Substituted 2-benz(o)ylpyridines, their preparation and their use as herbicides
    1.
    发明授权
    Substituted 2-benz(o)ylpyridines, their preparation and their use as herbicides 失效
    取代的2-苯并(o)吡啶,其制备及其作为除草剂的用途

    公开(公告)号:US06337305B1

    公开(公告)日:2002-01-08

    申请号:US09381033

    申请日:1999-09-15

    IPC分类号: C07D21330

    CPC分类号: C07D213/61 A01N43/40

    摘要: Substituted 2-benz(o)ylpyridines I and salts thereof where 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-haloalkyl, C1-C4-alkylthio, C1-C4-alkylsulfinyl, C1-C4-alkylsulfonyl; R2=H, halogen; R3=H, NO2, OH, halogen, C1-C4-alkoxy; R4=H, NO2, OH, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy; R5=H, NO2, CN, halogen, C1-C8-alkyl, C3-C8-alkenyl, C3-C8-alkynyl, C3-C8-cycloalkyl, C1-C8-haloalkyl, C2-C8-haloalkenyl, C2-C8-haloalkinyl, C1-C4-alkoxy-C1-C4-alkyl, C2-C4-alkenyloxy-C1-C4-alkyl, C2-C4-alkynyloxy-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-alkynyl, unsubstituted or 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, unsubstituted or substituted CHO, —O—CHO or —NH—CHO, —NH—CO—NH—R9, —O—CS—NH2, —O—CS—N(C1-C8-alkyl)2, —CO—N(R9,R10), —CS—N(R9,R10), —CO—NH—SO2—(C1-C4-alkyl).

    摘要翻译: 取代的2-苯并(o)吡啶I和其中n = 0,1; X = CO,CH 2,CH(C 1 -C 4 - 烷基),CH-OH,CH-CN,CH-卤素,C(卤素) CH-CONH 2,CH-CO-O(C 1 -C 4 - 烷基),CH-O(C 1 -C 4 - 烷基),C(CN)(C 1 -C 4 - 烷基); R 1 =卤素,C 1 -C 4卤代烷基, C 1 -C 4烷硫基,C 1 -C 4烷基亚磺酰基,C 1 -C 4烷基磺酰基; R 2 = H,卤素; R 3 = H,NO 2,OH,卤素,C 1 -C 4 - 烷氧基; R 4 = H,NO 2,OH,卤素, C 1 -C 4 - 烷基,C 1 -C 4 - 卤代烷基,C 1 -C 4 - 烷氧基; R 5 = H,NO 2,CN,卤素,C 1 -C 8烷基,C 3 -C 8 - 烯基,C 3 -C 8炔基,C 3 -C 8 - 环烷基,C 1 -C 8 - 卤代烷基,C 2 -C 8 - 卤代烯基,C 2 -C 8 - 卤代炔基,C 1 -C 4 - 烷氧基-C 1 -C 4烷基,C 2 -C 4 - 烯氧基-C 1 -C 4烷基,C 2 -C 4 - C 1 -C 4烷基,C 1 -C 4烷硫基-C 1 -C 4烷基,C 1 -C 4烷基亚磺酰基-C 1 -C 4烷基,C 1 -C 4烷基磺酰基-C 1 -C 4 - 烷基,氰基-C 1 -C 8烷基, 氰基-C 2 -C 8 - 烯基,氰基-C 3 -C 8 - 炔基,未取代或取代的OH,SH,SO-H,-SO 2 -H,COOH或NH-COOH,-SO 2 Cl,-N(R 9,R 10) NH-SO 2 - (C 1 -C 8 - 烷基),-N [-SO 2 - (C 1 -C 8 - 烷基)] 2,-N(C 1 -C 8 - 烷基) -SO 2 -N(R 9,R 10),-O-CO-NH-R 9,未取代的 取代的CHO,-O-CHO或-NH-CHO,-NH-CO-NH-R9,-O-CS-NH2,-O-CS-N(C1-

    Substituted 3-phenylpyrazoles
    3.
    发明授权
    Substituted 3-phenylpyrazoles 失效
    取代的3-苯基吡唑

    公开(公告)号:US06197973B1

    公开(公告)日:2001-03-06

    申请号:US09230838

    申请日:1999-02-01

    IPC分类号: C07D23114

    摘要: 3-phenylpyrazoles of formula I wherein R1 is cyano, alkyl or haloalkyl; R2 is cyano or is optionally halogenated alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R3 is hydrogen, cyano, halogen, alkyl or haloalkyl; R4 is hydrogen or halogen; R5 is cyano, halogen, or is optionally halogenated alkyl or alkoxy; R6, R7 independently of one another are optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl or phenyl, optionally substituted alkylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl or optionally halogenated alkylsulfonyl; X is a chemical bond, —C≡C—, —CH2—CH(R8)— or —CH═C(R8)—, wherein R8 is hydrogen, cyano, nitro, halogen, alkyl or haloalkyl; Y is oxygen or sulfur; their preparation and their use for controlling undesirable vegetation.

