公开(公告)号：EP0481289B1

公开(公告)日：1995-08-02

申请号：EP91116817

申请日：1991-10-02

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  KEIL MICHAEL DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR ,  KROHN KARSTEN PROF DR ,  FRANKE CLAUDIA

IPC: A01N37/26 ,  A01N37/30 ,  A01N37/38 ,  A01N37/40 ,  C07C233/91 ,  C07C235/88

CPC classification number: A01N37/38 ,  A01N37/30 ,  A01N37/40 ,  C07C235/88

公开(公告)号：HU226012B1

公开(公告)日：2008-02-28

申请号：HU0002178

申请日：1998-01-08

Applicant: BASF AG

Inventor： RHEINHEIMER JOACHIM DR ,  WALTER HELMUT DR ,  BAUMANN ERNST DR ,  MISSLITZ ULF DR ,  OTTEN MARTINA DR ,  HILL REGINA LUISE ,  ENGEL STEFAN ,  VON DEYN WOLFGANG ,  WITSCHEL MATTHIAS ,  WAGNER OLIVER DR ,  WESTPHALEN KARL-OTTO DR ,  MAYER GUIDO

IPC: C07D277/10 ,  A01N43/18 ,  C07D413/10 ,  A01N43/48 ,  A01N43/56 ,  A01N43/72 ,  A01N43/76 ,  A01N43/78 ,  A01N43/80 ,  C07D231/20 ,  C07D231/24 ,  C07D261/04 ,  C07D261/20 ,  C07D263/10 ,  C07D273/00 ,  C07D277/20 ,  C07D277/34 ,  C07D291/04 ,  C07D401/10 ,  C07D403/10 ,  C07D405/10 ,  C07D409/10 ,  C07D411/10 ,  C07D417/10 ,  C07D419/10 ,  C07D498/10

Abstract: 4-(3-Heterocyclyl-benzoyl)-pyrazole derivatives (I) and their salts are new: R1, R3 = H; NO2; halo; CN; 1-6C alkyl, 1-6C alkoxy, 1-6C alkylthio, 1-6C alkylsulphinyl or 1-6C alkylsulphonyl optionally substituted by halo; H2NSO2; (1-6C alkyl)NHSO2; (1-6C alkyl)2NSO2; (1-6C alkyl)SO2NH-; (1-6C haloalkyl-SO2)NH-; (1-6C alkyl)(1-6C alkyl-SO2)N-; or (1-6C haloalkyl)(1-6C alkyl-SO2)N-; R2 = optionally substituted 5- or 6-membered heterocycle containing 1-4 O, S and/or N atoms; R6 = 1-6C alkyl; R7 = 1-6C alkyl; 3-6C alkenyl or 3-6C alkynyl optionally substituted by halo; 3-6C cycloalkyl; 1-6C alkylcarbonyl; 2-6C alkenylcarbonyl; 2-6C alkynylcarbonyl; 3-6C cycloalkylcarbonyl; 1-6C alkoxycarbonyl; 3-6C alkenyloxycarbonyl; 3-6C alkynyloxycarbonyl; 1-6C alkyl-NH-CO-; 3-6C alkenyl-NH-CO-; 3-6C alkynyl-NH-CO-; (1-6C alkyl)2N-CO-; (3-6C alkenyl)(1-6C alkyl)N-CO-carbonyl; (3-6C alkynyl)(1-6C alkyl)N-CO-; (1-6C alkoxy)(1-6C alkyl)N-CO-; (3-6C alkenyl)(1-6C alkoxy)N-CO-; (3-6C alkynyl)(1-6C alkoxy)N-CO-; (1-6C alkyl)2N-CS-; 1-6C alkoxyimino-1-6C alkyl; 1-6C alkylamino imino-1-6C alkyl; or di(1-6C alkylamino)imino-1-6C alkyl (alkyl, cycloalkyl and alkoxy groups are optionally substituted by 1 or more halo and/or by 1-3 CN, OH, 1-4C alkoxy, 1-4C alkylthio, di(1-4C alkyl)amino, 1-4C alkylcarbonyl, 1-4C alkoxycarbonyl, 1-4C alkoxy-1-4C alkoxycarbonyl, (1-4C alkyl)2N-1-4C alkoxycarbonyl, COOH, 1-4C alkyl-NH-CO-, (1-4C alkyl)2N-CO-, CONH2; 1-4C alkylcarbonyloxy or 3-6C cycloalkyl); or Ar; Ar-1-6C alkyl; Ar-CO-1-6C alkyl; Ar-CO-; Ar-O-CO-; Ar-NH-CO-; (1-6C alkyl)(Ar)N-CO-; or Ar-2-6C alkenylcarbonyl; Ar = phenyl or heterocyclyl optionally substituted by 1 or more halo and/or by 1-3 NO2, CN or 1-4C alkyl or 1-4C alkoxy (optionally substituted by halo), and R8 = H, 1-6C alkyl or 1-6C haloalkyl.

