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    Carbamoyl carboxylic acid amide derivs.
    51.
    发明专利
    Carbamoyl carboxylic acid amide derivs. 未知

    公开(公告)号：DE4434462A1

    公开(公告)日：1996-03-28

    申请号：DE4434462

    申请日：1994-09-27

    Applicant: BASF AG

    Inventor： WAGNER OLIVER DR ,  MUELLER THOMAS DR ,  EICKEN KARL DR ,  HARREUS ALBRECHT DR ,  AMMERMANN EBERHARD DR ,  LORENZ GISELA DR

    IPC: C07C271/22 ,  C07C271/34 ,  C07C271/54 ,  C07C271/60 ,  A01N47/12 ,  C07C269/06

    Abstract: Carbamoyl carboxylic acid amide derivs. of formula (I) and their salts are new R1 = 1-8C alkyl, 2-8C alkenyl, or 2-8C alkynyl (these gps. being opt. partially or completely halogenated and/or mono-, di- or tri-substd. with T gps.); 3-7C cycloalkyl or 3-7C cycloalkyl (these last 2 gps. being opt. partially or completely halogenated and/or mono-, di- or tri-substd. with T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl) or with 1-4C alkyl or aryl(1-4C)alkyl (this last gp. itself opt. substd. with T gps. excluding cycloalkyl or cycloalkenyl)); a non-aromatic 4-8 membered ring contg. in the ring, in addition to C, 1 or 2 heteroatoms chosen from O, S and N (the ring C being opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl, T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl) and the second and any further N heteroatom carrying H or 1-4C alkyl); aryl or heteroaryl (these 2 gps. opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl or T gps. (excluding cycloalkyl and cycloalkenyl)) or W1W2C=N; W1 = 1-8C alkyl (opt. partially or completely halogenated and/or opt. mono-, di- or tri-substd. with T gps. (excluding alkoxycarbonyl, cycloalkyl and cycloalkenyl)), 2-8C alkenyl, 2-8C alkynyl (opt. partially or completely halogenated and opt. mono-, di- or tri-substd. with 1-4C alkyl or T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl), 3-7C cycloalkyl or 3-7C cycloalkenyl (opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl, aryl(1-4C)alkyl (this last gp. itself opt. substd. with halogen, 1-4C alkyl or T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl) or T gps. (excluding cycloalkyl, cycloalkenyl, aryloxy or heteroaryl)), aryl or heteroaryl (these last 2 gps. opt. substd. with T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl); W2 = H or a gp. W1; R2 = H, 1-8C alkyl or 3-7C cycloalkyl (these last 2 gps. opt. partially or completely halogenated); R3 = 1-8C alkyl, 3-7C cycloalkyl (opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl, phenyl(1-4C)alkyl (in which the Ph gp. is opt. mono-, di- or tri-substd. with halogen, 1-4C alkyl or T gps., excluding cycloalkyl, cycloalkenyl, aryl, aryloxy or heteroaryl)); R4 = one of the R3 gps.; or R3 and R4 together with the C atom to which they are attached form a 4-8 membered ring which contains, in addition to C, 1 or 2 heteroatoms chosen from O, S and N (the ring C being opt. mono- or di-substd. with halogen, 1-4C alkyl and T gps. (excluding cycloalkyl, cycloalkenyl and heteroaryl) and the N heteroatom carrying H or 1-4C alkyl); R5 = a R2 gp.; X = H, 1-8C alkyl and/or 2-8C alkenyl (these last 2 gps. opt. partially or completely halogenated and opt. mono-, di- or tri-substd. with T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl), 3-7C cycloalkyl and/or 3-7C cycloalkenyl (these 2 gps. opt. partially or completely halogenated and opt. mono-, di- or tri-substd. with 1-4C alkyl, aryl(1-4C) alkyl (this last opt. substd. with halogen, 1-4C alkyl and T gps., excluding cycloalkyl, cycloalkenyl and heteroaryl), or T gps. (excluding cycloalkyl, cycloalkenyl or heteroaryl)); m = 0-2; A = 3-7C cycloalkyl or 3-7C cycloalkenyl (opt. partially or completely halogenated and/or opt. mono-, di- or tri-substd. with 1-4C alkyl, aryl(1-4C)alkyl (thus last opt. mono-, di- or tri-substd. on aryl with halogen, 1-4C alkyl or T gps., excluding cycloalkyl, cycloalkenyl and heteroaryl) or T gps. excluding cycloalkyl, cycloalkenyl, aryloxy and heteroaryl); R6 = aryl or heteroaryl (these gps. opt. mono-, di- or tri-substd. with halogen or T gps., excluding cycloalkyl, cycloalkenyl or heteroaryl); T = CN, 1-4C alkoxyalkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy, 1-4C alkylthio, 1-4C alkoxycarbonyl, 3-7C cycloalkyl, 3-7C cycloalkenyl, aryl, aryloxy or heteroaryl, the cyclic gps. themselves being opt. mono-, di- or tri-substd. with halogen, CN, 1-4C alkyl, 1-4C alkoxy alkyl, 1-4C haloalkyl, 1-4C alkoxy, 1-4C haloalkoxy, 1-4C alkylthio, 1-4C alkoxycarbonyl, aryl, aryloxy or heteroaryl.

