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    Substituted 3-phenylisoxazolines
    3.
    发明授权
    Substituted 3-phenylisoxazolines 失效

    公开(公告)号：US6150303A

    公开(公告)日：2000-11-21

    申请号：US463246

    申请日：2000-01-21

    Applicant: Olaf Menke ,  Markus Menges ,  Gerhard Hamprecht ,  Robert Reinhard ,  Peter Schafer ,  Cyrill Zagar ,  Karl-Otto Westphalen ,  Ulf Misslitz ,  Helmut Walter

    Inventor： Olaf Menke ,  Markus Menges ,  Gerhard Hamprecht ,  Robert Reinhard ,  Peter Schafer ,  Cyrill Zagar ,  Karl-Otto Westphalen ,  Ulf Misslitz ,  Helmut Walter

    IPC: A01N43/80 ,  C07D261/04 ,  A01N43/72

    CPC classification number: C07D261/04

    Abstract: Substituted 3-phenylisoxazolines I, and their salts and enol ethers, are described as herbicides ##STR1## where X.dbd.--O--, --S--, --N(R.sup.9)--;R.sup.1 .dbd.CN, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylsulfonyl;R.sup.2 .dbd.H or unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkyl)carbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.2 -C.sub.6 -alkenyl, (C.sub.2 -C.sub.6 -alkenyl)carbonyl, C.sub.2 -C.sub.6 -alkynyl, (C.sub.2 -C.sub.6 -alkynyl)carbonyl;R.sup.3 .dbd.H, halogen;R.sup.4 .dbd.CN, halogen, C.sub.1 -C.sub.3 -haloalkyl;R.sup.5 .dbd.H, CN, halogen, C.sub.1 -C.sub.3 -haloalkyl;R.sup.6 .dbd.H, CN, halogen, C.sub.1 -C.sub.3 -haloalkyl or unsubstituted or substituted C.sub.1 -C.sub.6 -alkoxy;R.sup.7 .dbd.CN, halogen;R.sup.8 in position .alpha., R.sup.7 in this case being in position .beta., or in position .beta., R.sup.7 in this case being in position .alpha., is1) H, OH, SH, CN, NO.sub.2, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -haloalkylthio, C.sub.1 -C.sub.6 -alkylthio-(C.sub.1 -C.sub.6 -alkyl)carbonyl, (C.sub.1 -C.sub.6 -alkyl)iminooxycarbonyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxyamino-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkylamino-C.sub.1 -C.sub.6 -alkyl,2) unsubstituted or substituted C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.3 -C.sub.6 -cycloalkoxy, C.sub.3 -C.sub.6 -cycloalkylthio, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.2 -C.sub.6 -alkenylthio, C.sub.2 -C.sub.6 -alkynyloxy, C.sub.2 -C.sub.6 -alkynylthio, (C.sub.1 -C.sub.6 -alkyl)carbonyloxy, (C.sub.1 -C.sub.6 -alkyl)carbonylthio, (C.sub.1 -C.sub.6 -alkoxy)carboxyloxy, (C.sub.2 -C.sub.6 -alkenyl)carbonyloxy, (C.sub.2 -C.sub.6 -alkenyl)carbonylthio, (C.sub.2 -C.sub.6 -alkynyl)carbonyloxy, (C.sub.2 -C.sub.6 -alkynyl)carbonylthio, C.sub.1 -C.sub.6 -alkylsulfonyloxy or C.sub.1 -C.sub.6 -alkylsulfonyl,3) 29 further radicals;R.sup.9 .dbd.H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkoxy)carbonyl-C.sub.1 -C.sub.6 -alkyl, (C.sub.3 -C.sub.6 -alkenyloxy)carbonyl-C.sub.1 -C.sub.6 -alkyl, unsubstituted or substituted phenyl or phenyl-C.sub.1 -C.sub.6 -alkyl.

    Substituted herbicide tetrazolinonecarboxylic acid amides
    7.
    发明授权
    Substituted herbicide tetrazolinonecarboxylic acid amides 失效
    取代除草剂四唑啉酮羧酸酰胺

    公开(公告)号：US06277790B1

    公开(公告)日：2001-08-21

    申请号：US09463828

    申请日：2000-02-01

    Applicant: Cyrill Zagar ,  Gerhard Hamprecht ,  Markus Menges ,  Olaf Menke ,  Robert Reinhard ,  Peter Schäfer ,  Karl-Otto Westphalen ,  Martina Otten ,  Helmut Walter

    Inventor： Cyrill Zagar ,  Gerhard Hamprecht ,  Markus Menges ,  Olaf Menke ,  Robert Reinhard ,  Peter Schäfer ,  Karl-Otto Westphalen ,  Martina Otten ,  Helmut Walter

