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    • 31. 发明专利
    • BRPI0511888A
    • 2008-01-15
    • BRPI0511888
    • 2005-06-08
    • BASF AG
    • BLETTNER CARSTENGEWEHR MARKUSGRAMMENOS WASSILIOSGROTE THOMASHUENGER UDOMUELLER BERNDNIEDENBRUECK MATTHIASRHEINHEIMER JOACHIMSCHOFER PETERSCHIEWECK FRANKGLER ANJA SCHWWAGNER OLIVERRAPADO LILIANA PARRARACK MICHAELNAVE BARBARASCHERER MARIASTRATHMANN SIEGFRIEDFL ULRICH SCHSTIERL REINHARD
    • A01N43/90C07D487/04
    • The invention relates to the use of triazolopyrimidines of the formula I In which: R 1 , R 2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl, C 3 -C 6 -cycloalkynyl, phenyl, naphthyl, or a five- to ten-membered saturated, partially unsaturated or aromatic heterocycle which contains one, two, three or four heteroatoms from the group consisting of O, N and S, where R 1 , R 2 may be substituted as defined in the description or R 1 and R 2 together with the nitrogen atom to which they are attached may form five- to eight-membered heterocyclyl or heteroaryl which is attached via nitrogen and may contain one, two or three further heteroatoms from the group consisting of O, N and S as ring members and/or may be substituted as defined in the description; L independently of one another are halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyloxy, cyano, C(-O)A 1 , S(-O) m A 2 , NR c R d or NR c -(C-O)-R d , where A 1 , A 2 , R c , R d and m are as defined in the description; L 1 is halogen, alkyl or haloalkyl; L 2 is nitro, a group -C(S)NR 3 R 4 , a group -C(-N-OR 5 )(NR 6 R 7 ) or a group -C(-N-NR 8 R 9 )(NR 10 OR 11 ); X is halogen, cyano, alkyl, alkoxy, haloalkyl or haloalkoxy; R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 are independently of one another selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl and alkynyl, where the 4 last-mentioned radicals may be substituted as defined in the description; or R 3 and R 4 , or R 6 and R 7 , or R 8 and R 9 or R 10 and R 11 together with the nitrogen atom to which they are attached form a four, five, or six-membered saturated or partially unsaturated ring which may be substituted as defined in the description; n is 0, 1, 2 or 3; and the agriculturally acceptable salts thereof, novel triazolopyrimidines, crop protection compositions comprising at least one compound of the formula I and at least one solid or liquid carrier, and a method for controlling phytopathogenic harmful fungi.
    • 39. 发明专利
    • Fungicidal mixtures
    • AU2005237235B8
    • 2010-10-21
    • AU2005237235
    • 2005-04-23
    • BASF AG
    • GEWEHR MARKUSSTIERL REINHARDMUELLER BERNDNIEDENBRUECK MATTHIASSCHERER MARIAGROTE THOMASSCHOEFL ULRICHBLASCO JORDI TORMO ISUAREZ-CERVIERI MIGUEL OCTAVIOSTRATHMANN SIEGFRIED
    • A01N43/653
    • 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.