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Benzimidazolone derivative or salt acceptable to agricultural pharmacology and application of benzimidazolone derivative or salt acceptable to agricultural pharmacology

A technology of benzimidazolone and its derivatives, which is applied in the field of benzimidazolone derivatives or pesticide acceptable salts, and can solve the problems of increasing the difficulty of pest control, serious drug resistance and exchange resistance, etc.

Active Publication Date: 2020-11-24
SOUTH CHINA AGRI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the long-term use of existing insecticides has caused more serious problems of drug resistance and exchange resistance, which has increased the difficulty of pest control

Method used

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  • Benzimidazolone derivative or salt acceptable to agricultural pharmacology and application of benzimidazolone derivative or salt acceptable to agricultural pharmacology
  • Benzimidazolone derivative or salt acceptable to agricultural pharmacology and application of benzimidazolone derivative or salt acceptable to agricultural pharmacology
  • Benzimidazolone derivative or salt acceptable to agricultural pharmacology and application of benzimidazolone derivative or salt acceptable to agricultural pharmacology

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0083] Embodiment 1: the preparation of compound I-10

[0084]

[0085] Add 1-methylbenzimidazole (0.40mmol) to the sealed tube, Na 2 S 2 o 4 (0.80mmol), selenium powder (0.80mmol), and dissolved with 2mL dichloroethane (DCE), then added ethyl bromofluoroacetate (1.00mmol), sealed the reaction tube and placed it in an oil bath at 80°C to stir the reaction 24h. After the reaction was monitored by TLC, the reaction mixture was cooled to room temperature, and the SO produced by the reaction was treated with NaOH aqueous solution. 2 , the reaction mixture was extracted with ethyl acetate, and the combined organic phases were washed with anhydrous Na 2 SO 4 After drying, the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (eluted with a mixed solvent of ethyl acetate and n-hexane) to obtain a white solid product with a yield of 62%.

[0086] Compounds I-22-I-56 were prepared by referring to the method of compound I-10.

Embodiment 2

[0087] Embodiment 2: the preparation of compound I-11

[0088]

[0089] Preparation method: under the protection of nitrogen, add 1-pyridyl-3-n-butyl-1H-benzo[d]imidazolium bromide (0.50mmol) to the solution containing Na 2 Se 2 (0.25mmol) in tetrahydrofuran solution (5mL), stirred at room temperature for 6-8h, then potassium tert-butoxide (0.50mmol) was added to the reaction solution, and stirred for 5-7h. After the reaction was monitored by TLC, the reaction mixture was cooled to room temperature, quenched by adding 3 mL of water, and extracted with ether, the organic phases were combined, and washed with anhydrous Na 2 SO 4 Dry and evaporate the solvent under reduced pressure on a rotary evaporator to obtain a yellow oily product, yield: 90%.

[0090] Compound I-12 was prepared by referring to the method of compound I-11.

Embodiment 3

[0091] Embodiment 3: the preparation of compound 1-13

[0092]

[0093] Put 1,3-dibutyl-1H-benzo[d]imidazolium bromide (0.50mmol) and selenium powder (2.50mmol) in a single-necked bottle, add 6mL of ether to dissolve, and put it at –78℃ for low temperature reaction Stir in the tank for 5min. NaHMDS (2.50 mmol) was dissolved in 4 mL of ether, and added dropwise to the reaction solution under ice-bath stirring. After stirring at -78°C for 30 min, the stirring reaction was continued at room temperature for 16 h. After the reaction was monitored by TLC, the reaction solution was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (eluted with a mixed solvent of dichloromethane and n-hexane) to obtain a yellow solid with a yield of 76%.

[0094] Compound I-14 was prepared according to the method of compound I-13.

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Abstract

The invention discloses a benzimidazolone derivative or a salt acceptable to agricultural pharmacology and application of the benzimidazolone derivative or the agricultural pharmacology acceptable salt. The structure of the benzimidazolone derivative is shown as a general formula (I), and the definition of each substituent group in the formula is shown in the specification. The compound shown in the general formula (I) shows insecticidal activity on pests in agriculture and forestry and other fields, and meanwhile, the compound shown in the general formula (I) is used as an insecticide, namely, the compound shown in the general formula (I) is used for preparing drugs for preventing and treating pests in agriculture and forestry or other fields. Particularly, the derivative has good insecticidal activity and an excellent antifeedant effect on Lepidoptera pests such as Plutella xylostella, Spodoptera frugiperda, Spodoptera exigua, Spodoptera litura and the like, and has a relatively goodpoisoning effect on Meloidogyne incognita, sanitary insect pest Blattella germanica and the like.

Description

technical field [0001] The invention belongs to the field of agricultural insecticides, in particular to a benzimidazolone derivative (including benzimidazolone, benzimidazole thione, benzimidazole selenone derivative) or a pesticide acceptable salt thereof use. Background technique [0002] Nitrogen-heterocyclic pesticides have the advantages of high insecticidal activity, broad spectrum, and low toxicity, and have become the dominant framework for the creation of new pesticides. In recent years, newly developed pesticides such as cyclopyrid, cyantraniliprole, sulfoxaflor, flupyfuranone, flunicamid, cyflumetate, cyantraniliprole, spirotetramat, Flupyrimin, etc. All are nitrogen heterocyclic derivatives, mainly derived from nitrogen heterocyclic rings such as pyrazole or pyridine. However, the long-term use of existing insecticides has resulted in relatively serious drug resistance and exchange resistance problems, which has increased the difficulty of pest control. In pa...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D235/24C07D401/04C07D235/28C07D471/04C07D473/34C07D405/06C07D235/26A01N43/52A01N43/90A01P5/00A01P7/04
CPCC07D235/24C07D401/04C07D235/28C07D471/04C07D473/34C07D405/06C07D235/26A01N43/52A01N43/90
Inventor 汤日元郭雪莹徐汉虹
Owner SOUTH CHINA AGRI UNIV
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