Benzimidazole derivative and preparation method and application thereof
A technology of benzimidazoles and benzimidazoles, which is applied in the field of benzimidazole derivatives and their preparation, can solve the problems of lack of anti-drug addiction compounds and can only take medicines for life, etc., and achieves wide practicability and development value , reducing the relapse rate and suppressing the effects of morphine withdrawal symptoms
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Embodiment 1
[0037] Embodiment 1: A kind of benzimidazole derivative
[0038] The present invention specifically provides a benzimidazole derivative represented by general formula (I):
[0039]
[0040] Preferably, in general formula (I), R 1 =H.
[0041] Preferably, in general formula (I), R 2 =H or O.
[0042] Preferably, in the general formula (I), X═C or N or O or S.
[0043] Preferably, in the general formula (I), n=0 or 1.
[0044] Preferably, in general formula (I), R 1 It is any one of an alkyl substituent, a phenyl substituent, and a benzyl substituent.
[0045] Preferably, in general formula (I), R 2 Any of an alkyl substituent, a phenyl substituent, a benzyl substituent, and an acyl substituent.
Embodiment 2
[0046] Embodiment two: the preparation method of benzimidazole derivatives
[0047] Specifically adopt the following steps to prepare benzimidazole derivatives:
[0048]
Embodiment 3
[0049] Example 3: Preparation and structure identification of benzimidazole derivative TUP-01
[0050]Take a 30mL dried microwave tube, add 2-chlorobenzimidazole (0.457g, 3mmol), dissolve in 6mL of methanol, add tetrahydropyrrole (0.32mL, 3.9mmol), and react in microwave at 160°C for 2.5h. Spin to dry the solvent, add 200mL ethyl acetate to dissolve, wash with 200mL water and 200mL saturated brine respectively, and dry the organic phase with anhydrous sodium sulfate. The organic phase was spin-dried to obtain the benzimidazole derivative TUP-01, 0.274 g of white solid, with a yield of 41%. The structural formula of benzimidazole derivative TUP-01 is:
[0051]
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