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公开(公告)号:AP2006003778A0
公开(公告)日:2006-10-31
申请号:AP2006003778
申请日:2005-03-08
Applicant: BASF AG
Inventor: BLASCO TORMO I JORDI DR , BLETTNER CARSTEN DR , MUELLER BERND DR , GEWEHR MARKUS DR , GRAMMENOS WASSILIOS DR , GROTE THOMAS DR , RHEINHEIMER JOACHIM DR , SCHAEFER PETER DR , SCHIEWECK FRANK DR , SCHWOEGLER ANJA DR , WAGNER OLIVER
IPC: A01N43/90 , C07D487/04
Abstract: 5,6-Dialkyl-7-aminotriazolopyrimidines of the formula I in which the substituents are as defined below: R 1 is alkyl, alkoxymethylene or alkoxyethylene, where the aliphatic groups may be substituted as defined in the description; R 2 is n-propyl or n-butyl; processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.
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公开(公告)号:HU225014B1
公开(公告)日:2006-05-29
申请号:HU0002075
申请日:1998-05-15
Applicant: BASF AG
Inventor: MUELLER BERND DR , SAUTER HUBERT DR , LORENZ GISELA DR , LEYENDECKER JOACHIM DR , AMMERMANN EBERHARD DR , SCHELBERGER KLAUS , SAUR REINHOLD , STRATHMANN SIEGFRIED , SCHERER MARIA , BIRNER ERICH
Abstract: A fungicidal mixture, comprising at least one compound selected froma) carbamates of the formula I, where T is CH or N, n is 0, 1 or 2 and R is halogen, C1-C4-alkyl or C1-C4-haloalkyl, it being possible for the radicals R to be different if n is 2,a2) the oxime ether carboxylate of the formula II ora3) the oxime ether carboxamide of the formula III, andb) a compound of the formula IVin a synergistically effective amount.
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公开(公告)号:HU224639B1
公开(公告)日:2005-12-28
申请号:HU0002765
申请日:1998-05-20
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SAUR REINHOLD DR , SAUTER HUBERT DR , MUELLER BERND DR , BIRNER ERICH , LEYENDECKER JOACHIM , HAMPEL MANFRED DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
Abstract: Fungicidal mixtures comprisea.1) a carbamate of the formula I.a, in which X is CH or N, n is 0, 1 or 2 and R is halogen, alkyl or haloalkyl, ora.2) the oxime ether carboxamide of the formula I.b andb.1) 4-[2-methyl-3-(4-tert-butylphenyl)propyl]-2,6-dimethyl morpholine orb.2) 4-(C10-C13-alkyl)-2,6-dimethylmorpholine orb.3)(RS)-1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine andc) an active ingredient from the group of the azole fungicides (III),in a synergistically effective amount.