    IPC: A61N43713

    CPC classification number: C07D405/12 ,  A01N47/38 ,  C07D409/12

    Abstract: Tetrazolinonecarboxamides of formula I wherein Het is oxetan-3-yl, thietan-3-yl, tetrahydrofuran-3-yl, furan-3-yl, tetrahydrothiophen-3-yl, thiophen-3-yl, tetrahydro-2H-pyran-3-yl, tetrahydro-2H-thiopyran-3-yl, tetrahydro-2H-pyran-4-yl or tetrahydro-2H-thiopyran-4-yl, in each case with or without substitution; R1 is optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, phenyl, or 3- to 7-membered heterocyclyl; R2 is hydrogen, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, or is optionally substituted cycloalkyl, cycloalkylalkyl, phenyl, phenylalkyl, 3- to 7-membered heterocyclyl, or 3- to 7-membered heterocyclylalkyl, their preparation and herbicidal compositions comprising them.

    Abstract translation: 式I的四唑啉酮酰胺，其中Het是氧杂环丁烷-3-基，塞来赛汀-3-基，四氢呋喃-3-基，呋喃-3-基，四氢噻吩-3-基，噻吩-3-基，四氢-2H-吡喃-3-基 ，四氢-2H-噻喃-3-基，四氢-2H-吡喃-4-基或四氢-2H-噻喃-4-基，每种情况下具有或不具有取代; R 1是任选取代的烷基，烯基，炔基，环烷基 ，环烯基，苯基或3-至7-元杂环基; R 2是氢，烷基，卤代烷基，烯基，卤代烯基，炔基或任选取代的环烷基，环烷基烷基，苯基，苯基烷基，3-至7-元杂环基或3 至7元杂环基烷基，其制备和除草组合物包含它们。

    Substituted 2-phenylpyridines
    9.
    发明授权
    Substituted 2-phenylpyridines 失效
    取代的2-苯基吡啶

    公开(公告)号：US6100218A

    公开(公告)日：2000-08-08

    申请号：US117655

    申请日：1998-08-04

    Applicant: Cyrill Zagar ,  Peter Schafer ,  Gerhard Hamprecht ,  Elisabeth Heistracher ,  Markus Menges ,  Olaf Menke ,  Karl-Otto Westphalen ,  Ulf Misslitz ,  Helmut Walter

    Inventor： Cyrill Zagar ,  Peter Schafer ,  Gerhard Hamprecht ,  Elisabeth Heistracher ,  Markus Menges ,  Olaf Menke ,  Karl-Otto Westphalen ,  Ulf Misslitz ,  Helmut Walter

    IPC: A01N57/24 ,  C07F9/58 ,  C07F9/6558 ,  A01N57/08

    CPC classification number: A01N57/24 ,  C07F9/582 ,  C07F9/65583 ,  C07F9/65586

    Abstract: 2-Phenylpyridines I ##STR1## wherein X is a chemical bond, 1,2-ethynediyl or optionally substituted --(CH.sub.2).sub.1-3 --, --O--(CH.sub.2).sub.1-2 --, --s--(CH.sub.2).sub.1-2 --, --CH.sub.2 --O--CH.sub.2 --, --CH.sub.2 --S--CH.sub.2 -- or --CH.dbd.CH--;Y is oxygen or sulfur;Z.sup.1 is oxygen, sulfur or --N(R.sup.7)--;Z.sup.2 is oxygen, sulfur or --N(R.sup.8)--;R.sup.1, R.sup.2, R.sup.7 and R.sup.8 independently of one another are hydrogen, optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, phenyl or heterocyclyl; orR.sup.1 and R.sup.2 or R.sup.7, or R.sup.2 and R.sup.8 together are optionally substituted --(CH.sub.2).sub.2-5 -- or --(CH.sub.2).sub.2 --O--(CH.sub.2).sub.2 --, orR.sup.1 and R.sup.2 together are optionally substituted 1,2-phenylene;R.sup.3 is cyano, halogen, alkyl, haloalkyl, alkoxy or haloalkoxy;R.sup.4 and R.sup.5 are hydrogen or halogen;R.sup.6 is halogen or haloalkyl;n is zero or one;and their salts are suitable for controlling undesirable vegetation and as desiccants or defoliants.

