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Application of 2-aryl substituted pyrrole compound in medicine for killing oncomelania hupensis

A compound and aryl technology, applied in the field of schistosomiasis control, can solve the problems of slow efficacy of molluscicide, environmental pollution, and less research on killing effect.

Active Publication Date: 2018-12-18
JIANGSU INST OF PARASITIC DISEASES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Plant molluscicides have the advantages of low toxicity and easy degradation, but they are mainly used to kill several aquatic snails distributed in Europe, Africa and the Americas, and their killing effect on amphibious snails in my country and other Asian regions There are few studies, and the efficacy of molluscicide plants is slow, the extraction cost of active ingredients of molluscicide plants is high, and fresh plant water extracts are easy to cause environmental pollution

Method used

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  • Application of 2-aryl substituted pyrrole compound in medicine for killing oncomelania hupensis
  • Application of 2-aryl substituted pyrrole compound in medicine for killing oncomelania hupensis
  • Application of 2-aryl substituted pyrrole compound in medicine for killing oncomelania hupensis

Examples

Experimental program
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Effect test

Embodiment 1

[0061] Synthesis of compound 5

[0062]

[0063] (1) Synthesis of Triisopropylpyrrole

[0064] Measure 200mLTHF into a 1000mL three-neck flask, cool down to 0°C, slowly add 12.0g (0.500mol) sodium hydride, stir for 10min, add 17.0g (0.253mol) pyrrole dropwise to the suspension, and stir at 0°C for 1.5h , then slowly dropwise added 13.7g (0.259mol) triisopropylchlorosilane, after the addition was completed, stirred for 2h, added ice water, extracted with ethyl acetate, the extract was dried over anhydrous sodium sulfate, suction filtered and concentrated to obtain 51.7 g oil.

[0065] (2) Synthesis of 3-formaldehyde-1H-pyrrole

[0066] Preparation of Vilsmeier reagent: Weigh 3.9 g (0.876 mol) of DMF in a three-neck flask, cool down to 0°C, then weigh 89.6 g (0.584 mol) of phosphorus oxychloride and slowly add it dropwise to DMF. Stir at ℃ for 1.5h.

[0067] Measure an appropriate amount of dichloromethane to completely dissolve the prepared Vilsmeier reagent, cool down t...

Embodiment 2

[0073] Synthesis of compound 7

[0074]

[0075] (1) Synthesis of 2-phenylaziridine:

[0076] Dissolve 10.4g (100mmol) of styrene in 80mL of carbon tetrachloride, dissolve 16g (200mmol) of liquid bromine in 60mL of carbon tetrachloride, keep the styrene solution at 15-20°C in an ice-water bath, and slowly dissolve the liquid bromine solution Add it dropwise to the styrene solution, stir for 2 hours, wash with water, dry, and rotary evaporate under reduced pressure to obtain a white solid (1).

[0077] Dissolve the white solid (1) in 140 mL DMSO, add 9.8 g (150 mmol) sodium azide under nitrogen protection, and stir overnight at room temperature. Then 4 mL of an aqueous solution containing 4 g of sodium hydroxide was added to the mixture, and stirring was continued for 24 h. The reaction product was poured into 400 mL of 2% (wt%) sodium bicarbonate solution, extracted with dichloromethane, the organic layer was repeatedly washed with water, dried and then rotary evaporated ...

Embodiment 3

[0082] Synthesis of Compound 12

[0083]

[0084] Firstly, α-p-chlorophenylglycine was N-formylated with a mixture of formic acid and acetic anhydride, converted to the corresponding N-formyl derivative, and further reacted with 2-chloroacrylonitrile in the presence of acetic anhydride for 1 ,3-dipolar addition reaction to generate the corresponding N-formyl derivatives; further 1,3-dipolar addition reaction with 2-chloroacrylonitrile in the presence of acetic anhydride to generate arylpyrrolenitrile 12 As the main product, the total yield of the two-step reaction is 73.6%, and the product is light yellow solid powder with a melting point of 161-162°C; 1 H NMRδ(in acetone-D 6 ):6.59(t, J=2.7Hz, 1H), 7.05(t, J=2.8Hz, 1H), 7.55(d, J=8.5Hz, 2H, Ar-H), 7.84(d, J=8.3Hz , 2H, Ar-H), 11.30 (bs, 1H, N-H).

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Abstract

The invention relates to an application of 2-aryl substituted pyrrole compound in a medicine for killing oncomelania hupensis and belongs to the technical field of prevention and treatment of bilharziasis, and particularly provides the chemical structure of the 2-aryl substituted pyrrole compound and a preparation method of same. The 2-aryl substituted pyrrole compound, being an active component,is used for preparing the snail killing agent in the forms of suspending agents, emulsions and micro-emulsions for killing the oncomelania hupensis. Immersion killing use amount of the 2-aryl substituted pyrrole compound being the active component of the snail killing agent is 0.1-10.00 mg / l, and immersion killing time is 24-72 h. The use amount of spray application is 1-10 g / m<2> and action timeis 3-7 days. Experiment proves that the 2-aryl substituted pyrrole compound has killing activity on the oncomelania hupensis and is lower than a snail killing agent, niclosamide, in the prior art in toxicity on aquatic organisms. The compound can be processed to prepare the snail killing agents and applied in the field of prevention and treatment of bilharziasis.

Description

technical field [0001] The invention relates to the application of a 2-aryl substituted pyrrole compound in the preparation of snail-killing drugs, and belongs to the technical field of schistosomiasis prevention and control. Background technique [0002] Schistosoma, also known as Schistosoma, belongs to the flatworm phylum, mainly referring to all 19 species of the same genus classified under the genus Schistosoma. Among them, there are 6 species that can parasitize humans. There are three main species, which are prevalent in the Middle East, Asia and South America. They have a wide distribution and are the main three types of schistosomiasis that can infect humans; , Mekong River Basin, because most of them are zoophilic strains, the impact on people is small. The growth process of schistosomiasis must go through the parasitic stage in freshwater snails before it can infect other hosts. After schistosomiasis parasitizes, it usually chooses to settle in the veins and bloo...

Claims

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Application Information

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IPC IPC(8): A01N43/36A01P9/00C07D207/33C07D207/36C07D207/34C07D409/04C07D207/333
CPCA01N43/36C07D207/33C07D207/333C07D207/34C07D207/36C07D409/04
Inventor 邢云天戴建荣
Owner JIANGSU INST OF PARASITIC DISEASES
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