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1. 发明申请

WO2008049585A1 PYRIDAZINE DERIVATIVES 审中-公开
标题翻译：吡啶衍生物
公开(公告)号：WO2008049585A1
公开(公告)日：2008-05-02
申请号：PCT/EP2007/009189
申请日：2007-10-23
申请人： SYNGENTA PARTICIPATIONS AG , TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian
发明人： TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian
IPC分类号： C07D237/08 , C07D237/12 , C07D237/14 , C07D237/18 , C07D237/04 , C07D405/04 , C07D409/04 , C07D401/04 , C07D403/04 , C07D413/04 , C07D417/04 , C07D401/12 , C07D409/12 , C07D307/60
CPC分类号： C07D237/14 , A01N43/58 , C07D237/08 , C07D237/12 , C07D307/60 , C07D307/79 , C07D401/04 , C07D401/12 , C07D403/04 , C07D405/04 , C07D405/12 , C07D407/04 , C07D409/04 , C07D409/12 , C07D413/04 , C07D417/04
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R 1 is hydrogen, C 1 -C 6 alkyl, C 1 -C 8 haloalkyl or C 3 -C 6 cycloalkyl; R 2 is cycloalkyl, cycloalkylalkyl, halocycloalkyl, cycloalkoxy, halocycloalkoxy, cycloalkylalkoxy, halocycloalkylalkoxy, alkoxyalkyl, cycloalkoxyalkoxyalkyl, haloalkoxyalkyl, trialkylsilyl, alkylthioalkyl, haloalkylthioalkyl, cycloalkylthio, halocycloalkylthio, cycloalkylalkylthio, halocycloalkylalkylthio, alkylsulfinylalkyl, alkylsulfonylalkyl, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, optionally substituted arylsulfonyl, optionally substituted aryloxy, optionally substituted heteroaryloxy, optionally substituted arylthio, optionally substituted heteroarylthio; or R 2 together with an adjacent carbon atom forms an optionally substituted fused ring; R 3 is an optionally substituted aryl; R 4 is hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 8 alkoxy, C 1 -C 6 haloalkoxy, hydroxy or cyano; and n is a whole number from 1 to 4; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及式（I）的新颖哒嗪衍生物作为具有杀微生物活性，特别是杀真菌活性的活性成分：其中R 1是氢，C 1 -C C 1 -C 6烷基，C 1 -C 8卤代烷基或C 3 -C 6烷基，环烷基; R 2是环烷基，环烷基烷基，卤代环烷基，环烷氧基，卤代环烷氧基，环烷基烷氧基，卤代环烷基烷氧基，烷氧基烷基，环烷氧基烷氧基烷基，卤代烷氧基烷基，三烷基甲硅烷基，烷硫基烷基，卤代烷硫基烷基，环烷硫基，卤代环烷基硫基，环烷基烷硫基，卤代环烷基烷硫基，烷基亚磺酰基烷基，卤代烷基亚磺酰基，烷基磺酰基，卤代烷基磺酰基，C 2 -C 6亚烷基，C 2 -C 6 - 炔基，任选取代的芳基磺酰基，任选取代的芳氧基，任选取代的杂芳氧基，任选取代的芳硫基，任选取代的杂芳硫基; 或R 2与相邻碳原子一起形成任选取代的稠合环; R 3是任选取代的芳基; R 4是氢，卤素，C 1 -C 6烷基，C 1 -C 6烷基，C 1 -C 6烷基，C 1 -C 6烷基，C 1 -C 6 - 卤代烷基，C 1 -C 8烷氧基，C 1 -C 6卤代烷氧基，羟基或氰基; n为1〜4的整数; 或其农业化学上可用的盐形式。