    Abstract translation: PCT No.PCT / EP97 / 00735 Sec。 371日期：1998年8月4日 102（e）日期1998年8月4日PCT提交1997年2月17日PCT公布。 第WO97 / 30059号公报 日期：1992年8月21日 - 苯基吡啶I其中X为化学键，1,2-亚乙炔基或任选取代的 - （CH 2）1-3 - ， - O-（CH 2）1-2 - ， - 1-2-，-CH 2 -O-CH 2 - ， - CH 2 -S-CH 2 - 或-CH = CH-; Y是氧或硫; Z1是氧，硫或-N（R7） - ; Z2是氧，硫或-N（R8） - ; R 1，R 2，R 7和R 8彼此独立地是氢，任选取代的烷基，烯基，炔基，环烷基，苯基或杂环基; 或者R 1和R 2或R 7，或者R 2和R 8一起是任选取代的 - （CH 2）2-5 - 或 - （CH 2）2 -O-（CH 2）2 - ，或者R 1和R 2一起是任选取代的1,2- 亚苯基; R3是氰基，卤素，烷基，卤代烷基，烷氧基或卤代烷氧基; R4和R5是氢或卤素; R6是卤素或卤代烷基; n为零或一; 并且它们的盐适合于控制不期望的植物和干燥剂或脱叶剂。

    Substituted (4-brompyrazole-3-yl) benzazoles
    10.
    发明授权
    Substituted (4-brompyrazole-3-yl) benzazoles 失效

    公开(公告)号：US06482774B1

    公开(公告)日：2002-11-19

    申请号：US09673996

    申请日：2000-10-25

    Applicant: Cyrill Zagar ,  Gerhard Hamprecht ,  Markus Menges ,  Olaf Menke ,  Robert Reinhard ,  Peter Schäfer ,  Karl-Otto Westphalen ,  Martina Otten ,  Helmut Walter

    Inventor： Cyrill Zagar ,  Gerhard Hamprecht ,  Markus Menges ,  Olaf Menke ,  Robert Reinhard ,  Peter Schäfer ,  Karl-Otto Westphalen ,  Martina Otten ,  Helmut Walter

    IPC: C07D41704

    CPC classification number: C07D413/04 ,  A01N43/74 ,  C07D231/16 ,  C07D417/04 ,  C07D417/14 ,  C07F9/6541 ,  C07F9/65583

    Abstract: Substituted (4-bromopyrazol-3-yl)benzazoles I and their salts where R1=H, C1-C4-alkyl, C1-C4-haloalkyl; R2=CN, Cl-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, C1-C4-alkylsulfinyl, C1-C4-haloalkylsulfinyl, C1-C4-alkylsulfonyl, C1-C4-haloalkylsulfonyl; R4=H, halogen; R5=H, CN, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy; Z=—N═C(XR6)—O— or —N═C(XR6)—S—, attached to &agr; via the nitrogen, oxygen or sulfur; X=a chemical bond, oxygen, sulfur, —S(O)—, —SO2—, —NH— or —N(R7)—; R6, R7=Cl-C6-alkyl, Cl-C6-haloalkyl, cyano-Cl-C4-alkyl, hydroxy-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, cyano-C3-C6-alkynyl, C3-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkynyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-C1-C4-alkyl, amino-Cl-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di(C1-C4-alkyl)amino-C1-C4-alkyl, Cl-C4-alkylthio-C1-C4-alkyl, C1-C4-haloalkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkynylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-Cl-C4-alkyl, C1-C4-haloalkylsulfinyl-C1-C4-alkyl, C3-C4-alkenylsulfinyl-C1-C4-alkyl, C3-C4-alkynylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, C1-C4-haloalkylsulfonyl-C1-C4-alkyl, C3-C4-alkenylsulfonyl-C1-C4-alkyl, C3-C4-alkynylsulfonyl-C1-C4-alkyl, hydroxycarbonyl-C1-C4-alkyl, C1-C4-alkoxycarbonyl-C1-C4-alkyl, which may carry a CN or 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, unsubstituted or 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, where each cycloalkyl and each heterocyclyl ring may contain a CO or CS ring member; if X=a chemical bond, —O—, —S—, —NH— or —N(R7)—, R6 may also be C1-C4-alkylcarbonyl, C1-C4-haloalkylcarbonyl, C1-C4-alkoxycarbonyl, C1-C4-alkylsulfonyl or C1-C4-haloalkylsulfonyl; if X=a chemical bond, R6 may furthermore be CN, SH, NH2, halogen, —CH2—CH(halogen)-R8, —CH═CH—R8 or —CH═C(halogen)-R8, where R8=COOH, C1-C4-alkoxycarbonyl, C1-C4-alkylthiocarbonyl, CONH2, C1-C4-alkylaminocarbonyl, di(C1-C4-alkyl)aminocarbonyl or di(C1-C4-alkyl)phosphonyl; or R6+R7=an unsubstituted or substituted 1,3-propylene, tetramethylene, pentamethylene or ethyleneoxyethylene chain. Use: As herbicides; for the desiccation/defoliation of plants.

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