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    • 6. 发明申请
    • HERBICIDAL COMPOSITION
    • 除草组合物
    • WO2005077178A2
    • 2005-08-25
    • PCT/EP2005/001518
    • 2005-02-15
    • SYNGENTA PARTICIPATIONS AGHOLE, Stephen, JohnLÜTHY, ChristophBEAUDEGNIES, RenaudEDMUNDS, AndrewSCHAETZER, JürgenWENDEBORN, Sebastian
    • HOLE, Stephen, JohnLÜTHY, ChristophBEAUDEGNIES, RenaudEDMUNDS, AndrewSCHAETZER, JürgenWENDEBORN, Sebastian
    • A01N43/40
    • A01N43/76A01N25/32A01N43/40A01N43/44A01N43/50A01N43/54A01N43/56A01N43/653A01N43/713A01N43/80A01N43/82A01N61/00A01N2300/00
    • A herbicidal composition comprising a) a compound of formula I wherein the substituents are as defined in claim 1, or an agronomically acceptable salt of such a compound, and b) a synergistically effective amount of one or more compounds selected from pyridafol, dicamba and its salts, procarbazone, benflubutamid, tralkoxydim, mesosulfuron, chlorsulfuron, triasulfuron, flamprop-M, metoxuron, glufosinate, L-glufosinate, fluthiacet, imazamox, imazethapyr, nicosulfuron, primisulfuron-methyl, rimsulfuron, halosulfuron, cloransulam, clomazone, diclosulam, 2,4-D and its salts, florasulam, flumiclorac, bromoxynil, sethoxydim, ioxynil, tepraloxydim, carfentrazone, clethodim, sulfentrazone, imazaquin, sulcotrione, imazapyr, mesotrione, thifensulfuron, isoxaflutole, prosulfuron, isoxachlortole, bentazone, iodosulfuron, prohexadione, diflufenzopyr, flurtamone, butylate, flumioxazin, fentrazamide, benzfendizone, isopropazole, fluazolate, aclonifen, tritosulfuron, cinidon-ethyl, glyphosate and its potassium, isopropylammonium, sodium, trimesium, ammonium and diammonium salts, terbuthylazine, mesotrione + terbuthylazine, paraquat, ketospiradox, aminopyralid, amicarbazone, azafenidin, flufenpyr-ethyl, the compound of formula II and the compounds clodinafop-propargyl, prosulfocarb, picolinafen, pyrafIufan-ethyl, beflubutamid, fenoxaprop-P-ethyl, diclofop-methyl, amidosulfuron, flupyrsulfuron, flupyrsulfuron-methyl-sodium, metsulfuron-methyl, sulfosulfuron, tribenuron-methyl, imazamethabenz-methyl, flucarbazone, chiortoluron, isoproturon, methabenzthiazuron, bifenox, fluoroglycofen-ethyl, imazosuifuron, diflufenican, bilanafos, ethaifluralin, fluthiamide, isoxaben, trialiate, 2,4-DB, dichiorprop, MCPA, MCPB, mecoprop, MCPP, mecoprop-P, clopyralid, fluroxypyr, quinmerac, benazolin-ethyl, difenzoqual, cyhalofop-butyl, dithiopyr, quinclorac, prodiamine, benefin and trifluralin. The compositions according to the invention may also comprise a safener.
    • 一种除草组合物,其包含a)式I化合物,其中取代基如权利要求1所定义,或该化合物的农学上可接受的盐,和b)协同有效量的一种或多种选自吡哆酚,麦草畏及其它 盐酸盐,丙磺舒酮,苯磺隆,三唑磺隆,甲磺隆,氯磺隆,三磺嘧磺隆,磺胺磺隆,氯磺隆,氯磺隆,氯磺隆,氯磺隆, 4-D及其盐,氟草灵,氟氯氰菊酯,氯苯腈,樟脑酮,氯替芬,磺扎酮,咪草酮,磺草酮,咪草烟,甲基磺草酮,噻吩磺隆,异山梨醇,甲磺隆,异噻唑,苯达唑,碘磺隆, ,丁酸盐,氟咪嗪,氟哌嗪,苯并芬那唑,异丙唑,氟酸盐,aclonifen,三氯嘧磺隆,cinidon-乙基,草甘膦及其p 异丙基铵,钠,三甲基铵,铵和二铵盐,特丁津,甲基磺草酮+特丁津,百草枯,酮基吡唑,氨基吡啶,氨基吡嗪,azafenidin,flufenpyr-乙基,式II化合物和化合物clodinafop-propargyl,prosulfocarb,picolinafen,pyrafIufan - 甲基,甲磺隆,甲磺隆,甲磺隆,甲磺隆,异丙隆,甲基噻唑隆,异丙隆,甲苯磺隆,二氟甲磺隆,氟磺草酮,甲苯磺隆,氟磺草隆, - 乙基,咪唑苏氟脲,氟磺草胺,双胍,乙醛酸,氟噻胺,异恶草酮,三钠,2,4-DB,二氯丙酸,MCPA,MCPB,mecoprop,MCPP,mecoprop-P,clopyralid,氟草吡啶,quinmerac,benazolin-ethyl,difenzoqual, 丁基,二硫代吡啶,喹氯林,丙二胺,益生菌和氟乐灵。 根据本发明的组合物还可以包含安全剂。
    • 9. 发明申请
    • PYRIDAZINE DERIVATIVES
    • 吡啶衍生物
    • WO2008049585A1
    • 2008-05-02
    • PCT/EP2007/009189
    • 2007-10-23
    • SYNGENTA PARTICIPATIONS AGTRAH, StephanLAMBERTH, ClemensWENDEBORN, Sebastian
    • TRAH, StephanLAMBERTH, ClemensWENDEBORN, Sebastian
    • C07D237/08C07D237/12C07D237/14C07D237/18C07D237/04C07D405/04C07D409/04C07D401/04C07D403/04C07D413/04C07D417/04C07D401/12C07D409/12C07D307/60
    • C07D237/14A01N43/58C07D237/08C07D237/12C07D307/60C07D307/79C07D401/04C07D401/12C07D403/04C07D405/04C07D405/12C07D407/04C07D409/04C07D409/12C07D413/04C07D417/04
    • 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.
    • 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。