2. 发明申请

WO2009090038A1 FUNGICIDAL COMPOSITIONS 审中-公开
标题翻译：杀真菌剂
公开(公告)号：WO2009090038A1
公开(公告)日：2009-07-23
申请号：PCT/EP2009/000165
申请日：2009-01-14
申请人： SYNGENTA PARTICIPATIONS AG , GODWIN, Jeremy, R. , TRAH, Stephan , LAMBERTH, Clemens , DUMEUNIER, Raphael , WENDEBORN, Sebastian, Volker , GRASSO, Valeria
发明人： GODWIN, Jeremy, R. , TRAH, Stephan , LAMBERTH, Clemens , DUMEUNIER, Raphael , WENDEBORN, Sebastian, Volker , GRASSO, Valeria
IPC分类号： A01N43/58 , A01P3/00
CPC分类号： A01N43/58 , A01N37/34 , A01N43/54 , A01N43/653 , A01N47/14 , A01N51/00 , A01N2300/00
摘要： A fungicidal composition suitable for control of diseases caused by phytopathogens comprising (A) a compound of formula (I), wherein R 1 is methyl, ethyl or isopropyl; R 2 is 2-chloro-6-fluoro-phenyl, 2,4,6-trifluorophenyl or 2,6-difluoro-4-methoxy-phenyl; R 3 is chloro, fluoro or methoxy; and (B) a compound selected, for example, from the group consisting of (B1) a strobilurin fungicide, (B2) an azole fungicide, (B3) a morpholine fungicide, and (B4) an anilinopyrimidine fungicide.
摘要翻译：一种适于控制由植物病原体引起的疾病的杀真菌组合物，其包含（A）式（I）化合物，其中R 1为甲基，乙基或异丙基; R2是2-氯-6-氟 - 苯基，2,4,6-三氟苯基或2,6-二氟-4-甲氧基 - 苯基; R3是氯，氟或甲氧基; 和（B）选自例如（B1）嗜球果伞素杀真菌剂，（B2）唑类杀真菌剂，（B3）吗啉杀真菌剂和（B4）苯胺基嘧啶杀真菌剂的组合的化合物。

3. 发明申请

WO2009080314A1 PYRIDAZINE DERIVATIVES USEFUL AS FUNGICIDES AND FOR THE TREATMENT OF CANCER 审中-公开
标题翻译：用作杀真菌剂和治疗癌症的吡咯烷酮衍生物
公开(公告)号：WO2009080314A1
公开(公告)日：2009-07-02
申请号：PCT/EP2008/010928
申请日：2008-12-19
申请人： SYNGENTA PARTICIPATIONS AG , LAMBERTH, Clemens , TRAH, Stephan , DUMEUNIER, Raphael , WENDEBORN, Sebastian, Volker
发明人： LAMBERTH, Clemens , TRAH, Stephan , DUMEUNIER, Raphael , WENDEBORN, Sebastian, Volker
IPC分类号： C07D237/12 , C07D237/14 , A01N43/58 , A01P3/00 , A61K31/50 , A61P35/00
CPC分类号： C07D237/12 , A01N43/58 , C07D237/14
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: formula (I) wherein R 1 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 3 -C 6 cycloalkyl; R 2 is hydrogen or an optionally substituted alkyl, aryl or heteroaryl; R 3 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 haloalkyl; R 4 is hydrogen, C 1 -C 6 alkyl or C 1 -C 6 haloalkyl; or R 3 and R 4 together can be part of a carbocyclic or heterocyclic 3- to 8-membered ring; R 5 is optionally substituted aryl or heteroaryl; and R 6 is hydroxy, halogen, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio or C 1 -C 6 haloalkylthio; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及具有杀微生物活性，特别是杀真菌活性的作为活性成分的式（I）的新哒嗪衍生物：式（I）其中R1是C1-C6烷基，C1-C6卤代烷基或C3-C6环烷基; R 2是氢或任选取代的烷基，芳基或杂芳基; R3是氢，C1-C6烷基或C1-C6卤代烷基; R4是氢，C1-C6烷基或C1-C6卤代烷基; 或者R 3和R 4一起可以是碳环或杂环的3至8元环的一部分; R5是任选取代的芳基或杂芳基; R 6为羟基，卤素，C 1 -C 6烷氧基，C 1 -C 6卤代烷氧基，C 1 -C 6烷硫基或C 1 -C 6卤代烷硫基; 或其农业化学上可用的盐形式。