公开(公告)号：CZ292267B6

公开(公告)日：2003-08-13

申请号：CZ50098

申请日：1996-08-26

Applicant: BASF AG

Inventor： WETTERICH FRANK DR ,  WAGNER OLIVER DR ,  EICKEN KARL DR ,  DITRICH KLAUS DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR ,  STRATHMANN SIEGFRIED DR

IPC: C07C269/04 ,  A01N47/12 ,  C07C269/06 ,  C07C271/22

Abstract: In the present invention there are disclosed carbamoyl carboxylic acid amides of the general formula I, in which Re1 represents an optionally substituted alkyl containing 1 to 8 carbon atoms, alkenyl containing 2 to 8 carbon atoms or alkynyl containing 2 to 8 carbon atoms a Re2 denotes hydrogen, a halogen, cyano, nitro, alkyl containing 1 to 8 carbon atoms, alkoxyalkyl containing 1 to 4 carbon atoms in the alkoxy moiety, haloalkyl containing 1 to 4 carbon atoms, alkoxy containing 1 to 4 carbon atoms, haloalkoxy containing 1 to 4 carbon atoms, alkylthio containing 1 to 4 carbon atoms, haloalkylthio containing 1 to 4 carbon atoms, or a phenyl group bound through oxygen or sulfur. Further disclosed is a process of their preparation, which process is characterized by bringing a corresponding carbamoyl carboxylic acid into reaction a relevant amine. Said amides can be used for fighting harmful fungi and molds wherein the compositions for controlling harmful fungi and molds contain an effective amount of at least one above-indicated amide and at least one general preparation. When controlling the harmful fungi and molds the harmful fungi and molds, or a place of their incidence or plants, area, material or surfaces are treated with an effective amount of at least one aforementioned compound or the above-indicated composition.

公开(公告)号：ES2166129T3

公开(公告)日：2002-04-01

申请号：ES98123304

申请日：1995-12-05

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  EICKEN KARL DR ,  BAYER HERBERT DR ,  SAUTER HUBERT DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

IPC: C07D215/22 ,  A01N37/10 ,  A01N37/18 ,  A01N37/36 ,  A01N37/50 ,  A01N43/36 ,  A01N43/42 ,  A01N43/54 ,  A01N43/653 ,  A01P3/00 ,  C07D207/34 ,  C07D405/06

Abstract: Fungicidal mixt. comprises a synergistic amt. of a cpd. of formula (I) (or an N-oxide or salt), (II), (III) (or a salt), (IV) or (V) (sic). Ar = phenyl (opt. substd. by 1-3 OH, CN, NO2, halo, 1-7C alkyl (opt. substd. by OH or halo), 1-7C alkoxy, 1-7C haloalkoxy, 1-7C alkylthio, 1-7C haloalkylthio, 2-4C acyl, Ar' or OAr'; Ar' = aryl (opt. substd. by 1-3gps. CN, NO2, halo, OR or SR); R1-R4 = H, halo, OH, NO2, OR or SR; R8 = phenyl (opt. substd. by 1-3 CN, halo, 1-4C alkyl, 1-2C haloalkyl or 1-4C alkoxy), or pyrimidyl (opt. substd. by a 1-3C alkyl and/or OPh); Ph = phenyl (opt. substd. by 1-3 CN, halo, 1-4C alkyl, 1-2C haloalkyl or 1-4C alkoxy); A = O or CH2; X = CH or N; Y = O or NR5; R5 = H, 1-3C alkyl or 1-3C alkoxy; R9 = Me, propyn-1-yl or cyclopropyl; R' = F or Cl; R" = CF3 or Cl; or R'+R" = OCF2O; R = 1-4C alkyl (opt. substd. by halo). Also claimed is a process for combating harmful fungi by treatment with one cpd. (I) and one of the cpds. (II)-(V), applied together or separately.

