Bio-oil fractions composition derived from bio-oil
US-2024381867-A1 · Nov 21, 2024 · US
US10986840B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10986840-B2 |
| Application number | US-201916590006-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 1, 2019 |
| Priority date | Aug 7, 2015 |
| Publication date | Apr 27, 2021 |
| Grant date | Apr 27, 2021 |
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The invention relates to novel compounds of the formula (I) in welcher R 1 , R 2 , R 3 , A 1 , X and n have the meanings given above, to their use as acaricides and/or insecticides for controlling animal pests and to processes and intermediates for their preparation.
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The invention claimed is: 1. A compound of formula (I), wherein A 1 represents nitrogen, R 1 represents methyl, ethyl, n-propyl, isopropyl or cyclopropyl, R 2 represents a group selected from-NR 11 R 12 (G10), where R 11 is hydrogen and R 12 is hydrogen or oxetanyl or —NR 11 —C(═O)—R 8 (G12), where R 11 represents hydrogen and R 8 represents hydrogen, methyl, ethyl, isopropyl, tert-butyl, trifluoromethyl, difluoromethyl, tetrafluoroethyl, pentafluoroethyl, cyclopropyl, cyclopropylmethyl, methylsulphanylmethyl methylsulphonylpropan-2-yl or 1-(methylsulphanyl)propan-2-yl or —C(═O)—NR 11 R 12 (G3), where R 11 represents hydrogen and R 12 represents methyl, ethyl, isopropyl, cyclopropyl or tert-butyl, R 3 represents hydrogen, X represents a heteroaromatic 9-membered or 12-membered fused bicyclic or tricyclic ring system selected from the group consisting of H1, H2, H5, H15, H16, H17 and H19, R 5 represents fluorine, chlorine, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, tetrafluoroethyl, pentafluoroethyl, trifluoromethoxy, difluorochloromethoxy, dichlorofluoromethoxy, trifluoromethylthio, trifluoromethylsulphonyl or trifluoromethylsulphinyl, R 6 represents hydrogen, R 7 represents methyl, ethyl, isopropyl, methoxymethyl or methoxyethyl, n represents 0, 1 or 2, where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5. 2. The compound of formula (I) according to claim 1 wherein A 1 represents nitrogen, R 1 represents ethyl, R 2 represents a group selected from G10, where R 11 represents hydrogen and R 12 represents hydrogen or oxetanyl, G12, where R 11 represents hydrogen and R 8 represents methyl, trifluoromethyl, cyclopropyl,—CH 2 SCH 3 ,—CH(CH 3 )CH 2 SCH 3 or —CH(CH 3 )CH 2 SO 2 CH 3 , and G3, where R 11 represents hydrogen and R 12 represents methyl, R 3 represents hydrogen, X represents a heteroaromatic 9-membered or 12-membered fused bicyclic or tricyclic ring system selected from the group consisting of H1, H2, H5, H15, H16, H17 and H19, R 5 represents trifluoromethyl R 6 represents hydrogen, R 7 represents methyl, n represents 0, 1 or 2, where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5. 3. The compound of formula (I) according to claim 1 wherein A 1 , R 1 , R 3 , R 5 , R 6 , R 7 , X and n have the meanings given above and R 2 represents a radical from the following series: where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5. 4. The compound of formula (I) according to claim 1 wherein A 1 , R 1 , R 2 , R 3 , R 5 , R 6 , R 7 and n have the meanings given above and X represents a radical from the following series: where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5. 5. An agrochemical formulation comprising the compound of formula (I) according to claim 1 and one or more extenders and/or surfactants. 6. The agrochemical formulation according to claim 5 , additionally comprising a further agrochemically active compound. 7. A method for controlling one or more animal pests, comprising allowing the compound of formula (I) according to claim 1 or an agrochemical formulation thereof to act on the animal pests and/or a habitat thereof. 8. The compound of formula (I) according to claim 1 , where the substituents R 1 , R 2 , R 3 , A 1 , X and n have the meanings given in the table below and where the bond from X and R 2 to the remainder of the molecule is characterized by a wavy line: Ex. R 1 n A 1 R 3 X R 2 Ex. I-7 —CH 2 CH 3 2 N H Ex. I-8 —CH 2 CH 3 2 N H Ex. I-31 —CH 2 CH 3 2 N H Ex. I-32 —CH 2 CH 3 2 N H Bsp-I-34 —CH 2 CH 3 2 N H
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