发明名称 Haloalky-substituted amides as insecticides and acaricides
摘要 The present invention relates to halogen-substituted amide derivatives of the general formula (I);in which R1 to R6, Q1 to Q8, A, V, W, X, Y, n and m are each defined as described in the description—and to a process for preparation thereof and to the use thereof as insecticides and acaricides.
申请公布号 US8889878(B2) 申请公布日期 2014.11.18
申请号 US201012913251 申请日期 2010.10.27
申请人 Bayer CropScience AG 发明人 Heil Markus;Heilmann Eike Kevin;Sudau Alexander;Kapferer Tobias;Mühlthau Friedrich August;Jeschke Peter;Voerste Arnd;Görgens Ulrich;Raming Klaus;Ebbinghaus-Kintscher Ulrich;Drewes Mark;Adamczewski Martin;Becker Angela
分类号 A01N43/40;C07D211/70;A01N43/653;C07D331/04;C07C281/02;C07C233/83;C07C237/20;A01N37/18;A01N37/30;C07C317/32;A01N43/38;C07C311/14;C07C237/22;C07D213/82;A01N43/16;C07C323/41;A01N43/58;C07D209/42;A01N43/56;C07C233/66;A01N43/12;C07D401/12;A01N43/08;C07C255/57;C07D405/12;C07C255/24;A01N43/10;A01N43/60;C07D249/08;A01N41/06;C07D409/12;C07D213/40;A01N43/02;C07C233/13;A01N43/54;A01N43/82;A01N43/50;C07D307/85;C07D213/56;C07C233/65;C07C233/74;C07D271/06;A01N37/34 主分类号 A01N43/40
代理机构 Sterne, Kessler, Goldstein & Fox P.L.L.C. 代理人 Sterne, Kessler, Goldstein & Fox P.L.L.C.
主权项 1. A compound of formula (I) or a diastereomer, enantiomer, E/Z isomer, or salt thereof where R1 is hydrogen, halogen, nitro, cyano, optionally monosubstituted or identically or differently polysubstituted C1-C4-alkyl, C2-C6-alkenyl, C2-C4-alkynyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-alkylsulphinyl, C1-C4-lkylsulphonyl, C3-C4-cycloalkyl, C1-C4-alkylcarbonyl, C1-C4-alkoxycarbonyl, C1-C4-alkylaminocarbonyl, C1-C4-dialkylaminocarbonyl or C1-C4-alkylaminosulphonyl, where the substituents are each independently halogen, cyano, nitro, hydroxyl, C1-C4-alkyl, C1-C4-alkoxy, C3-C4-cycloalkyl, C1- C4-haloalkoxy or C1-C4-alkylthio, n is 1, 2 or 3, R2 is hydrogen, cyano, hydroxyl, amino, optionally monosubstituted to identically or differently trisubstituted C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-alkoxy or C3-C6-cycloalkyl, where the substituents are each independently halogen, cyano, nitro, hydroxyl, amino, C1-C4-alkyl or C1-C4-alkoxy, R3 is hydrogen, optionally monosubstituted or identically or differently polysubstituted C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C3-C4-cycloalkyl, aryl-C1-C4-alkyl, C1-C4-alkylcarbonyl, C1-C4-alkylsulphonyl, arylcarbonyl, hetarylcarbonyl, C1-C4-alkoxycarbonyl or aryloxycarbonyl, where the substituents are each independently halogen, cyano, nitro, hydroxyl, C1-C6-alkyl, C1-C6-alkoxy, C3-C6-cycloalkyl, C1- C6-haloalkoxy, C1-C6-alkylthio, C1-C4-alkoxycarbonyl, aminocarbonyl, C1-C4-alkylaminocarbonyl or C1-C4-dialkylaminocarbonyl, V is R4,where R4 is hydrogen, halogen or optionally monosubstituted or identically or differently polysubstituted C1-C4-alkyl, where the substituents are each independently halogen, C1-C4-alkyl or C1-C4-alkoxy, R5 is hydrogen, halogen or optionally monosubstituted or identically or differently polysubstituted C1-C4-alkyl, where the substituents are each independently halogen or C1-C4-alkyl, R6 is hydrogen, halogen, nitro, cyano, amino, hydroxyl, optionally monosubstituted or identically or differently polysubstituted C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C3-C5-cycloalkyl, C1-C4-alkoxy, (C1-C4-alkoxy)carbonyl, C1-C4-alkylamino, formyl, (C1-C4-alkyl)carbonyl, C1-C4alkoxyimino-C1-C4-alkyl, C1-C4-dialkylamino, (C1-C4-alkylamino)carbonyl, (C1-C4-dialkylamino)carbonyl, C1-C4-alkylthio, C1-C4-alkylsulphinyl, C1-C4-alkylsulphonyl, C1-C4-alkylaminosulphonyl or C1-C4-alkylsulphonylamino, where the substituents are each independently halogen, cyano, nitro, hydroxyl, amino, C1-C6-alkyl, C1-C6-alkoxy, C3-C6-cycloalkyl, C1-C6-haloalkoxy or C1-C6-alkylthio, m is 0, 1, 2, or 3, X is unsubstituted C1-C4-haloalkyl, W is O, A-Y together are cyano or are optionally monosubstituted