SUBSTITUTED HERBICIDE TETRAZOLINONECARBOXYLIC ACID AMIDES

    公开(公告)号:CA2299502A1

    公开(公告)日:1999-02-18

    申请号:CA2299502

    申请日:1998-07-20

    Applicant: BASF AG

    Abstract: The invention concerns tertrazonlinonecarboxylic acid amides of formula (I) and amide-containing herbicides. In formula (I), Het represents oxetan-3-yl, thietan-3-yl, tetrahydrofuran-3-yl, furan-3-yl, tetrahydrothiophene-3-yl, thiophene-3-yl, tetrahydro-2H-pyran-3-yl, tetrahydro-2H-thiopyran-3-yl, tetrahydro-2H-pyran-4-yl or tetrahydro-2H-thiopyran-4-yl, each being possibly substituted; R1 represents alkyl C1-C6, alkyl halide C1-C6, cyanoalkyl C1-C4, alcoxy C1-C6 alkyl C1-C4, alkyl halide C1-C4 alkyl C1-C4, alkylthio C1-C4 alkyl C1-C4, alkylthio halide C1-C4 alkyl C1-C4, alkylsulfonyl C1-C4 alkyl C1C4, alkylsulfonyl halide C1-C4 alkyl C1-C4, alcenyl C2-C6, cyanoalcenyl C3-C6, alcenyl halide C2-C6, alcinyl C3-C6, cycloalyl C3-C8, cycloalkyl C3-C8 alkyl C1-C4, cycloalcenyl C5-C8, cycloalcenyl C5-C8 alkyl C1-C4, phenyl, phenylakyl C1-C4, heterocyclyl having 3 to 7 links and capable of containing one carbonyl or thiocarbonyl cycle, or heterocyclylakyl C1-C4 having 3 to 7 links and capable of containing one carbonyl or thiocarbonyl cycle, the cycloalkyl, cycloalcenyl, phenyl or heterocyclyl cycles being possibly substituted; R2 represents hydrogen, alkyl C1-C6, alkyl halide C1-C6, alcenyl C3-C6, alcenyl halide C3-C6, alcinyl C3-C6, cycloalkyle C3-C8, cycloalkyl C3-C8 alkyl C1-C4, phenyl, phenylakyl C1-C4, heterocyclyl having 3 to 7 links and capable of containing one carbonyl or thiocarbonyl cycle, or heterocyclylalkyl C1-C4 having 3 to 7 links and capable of containing a carbonyl or thiocarbonyl cycle, the cylcoakyl, phenyl or heterocyclyl cycles being possibly substituted.

