71.
    发明专利
    未知

    公开(公告)号:AT204259T

    公开(公告)日:2001-09-15

    申请号:AT94115579

    申请日:1994-10-04

    Applicant: BASF AG

    Abstract: Naphthyl ethers of the formula I in which the index and the substituents have the following meaning: A is optionally substituted phenyl or optionally substituted 5- to 6-membered heteroaryl which, in addition to carbon ring members, can contain one to three nitrogen atoms or one or two nitrogen atoms and an oxygen or sulphur atom or an oxygen or sulphur atom as further ring members; n is 0 or 1; X is oxygen, sulphur or nitrogen, the nitrogen atom carrying one of the following radicals: hydrogen, C1-C4-alkyl, C1-C4-alkoxy, C3-C6-cycloalkyl, optionally substituted phenyl or optionally substituted benzyl; Y is oxygen or in the case where Z is NOCH3: oxygen or nitrogen, where the nitrogen atom carries one of the following radicals: hydrogen, C1-C4-alkyl or C1-C4-alkoxy; Z is CHOCH3, NOCH3, CHCH3 or CHCH2CH3; R is C1-C4-alkyl; R is optionally substituted C1-C6-alkyl, C3-C6-cycloalkyl, C2-C6-alkenyl or C3-C6-alkynyl; optionally substituted phenyl; optionally substituted 5- or 6-membered heteroaryl containing, in addition to carbon ring members, one to three nitrogen atoms or one or two nitrogen atoms and an oxygen or sulphur atom as further ring members; or in the case where the value of n is 0 additionally to the above meanings: halogen, C1-C6-alkoxy, C1-C4-alkylsulphoxyl or phenylsulphoxyl, where the phenyl ring can in turn carry substituents, process for the preparation of the naphthyl ethers I, compositions containing them and their use for the control of animal pests or harmful fungi.

    76.
    发明专利
    未知

    公开(公告)号:DE59502205D1

    公开(公告)日:1998-06-25

    申请号:DE59502205

    申请日:1995-03-17

    Applicant: BASF AG

    Abstract: Oximino-substd benzyloxybenzene derivs of formula (I) are new. Ra = a gp. of formula (i); X = CHOMe, CH-Me or N-OMe; R1 = 1-6C alkyl (opt substd by halo, 1-4C alkoxy, CN, 1-6C alkoxycarbonyl, aryl, aryloxy or heteroaryl); 2-6C alkenyl; 3-6C alkynyl or haloalkenyl; 3-6C cycloalkyl; 3-6C cycloalkyl(1-4C)alkyl; aryl(3-6C)alkenyl; satd or unsatd 4-6 membered heterocyclyl or heterocyclyl(1-4C)alkyl where the heterocyclic rings includes 1 or 2 ring members selected from one O or S and one or two N and one or two NMe gps.; and carbocyclic or heterocyclic rings are opt substd by 1 or more halo, 1-4C alkyl or alkoxy, 1-2C haloalkyl or haloalkoxy, 3-6C cycloalkyl, aryl or aryloxy; R2 and R3 = H, halo, CN, NO2, 1-4C alkyl or alkoxy, 1-2C haloalkyl or haloalkoxy, or if on adjacent C atoms are together oxy(m)ethylideneoxy (opt substd on each C by 1 or 2 halo and/or Me); R4 = CN, Cl, Br, 1-6C alkoxy or alkylthio, 1-4C haloalkoxy, 1-4C alkoxy(1-4C)alkoxy, 3-6C cycloalkyl(1-2C)alkoxy, mon o or di(1-6C)alkylamino, 3-6C alkenyloxy or alkynyloxy, aryloxy or arylthio (aromatic rings opt substd by 1-3 of 1-4C(halo)alkyl, (halo)alkoxy or alkylthio, and additionally by halo atoms to a total no of 4 or 5 substits); R5 = NO2, CN, halo, 1-4C(halo)alkyl, (halo)alkoxy or alkylthio, phenyl or phenoxy (opt substd as aromatic rings in R4); or 2 R5 on adjacent C form a 1,3-butadiene-1,4-diyl gp. (i.e. a fused benzene ring), opt. substd by 1 or 2 halo, and opt. also by 1 or 2 of NO2, CN, halo, 1-4C haloalkyl, (halo)alkoxy or alkylthio; n = 0-4 (R5 same or different if n = 2 or more); Y = O, NH or NMe; R6 = H or 1-4C alkyl. Also new are intermediates of formulae (XI') and (IVb'). Y' = NH or NMe; R2 and R3 are above except that in (X1') they do not represent alkylenedioxy; in (IVb') Y is limited to Y'.

