮和硫的杂原子，其中苯基或5- 至6元杂芳环或相应的稠环体系可以是未取代的或被1至6个任选取代的基团R 3 3的任何组合取代，其中R 3是卤素，氰基，硝基，羟基，巯基，氨基，烷基，烯基，炔基，环烷基，环烯基，卤代烷基，卤代烯基，卤代炔基，卤代环烷基，卤代环烯基，烷氧基，烯氧基，炔氧基，卤代烷氧基，卤代烯氧基，卤代炔氧基，烷硫基，烯硫基，炔硫基，卤代烷硫基， H 烯基氨基，炔基氨基，二烷基氨基，二链烷基氨基，二炔基氨基，烷基 - 链烯基氨基，烷基 - 炔基氨基，烯基 - 炔基氨基，三烷基甲硅烷基或苯基或5至7元饱和或部分不饱和的杂环，至3个选自氧，硫和氮的杂原子或5至6元杂芳环体系，其可以含有1至4个选自氧，氮和硫的杂原子，该苯基和杂芳环可以通过氧或硫原子或-C（= G）R a，-C（= G）OR a，-C（= G）NR a 2，-C（= G）[N = SR a 2] （= NORa）NRa2，-C（= NNRa2）Ra，-OC（= G）-OC（= G）ORa，N = SRa2，-NRaC（= G）Ra，-N [C（= G）Ra] 2，-NR a C（= G）OR a，-C（= G）NR a -NR a 2，-C（= G）NR a -NR a [C（= G）R a] -NRaC（= G）Ra，-NRa-N [C（= G）Ra] 2，-N [（C = G）Ra] -NRa2，-NRa-NRa [（C = G） [（C = G）NRa2，-NRa [C = NRa] Ra，-NRa（C = NRa）NRa2，-O-NRa2，-O-NRa（C = G）Ra，-SO2NRa2，-NRaSO2Ra，-S （= O）R a，-S（= O）2 R a，-SO 2 OR a或-O SO 2 R a，其中G是氧或硫，Ra如说明书中所定义，R 2是氢，卤素，氰基，烷基，卤代烷基，烯基，卤代烯基，炔基，卤代炔基，烷氧基或卤代烷氧基， x是2,3,4,5,6或7，或其非对映异构体，对映异构体，盐或N-氧化物，条件是R 1不是5-氯-2,2 ，当R 2是氢并且x是3或4时，制备化合物I的方法和中间体，使用化合物I，其中R 1，R 2，R 3，用于防治昆虫，螨虫或线虫，以及用化合物I治疗，控制，预防或保护动物免受寄生虫侵袭或感染的方法。

18. 发明申请

WO2006056433A2 NOVEL 2-CYANO-3-(HALO)ALKOXY-BENZENESULFONAMIDE COMPOUNDS FOR COMBATING ANIMAL PESTS 审中-公开
标题翻译：新型2-氰基-3-（卤代）烷氧基苯磺酰胺化合物用于防治动物病虫害
公开(公告)号：WO2006056433A2
公开(公告)日：2006-06-01
申请号：PCT/EP2005012561
申请日：2005-11-24
申请人： BASF AG , DEYN WOLFGANG VON , BASTIAANS HENRICUS MARIA MARTI , POHLMAN MATTHIAS , RACK MICHAEL , BAUMANN ERNST , PUHL MICHAEL , HOFMANN MICHAEL , TEDESCHI LIVIO , KORDES MARKUS , KORADIN CHRISTOPHER , ANSPAUGH DOUGLAS D , CULBERTSON DEBORAH L , COTTER HENRY VAN TUYL , OLOUMI-SADEGHI HASSAN
发明人： VON DEYN WOLFGANG , BASTIAANS HENRICUS MARIA MARTI , POHLMAN MATTHIAS , RACK MICHAEL , BAUMANN ERNST , PUHL MICHAEL , HOFMANN MICHAEL , TEDESCHI LIVIO , KORDES MARKUS , KORADIN CHRISTOPHER , ANSPAUGH DOUGLAS D , CULBERTSON DEBORAH L , COTTER HENRY VAN TUYL , OLOUMI-SADEGHI HASSAN
IPC分类号： C07C311/16 , A01N41/06 , C07C311/29 , C07C311/39 , C07C319/20 , C07C323/32
CPC分类号： C07C319/20 , A01N41/06 , C07C311/29 , C07C323/62
摘要： The invention relates to 2-cyano-3-(halo)alkoxy-benzenesulfonamide compounds (I), where the variables Alk and R1 to R5 are as defined in claim 1, and/or to their agriculturally useful salts. Moreover, the present invention relates to: the use of compounds (I) and/or their salts for combating animal pests; agricultural compositions comprising such an amount of at least one compound of the general formula (I) and/or at least one agriculturally useful salt of (I) and at least one inert liquid and/or solid agronomically acceptable carrier that it has a pesticidal action and, if desired, at least one surfactant; and a method of combating animal pests which comprises contacting the animal pests, their habit, breeding ground, food supply, plant, seed, soil, area, material or environment in which the animal pests are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from animal attack or infestation with a pesticidally effective amount of at least one2-cyano-3-(halo)alkoxy-benzenesulfonamide compound of the formula (I) and/or at least one agriculturally acceptable salt thereof; a method for the for the protection of seeds from soil insects and of the resulting plant's roots and shoots from soil and foliar insects comprising contacting the seeds before sowing and/or after pregermination with a 2-cyano-3-(halo)alkoxy-benzenesulfonamide compound of the general formula (I).
摘要翻译：本发明涉及2-氰基-3-（卤代）烷氧基 - 苯磺酰胺化合物（I），其中变量Alk和R1-R5如权利要求1中所定义，和/或其可农用盐。此外，本发明涉及：化合物（I）和/或其盐用于对抗动物害虫的用途; 包含这种量的至少一种通式（I）的化合物和/或至少一种（I）的农业上有用的盐和至少一种惰性液体和/或固体农艺上可接受的载体的农业组合物，其具有杀虫作用和如果需要的话，至少一种表面活性剂; 以及防治动物害虫的方法，其包括使动物害虫，其习性，繁殖场，食物供应，植物，种子，土壤，面积，动物害虫正在生长或可能生长的材料或环境，或材料，植物（I）的至少一种2-氰基-3-（卤代）烷氧基 - 苯磺酰胺化合物和/或至少一种农业上受到保护的种子，土壤，表面或空间免于动物攻击或侵染其可接受的盐; 一种用于保护种子免受土壤昆虫以及所得植物的根和茎由土壤和叶面昆虫引起的方法，包括在播种之前和/或在萌芽后使种子与2-氰基-3-（卤代）烷氧基 - 苯磺酰胺通式（I）的化合物。