    SUBSTITUTED 2-BENZ(O)YLPYRIDINES, THEIR PREPARATION AND THEIR USE AS HERBICIDES

    公开(公告)号:CA2283981A1

    公开(公告)日:1998-10-01

    申请号:CA2283981

    申请日:1998-03-09

    Applicant: BASF AG

    Abstract: Substituted 2-benz(o)ylpyridines of formula (I) and the salts thereof, wherein n = 0, 1; x = CO, CH2, CH(C1-C4-alkyl), CH-OH, CH-CN, CH-halogen, C(halogen)2, CH-CONH2, CH-CO-O(C1-C4-alkyl), CH-O(C1-C4-alkyl), C(CN) (C1-C4-alkyl); R1 = halogen, C1-C4-halogen alkane, C1-C4-alkylthio, C1-C4-alkyl sulfinyl, C1-C4-alkyl sulfonyl; R2 = H, halogen; R3 = H, NO2, OH, halogen, C1-C4-alkoxy; R4 = H, NO2, OH, halogen, C1-C4-alkyl, C1-C4 halogen alkane, C1-C4-alkoxy; R5 = H, NO2, CN, halogen, C1-C8-alkyl, C3-C8-alkenyl,C3-C8-alkinyl, C3-C8-cycloalkyl, C1-C8-halogen alkane, C2-C8-halogen alkenyl, C2-C8-halogen alkane, C1-C4-alkoxy-C1-C4-alkyl, C2-C4-alkenyloxy-C1-C4-alkyl, C2-C4-alkinyloxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, cyano-C1-C8-alkyl, cyano-C2-C8-alkenyl, cyano-C3-C8-alkinyl, optionally substituted OH, SH, SO-H, -SO2-H, COOH or NH-COOH, -SO2Cl, -N(R9, R10), -NH-SO2-(C1-C8-alkyl), -N¢-SO2-(C1-C8-alkyl)!2, -N(C1-C8-alkyl) ¢SO2-(C1-C8-alkyl)!, -SO2-N(R9, R10), -O-CO-NH-R9, optionally substituted CHO, O-CHO or -NH-CHO, NH-CO-NH-R9, -O-CS-NH2, -OCS-N(C1-C8-alkyl)2, -CO-N(R9, R10), -CS-N (R9, R10), -CO-NH-SO2-(C1-C4-alkyl), -CO-N(C1-C4-alkyl), -SO2-(C1-C4-alkyl), hydroxycarbonyl-C1-C8-alkyl, (C1-C8-alkoxy)carbonyl-C1-C6-alkyl, CH2-CH(halogen)-CO-N(R9, R10), -CH2-CH(halogen)-CN, -CH2-CH(halogen)-CO-(C1-C4-alkyl), optionally substituted -CH2-CH(halogen-COOH, -CH=C(halogen)-COOH or CH=C(C1-C4-alkyl)-COOH, optionally substituted -CH=N-OH or -CH(-Y-R15, -Z-R15), (II) or (III); R9, R10 = H, C1-C8-alkyl, C3-C8-cycloalkyl, C2-C8-alkenyl, C3-C8-alkinyl, C1-C8-halogen alkane, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, cyano-C1-C8-alkyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C1-C4-alkyl, (C3-C6-cycloalkoxy)carbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C3-C7-cycloalkyl, C1-C4-alkoxy-(C1-C4)alkoxy)-carbonyl-C1-C4-alkyl, C1-C6-alkoxy, optionally substituted phenyl or phenyl-C1-C4-alkyl or R9 + R10 together = optionally substituted tetramethylene, pentamethylene or ethylene oxyethylene chain; Y, Z = O, S; R15 = C1-C8-alkyl, C1-C8 halogen alkane, C1-C4-alkoxy-C1-C4-alkyl; R16-R21 = H, CN, C1-C8-alkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C8-alkoxy, C1-C4-alkoxy-C1-C4-alkoxy, COOH, (C1-C8-alkoxy)carbonyl, CONH2, (C1-C8-alkyl)aminocarbonyl, di(C1-C8-alkyl)aminocarbonyl; R6 = H, NO2, halogen, optionally substituted OH or COOH; R7 = H, NO2, halogen, optionally substituted OH; excluding those compounds in (I) in wherein X = CH2 and R5 = optionally substituted OH as well as R3, R7 = H or R1 = halogen as well as R3, R4, R6, R7 = H. The invention further relates to the use of said substances as herbicides and for dessication/defoliation of plants.

    SUBSTITUTED PYRAZOLE-3-YL BENZAZOLES

    公开(公告)号:CA2275611A1

    公开(公告)日:1998-06-25

    申请号:CA2275611

    申请日:1997-12-01

    Applicant: BASF AG

    Abstract: The invention concerns substituted pyrazole-3-yl benzazoles of formula (I) and salts thereof, in the formula R1 designating H, C1-C4 alkyl, C1-C4 alkyl halide; R2 designating CN, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, C1-C4-alkylsulphinyl, C1-C4-haloalkylsulphinyl, C1-C4-alkylsulphonyl, C1-C4-haloalkylsulphonyl; R3 = H, CN, NO2, halogen, C1-C4-alkyl, C1-C4-haloalkyl; R4 designating H, halogen; R5 designating H, CN, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1C4-haloalkoxy; Z designating -N=C(XR6)-O- or -N=C(XR6)-S-, bonded to .alpha. by the nitrogen, oxygen or sulphur; X designating a chemical bond, oxygen, sulphur, -S(O)-, -SO2-, -NH- or -N(R7); R6, R7 designating C1-C6-alkyl, C1-C6-haloalkyl, cyano-C1-C4-alkyl, hydroxy-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkinyl, cyano-C3-C6-alkinyl, C3-C6-haloalkinyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-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, C1-C4-haloalkylthio-C1-C4-alkyl, C3-C4-alkenylthio- C1-C4-alkyl, C3-C4-alkinylthio-C1-C4-alkyl, C1-C4-alkyl-sulphinyl-C1-C4-alkyl, C1-C4-haloalkylsulphinyl-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphonyl-C1-C4-alkyl, C1-C4-haloalkylsulphonyl-C1-C4-alkyl, C3-C4-alkenylsulphonyl-C1-C4-alkyl, C3-C4-alkinylsulphonyl-C1-C4-alkyl, hydroxycarbonyl-C1-C4-alkyl, C1-C4-alkoxycarbonyl-C1-C4-alkyl, which can carry a CN oder C1-C4-alkoxycarbonyl group, C1-C4-alkylthiocarbonyl-C1-C4-alkyl, aminocarbonyl-C1-C4-alkyl, C1-C4-alkylaminocarbonyl-C1-C4-alkyl, di(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, di(C1-C4-alkyl)-phosphonyl-C1-C4-alkyl, C1-C4-alkoxyimino-C1-C4-alkyl, C3-C4-alkenyloxyimino-C1-C4-alkyl, optionally substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, 3- to 7-member heterocyclic or heterocyclyl-C1-C4-alkyl, wherein each cycloalkyl ring and each heterocyclyl ring contain a CO or CS ring member; if X is a chemical bond, -O-, -S-, -NH- or -N(R7)-, R6 also being C1C4 alkylcarbonyl, C1-C4 haloalkylcarbonyl, C1-C4 alkoxycarbonyl, C1-C4 alkylsulphonyl or C1-C4 haloalkylsulphonyl; if X is a chemical bond, R6 additionally designating CN, SH, NH2, halogen, -CH2-CH(halogen)-R8, -CH=CH-R8 or -CH=C(halogen)-R8, R8 designating COOH, C1-C4 alkoxycarbonyl, C1-C4 alkylthiocarbonyl, CONH2, C1-C4 alkylaminocarbonyl, di(C1-C4 alkyl)aminocarbonyl or di(C1-C4 alkyl)phosphonyl; or R6 plus R7 designating an optionally substituted 1,3-propylene, tetramethylene, pentamethylene or ethylene oxyethylene chain. The invention alsoEncerns the use of these substances as herbicides and for the desiccation and/or defoliation of plants.