公开(公告)号：ES2166128T3

公开(公告)日：2002-04-01

申请号：ES98123303

申请日：1995-12-05

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  EICKEN KARL DR ,  BAYER HERBERT DR ,  SAUTER HUBERT DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

IPC: C07D215/22 ,  A01N37/10 ,  A01N37/18 ,  A01N37/36 ,  A01N37/50 ,  A01N43/36 ,  A01N43/42 ,  A01N43/54 ,  A01N43/653 ,  A01P3/00 ,  C07D207/34 ,  C07D405/06

Abstract: Fungicidal mixt. comprises a synergistic amt. of a cpd. of formula (I) (or an N-oxide or salt), (II), (III) (or a salt), (IV) or (V) (sic). Ar = phenyl (opt. substd. by 1-3 OH, CN, NO2, halo, 1-7C alkyl (opt. substd. by OH or halo), 1-7C alkoxy, 1-7C haloalkoxy, 1-7C alkylthio, 1-7C haloalkylthio, 2-4C acyl, Ar' or OAr'; Ar' = aryl (opt. substd. by 1-3gps. CN, NO2, halo, OR or SR); R1-R4 = H, halo, OH, NO2, OR or SR; R8 = phenyl (opt. substd. by 1-3 CN, halo, 1-4C alkyl, 1-2C haloalkyl or 1-4C alkoxy), or pyrimidyl (opt. substd. by a 1-3C alkyl and/or OPh); Ph = phenyl (opt. substd. by 1-3 CN, halo, 1-4C alkyl, 1-2C haloalkyl or 1-4C alkoxy); A = O or CH2; X = CH or N; Y = O or NR5; R5 = H, 1-3C alkyl or 1-3C alkoxy; R9 = Me, propyn-1-yl or cyclopropyl; R' = F or Cl; R" = CF3 or Cl; or R'+R" = OCF2O; R = 1-4C alkyl (opt. substd. by halo). Also claimed is a process for combating harmful fungi by treatment with one cpd. (I) and one of the cpds. (II)-(V), applied together or separately.

公开(公告)号：DK0910950T3

公开(公告)日：2001-11-19

申请号：DK98123304

申请日：1995-12-05

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  EICKEN KARL DR ,  BAYER HERBERT DR ,  SAUTER HUBERT DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

IPC: C07D215/22 ,  A01N37/10 ,  A01N37/18 ,  A01N37/36 ,  A01N37/50 ,  A01N43/36 ,  A01N43/42 ,  A01N43/54 ,  A01N43/653 ,  A01P3/00 ,  C07D207/34 ,  C07D405/06

Abstract: Fungicidal mixt. comprises a synergistic amt. of a cpd. of formula (I) (or an N-oxide or salt), (II), (III) (or a salt), (IV) or (V) (sic). Ar = phenyl (opt. substd. by 1-3 OH, CN, NO2, halo, 1-7C alkyl (opt. substd. by OH or halo), 1-7C alkoxy, 1-7C haloalkoxy, 1-7C alkylthio, 1-7C haloalkylthio, 2-4C acyl, Ar' or OAr'; Ar' = aryl (opt. substd. by 1-3gps. CN, NO2, halo, OR or SR); R1-R4 = H, halo, OH, NO2, OR or SR; R8 = phenyl (opt. substd. by 1-3 CN, halo, 1-4C alkyl, 1-2C haloalkyl or 1-4C alkoxy), or pyrimidyl (opt. substd. by a 1-3C alkyl and/or OPh); Ph = phenyl (opt. substd. by 1-3 CN, halo, 1-4C alkyl, 1-2C haloalkyl or 1-4C alkoxy); A = O or CH2; X = CH or N; Y = O or NR5; R5 = H, 1-3C alkyl or 1-3C alkoxy; R9 = Me, propyn-1-yl or cyclopropyl; R' = F or Cl; R" = CF3 or Cl; or R'+R" = OCF2O; R = 1-4C alkyl (opt. substd. by halo). Also claimed is a process for combating harmful fungi by treatment with one cpd. (I) and one of the cpds. (II)-(V), applied together or separately.