19. 发明申请

WO03008417A9 SUBSTITUTED 6-(2-TOLYL)-TRIAZOLOPYRIMIDINES AS FUNGICIDES 审中-公开
标题翻译：取代的6-（2-甲苯基） - 三唑并嘧啶作为杀真菌剂
公开(公告)号：WO03008417A9
公开(公告)日：2003-10-30
申请号：PCT/EP0207578
申请日：2002-07-08
申请人： BASF AG , TORMO I BLASCO JORDI , SAUTER HUBERT , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , RACK MICHAEL , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
发明人： TORMO I BLASCO JORDI , SAUTER HUBERT , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , ROSE INGO , SCHAEFER PETER , SCHIEWECK FRANK , RACK MICHAEL , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD
IPC分类号： A01N43/90 , C07D487/04
CPC分类号： C07D487/04 , A01N43/90
摘要： Substituted 6-(2-tolyl)-triazolopyrimidines of formula (I) in which R and R independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R and R radicals may be unsubstituted or substituted as defined in the description, or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; R is halogen, cyano, alkyl, alkoxy, haloalkyl, or C(=O)A, wherein A is hydrogen, hydroxy, alkyl, amino, or mono- or dialkyl-amino; n is an integer from 1 to 4; and X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
摘要翻译：式（I）的取代的6-（2-甲苯基） - 三唑并嘧啶，其中R 1和R 2独立地表示氢或烷基，烯基，炔基或链二烯基，卤代烷基，卤代烯基，环烷基，苯基，萘基或含有1至4个氮原子或1至3个氮原子和1个硫或氧原子的5-或6-元杂环基，或者含有1-4个氮原子或1-3个氮原子的5-或6-元杂芳基，硫或氧原子，或者其中R 1和R 2基团可以如说明书中所定义的那样未被取代或被取代，或者R 1和R 2与中间的氮原子一起表示5或6 - 含有1至4个氮原子或1至3个氮原子和1个硫或氧原子的可被取代的 - 元杂环; R 3是卤素，氰基，烷基，烷氧基，卤代烷基或C（= O）A，其中A是氢，羟基，烷基，氨基或单或二烷基氨基; n是1至4的整数; X是卤素，氰基，烷基，烷氧基，卤代烷氧基或烯氧基; 它们的制备方法，含有它们的组合物以及它们用于防治植物病原性真菌的用途。

20. 发明申请

WO0031042A3 METHOD FOR PRODUCING 1-SUBSTITUTED 5- OR 3-HYDROXYPYRAZOLES 审中-公开
标题翻译：制备1-取代的5-或3-羟基吡唑的方法
公开(公告)号：WO0031042A3
公开(公告)日：2000-10-26
申请号：PCT/EP9908516
申请日：1999-11-06
申请人： BASF AG , MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
发明人： MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
IPC分类号： C07D231/20
CPC分类号： C07D231/20
摘要： The invention relates to a method for producing 1-substituted 5- and/or 3-hydroxypyrazoles of formulas (I) and (II), wherein R represents C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkinyl, C3-C6-cycloalkyl or C1-C4-alkoxy, whereby these groups can be substituted by halogen, C1-C4-alkoxy, phenoxy, C1-C6-alkoxycarbonyl, C1-C6-alkylthiocarbonyl or a cyclic ring system with 3-14 ring atoms, by reacting a 3-alkoxyacrylic acid alkyl ester of formula (III), wherein R , R independently mean C1-C6-alkyl or C3-C6-cycloalky, with a hydrazine of formula (IV), wherein R has the above cited meaning, a) at a pH value of 6-11 to form 5-hydroxypyrazoles of formula (I), or b) at a pH value of 11-14 to form 3-hydroxypyrazoles of formula (II).
摘要翻译：本发明涉及一种制备1-取代的5和/或所述式（I）和（II），其中R <1> C1-C6-烷基，C2-C6链烯基，C2-C6的3-羟基吡炔基，C3-C6环烷基或C1-C4烷氧基，其中这些基团被卤素，C1-C4烷氧基，苯氧基，C1-C6烷氧羰基，C1-C6烷硫基羰基或具有3-14个环原子的环系可以由式（III）的烷基3- alkoxyacrylates被取代，其中R <2>，R <3>独立地是C1-C6烷基或C3-C6环烷基与式的肼（Ⅳ）其中R <1>具有上面给出的含义，a）在pH值下式I）的6-11（约5-羟基吡唑反应而，或b）在pH为11-14，得到3- hydroxypyrazoles 的式（II）。

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