    SUBSTITUTED 3-PHENYL PYRAZOLES
    28.
    发明专利

    公开(公告)号:CA2261615A1

    公开(公告)日:1998-02-12

    申请号:CA2261615

    申请日:1997-07-21

    Applicant: BASF AG

    Abstract: Compounds having the formula (I) and their salts are useful as herbicides. In the formula {R1 = C1-C4-alkyl, halogenated C1-C4-alkyl, R2 = CN, C1-C4-alkyl, halogenated C1-C4-alkyl, C1-C4-alkoxy, halogenated C1-C4-alkoxy, C1-C4-alkylthio, halogenated C1-C4-alkylthio, C1-C4-alkylsulphinyl, halogenated C1C4-alkylsulphinyl, C1-C4-alkylsulphonyl, halogenated C1-C4-alkylsulphonyl; R3 = H, CN, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl; R4 = H, halogen; R5 = CN, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl, C1-C4-alkoxy, halogenated C1-C4-alkoxy; R6, R7 = C1-C6-alkyl, halogenated C1-C6-alkyl, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, halogenated C1-C4-alkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-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, halogenated C1C4-alkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkinylthio-C1-C4-alkyl, C1-C4-alkylsulphinil-C1-C4-alkyl, halogenated C1-C4-alkylsulphinyl-C1-C4-alkyl, C3-C4-alkenylsulphinyl-C1-C4-alkyl, C3-C4-alkinylsulphinyl-C1-C4-alkyl, C1-C4-alkylsulphonyl-C1-C4-alkyl, halogenated C1-C4-alkylsulphonyl-C1-C4-alkyl, C3-C4-alkenylsulphonyl-C1-C4-alkyl, C3-C4-alkinylsulphonyl-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, halogenated C3-C6-alkenyl, C3-C6-alkinyl, cyano-C3-C6-alkinyl, halogenated cyano-C3-C6-alkinyl, (C1-C4-alkyl)carbonyl, (halogenated C1-C4-alkyl)carbonyl, (C1-C4-alkoxy)carbonyl, H2NCO, (C1-C4-alkyl)NH-CO; (C1-C4-alkyl)2N-CO, (C1-C4-alkoxy- C1-C4-alkyl)carbonyl, C1-C4-alkyl-SO2-, halogenated C1-C4-alkyl-SO2-, (C1-C4-alkyl)carbonyl- C1-C4-alkyl, (halogenated C1-C4-alkyl)-carbonyl- C1-C4-alkyl, (C3-C8-cycloalkyl)carbonyl- C1-C4-alkyl, (C1-C4-alkoxy)imino- C1-C4-alkyl, (C3C4-alkenyloxy)imino- C1-C4-alkyl, hydroxycarbonyl- C1-C4-alkyl, optionally substituted (C1-C4-alkoxy)carbonyl- C1-C4-alkyl, (halogenated C1-C4-alkoxy)-carbonyl- C1-C4-alkyl, (C1-C4-alkylthio)carbonyl- C1-C4-alkyl, H2NCO- C1-C4-alkyl, (C1-C4-alkylamino)carbonyl- 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-membered heterocyclyl or heterocyclyl- C1-C4-alkyl, whereas all cycloalkyl or heterocyclyl rings may contain CO or Cs; X stands for a bond, -CC-, *-CH2-CH(R8)- or *-CH=C(R8)- (asterisk = bond with the phenyl ring; R8 = H, CN, NO2, halogen, C1-C4-alkyl, halogenated C1-C4-alkyl); and Y = O, S}

Patent Agency Ranking