4. 发明申请

WO2009053101A1 NOVEL IMIDAZOLE DERIVATIVES 审中-公开
标题翻译：新咪唑衍生物
公开(公告)号：WO2009053101A1
公开(公告)日：2009-04-30
申请号：PCT/EP2008/009042
申请日：2008-10-24
申请人： SYNGENTA PARTICIPATIONS AG , DUMEUNIER, Raphael , LAMBERTH, Clemens , TRAH, Stephan , WENDEBORN, Sebastian, Volker
发明人： DUMEUNIER, Raphael , LAMBERTH, Clemens , TRAH, Stephan , WENDEBORN, Sebastian, Volker
IPC分类号： C07D401/04 , C07D401/14 , C07D409/04 , C07D409/14 , A01N43/50 , A61K31/4439 , A61P35/00
CPC分类号： C07D233/61 , C07D233/68 , C07D401/04 , C07D401/14 , C07D409/04 , C07D409/14
摘要： The present invention relates to novel imidazole derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R 1 is halogen, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl; R 2 is an optionally substituted aryl or heteroaryl; R 3 is halogen; R 4 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, hydroxyl, C 1 -C 4 alkoxy, OR 6 , C 1 -C 4 haloalkoxy or cyano; R 5 is halogen; R 6 is hydrogen, C 3 -C 7 cycloalkyl, C 3 -C 10 alkylcycloalkyl, C 1 -C 6 haloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 3 -C 7 cycloalkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkynyl or C 2 -C 6 alkyloxyalkyl; X is N or C(R); and R is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 aIkoxy, C 1 -C 4 haIoaIkoxy or cyano; or an agrochemically usable salt form thereof; provided that when X is C(R), R 2 cannot be an optionally substituted aryl.
摘要翻译：本发明涉及式（I）的新咪唑衍生物作为具有杀微生物活性，特别是杀真菌活性的活性成分：其中R1是卤素，C1-C4烷基或C1-C4卤代烷基; R2是任选取代的芳基或杂芳基; R3是卤素; R4是氢，卤素，C1-C4烷基，C1-C4卤代烷基，羟基，C1-C4烷氧基，OR6，C1-C4卤代烷氧基或氰基; R5是卤素; R6是氢，C3-C7环烷基，C3-C10烷基环烷基，C1-C6卤代烷基，C2-C6烯基，C2-C6卤代烯基，C3-C7环烯基，C2-C6炔基，C2-C6卤代炔基或C2-C6烷氧基烷基; X是N或C（R）; 且R为氢，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卤代烷氧基或氰基; 或其农业化学可用的盐形式; 条件是当X是C（R）时，R 2不能是任选取代的芳基。

5. 发明申请

WO2008049584A1 NOVEL PYRIDAZINE DERIVATIVES 审中-公开
标题翻译：新的吡咯烷酮衍生物
公开(公告)号：WO2008049584A1
公开(公告)日：2008-05-02
申请号：PCT/EP2007/009188
申请日：2007-10-23
申请人： SYNGENTA PARTICIPATIONS AG , TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian
发明人： TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian
IPC分类号： C07D237/12 , C07D237/24 , C07D237/14 , A01N43/58
CPC分类号： C07D237/12 , A01N43/58 , C07D237/14 , C07D237/24
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R 1 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 3 -C 6 cycloalkyl; R 2 is halogen, nitro, cyano, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 1 -C 4 alkylthio or C 1 -C 4 haloalkylthio; R 3 is an optionally substituted aryl; R 4 is fluoro, cyano, C 1 -C 6 haloalkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio or C 1 -C 6 haloalkylthio; and n is a whole number from 1 to 4; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及式（I）的新颖哒嗪衍生物作为具有杀微生物活性，特别是杀真菌活性的活性成分：其中R 1是氢，C 1 -C C 1 -C 6烷基，C 1 -C 6卤代烷基或C 3 -C 6烷基，C 1 -C 6烷基，C 1 -C 6 - 环烷基; R 2是卤素，硝基，氰基，C 1 -C 4烷基，C 1 -C 3 卤代烷基，C 1 -C 4烷氧基，C 1 -C 4卤代烷氧基，C 1 -C 4卤代烷氧基， C 1 -C 4烷硫基或C 1 -C 4卤代烷硫基; C 1 -C 4烷基硫基或C 1 -C 4卤代烷硫基; R 3是任选取代的芳基; R 4是氟，氰基，C 1 -C 6卤代烷基，C 3 -C 6 环烷基，C 1 -C 6卤代烷氧基，C 1 -C 6烷硫基或C 1 -C 6烷基， SUB> 1 -C _{6 卤代烷硫基; n为1〜4的整数; 或其农业化学上可用的盐形式。}