    摘要翻译: 式I的3-苯基吡唑,其中R1是氰基,烷基或卤代烷基; R2是氰基或任选被卤代烷基,烷氧基,烷硫基,烷基亚磺酰基或烷基磺酰基; R3是氢,氰基,卤素,烷基或卤代烷基; R4是氢或卤素; R5是 氰基,卤素或任选卤代烷基或烷氧基; R 6,R 7彼此独立地是任选取代的烷基,烯基,炔基,环烷基,杂环基或苯基,任选取代的烷基羰基,烷氧基羰基,氨基羰基,烷基氨基羰基,二烷基氨基羰基或任选卤代烷基磺酰基; X是化学键,-C = C-,-CH 2 -CH(R 8) - 或-CH = C(R 8) - ,其中R 8是氢,氰基,硝基,卤素,烷基或卤代烷基; Y是氧或硫 ;他们的准备和用于控制不良植被的用途。

    Substituted 2-phenyl-3(2H)-pyridazinones
    7.
    发明授权
    Substituted 2-phenyl-3(2H)-pyridazinones 失效
    取代的2-苯基-3(2H) - 哒嗪酮

    公开(公告)号:US06225313B1

    公开(公告)日:2001-05-01

    申请号:US09508781

    申请日:2000-03-16

    IPC分类号: C07D23718

    摘要: Substituted 2-phenyl-3(2H)-pyridazinones I and salts thereof, where n=0, 1, 2; R1=C1-C4-alkyl, C1-C4-haloalkyl; R2=H, halogen; R3=halogen, CN; R4=H, NO2, CN, CHO, NH—OH, C1-C4-alkyl, C1-C4-halogenalkyl, —OR5, —CH═N—OR6, —CH═C(R7)—CO—OR8, —CO—OR9, C1-C6-alkyl-SO2—NH, di(C1-C6-alkylsulfonyl)amino or R5=C1-C6-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, (C1-C6-alkoxy)carbonyl-C1-C4-alkyl, (C3-C6-alkenyloxy)carbonyl-C1-C4-alkyl, (C3-C6-alkynyloxy)carbonyl-C1-C4-alkyl, C1-C4-alkoxy(C1-C4-alkoxy)carbonyl-C1-C4-alkyl; R6=H, C1-C4-alkyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)carbonyl-C1-C4-alkyl; R7=H, halogen, C1-C4-alkyl; R8=H, C1-C6-alkyl; R9=H, C1-C6-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C4-alkoxy-C1-C4-alkoxy, hydroxycarbonyl-C1-C4-alkyl, (C1-C6-alkoxy)carbonyl-C1-C4-alkyl, (C3-C6-alkenyloxy)carbonyl-C1-C4-alkyl, (C3-C6-alkynyloxy)carbonyl-C1-C4-alkyl, C1-C4-alkoxy-(C1-C4-alkoxy)carbonyl-C1-C4-alkyl; R10=H, C1-C6-alkyl, COOH, (C1-C6-alkoxy)carbonyl; and their use as herbicides and for the desiccation/defoliation of plants are described.

    摘要翻译: 取代的2-苯基-3(2H) - 哒嗪酮I和其盐,其中n = 0,1,2; R1 = C1-C4-烷基,C1-C4卤代烷基; R2 = H,卤素; R3 =卤素,CN; R4 = H,NO2,CN,CHO,NH-OH,C1-C4-烷基,C1-C4-卤代烷基,-OR5,-CH = N-OR6,-CH = C(R7) CO-OR 8,-CO-OR 9,C 1 -C 6烷基-SO 2 -NH,二(C 1 -C 6烷基磺酰基)氨基或R 5 = C 1 -C 6烷基,C 3 -C 6 - 烯基,C 3 -C 6炔基,(C 1 C 3-6 - 烷氧基)羰基-C 1 -C 4烷基,(C 3 -C 6 - 烯氧基)羰基-C 1 -C 4 - 烷基,(C 3 -C 6 - 炔氧基)羰基-C 1 -C 4烷基,C 1 -C 4 - C 1 -C 4 - 烷氧基)羰基-C 1 -C 4 - 烷基; R 6 = H,C 1 -C 4 - 烷基,羟基羰基-C 1 -C 4 - 烷基,(C 1 -C 4 - 卤素,C 1 -C 4 - 烷基; R8 = H,C1-C6-烷基; R9 = H,C1-C6-烷基,C3-C6-烯基,C3-C6-炔基,C1-C4-烷氧基-C1-C4-烷氧基,羟基羰基C1-C4- 烷基,(C 1 -C 6 - 烷氧基)羰基-C 1 -C 4 - 烷基,(C 3 -C 6 - 烯氧基)羰基-C 1 -C 4烷基,(C 3 -C 6 - 炔氧基)羰基-C 1 -C 4烷基,C 1 -C 4 - 烷氧基 - (C 1 -C 4 - 烷氧基)羰基-C 1 -C 4烷基; R 10 = H,C 1 -C 6烷基,COOH,(C 1 -C 6 - 烷氧基)羰基;及其作为除草剂和干燥/ 的植物被描述。

