Benzimidazole derivative containing alkoxy acetamide substituted pyridine
A technology of drugs and compounds, applied in the field of medicine, can solve the problems of reducing the surgical operation rate, large individual differences in pharmacokinetics, and insufficient drug efficacy
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Embodiment 1
[0100] The preparation of embodiment 1 2-mercapto-benzimidazole
[0101] Put 6.5g (60mmol) of phthalic diamine into the reaction flask, add 200ml of 95% ethanol solution, then add 12.8g (80mmol) of potassium ethoxysulfonate, and heat to reflux at 80°C for 4h. After the reaction was completed, cool to room temperature, pour the reaction solution into 200ml of ice water, stir evenly, adjust the pH to 3-4 with 4N hydrochloric acid, precipitate a solid, filter, wash with water until neutral, and vacuum-dry the filter cake to obtain 7.2g of the product. Rate: 79.7%.
Embodiment 2
[0102] Example 2 Preparation of 2-mercapto-5-methoxy-benzimidazole
[0103] Preparation method Referring to Example 1, 8.3 g (60 mmol) of 4-methoxy o-phenylenediamine and 12.8 g (80 mmol) of potassium ethoxysulfonate were cast. 8.2 g of the product was obtained, yield: 75.4%.
Embodiment 3
[0104] Example 3 Preparation of 2-mercapto-5-difluoromethoxy-benzimidazole
[0105] Preparation method Referring to Example 1, 10.4 g (60 mmol) of 4-difluoromethoxy o-phenylenediamine and 12.8 g (80 mmol) of potassium ethoxysulfonate were injected. 9.5 g of the product was obtained, yield: 73.5%.
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