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公开(公告)号:AT248142T
公开(公告)日:2003-09-15
申请号:AT01115054
申请日:2001-06-21
Applicant: BASF AG
Inventor: GYPSER ANDREAS DR , GROTE THOMAS DR , RHEINHEIMER JOACHIM DR , ROSE INGO DR , CULLMANN OLIVER DR , GEWEHR MARKUS DR , GRAMMENOS WASSILIOS DR , TORMO I BLASCO JORDI DR , MUELLER BERND DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , STRATHMANN SIEGFRIED DR , LORENZ GISELA DR , STIERL REINHARD DR
IPC: C07C251/80 , A01N33/26 , A01N37/50 , C07C249/16 , C07C251/86
Abstract: Hydrazonomethyl-salicylic acid (I) derivatives are new. The hydrazonomethyl-salicylic acid derivatives are compounds of formula (I). X = halo, NO2, CN, 1-4C alkyl, or 1-4C alkoxy; m = 0-3; A = OH, 1-4C alkoxy, NH2, NHCH3, or N(CH3)2; R = phenyl, naphthyl, 3-10C cycloalkyl, 5- or 6-membered heteroaryl or heterocyclyl containing 1-3 N and/or 1 O or S or 1 or 2 O and/or S (each optionally substituted with 1-3 Ra); Ra = CN, NO2, NH2, H2NCO-, H2NCS-, halo, OH, 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo), 1-6C alkylcarbonyl, 1-6C alkylsulfonyl, 1-6C alkylsulfoxyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 1-6C alkyl-NH-CO-, (1-6C alkyl)2N-CO-, 1-6C alkyl-NH-CS-, (1-6C alkyl)2N-CS-, 2-6C alkenyl, 2-6C alkenyloxy, phenyl, phenoxy, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, heteroaryl or heteroaryloxy, C(=NOR alpha )-OR beta , or OC(R alpha )2-C(R beta )=NOR beta , and cyclic groups are optionally substituted with 1-3 Rb; Rb = CN, NO2, NH2, H2NCO-, H2NCS-, halo, OH, 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo), 1-6C alkylcarbonyl, 1-6C alkylsulfonyl, 1-6C alkylsulfoxyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 1-6C alkyl-NH-CO-, (1-6C alkyl)2N-CO-, 1-6C alkyl-NH-CS-, (1-6C alkyl)2N-CS-, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C cycloalkenyl, phenyl, phenoxy, phenylthio, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, heteroaryl or heteroaryloxy, or C(=NOR alpha )-OR beta ; R alpha and R beta = H or 1-6C alkyl; R = H, CN, or 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl, 1-6C haloalkyl, 1-6C alkoxy or 1-6C alkylthio (each optionally substituted with 1 or more halo and/or 1-3 Rc); Rc = halo, CN, NO2, OH; 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo); 1-6C alkylcarbonyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 2-6C alkenyl, 3-6C alkenyloxy, 3-6C alkynyloxy, or 1-4C alkylenedioxy (optionally halogenated). An Independent claim is also included for the preparation of compounds (I).
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公开(公告)号:HU0004838A2
公开(公告)日:2001-05-28
申请号:HU0004838
申请日:1998-05-13
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD DR , BIRNER ERICH , LEYENDECKER JOACHIM DR , LORENZ GISELA DR , MUELLER BERND DR , SAUR REINHOLD DR , SAUTER HUBERT DR , SCHELBERGER KLAUS DR , SCHERER MARIA , STRATHMANN SIEGFRIED
IPC: A01N20060101 , A01N37/18 , A01N37/20 , A01N37/34 , A01N37/50 , A01N43/50 , A01N43/64 , A01N47/24 , A01N47/46 , A01N47/48 , C07C233/76 , C07C235/44 , C07C251/48 , C07C255/57 , C07C331/04 , C07C331/18 , C07D231/20 , C07D249/12
Abstract: A fungicidal mixture comprisesa) a phenyl benzyl ether derivative of the formula I.a, I.b or I.c, and/or a carbamate of the formula Idwhere X is CH or N, n is 0, 1 or 2 and R is halogen, C1-C4-alkyl or C1-C4-haloalkyl, it being possible for the radicals R to be different if n is 2, or a salt or adduct thereof,and(b) a N-acetonylbenzamide of the formula II where:R1 and R3 independently of one another are each halogen or C1-C4-alkyl;R2 is cyano, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl or C1-C4-alkoxy;R4 is hydrogen or C1-C4-alkyl;R5 is C2-C4-alkyl;R6 is thiocyano, isothiocyano or halogen,or a salt or adduct thereof,in a synergistically effective amount.