heterocyclyl or oxoheterocyclyl selected from the group consisting of pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, tetrazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, pyrrolidinyl, isoxazolidinyl, pyrazolidinyl, oxazolidinyl, thiazolidinyl, imidazolinyl, imidazolidinyl, 1,2,4-oxadiazolidinyl, 1,2,4-thiadiazolyl, 1,2,4-triazolidinyl, 1,3,4-oxadiazolidinyl, 1,3,4-thiadiazolidinyl, 1,3,4-triazolidinyl, pyrrolinyl, isoxazolinyl, 2,3-dihydropyrazolyl, 3,4-dihydropyrazolyl, 4,5-dihydropyrazolyl, 2,3-dihydrooxazolyl, 3,4-dihydrooxazolyl, piperidinyl, oxopyrrolidinyl, 3-oxo-1,2,4-triazolidinyl, 5-oxo-1,2,4-triazolidinyl, dioxopyrrolidinyl, oxomorpholinyl, oxopiperidinyl and oxopiperazinyl, where the substituents are halogen, nitro, cyano, amino, hydroxyl, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkoxy-C1-C6alkyl, C1-C6-alkylcarbonyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C1-C6-alkylthio, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, C1-C6-alkoxycarbonyl or C1-C6-alkylaminocarbonyl, or A is a bivalent chemical moiety which is —NR13C(═O)—, —C(R11)(R12)NR13C(═O)—, —C(═O)NR13—, —C(═O)N(R13)—O—, —C(═O)NR13CH2—, —C(═O)O—, —C(═O)NR13CH2C(═O)NR14—, —C(═O)NR14—, —C(R11)(R12)NR13—, —S(═O)2NR13—, or —C(R11)(R12)NR13S(═O)2—, where the first (left-hand) connection site in the bivalent chemical moieties in each case is connected to the ring at one of positions Q4 to Q8 and the second (right-hand) connection site in each case to Y, where R11 and R12 are each independently hydrogen, cyano or optionally monosubstituted to identically or differently trisubstituted C1-C4-alkyl or C3-C6-cycloalkyl, where the substituents are each independently selected from halogen, cyano, nitro, hydroxyl, C1-C6-alkyl or C1-C6-alkoxy, and where R13 and R14 are each independently hydrogen, optionally monosubstituted or identically or differently polysubstituted C1-C4-alkyl or C3-C6-cycloalkyl, C1-C4-alkylcarbonyl, C1-C4-alkoxycarbonyl or aryloxycarbonyl, where the substituents are each independently halogen, cyano, nitro, hydroxyl, C1-C4-alkyl or C1-C4-alkoxy, Y is hydrogen or optionally monosubstituted C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C3-C6-cycloalkenyl, is an optionally monosubstituted phenyl, or Y is an optionally monosubstituted heterocycle selected from the group consisting of thienyl, furanyl, pyrrolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4,-triazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, tetrazolyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, pyrrolidinyl, isoxazolidinyl, pyrazolidinyl, oxazolidinyl, thiazolidinyl, imidazolidinyl, 1,2,4-oxadiazolidinyl, 1,2,4-thiadiazolidinyl, 1,2,4-triazolidinyl, 1,3,4-oxadiazolidinyl, 1,3,4-thiadiazolidinyl, 1,3,4-triazolidinyl, pyrrolinyl, isoxazolinyl, 2,3-dihydropyrazolyl, 3,4-dihydropyrazolyl, 4,5-dihydropyrazolyl, 2,3-dihydrooxazolyl, 3,4-dihydrooxazolyl, piperidinyl, tetrahydrothienyl, piperazinyl, morpholinyl, thiomorpholinyl, dihydropyranyl, tetrahydropyranyl, tetrahydrothienyl, 1,4-dioxanyl, 1,3-dioxanyl, dioxolanyl, dioxolyl, tetrahydrofuranyl, dihydrofuranyl, oxetanyl, thietanyl, oxidothietanyl, dioxidothietanyl, oxiranyl, azetidinyl, oxazetidinyl, oxaziridinyl, oxazepanyl, oxazinanyl, azepanyl, 5 oxopyrrolidinyl, dioxopyrrolidinyl, oxomorpholinyl, oxopiperidinyl, oxopiperazinyl and oxotetrahydrofuranyl, where the substituents are halogen, nitro, cyano, hydroxyl, amino, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylcarbonyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl, C1-C6-alkylthio, C1-C6-alkylsulphinyl, C1-C6-alkylsulphonyl, or C1-C6-alkoxycarbonyl, Q1 to Q3 are each independently a carbon atom which is substituted by hydrogen or by R1 , Q4 is a carbon atom which is substituted by hydrogen or R6, and Q5 to Q8 are each independently a carbon atom which is substituted by hydrogen, R6 or A-Y, where exactly one of Q5, Q6, Q7, Q8 is substituted by A-Y.
地址 Monheim DE