6. 发明申请

WO2008031566A2 NOVEL PYRIDOPYRAZINE DERIVATIVES 审中-公开
标题翻译：新型吡咯烷酮衍生物
公开(公告)号：WO2008031566A2
公开(公告)日：2008-03-20
申请号：PCT/EP2007/007912
申请日：2007-09-11
申请人： SYNGENTA PARTICIPATIONS AG , SYNGENTA LIMITED , CROWLEY, Patrick, Jelf , LAMBERTH, Clemens , WENDEBORN, Sebastian, Volker , TRAH, Stephan
发明人： CROWLEY, Patrick, Jelf , LAMBERTH, Clemens , WENDEBORN, Sebastian, Volker , TRAH, Stephan
CPC分类号： C07D471/04 , A01N43/90
摘要： The present invention relates to novel N -oxide derivatives of pyridopyrazines of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity :wherein X is N + -O" and Y is N; or X is N and Y is N + -O"; or X and Y are both N + -O"; R is for example H, halo, cyano, C 1-6 alkyl or C 1-6 alkoxy; R 1 is optionally substituted aryl or heteroaryl; R 2 is for example halo, C 1-8 alkyl, C 3-8 CycloaIkyI, aryl, or heteroaryl; R 3 and R 4 independently of each other are for example H, C 1-8 alkyl, halo(d-8)alkyl, C 2-8 alkenyl, C 2-8 alkynyl or aryl; or R 3 and R 4 together with the nitrogen atom to which they are attached form a C 3-10 alkylene chain or C 3-7 alkenylene chain optionally substituted with halo, C 1-4 alkyl, C 1-4 haloalkyl, C1-4 alkoxy; or R 3 and R 4 together with the nitrogen atom to which they are attached form for example a morpholine, thiomorpholine or thiomorpholine S-oxide ring; or R 3 and R 4 together with the nitrogen atom to which they are attached form a bicyclic annelated or fused ring; and R 7 and R 8 independently of each other are for example H, halo, cyano, C 1-4 alkyl, C 1-4 aIkoxy or halo(C 1-4 )alkyl.
摘要翻译：本发明涉及式（I）吡啶并吡嗪的新型N-氧化物衍生物作为具有杀微生物活性，特别是杀真菌活性的活性成分：其中X为N + -O，Y为N; 或X为N且Y为N + O“; 或X和Y均为N + O-O“; R为例如H，卤素，氰基，C 1-6烷基或C 1-6烷基， R 1是任选取代的芳基或杂芳基; R 2是例如卤素，C 1-8烷基，C 1-4烷基，环烷基，芳基或杂芳基; R 3和R 4彼此独立地是例如H，C 1〜烷基，卤代（C 1-8）烷基，C 2-8链烯基，C 2-8炔基或芳基;或R 3， R 4和R 4与它们所连接的氮原子一起形成C 3-10亚烷基链或C 3-7亚烷基，任选被卤素取代的亚烯基链，C 1-4烷基，C 1-4卤代烷基，C 1-4烷氧基或R 3和R 3 与它们所连接的氮原子一起形成例如吗啉，硫代吗啉或硫代吗啉S-氧化物环;或R 3和R 4， SUP与它们所连接的氮原子一起形成a 双环环或稠环; R 7和R 8彼此独立地是例如H，卤素，氰基，C 1-4烷基，C 1 -C 4烷基， 1-4烷氧基或卤代（C 1-4烷基）烷基。

