Benzimidazole derivative, preparation method thereof and application of benzimidazole derivative to tumor resistance
A technology of benzimidazoles and derivatives, which is applied in its preparation method and its application in anti-tumor. In the field of benzimidazole derivatives, it can solve the problems of limited application and limited types of topoisomerase inhibitors.
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[0063] The present invention also provides a kind of preparation method of benzimidazole derivatives, comprising the following steps:
[0064] performing a first condensation reaction on rhodanine or its derivatives with a first compound having a structure represented by formula (II), to obtain a benzimidazole derivative having a structure represented by formula (I);
[0065]
[0066] Among them, R 1 and R 2 Independently selected from one of hydrogen, halogen, alkyl, alkoxy, haloalkyl, nitro and nitrile; preferably independently selected from hydrogen, halogen, alkyl with 1 to 5 carbon atoms, carbon atoms One of an alkoxy group with a number of 1 to 5, a haloalkyl group with a carbon number of 1 to 5, a nitro group, and a nitrile group; more preferably independently selected from hydrogen, chlorine, fluorine, bromine, iodine, and methoxy One of , methyl, trifluoromethyl, nitro and nitrile;
[0067] R 3 is carboxyl, alkyl, phenyl or cyano; preferably carboxyl, alkyl wit...
Embodiment 1
[0112] Synthesis of compounds A2, b2, c2, d2, e2, f2, g2, h2, i2, j2, k2
[0113] The molar ratio of 1:1.5 o-phenylenediamine or its derivatives and glycolic acid was catalyzed by 4N hydrochloric acid, and reacted at 100°C for 6h. After the reaction, cool to room temperature, adjust the pH to 8 with sodium bicarbonate solution, precipitate a solid, filter it with suction, and dry it by infrared.
[0114]
Embodiment 2
[0116] Synthesis of Compounds A3~A22
[0117] Benzyl bromide with a molar ratio of 1:1 and compound A2 were dissolved in DMF, and a potassium carbonate solid with a molar ratio of benzyl bromide of 1:5 was reacted at room temperature for 8 h. After the reaction, extract with ethyl acetate and water, collect the organic phase, and purify with a silica gel column to obtain a white solid with a yield of 80-93%.
[0118]
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