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公开(公告)号:DE19900571A1
公开(公告)日:1999-07-29
申请号:DE19900571
申请日:1999-01-09
Applicant: BASF AG
Inventor: GEWEHR MARKUS DR , SAUTER HUBERT DR , BAYER HERBERT DR , GROTE THOMAS DR , GRAMMENOS WASSILIOS DR , GYPSER ANDREAS DR , PTOCK ARNE DR , MUELLER BERND DR , GOETZ ROLAND DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
IPC: A01N43/713 , A01N43/76 , A01N43/80 , C07D257/04 , C07D401/12 , C07D403/12 , C07D413/12
Abstract: 1-(2-(N-(1-Oximino-2-alkylidene)-aminooxymethyl)-phenyl)-1,4-dihydro-5 H-tetrazol-5-one derivatives (I) are new. Phenyl tetrazolinones of formula (I) are new. Ra = H, alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, alkylcarbonyl or alkoxycarbonyl; Y = halo, 1-4C alkyl, haloalkyl or alkoxy; n = 0-2; R1 = H, CN, halo, alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy or cycloalkoxy; R2 = H, alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkylalkyl, alkoxyalkyl or cycloalkoxyalkyl; R3 = alkoxyalkyl or -C(R3a)=NOR3b; or (all optionally substituted) aryl, heteroaryl, C-bonded 3-, 5- or 6-membered heterocyclyl, aryloxy, heteroaryloxy, arylthio, heteroarylthio, arylsulfinyl, heteroarylsulfinyl, arylsulfonyl, heteroarylsulfonyl, arylalkyl, heteroarylalkyl, 3-, 5- or 6-membered heterocyclylalkyl, aryloxyalkyl, heteroaryloxyalkyl, arylamino, heteroarylamino diarylamino, diheteroarylamino, arylalkylamino or heteroarylalkylamino; R3a = as R3b; or (all optionally substituted) 3-, 5- or 6-membered heterocyclyl, aryl, heteroaryl, arylalkyl or heteroarylalkyl; R3b = H, alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl, cycloalkylakyl, alkoxyalkyl or cycloalkoxyalkyl; alkyl moieties = 1-6C, alkenyl or alkynyl moieties 2-6C and cycloalkyl moieties 3-6C unless specified otherwise. An Independent claim is included for the preparation of (I).
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公开(公告)号:DE19732693C1
公开(公告)日:1999-03-11
申请号:DE19732693
申请日:1997-07-30
Applicant: BASF AG
Inventor: WINGERT HORST DR , GOETZ NORBERT DR , KEIL MICHAEL DR , MUELLER BERND DR
IPC: C07B39/00 , C07C17/14 , C07C25/02 , C07C67/307 , C07C69/76 , C07C201/12 , C07C205/11 , C07C253/30 , C07C255/50
Abstract: The invention concerns a method for preparing substituted benzyl bromides of general formula (I), wherein at least one substituent R represents an electroattractive group, such as fluorine, chlorine, bromine, C1-C4 alkoxycarbonyl, cyano or nitro, and the remaining R substituents represent hydrogen or methyl, by bromination of substituted toluenes of general formula (II) with a bromination agent at temperatures from 20 to 95 DEG C.
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公开(公告)号:DE19724200A1
公开(公告)日:1998-12-10
申请号:DE19724200
申请日:1997-06-09
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , BAYER HERBERT DR , GROTE THOMAS DR , SAUTER HUBERT DR , GYPSER ANDREAS DR , KIRSTGEN REINHARD DR , MUELLER BERND DR , PTOCK ARNE DR , ROEHL FRANZ DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , STRATHMANN SIEGFRIED DR , HARRIES VOLKER DR
IPC: A01N43/653 , A01N43/80 , C07D249/12 , C07D261/12
Abstract: The invention relates to bisimino-substituted phenyl compounds of formula (I) wherein the constituents have the following meaning: X is a group A or B, # representing the bond with the phenyl ring and R standing for halogen, alkyl, or alkoxy; Y is halogen, alkyl, alkyl halide or alkoxy; n is 0, 1 or 2 and the radicals Y can be different when n = 2, R is alkyl, R is alkyl, alkyl halide, alkenyl, halogen alkenyl, alkynyl or halogen alkynyl; R is hydrogen, alkyl, alkyl halide or optionally substituted phenyl and R =CR R or =N-OR , R and R being independently of each other hydrogen, alkyl or optionally substituted phenyl, and R being one of the radicals given for R . The invention also relates to a method and intermediate products for producing the inventive compounds, and to their use in combating harmful fungi and animal pests.
