Title (en) Fungicidal mixtures

Title (de) Fungizide Mischungen

Title (fr) Mélanges fongicides

Publication EP 2255628 A2 20101201 (DE)

Application EP 10174033 A 20050423

Priority • EP 05734026 A 20050423 • DE 102004025032 A 20040518 • DE 102004021766 A 20040430

Abstract (en) A fungicidal composition (A) comprising synergistic amounts of a 3-indolylsulfonyl-1-aminosulfonyl-triazole derivative (I) and a second active agent (2), is new. Fungicidal composition (A) comprising synergistic amounts of a 3-indolylsulfonyl-1-aminosulfonyl-triazole derivative of formula (I) and a second active agent (2), where (2) is any of: azoles (e.g. cyproconazole, difenoconazole, enilconazole, epoxiconazole, fluquiconazole, flusilazol, hexaconazole, imazalil, metconazole, mycolbutanil, penconazole, prochloraz, prothioconazole, tebuconazole, triadimefon, triadimenol or triflumizole); strobilurines (e.g. azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, cresoxime-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin or trifloxystrobin); acylalanines (e.g. benalaxyl, metalaxyl, mefenoxam, ofurace and oxadixyl); amine derivatives, e.g. spiroxamine; aniliniopyrimidines (e.g. pyrimethanil, mepanipyrim or cyprodinil); dicarboximides (e.g. iprodione, procymidone or vinclozolin); cinnamic acid amide and analogs (e.g. dimethomorph, flumetover or flumorph); dithiocarbamates (e.g. ferbam, nabam, maneb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb); heterocyclic compounds (e.g. benomyl, boscalide, carbendazim, dithianon, famoxadon, fenamidon, pentiopyrad, quinoxyfen, thiophanate-methyl, triforine); 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)[1,2,4]triazolo[1,5-a]pyrimidine (II); sulfur or copper fungicides (e.g. Bordeaux mixture, copper acetate, copper oxychloride or basic copper sulfate); nitrophenyl derivatives (e.g. dinocap); phenylpyrroles (e.g. fenpiclonil or fludioxonil); sulfenic acid derivatives (e.g. captafol, dichlorofluanide or tolylfluanide); other fungicides (e.g. benthiavalicarb, chlorothalonil, cyflufenamide, diclofluanide, ethaboxam, fenhexamide, fluazinam, iprovalicarb, namdipropamide, metrafenon, zoxamide); oxime-ether derivatives of formula (III) or heterocyclic compounds of formula (IV). R 1>= hydrogen, halo, cyano, 1-4C alkyl, alkoxy, alkylthio or alkoxycarbonyl, 1-2C haloalkyl, phenyl, benzyl, formyl or CH=NOA; A in (I)= hydrogen, 1-4C alkyl or alkylcarbonyl; R 2>= hydrogen, halo, cyano, 1-4C alkyl, 1-2C haloalkyl or 1-6C alkoxycarbonyl; R 3>= halo, cyano, nitro, 1-4C alkyl, alkoxy, alkylthio or alkoxycarbonyl, 1-2C haloalkyl, formyl or CH=NOA; n in (I)= 0-4; R 4>= hydrogen, halo, cyano, 1-4C alkyl or 1-2C haloalkyl; X= 1-4C haloalkoxy; n in (III)= 0-3; R= halo, 1-4C (halo) alkyl or (halo)alkoxy; A in (IV)= O or N; B= N or direct bond; G= C or N; R 41>= 1-4C alkyl; R 42>= 1-4C alkoxy; and R 43>= halo. An independent claim is also included for seeds treated with 1-1000 g (A) per 100 kg. [Image] [Image] [Image] ACTIVITY : Plant Antifungal. MECHANISM OF ACTION : None given.

Abstract (de) Fungizide Mischungen, enthaltend als aktive Komponenten 1) eine Sulfamoylverbindung der Formel I, in der die Substituenten folgende Bedeutung haben: R 1 Wasserstoff, Halogen, Cyano, Alkyl, Halogenalkyl, Alkoxy, Alkylthio, Alkoxycarbonyl, Phenyl, Benzyl, Formyl oder CH=NOA; A Wasserstoff, Alkyl, Alkylcarbonyl; R 2 Wasserstoff, Halogen, Cyano, Alkyl, Halogenalkyl, Alkoxycarbonyl; R 3 Halogen, Cyano, Nitro, Alkyl, Halogenalkyl, Alkoxy, Alkylthio, Alkoxycarbonyl, Formyl oder CH=NOA; n 0, 1, 2, 3 oder 4; R 4 Wasserstoff, Halogen, Cyano, Alkyl oder Halogenalkyl; und 2) mindestens einen Wirkstoff ausgewählt aus der Gruppe G) Zimtsäureamide; gemäß der Beschreibung; in einer synergistisch wirksamen Menge, Verfahren zur Bekämpfung von Schadpilzen mit Mischungen einer Verbindung I mit Wirkstoffen aus der Gruppe G) und die Verwendung der Verbindungen I mit Wirkstoffen aus der Gruppe G) zur Herstellung derartiger Mischungen sowie Mittel, die diese Mischungen enthalten.

IPC 8 full level A01N 43/653 (2006.01); A01N 43/90 (2006.01); A01N 37/38 (2006.01); A01N 47/38 (2006.01)

CPC (source: EP KR) A01N 43/653 (2013.01 - EP KR)

C-Set (source: EP) A01N 43/653 + A01N 35/04 + A01N 37/20 + A01N 37/24 + A01N 37/34 + A01N 37/36 + A01N 37/52 + A01N 43/16 + A01N 43/40 + A01N 43/42 + A01N 43/54 + A01N 43/78 + A01N 43/86 + A01N 43/90 + A01N 47/04 + A01N 47/12 + A01N 47/18 + A01N 47/20 + A01N 47/38

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Cited by US8802708B2

Designated contracting state (EPC) AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR

DOCDB simple family (publication) WO 2005104847 A1 20051110; AR 048639 A1 20060510; AU 2005237235 A1 20051110; AU 2005237235 B2 20100722; AU 2005237235 B8 20101021; BR PI0509124 A 20070828; CA 2560341 A1 20051110; EA 011813 B1 20090630; EA 013507 B1 20100630; EA 200601882 A1 20070427; EA 200800989 A1 20081230; EP 1744629 A1 20070124; EP 1744629 B1 20121205; EP 2255627 A2 20101201; EP 2255627 A3 20120926; EP 2255628 A2 20101201; EP 2255628 A3 20120919; EP 2255629 A2 20101201; EP 2255629 A3 20120919; EP 2255630 A2 20101201; EP 2255630 A3 20120926; ES 2396418 T3 20130221; IL 177899 D0 20061231; JP 2007532608 A 20071115; KR 20070011548 A 20070124; PT 1744629 E 20130131; TW 200605787 A 20060216; US 2008064597 A1 20080313; US 7601673 B2 20091013

DOCDB simple family (application) EP 2005004387 W 20050423; AR P050101728 A 20050429; AU 2005237235 A 20050423; BR PI0509124 A 20050423; CA 2560341 A 20050423; EA 200601882 A 20050423; EA 200800989 A 20050423; EP 05734026 A 20050423; EP 10174032 A 20050423; EP 10174033 A 20050423; EP 10174036 A 20050423; EP 10174037 A 20050423; ES 05734026 T 20050423; IL 17789906 A 20060905; JP 2007507781 A 20050423; KR 20067025091 A 20061129; PT 05734026 T 20050423; TW 94113950 A 20050429; US 57908505 A 20050423