    77.
    发明专利
    未知

    公开(公告)号:AT166341T

    公开(公告)日:1998-06-15

    申请号:AT95103942

    申请日:1995-03-17

    Applicant: BASF AG

    Abstract: Oximino-substd benzyloxybenzene derivs of formula (I) are new. Ra = a gp. of formula (i); X = CHOMe, CH-Me or N-OMe; R1 = 1-6C alkyl (opt substd by halo, 1-4C alkoxy, CN, 1-6C alkoxycarbonyl, aryl, aryloxy or heteroaryl); 2-6C alkenyl; 3-6C alkynyl or haloalkenyl; 3-6C cycloalkyl; 3-6C cycloalkyl(1-4C)alkyl; aryl(3-6C)alkenyl; satd or unsatd 4-6 membered heterocyclyl or heterocyclyl(1-4C)alkyl where the heterocyclic rings includes 1 or 2 ring members selected from one O or S and one or two N and one or two NMe gps.; and carbocyclic or heterocyclic rings are opt substd by 1 or more halo, 1-4C alkyl or alkoxy, 1-2C haloalkyl or haloalkoxy, 3-6C cycloalkyl, aryl or aryloxy; R2 and R3 = H, halo, CN, NO2, 1-4C alkyl or alkoxy, 1-2C haloalkyl or haloalkoxy, or if on adjacent C atoms are together oxy(m)ethylideneoxy (opt substd on each C by 1 or 2 halo and/or Me); R4 = CN, Cl, Br, 1-6C alkoxy or alkylthio, 1-4C haloalkoxy, 1-4C alkoxy(1-4C)alkoxy, 3-6C cycloalkyl(1-2C)alkoxy, mon o or di(1-6C)alkylamino, 3-6C alkenyloxy or alkynyloxy, aryloxy or arylthio (aromatic rings opt substd by 1-3 of 1-4C(halo)alkyl, (halo)alkoxy or alkylthio, and additionally by halo atoms to a total no of 4 or 5 substits); R5 = NO2, CN, halo, 1-4C(halo)alkyl, (halo)alkoxy or alkylthio, phenyl or phenoxy (opt substd as aromatic rings in R4); or 2 R5 on adjacent C form a 1,3-butadiene-1,4-diyl gp. (i.e. a fused benzene ring), opt. substd by 1 or 2 halo, and opt. also by 1 or 2 of NO2, CN, halo, 1-4C haloalkyl, (halo)alkoxy or alkylthio; n = 0-4 (R5 same or different if n = 2 or more); Y = O, NH or NMe; R6 = H or 1-4C alkyl. Also new are intermediates of formulae (XI') and (IVb'). Y' = NH or NMe; R2 and R3 are above except that in (X1') they do not represent alkylenedioxy; in (IVb') Y is limited to Y'.

    New imino:oxy:phenyl:acetic acid derivatives

    公开(公告)号:DE19622332A1

    公开(公告)日:1997-12-11

    申请号:DE19622332

    申请日:1996-06-04

    Applicant: BASF AG

    Abstract: 2-Iminooxyphenylacetic acid derivatives of formula (I) and their salts are new. R = C(CO2Me)=NOMe, C(CONHMe)=NOMe, C(CONH2)=NOMe, C(CO2Me)=COMe or C(CO2Me)=CHMe; R2 = CN, NO2, halo, 1-4C alkyl, 1-4C haloalkyl or 1-4C alkoxy; m = 0-2; R3 = H, CN, OH, halo, 1-6C alkyl (optionally substituted by halo or 1-6C alkoxy) 1-6C alkoxy, 1-6C haloalkoxy, 1-6C alkylthio, cyclopropyl, 2-6C alkenyl, or aryloxy-1-6C alkyl, benzyl or benzyloxy (all optionally ring-substituted by 1-3 CN, NO2, halo, 1-6C alkyl, 1-6C alkoxy, 1-6C haloalkyl or 1-6C haloalkoxy) or C(Me)=N-Y-Ra; Ra = 1-6C alkyl; Y = O, NH or NRa; R4 = H, CN, -Qp-C(R5)=N-Y'-R6 or -Q-O-N=CR7R8; or alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, alkoxy, alkenyloxy, alkynyloxy, cycloalkoxy, heterocyclyloxy, aryloxy, heteroaryloxy, arylthio or heteroarylthio (all optionally substituted); or CR3R4 = 4-8 membered ring containing C atoms an optionally 1 or 2 of O, S, NH and/or N(1-4C alkyl) (optionally substituted on C by halo, 1-6C alkyl or 1-4C alkoxyimino), provided R3 and R4 are not both bonded to C via hetero atoms; Q = bond, CH2, CH(Me), CH(Et) or 1,1-cyclopropyl; p = 0 or 1; Y' = O, NH or N(1-4C alkyl); R5 = as for R3 or optionally substituted cycloalkoxy, heterocyclyloxy, aryloxy, heteroaryloxy, arylthio or heteroarylthio; R6 = optionally substituted 1-10C alkyl, 3-6C cycloalkyl, 2-10C alkenyl, 2-10C alkynyl, 1-10C alkylcarbonyl, 2-10C alkenylcarbonyl, 2-10C alkynylcarbonyl, 1-10C alkylsulphonyl, aryl, heteroaryl, arylcarbonyl, heteroarylcarbonyl, arylsulphonyl or heteroarylsulphonyl; R7, R8 = Me, Et, Ar or CH2Ar; Ar = phenyl (optionally mono-, di- or trisubstituted by CN, NO2, halo, 1-6C alkyl, 1-6C alkoxy, 1-6C haloalkyl or 1-6C haloalkoxy.

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