公开(公告)号：HUT58184A

公开(公告)日：1992-02-28

申请号：HU189691

申请日：1991-06-06

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  ZIPPERER BERNHARD ,  GOETZ NORBERT ,  KEIL MICHAEL ,  LORENZ GISELA ,  AMMERMANN EBERHARD

IPC: A01N43/40 ,  C07D213/26 ,  C07D213/30 ,  C07D213/48 ,  C07D213/50 ,  C07D213/53 ,  C07D213/16 ,  C07D213/89

Abstract: Beta-picoline derivs. (I) and their N-oxides and addn. salts are new. In (I), A = CR1R2; R1, R2 = H, 1-6C alkyl, 2-6C alkenyl or 2-6C alkynyl; or R1+R2 = 2-6C n-alkylene; B = CH2, CHOR3, CHR4 or C=NOR5; R3 = H, 1-6C alkyl, 1-6C haloalkyl, 3-8C cycloalkyl, 3-6C alkenyl, 2-6C acyl or phenyl, benzyl or benzoyl opt. mono-, di- or tri-substd. in the ring by 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy, halogen, cyano or nitro; R4 = H, F, Cl, Br or I; R5 = H, 1-6C alkyl, 1-6C haloalkyl, 3-7C cycloalkyl, 3-6C alkenyl or aryl-1-4C alkyl opt. mono-, di- or tri-substd. in the aryl ring by 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, halogen, cyano or nitro; Ar = phenyl or naphthyl opt. mono-, di- or tri-substd. by halogen, 1-6C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy, phenyl, phenoxy, halophenyl, halophenoxy or benzyloxy; except 1-phenyl-3-(3-pyridyl) propan-1-one (IA). The use of cpd. (IA), which is known from J. Org. Chem. 43 (1978), 3396 and Arch. Pharm. 307 (1974), 550, for the control of fungi is also claimed. Further, intermediates (II) are claimed except where A = CH2 or CH(CH3). 3 Cpds. (I), e.g., 2-ethyl-1-(4-fluorophenyl) -2-(pyridyl-3-methyl)butan-1-ol, are specifically claimed.

公开(公告)号：DE4018260A1

公开(公告)日：1991-12-12

申请号：DE4018260

申请日：1990-06-07

Applicant: BASF AG

Inventor： WAGNER OLIVER DR ,  ZIPPERER BERNHARD DR ,  GOETZ NORBERT DR ,  KEIL MICHAEL DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

IPC: A01N43/40 ,  C07D213/26 ,  C07D213/30 ,  C07D213/48 ,  C07D213/50 ,  C07D213/53

Abstract: Beta-picoline derivs. (I) and their N-oxides and addn. salts are new. In (I), A = CR1R2; R1, R2 = H, 1-6C alkyl, 2-6C alkenyl or 2-6C alkynyl; or R1+R2 = 2-6C n-alkylene; B = CH2, CHOR3, CHR4 or C=NOR5; R3 = H, 1-6C alkyl, 1-6C haloalkyl, 3-8C cycloalkyl, 3-6C alkenyl, 2-6C acyl or phenyl, benzyl or benzoyl opt. mono-, di- or tri-substd. in the ring by 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy, halogen, cyano or nitro; R4 = H, F, Cl, Br or I; R5 = H, 1-6C alkyl, 1-6C haloalkyl, 3-7C cycloalkyl, 3-6C alkenyl or aryl-1-4C alkyl opt. mono-, di- or tri-substd. in the aryl ring by 1-4C alkyl, 1-4C alkoxy, 1-4C haloalkyl, halogen, cyano or nitro; Ar = phenyl or naphthyl opt. mono-, di- or tri-substd. by halogen, 1-6C alkyl, 1-4C alkoxy, 1-4C haloalkyl, 1-4C haloalkoxy, phenyl, phenoxy, halophenyl, halophenoxy or benzyloxy; except 1-phenyl-3-(3-pyridyl) propan-1-one (IA). The use of cpd. (IA), which is known from J. Org. Chem. 43 (1978), 3396 and Arch. Pharm. 307 (1974), 550, for the control of fungi is also claimed. Further, intermediates (II) are claimed except where A = CH2 or CH(CH3). 3 Cpds. (I), e.g., 2-ethyl-1-(4-fluorophenyl) -2-(pyridyl-3-methyl)butan-1-ol, are specifically claimed.

公开(公告)号：ES2166127T3

公开(公告)日：2002-04-01

申请号：ES98123302

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：DE59509762D1

公开(公告)日：2001-11-29

申请号：DE59509762

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：DE59509761D1

公开(公告)日：2001-11-29

申请号：DE59509761

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：AT207293T

公开(公告)日：2001-11-15

申请号：AT98123303

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：AT207292T

公开(公告)日：2001-11-15

申请号：AT98123302

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：CZ9701823A3

公开(公告)日：1998-05-13

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

CPC classification number: A01N43/42 ,  A01N43/653 ,  A01N43/54 ,  A01N43/36 ,  A01N37/50 ,  A01N2300/00

公开(公告)号：DE59405370D1

公开(公告)日：1998-04-09

申请号：DE59405370

申请日：1994-11-04

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.

公开(公告)号：CZ227097A3

公开(公告)日：1998-02-18

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: PCT No. PCT/EP96/00170 Sec. 371 Date Jul. 7, 1997 Sec. 102(e) Date Jul. 7, 1997 PCT Filed Jan. 17, 1996 PCT Pub. No. WO96/22967 PCT Pub. Date Aug. 1, 1996A process for preparing aromatic or heteroaromatic hydroxylamines of the general formula I (I) where R1 is an unsubstituted or substituted aryl radical or an unsubstituted or substituted hetaryl radical from the pyridine or quinoline groups, by hydrogenation of nitro compounds of the general formula IIR1-NO2(II)where R1 has the meaning indicated above, in the presence of a platinum catalyst on an activated carbon support or in the presence of a palladium catalyst doped with sulfur or selenium on an activated carbon support, by carrying out the reaction in the presence of a nitrogen-substituted morpholine compound of the general formula III (III) R2 being alkyl radicals having 1 to 5 carbon atoms and R3 to R10 being hydrogen atoms or alkyl radicals having 1 to 5 carbon atoms is described.