7. 发明申请

WO2008014955A2 FUNGICIDAL COMPOUNDS AND COMPOSITIONS 审中-公开
标题翻译：杀真菌化合物和组合物
公开(公告)号：WO2008014955A2
公开(公告)日：2008-02-07
申请号：PCT/EP2007/006720
申请日：2007-07-30
申请人： SYNGENTA PARTICIPATIONS AG , GODWIN, Jeremy, R. , TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian, Volker
发明人： GODWIN, Jeremy, R. , TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian, Volker
CPC分类号： C07D237/12 , A01N43/58
摘要： The present invention relates, inter alia , to a compound having the formula (I):-wherein (R)n is selected from the group consisting of 4-Br, 4-OCH 2 CH 3 , 4-OCH 2 CF 3 , 2-CH 3 -4-C1, 2-CH 3 -4-OCH 3 , 2-CH 3 -4-OCF 3 , 2-F-4-Br, 2-F-4-CF 3 , 3-CH 3 -4-Br, 3-F-4-C1, 3-F-4-CH 3 , 3-F-4-Br, 3-F-4-OCH 3 and 3-F-4-F. The present invention further relates to a fungicidal composition comprising a compound having the formula (I) - and also to fungicidal compositions comprising compounds having the formula (II) and/or (III):Furthermore, the present invention relates to methods for controlling pathogenic organisms using the compositions.
摘要翻译：本发明尤其涉及具有式（I）的化合物：其中（R）n选自4-Br， 4-OCH 2 CH 3，4-OCH 2 CF 3，2-CH 3， 4-Cl-2-CH 3 -4-OCH 3，2-CH 3 -4-OCF 4， 2-F-4-Br，2-F-4-CF 3 3，3-CH 3 -4-Br，3-F- 4-Cl，3-F-4-CH 3，3-F-4-Br，3-F-4-OCH 3和3-F-4- F。本发明进一步涉及包含具有式（I）的化合物的杀真菌组合物，并且还涉及包含具有式（II）和/或（III）的化合物的杀真菌组合物：此外，本发明涉及用于防治致病性使用该组合物的有机体。

8. 发明申请

WO2008009405A2 NOVEL PYRIDAZINE DERIVATIVES 审中-公开
标题翻译：新的哒嗪衍生物
公开(公告)号：WO2008009405A2
公开(公告)日：2008-01-24
申请号：PCT/EP2007/006303
申请日：2007-07-16
申请人： SYNGENTA PARTICIPATIONS AG , TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian, Volker
发明人： TRAH, Stephan , LAMBERTH, Clemens , WENDEBORN, Sebastian, Volker
IPC分类号： C07D401/14 , C07D403/14 , C07D405/14 , C07D407/14 , C07D409/14 , C07D417/14 , A01N43/58
CPC分类号： C07D401/14 , A01N43/58 , C07D403/14 , C07D405/14 , C07D407/14 , C07D409/14 , C07D417/14
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R 1 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 3 -C 6 cycloalkyl; R 2 is an optionally substituted hereroaryl; R 3 is an optionally substituted heteroaryl; and R 4 is hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, hydroxy or cyano; or an agrochemically usable salt form thereof.
摘要翻译：本发明涉及作为活性成分的式（I）的新型哒嗪衍生物，其具有杀微生物活性，特别是杀真菌活性：其中R 1为氢，C _{6 环烷基; R 2是任选取代的杂芳基; R 3是任选取代的杂芳基; 并且R 4为氢，卤素，C 1 -C 6烷基，C 1 -C 4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，羟基或氰基; 或其农业化学可用的盐形式。}

