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    12.
    发明专利
    未知

    公开(公告)号：BRPI0513032A

    公开(公告)日：2008-04-22

    申请号：BRPI0513032

    申请日：2005-07-06

    Applicant: BASF AG

    Inventor： BLETTNER CARSTEN ,  GEWEHR MARKUS ,  GRAMMENOS WASSILIOS ,  GROTE THOMAS ,  HUENGER UDO ,  MUELLER BERND ,  NIEDENBRUECK MATTHIAS ,  RHEINHEIMER JOACHIM ,  SCHOFER PETER ,  SCHIEWECK FRANK ,  SCHWOEGLER ANJA ,  WAGNER OLIVER ,  NAVE BARBARA ,  SCHERER MARIA ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  STIERL REINHARD

    IPC: C07D487/04 ,  A01N43/90

    Abstract: Substituted triazolopyrimidines of the formula I in which the substituents are as defined below: R 1 is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, cycloalkenyl, halocycloalkenyl, alkynyl, haloalkynyl or phenyl, naphthyl, or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle comprising one to four heteroatoms from the group consisting of O, N and S, R 2 is hydrogen or a group R 1 , R 1 and R 2 together with the nitrogen atom, to which they are attached, may also form a five- or six-membered heterocyclyl or heteroaryl which is attached via N and which may comprise one to three further heteroatoms from the groups consisting of O, N and S as ring member and/or may be substituted according to the description; L is fluorine, chlorine or methyl; X is cyano, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy or C 1 -C 2 -haloalkoxy, where X is not methyl if R 1 and R 2 together are n-pentylene or 3-methyl-n-pentylene and L is fluorine, or R 1 and R 2 together are 3-methyl-n-pentylene and L is chlorine; processes and intermediates for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

    13.
    发明专利
    未知

    公开(公告)号：BRPI0509124A

    公开(公告)日：2007-08-28

    申请号：BRPI0509124

    申请日：2005-04-23

    Applicant: BASF AG

    Inventor： BLASCO JORDI TORMO I ,  GROTE THOMAS ,  SCHERER-STRASSE MARIA ,  STIERL REINHARD ,  STRATHMANN SIEGFRIED ,  SCHOEFL ULRICH ,  GEWEHR MARKUS ,  MUELLER BERND ,  SUAREZ-CERVIERI MIGUEL OCTAVIO ,  NIEDENBRUECK MATTHIAS

    IPC: A01N43/653 ,  A01N43/90

    Abstract: 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.

    METHOD FOR INCREASING A ETHABOXAM EFFECTIVENESS
    19.
    发明专利
    METHOD FOR INCREASING A ETHABOXAM EFFECTIVENESS 未知

    公开(公告)号：CA2586441A1

    公开(公告)日：2006-06-01

    申请号：CA2586441

    申请日：2005-11-23

    Applicant: BASF AG

    Inventor： BECK CHRISTINE ,  GEWEHR MARKUS ,  BRIX HORST DIETER ,  STRATHMANN SIEGFRIED ,  NIEDENBRUECK MATTHIAS ,  STIERL REINHARD ,  SCHERER MARIA ,  TORMO I BLASCO JORDI

    IPC: A01N43/78 ,  A01N37/20 ,  A01N37/34 ,  A01N37/38 ,  A01N37/46 ,  A01N37/50 ,  A01N41/06 ,  A01N43/32 ,  A01N43/40 ,  A01N43/76 ,  A01N43/90 ,  A01N47/04 ,  A01N47/14 ,  A01N47/24 ,  A01N47/34 ,  A01P3/00

    Abstract: Method for increasing a fungicidal efficiency of ethaboxam (I) (active substance I) comprises simultaneously applying (I) or jointly with at least one active substance II (comprising e.g. dithiocarbamates, sulfenic acid derivatives and strobilurin derivatives) by spraying or powdering seeds, plants or grounds. Method for increasing a fungicidal efficiency of ethaboxam of formula (I) (active substance I) comprises simultaneously applying (I) or jointly with at least one active substance II (comprising dithiocarbamates such as maneb, mancozeb, metam or metiram, sulfenic acid derivatives such as captan or folpet, strobilurin derivatives such as kresoxim-methyl or pyraclostrobin, cinnamic acid amides and analogs such as dimethomorph or flumorph, or dithianon, famoxadone, cymoxanil, fluazinam, zoxamide, mefenoxam or chlorothalonil, N-(2-{4-[3-(4-chloro-phenyl)-prop-2-inyloxy]-3-methoxy-phenyl}-ethyl)-2-methansulfonylamino-3-methyl-butyramide, N-(2-{4-[3-(4-chloro-phenyl)-prop-2-inyloxy]-3-methoxy-phenyl}-ethyl)-2-methansulfonylamino-3-methyl-butyramide or 5-chloro-7-(4-methyl-piperidine-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine) by spraying or powdering seeds, plants or grounds prior to or after sowing plants or prior to or after the plant growth, where polyoxyalkylene-alkylether is not used as an adjuvant. Independent claims are also included for: (1) a fungicidal mixture (Ia) containing (I), as active substance I and a compound such as maneb, metam, metiram, captan, kresoxim-methyl or pyraclostrobin, flumorph or zoxamide, as an active substance II, or 5-chloro-7-(4-methyl-piperidin-1-yl)-6-(2,4,6-trifluorphenyl)-[1,2,4]triazolo[1,5-a]pyrimidine; (2) a temare fungicidal mixture (Ib), containing (I), active substance II, and an active substance III or phosphoric acid, its alkali- or alkaline-earth salts or it eliminating derivatives, or copper fungicides; (3) an agent containing a liquid or solid carrier material and (Ia) and (Ib); (4) a procedure for combating harmful fungus comprising treating the soil or seeds with (Ia) or (Ib), where (Ia) or (Ib) is applied before fungal attack; and (5) a seed containing (Ia) or (Ib) (1-1000 g/100 kg). [Image] ACTIVITY : Fungicide. MECHANISM OF ACTION : None given.

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