公开(公告)号：CZ289091B6

公开(公告)日：2001-10-17

申请号：CZ227097

申请日：1996-01-17

Applicant: BASF AG

Inventor： GOTZ NORBERT DR ,  MULLER BERND DR ,  SAUTER HUBERT DR ,  GEBHARDT JOACHIM DR ,  WAGNER OLIVER DR

IPC: B01J23/42 ,  B01J23/44 ,  C07B61/00 ,  C07C239/10 ,  C07C239/12 ,  C07C251/48 ,  C07C253/30 ,  C07C255/64 ,  C07D213/76 ,  C07D213/80 ,  C07D215/38 ,  C07D215/40 ,  C07D215/42 ,  C07D231/22 ,  C07D239/54 ,  C07D249/12 ,  C07D471/04

Abstract: The present invention relates to a process for preparing aromatic or heteroaromatic hydroxylamines of the general formula I, in which Re1 represents unsubstituted or substituted aryl radical or unsubstituted or substituted hetaryl radical being selected from a group comprising pyridines and quinolines, by hydrogenation of nitro compounds of the general formula II, wherein Re1 is as specified above, in the presence of a platinum catalyst supported on activated charcoal or in the presence of a sulfur or selenium doped palladium catalyst supported on activated charcoal. The preparation process is characterized in that the reaction is carried out in the presence of nitrogen-substituted morpholine compound of the general formula III, wherein Re2 represents an alkyl radical containing 1 to 5 carbon atoms and Re3 through a Re10 represent each a hydrogen atom or an alkyl radical having 1 to 5 carbon atoms.

公开(公告)号：CZ288779B6

公开(公告)日：2001-08-15

申请号：CZ182397

申请日：1995-12-05

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  EICKEN KARL DR ,  BAYER HERBERT DR ,  SAUTER HUBERT DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

IPC: C07D215/22 ,  A01N37/10 ,  A01N37/18 ,  A01N37/36 ,  A01N37/50 ,  A01N43/36 ,  A01N43/42 ,  A01N43/54 ,  A01N43/653 ,  A01P3/00 ,  C07D207/34 ,  C07D405/06

Abstract: In the present invention there is disclosed a mixed fungicidal agent containing in synergetically effective amount a) the compound of the general formula I, N-oxide or a salt thereof, wherein the symbols Re1, Re2, Re3, Re4, Re5, Re6, Re7 have specific meaning and b) the compound of the general formula II, wherein the symbols Re8, A, X and Y have specific meaning or c) a pyridine derivative of the general formula III or a salt thereof, whereby Re9 represents methyl, propin-1-yl or cyclopropyl, or d) (2RS,3SR)-1-[3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiran-2-yl-methyl]-1H-1,2,4-triazole of the general formula IV, or e) the compound of the general formula V, wherein the symbols Re10 and Re11 have specific meaning. In the present invention there is also claimed a method of fighting harmful fungi and which is characterized by treating the attacked areas with a fungicidally effective amount of the above specified mixed fungicidal agent.

公开(公告)号：CZ9801610A3

公开(公告)日：1998-10-14

申请号：CZ161098

申请日：1996-11-18

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  AMMERMANN EBERHARD DR ,  STRATHMANN SIEGFRIED DR ,  LORENZ GISELA DR

IPC: A01N37/24 ,  A01N37/50 ,  A01N43/54

CPC classification number: A01N37/24 ,  A01N61/00 ,  A01N37/50 ,  A01N43/54 ,  A01N2300/00

公开(公告)号：GR3026397T3

公开(公告)日：1998-06-30

申请号：GR980400594

申请日：1998-03-17

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  EICKEN KARL DR ,  GOETZ NORBERT DR ,  RANG HARALD DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

IPC: A01N37/24 ,  A01N47/06 ,  A01N47/22 ,  C07C233/24 ,  C07C233/25 ,  C07C233/29 ,  C07C269/02 ,  C07C271/44 ,  C07C271/46 ,  C07C271/58

Abstract: p-Hydroxyaniline derivatives of the formula I in which the substituents have the following meanings: R is hydrogen or optionally substituted alkyl; R and R independently of one another are halogen, alkyl, haloalkyl, alkoxy and haloalkoxy; R is optionally substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl or aryl, OR or NR R , where R and R are optionally substituted alkyl, alkenyl, cycloalkyl, cycloalkenyl or aryl and R is hydrogen or alkyl, and salts thereof, their preparation, compositions comprising them, and their use as fungicides or pesticides; furthermore compounds of the formula VI and salts thereof, processes for their preparation, compositions comprising them, and their use as intermediates and as pesticides.