    Benzylhydroxylamines and intermediates used to prepare them

    公开(公告)号:US6057269A

    公开(公告)日:2000-05-02

    申请号:US973780

    申请日:1998-01-05

    摘要: Benzylhydroxylamines I ##STR1## (X=--N(R.sup.7)--O--; Y=O, S; R.sup.1 =halogen, CN, NO.sub.2, CF.sub.3 ; R.sup.2 =H, halogen; R.sup.3 =H, NH.sub.2, CH.sub.3 ;R.sup.4 =H, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylsulfinyl or C.sub.1 -C.sub.6 -alkylsulfonyl;R.sup.5 =H, halogen, C.sub.1 -C.sub.6 -alkyl;R.sup.6 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.2 -C.sub.6 -alkenyl;R.sup.7 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.3 -C.sub.6 -alkenylcarbonyl, C.sub.3 -C.sub.6 -alkynylcarbonyl, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.2 -C.sub.8 -alkenyloxycarbonyl, C.sub.2 -C.sub.6 -alkynyloxycarbonyl, C.sub.1 -C.sub.6 -alkylthiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylcarbamoyl, it being possible for the 14 last-mentioned radicals to have attached to them 1-3 substituents:NO.sub.2, CN, halogen, C.sub.3 -C.sub.8 -cycloalkyl, OH, C.sub.1 -C.sub.6 -alkoxy, C.sub.3 -C.sub.8 -cycloalkoxy, C.sub.3 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylcarbonyloxy, C.sub.1 -C.sub.6 -alkylsulfinyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylideneaminoxy, C.sub.1 -C.sub.6 -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--Z.sup.1 R.sup.9, --OCO--Z.sup.1 R.sup.9, --N(R.sup.9)R.sup.10 orR.sup.7 =unsubstituted or substituted cycloalkylcarbonyl, phenylcarbonyl, phenylsulfonyl, phenylcarbamoyl;R.sup.8 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl or C.sub.3 -C.sub.6 -alkynyl, it being possible for each of the 5 last-mentioned radicals to have attached to it 1-3 substituents:NO.sub.2, CN, halogen, C.sub.3 -C.sub.8 -cycloalkyl, OH, C.sub.1 -C.sub.6 -alkoxy, C.sub.3 -C.sub.8 -cycloalkoxy, C.sub.3 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylsulfinyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -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--Z.sup.2 R.sup.11, --OCO--Z.sup.2 R.sup.11, --N(R.sup.11)R.sup.12 ;Z.sup.1 a chemical bond, oxygen, sulfur or --N(R.sup.10)--;Z.sup.2 =a chemical bond, oxygen, sulfur or --N(R.sup.12)--;R.sup.9, R.sup.11 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.8 -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, unsubstituted or substituted phenyl or phenyl-C.sub.1 -C.sub.6 -alkyl,orZ.sup.1 and R.sup.9 and/or Z.sup.2 and R.sup.11 together=a 3- to 7-membered heterocycle having 1-3 hetero atoms and bonded via nitrogen, it being possible for this heterocycle to be saturated, unsaturated or aromatic and, if desired, to have attached to it one to three substituents,R.sup.10, R.sup.12 =H, OH, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy)and the salts of I where R.sup.3, R.sup.7 and/or R.sup.8 =hydrogenare used as herbicides and for the desiccation/defoliation of plants.

    Substituted 3-phenylisoxazolines
    10.
    发明授权

    公开(公告)号:US6150303A

    公开(公告)日:2000-11-21

    申请号:US463246

    申请日:2000-01-21

    CPC分类号: C07D261/04

    摘要: 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.