9. 发明申请

WO2009090039A1 PYRIDAZINE FUNGICIDES 审中-公开
标题翻译：吡咯烷类杀真菌剂
公开(公告)号：WO2009090039A1
公开(公告)日：2009-07-23
申请号：PCT/EP2009/000166
申请日：2009-01-14
申请人： SYNGENTA PARTICIPATIONS AG , TRAH, Stephan , LAMBERTH, Clemens , DUMEUNIER, Raphael , WENDEBORN, Sebastian, Volker
发明人： TRAH, Stephan , LAMBERTH, Clemens , DUMEUNIER, Raphael , WENDEBORN, Sebastian, Volker
IPC分类号： C07D401/04 , A01N43/58 , A61P35/00
CPC分类号： C07D401/04
摘要： The present invention relates to novel pyridazine derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R 1 is methyl, ethyl or isopropyl; R 2 is chloro, fluoro, hydroxy or C 1 -C 2 alkoxy; R 3 is H, chloro, fluoro, methoxy or C 1 -C 3 alkyl; R 4 is chloro, fluoro or bromo; and R 5 is H, fluoro or methoxy; or an agrochemically usable salt form thereof; with the proviso that when R 1 is methyl, R 2 is chloro and R 3 is H, then R 4 or R 5 is different from fluoro.
摘要翻译：本发明涉及式（I）的新的哒嗪衍生物作为具有杀微生物活性的活性成分，特别是杀真菌活性：其中R1是甲基，乙基或异丙基; R2是氯，氟，羟基或C1-C2烷氧基; R3是H，氯，氟，甲氧基或C1-C3烷基; R4是氯，氟或溴; R5为H，氟或甲氧基; 或其农业化学可用的盐形式; 条件是当R 1为甲基时，R 2为氯且R 3为H，则R 4或R 5不同于氟。

10. 发明申请

WO2009053102A1 NOVEL IMIDAZOLE DERIVATIVES 审中-公开
标题翻译：新咪唑衍生物
公开(公告)号：WO2009053102A1
公开(公告)日：2009-04-30
申请号：PCT/EP2008/009043
申请日：2008-10-24
申请人： SYNGENTA PARTICIPATIONS AG , DUMEUNIER, Raphael , LAMBERTH, Clemens , TRAH, Stephan , WENDEBORN, Sebastian
发明人： DUMEUNIER, Raphael , LAMBERTH, Clemens , TRAH, Stephan , WENDEBORN, Sebastian
IPC分类号： C07D401/04 , C07D401/14 , C07D409/04 , C07D409/14 , A01N43/50 , A61P35/00 , A61K31/4439
CPC分类号： C07D233/54 , C07D233/61 , C07D233/68 , C07D401/04 , C07D409/04 , C07D409/14
摘要： The present invention relates to novel imidazole derivatives of formula (I) as active ingredients which have microbiocidal activity, in particular fungicidal activity: wherein R 1 is halogen, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl; R 2 is an optionally substituted aryl or heteroaryl; R 3 is halogen; R 4 is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy or cyano; R 5 is halogen; X is N or C(R); and R is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy or cyano; or an agrochemically usable salt form thereof; provided that when X is C(R), R 2 cannot be an optionally substituted aryl.
摘要翻译：本发明涉及式（I）的新咪唑衍生物作为具有杀微生物活性，特别是杀真菌活性的活性成分：其中R1是卤素，C1-C4烷基或C1-C4卤代烷基; R2是任选取代的芳基或杂芳基; R3是卤素; R4是氢，卤素，C1-C4烷基，C1-C4卤代烷基，C1-C4烷氧基，C1-C4卤代烷氧基或氰基; R5是卤素; X是N或C（R）; 且R为氢，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卤代烷氧基或氰基; 或其农业化学可用的盐形式; 条件是当X是C（R）时，R 2不能是任选取代的芳基。

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