    New N-acyl fumaramic acid derivs.
    54.
    发明专利
    New N-acyl fumaramic acid derivs. 未知

    公开(公告)号：DE4036692A1

    公开(公告)日：1992-05-21

    申请号：DE4036692

    申请日：1990-11-17

    Applicant: BASF AG

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

    IPC: A01N37/30 ,  A01N37/38 ,  A01N37/40 ,  C07C235/88

    Abstract: (A) N-acyl fumaramic acid derivs. of formula (I) are new. A= OR3 or NR4R5; R3-R5= H, 1-6C alkyl, 1-4C haloalkyl, 2-6C alkenyl, 2-6C alkynyl, or aryl(1-4C)alkyl opt. ring-substd. by 1-3 of alkyl, alkoxy, haloalkyl, haloalkoxy, halogen, CN or NO2; R1 and R2= H or 1-6C alkyl or R1+R2= (CH2)m; M= 2-6. Ar= mono- or bicyclic aryl opt. substd. by 1-3 of alkyl, alkoxy, haloalkyl, phenoxy, halophenoxy, benzyloxy, phenyl, haloalkoxy, OH, halogen or NO2; n= 0-3; provided that: (a) Ar is not phenyl or 4-nitrophenyl when A= NH2; (b) Ar is not phenyl when A= OEt or MNe2. (B) Fungicidal compsns. contg. cpds. (I) including those excluded by the above provisos, are also new.

    55.
    发明专利
    未知

    公开(公告)号：DE59509759D1

    公开(公告)日：2001-11-29

    申请号：DE59509759

    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.

    56.
    发明专利
    未知

    公开(公告)号：DK0910949T3

    公开(公告)日：2001-11-19

    申请号：DK98123303

    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.

    Use of aryl-alkylamino-pyrimidine compounds
    57.
    发明专利
    Use of aryl-alkylamino-pyrimidine compounds 未知

    公开(公告)号：DE19827611A1

    公开(公告)日：1999-01-28

    申请号：DE19827611

    申请日：1998-06-20

    Applicant: BASF AG

    Inventor： WAGNER OLIVER DR ,  HARRIES VOLKER DR ,  KRAMER JACOBUS-JAN DE DR

    IPC: A01N43/54

    Abstract: Use of arylalkylamino-pyrimidine compounds of formula (I), as insecticides, is new: R1 = H, halo, T, T', 3-7C cycloalkyl, TO,NH2 (optionally substituted by T), or 6-14C aryl (optionally substituted by 1-3 halo, R, RO or R'O); R2, R3 = H, halo or T; or R2+R3 = a 5-6 membered saturated or unsaturated ring which contains 1-2 N or S atoms; R4 = H, T, 3-7C cycloalkyl or R'; n = 1 or 2; R6 = H, halo, T, R' or TO; R5 = (a) when R6 is H: a group O-A1-CN or O-S(O)2R7; or (b) when R6 is H, halo, T, R' or TO: a group S(O)mR8; or R5+R6 = O-A2-O at positions 3 and 4 of the phenyl ring; A1 = 1-6C alkylene; R7 = T, R', 6-14C aryl, benzyl, styryl, or NH2 (optionally substituted by T); R8 = T (optionally substituted by RS or TO) or CF2R9; R9 = H or halo; A2 = methylene or ethylene (optionally substituted by 1-4 halo); T, T', R, R' = 1-6C alkyl, 1-6C haloalkyl, 1-4C alkyl and 1-4C haloalkyl respectively; m =0-2; provided that R4 is not a group R if R5 and R6 = O-A2- O.

    58.
    发明专利
    未知

    公开(公告)号：ES2114113T3

    公开(公告)日：1998-05-16

    申请号：ES94117400

    申请日：1994-11-04

    Applicant: BASF AG

    Inventor： WAGNER OLIVER DR ,  EICKEN KARL DR ,  GOTZ 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.

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