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公开(公告)号:DE19722225A1
公开(公告)日:1998-12-03
申请号:DE19722225
申请日:1997-05-28
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SCHERER MARIA , SAUR REINHOLD DR , SAUTER HUBERT DR , MUELLER BERND DR , BIRNER ERICH , LEYENDECKER JOACHIM DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
Abstract: The invention relates to a fungicidal mixture containing a synergistically active quantity of a) a carbamate of formula (I) in which T is CH or N, n is 0, 1 or 2 and R is a halogen, C1-C4-alkyl or C1-C4 halogen alkyl, where the R radicals can be different if n equals 2; and b) an active ingredient of the formula (II) in which the substituents have the following meanings: Y is hydrogen, a metal from main groups I to III of the periodic table of elements or an NR R R R group; R is hydrogen, a C1-C18 alkyl group which can be substituted with halogen or a nitro-group, a C2-C8-alkenyl or C2-C8-alkynyl group which can be substituted with halogen or a nitro-group, a C1-C8-alkoxy-C1-C8-alkyl or a C2-C8-alkenyl-C1-C8-alkyl group, an optionally substituted aryl group with between 6 and 14 C-atoms, a C3-C7-cycloalkyl group, a C1-C4-alkyl aryl group or a heterocyclic group with 5 or 6 ring atoms and a heteroatom from the group N, O or S, whereby the heterocyclic group is linked to the oxygen atom directly or via an aliphatic chain; R -R independently of each other are a C1-C4-alkyl group or a C1-C4 hydroxy alkyl group.
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公开(公告)号:DE19722223A1
公开(公告)日:1998-12-03
申请号:DE19722223
申请日:1997-05-28
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SCHERER MARIA , SAUR REINHOLD DR , SAUTER HUBERT DR , MUELLER BERND DR , BIRNER ERICH , LEYENDECKER JOACHIM DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , STRATHMANN SIEGFRIED DR
Abstract: The invention relates to a fungicidal mixture containing a synergistically active quantity of at least one compound chosen from a) carbamates of formula (I) in which T is CH or N, n is 0, 1 or 2 and R is a halogen, C1-C4-alkyl or C1-C4-halogen alkane, whereby the R radicals can be different if n equals 2; a2) the oxime ether carboxylic acid ester of formula (II); or a3) the oxime ether carboxylic acid amine of formula (III); and b) a compound of formula (IV), wherein the substituents X to X and R to R have the following meaning: X to X independently of each other are hydrogen, halogen, C1-C4-alkyl, C1-C4-halogen alkane, C1-C4-alkoxy, C1-C4-halogen alkoxy, C1-C4-alkylthio, C1-C4-thioalkoxy, C1-C4-sulfonyl alkyl, nitro, amino, N-C1-C4-carboxyl amino, N-C1-C4-alkyl amino; R is C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-alkyl-C3-C7-cycloalkyl, whereby these radicals may carry substituents selected from among halogen, cyano and C1-C4-alkoxy; R is a phenyl radical or a 5- to 6-membered saturated or unsaturated heterocyclyl radical with at least one heteroatom selected from among the group N, O and S, whereby the cyclic radicals can have between one and three substituents selected from the group of halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogen alkane, C1-C4-halogen alkoxy, C1-C4-alkoxy-C2-C4-alkenyl and C1-C4-alkoxy-C2-C4-alkynyl; R and R independently of each other are hydrogen, halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylthio, N-C1-C4-alkyl amino, C1-C4-halogen alkane or C1-C4-halogen alkoxy or R and R together form a =O group.
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