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    164.
    发明专利
    未知

    公开(公告)号：DE59600551D1

    公开(公告)日：1998-10-22

    申请号：DE59600551

    申请日：1996-02-16

    Applicant: BASF AG

    Inventor： RHEINHEIMER JOACHIM DR ,  MISSLITZ ULF DR ,  KARDORFF UWE DR ,  WESTPHALEN KARL-OTTO DR ,  WALTER HELMUT DR

    IPC: A01N43/16 ,  C07D309/30

    Abstract: (2-Hydroxy-4-(2-oxotetrahydro-pyran-4-yl)-6-oxo-1-cyclohexenyl)ketoxime ethers of formula (I) and their salts and esters with 1-10C carboxylic acids or inorganic acids are new. R1 = 1-6C alkyl; R2 = 1-4C alkyl, 3-4C alkenyl or 3-4C alkynyl (all opt. substd. by halogen, 1-3C alkyl, phenyl (opt. mono- to tri-substd. by NO2, CN, halogen, 1-4C alkyl, 1-4C haloalkyl, phenyl and phenoxy) or OPh) or Ph; Ph = phenyl (opt. mono- to tri-substd. by NO2, CN, halogen, 1-4C alkyl and 1-4C haloalkyl).

    BENZYLHYDROXYLAMINES AND INTERMEDIATES FOR THEIR PREPARATION
    169.
    发明专利
    BENZYLHYDROXYLAMINES AND INTERMEDIATES FOR THEIR PREPARATION 未知

    公开(公告)号：CZ2698A3

    公开(公告)日：1998-07-15

    申请号：CZ2698

    申请日：1996-06-27

    Applicant: BASF AG

    Inventor： KLINTZ RALF DR ,  HAMPRECHT GERHARD DR ,  HEISTRACHER ELISABETH DR ,  SCHAFER PETER DR ,  ZAGAR CYRILL DR ,  WESTPHALEN KARL-OTTO DR ,  WALTER HELMUT DR ,  MISSLITZ ULF DR ,  MENKE OLAF DR ,  MENGES MARKUS DR

    IPC: A01N43/54 ,  A01N47/12 ,  A01N47/24 ,  A01N47/30 ,  A01N53/00 ,  C07C239/08 ,  C07C239/10 ,  C07C239/16 ,  C07C239/20 ,  C07C265/12 ,  C07C271/22 ,  C07C271/28 ,  C07C271/54 ,  C07C271/58 ,  C07C275/32 ,  C07C275/40 ,  C07D239/54 ,  C07D405/12

    Abstract: PCT No. PCT/EP96/02805 Sec. 371 Date Jan. 5, 1998 Sec. 102(e) Date Jan. 5, 1998 PCT Filed Jun. 27, 1996 PCT Pub. No. WO97/02253 PCT Pub. Date Jan. 23, 1997Benzylhydroxylamines I (X=-N(R7)-O-; Y=O, S; R1=halogen, CN, NO2, CF3; R2=H, halogen; R3=H, NH2, CH3; R4=H, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkylthio, C1-C6-alkylsulfinyl or C1-C6-alkylsulfonyl; R5=H, halogen, C1-C6-alkyl; R6=H, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C2-C6-alkenyl; R7=H, C1-C6-alkyl, C3-C8-cycloalkyl, C1-C6-haloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkylcarbonyl, C3-C6-alkenylcarbonyl, C3-C6-alkynylcarbonyl, C1-C6-alkoxycarbonyl, C2-C8-alkenyloxycarbonyl, C2-C6-alkynyloxycarbonyl, C1-C6-alkylthiocarbonyl, C1-C6-alkylsulfonyl, C1-C6-alkylcarbamoyl, it being possible for the 14 last-mentioned radicals to have attached to them 1-3 substituents: NO2, CN, halogen, C3-C8-cycloalkyl, OH, C1-C6-alkoxy, C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkynyloxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylcarbonyl, C1-C6-alkylcarbonyloxy, C1-C6-alkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-alkylideneaminoxy, C1-C6-alkylcarbamoyl, unsubstituted or substituted phenyl, phenoxy or phenylsulfonyl, a 3- to 7-membered heterocyclyl or heterocyclyloxy group having 1-3 hetero atoms, it being possible for this group to be saturated, unsaturated or aromatic and to have attached to it 1-3 substituents, -CO-Z1R9, -OCO-Z1R9, -N(R9)R10 or R7=unsubstituted or substituted cycloalkylcarbonyl, phenylcarbonyl, phenylsulfonyl, phenylcarbamoyl; R8=H, C1-C6-alkyl, C3-C8-cycloalkyl, C1-C6-haloalkyl, C3-C6-alkenyl or C3-C6-alkynyl, it being possible for each of the 5 last-mentioned radicals to have attached to it 1-3 substituents: NO2, CN, halogen, C3-C8-cycloalkyl, OH, C1-C6-alkoxy, C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkynyloxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-alkylideneaminoxy, unsubstituted or substituted phenyl- [sic], phenoxy-[sic] or phenylsulfonyl, a 3- to 7-membered heterocyclyl or heterocyclyloxy group having 1-3 hetero atoms, it being possible for this group to be saturated, unsaturated or aromatic and to have attached to it 1-3 substituents, -CO-Z2R11, -OCO-Z2R11, -N(R11)R12; Z1 a chemical bond, oxygen, sulfur or -N(R10)-; Z2=a chemical bond, oxygen, sulfur or -N(R12)-; R9, R11=H, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl, (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, unsubstituted or sub

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