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    Substituted 2-phenylpyridines.
    46.
    发明专利
    Substituted 2-phenylpyridines. 未知

    公开(公告)号：ZA966699B

    公开(公告)日：1998-02-09

    申请号：ZA966699

    申请日：1996-08-07

    Applicant: BASF AG

    Inventor： SCHAEFER PETER ,  HEISTRACHER ELISABETH ,  MENKE OLAF ,  HAMPRECHT GERHARD ,  ZAGAR CYRILL ,  RACK MICHAEL ,  GOETZ NORBERT ,  HARREUS ALBRECHT ,  WESTPHALEN KARL-OTTO ,  WALTER HELMUT ,  MISLITZ ULF

    IPC: A01N43/40 ,  C07D213/61 ,  C07D405/12 ,  A01N ,  C07D

    Abstract: PCT No. PCT/EP96/03243 Sec. 371 Date Jan. 20, 1998 Sec. 102(e) Date Jan. 20, 1998 PCT Filed Jul. 23, 1996 PCT Pub. No. WO97/06143 PCT Pub. Date Feb. 20, 1997Substituted 2-phenylpyridines I where n is 0, 1; R1 is halogen, C1-C6-haloalkyl; R2 and R3 are H, halogen; R4 is cyano, halogen; X and Y are -O-, -S-; R5 and R6 are H, C1-C4-alkyl or together are a 1,2-ethylene, 1,3-propylene, 1,4-tetramethylene or 1,5-pentamethylene chain; R7 is C1-C6-haloalkyl, C3-C6-haloalkenyl, C2-C6-alkenyloxy-C1-C4-alkyl, C2-C6-alkenyloxy-C1-C4-alkoxy-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-alkadienyl, C3-C6-alkynyl, C3-C6-cycloalkyl, C5-C6-cycloalkenyl, 3-oxetanyl, 3-thietanyl, phenyl, phenyl-C1-C4-alkyl or 5/6-membered heteroaryl having 1 to 3 hetero atoms selected from the group consisting of two oxygen atoms, two sulfur atoms and 3 nitrogen atoms, or R6 and R7 together are a 1,2-ethylene or 1,3-propylene chain which can have attached to it one or two C1-C4-alkyl substituents are used as herbicides and for the desiccation/defoliation of plants.

    SUBSTITUTED 2-PHENYLPYRIDINES
    48.
    发明专利
    SUBSTITUTED 2-PHENYLPYRIDINES 未知

    公开(公告)号：CA2245541A1

    公开(公告)日：1997-08-21

    申请号：CA2245541

    申请日：1997-02-17

    Applicant: BASF AG

    Inventor： WALTER HELMUT ,  ZAGAR CYRILL ,  MISLITZ ULF ,  HEISTRACHER ELISABETH ,  MENKE OLAF ,  HAMPRECHT GERHARD ,  SCHAEFER PETER ,  MENGES MARKUS ,  WESTPHALEN KARL-OTTO

    IPC: A01N57/24 ,  A01N57/32 ,  C07F9/58 ,  C07F9/6558

    Abstract: The invention concerns substituted 2-phenylpyridines of formula (I) and their salts, in which X = a bond, 1,2-ethinediyl, an optionally substituted methylene-, 1,2-ethanediyl- or 1,3-propylene bridge, optionally substituted methyleneoxymethylene, methylenethiamethylene, ethene-1,2-diyl, optionally substituted oxymethylene, thiamethylene, oxyethylene or thiaethylene bonded to the phenyl ring via the heteroatom; Y = -O-, -S-; -Z1 = -O-, -S-, -N(R7)-; Z2 = -O2-, -S-, -N(R8)-; R1, R2, R7, R8 = H, C1-C6-alkyl, C1-C6-alkyl halide, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4alkoxy-C1-C4alkyl, C1-C4alkoxy halide-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkoxy-C1-C4-alkyl, amino-C1-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di-(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1C4-alkylthiohalide-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3C4alkinylthio-C1-C4-alkyl, C1-C4-alkylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphinylhalide-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphonyl-C1-C4-alkyl, C1-C4-alkylsulphonyl halide-C1-C4-alkyl, C3-C4-alkenylsulphonyl-C1-C4-alkyl, C3-C4-alkinylsulphonyl-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-alkenyl halide, cyano-C3-C6-alkenyl, C3-C6-alkinyl, C3-C6-alkinyl halide, cyano-C3-C6-alkinyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)-carbonyl-C1-C4-alkyl, (C1-C4-alkylthio)carbonyl-C1-C4-alkyl, amino-carbonyl-C1-C4-alkyl, (C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, di-(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, optionally substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, 3- to 7-members heterocyclyl or heterocyclyl-C1-C4-alkyl, wherein all the heterocycles can contain a (thio)carbonyl ring member, or R1 + R2 and/or R1 + R7 and/or R2 + R8 together in each case are an optionally substituted 1,2-ethanediyl-, 1,3-propylene-, tetramethylene-, pentamethyleneor ethyleneoxyethylene chain; or R1 + R2 together are optionally substituted 1,2-phenylene; R3 = CN, halogen, C1-C4-alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C4 halkoxy halide; R4, R5 are H, halogen; R6 is halogen, C1-C4 alkyl halide; and n = 0,1. The invention further concerns the use of these substances as herbicides and for desiccating/defoliating plants.

    Benzylhydroxylamines and intermediates used to prepare them
    50.
    发明专利
    Benzylhydroxylamines and intermediates used to prepare them 未知

    公开(公告)号：AU6305696A

    公开(公告)日：1997-02-05

    申请号：AU6305696

    申请日：1996-06-27

    Applicant: BASF AG

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

    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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