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Application of quinidine or quinidine derivatives, botanical insecticide, quinidine derivatives and preparation method thereof

A technology of plant-derived insecticides and derivatives, applied in the field of plant-derived pesticides, can solve the problems of less research on insecticidal activity and no reports of preventive effects

Active Publication Date: 2021-10-26
HENAN UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, at present, there are few studies on the insecticidal activity of quinidine alkaloids and their derivatives, and there is no report on the preventive effect of quinidine alkaloids on agricultural pests of Lepidoptera

Method used

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  • Application of quinidine or quinidine derivatives, botanical insecticide, quinidine derivatives and preparation method thereof
  • Application of quinidine or quinidine derivatives, botanical insecticide, quinidine derivatives and preparation method thereof
  • Application of quinidine or quinidine derivatives, botanical insecticide, quinidine derivatives and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1-21

[0047] Example 1-21 9S-acyloxyquinidine derivatives 3a-u

[0048] According to the corresponding substituent R in Table 1 in the general structural formula I, 9S-acyloxyquinidine derivatives 3a-u can be obtained.

[0049]

[0050] Table 1: 9S-acyloxyquinidine derivatives 3a-u corresponding substituents R

[0051]

[0052]

Embodiment 22

[0054] The preparation method of 9S-acyloxyquinidine derivatives in Example 1-21 is as follows:

[0055] Weigh quinidine 1 (0.5mmol), corresponding carboxylic acid 2a-u (0.6mmol), N,N'-dicyclohexylcarbodiimide DCC (0.6mmol) and 4-(N,N-dimethyl Amino)pyridine DMAP (0.1 mmol) was placed in a 50 mL flask, and 10 mL of dichloromethane (calcium hydride dried and ready for use) was added to the above reaction solution, and the esterification reaction was carried out at room temperature for 24-96 h.

[0056] During the esterification reaction, TLC tracked and detected until the reaction of the raw materials was complete. A large amount of urea in the reaction solution was removed by filtration, and the filtrate was diluted with dichloromethane (40 mL). The diluted solution was successively washed once with 0.1 mol / L hydrochloric acid (25 mL), saturated sodium bicarbonate (25 mL) and saturated brine (25 mL), and dried over anhydrous sodium sulfate. The solvent was removed under redu...

Embodiment 23

[0210] A botanical insecticide, prepared from compound 3a and acetone in Example 1, the concentration of compound 3a is 1mg / mL.

[0211] In other embodiments of the plant pesticide, the active ingredient includes any one of the compounds 3b-u in the embodiments 2-21.

[0212] In other embodiments of the plant pesticide, the active ingredient only needs to include quinidine.

[0213] It can be made into powders, sprays, etc. by referring to the application methods of existing botanical insecticides, and can also be compounded with other types of insecticides.

[0214] The botanical insecticides in the present invention have little impact on the natural environment, and can be used alternately with other types of insecticides to improve the insecticidal effect.

[0215] The application of quinidine and 9S-acyloxyquinidine derivatives in the prevention and control of Lepidoptera pests in the present invention is realized through the following test examples.

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Abstract

The invention relates to the application of quinidine or quinidine derivatives, botanical pesticides, quinidine derivatives and a preparation method thereof, belonging to the technical field of botanical pesticides. In the prior art, quinidine is mainly used to treat heart-related diseases. In the present invention, it is found that quinidine and 9S-acyloxyquinidine derivatives also have a good control effect on lepidopteran agricultural pests. Effective against armyworms. The 9S-acyloxyquinidine derivatives of the present invention are prepared by esterification of quinidine and R-COOH, which have significant insecticidal activity against Lepidoptera agricultural pests, and have significant insecticidal activity against Lepidoptera The control effect of armyworms is remarkable, and the control effect of some 9S-acyloxyquinidine derivatives on armyworms has surpassed the commercial botanical insecticide toosendanin, which can be used to prepare plant-derived Lepidoptera agricultural pest killers. Insecticide.

Description

technical field [0001] The invention relates to the application of quinidine or quinidine derivatives, botanical pesticides, quinidine derivatives and a preparation method thereof, and belongs to the technical field of botanical pesticides. Background technique [0002] Compared with organic synthetic pesticides, botanical pesticides have the advantages of high selectivity, low toxicity, easy degradation, and resistance to pests, which represent the direction and trend of modern pesticide development. Compared with traditional mass synthesis and random screening methods, this method has a shorter development period, lower investment, and higher probability of success (He Jun, Ma Zhiqing, Zhang Xing, Overview of Botanical Pesticides, Journal of Northwest A&F University, 2006 , 34(9):79-85). [0003] Studies have shown that the roots and stems of C.calisaya are toxic to melon silk borer (Diaphania hyalinata L.) and diamondback moth (Plutella xylostella L.); Function; the ste...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A01N43/90A01P7/04C07D453/04
CPCA01N43/90C07D453/04
Inventor 车志平田月娥孙迪杨进明刘圣明陈根强林晓民
Owner HENAN UNIV OF SCI & TECH