FIELD: organic chemistry, chemical technology, medicine, gastroeneterology, pharmacy. SUBSTANCE: invention relates to the improved method of synthesis of omeprazole that is the first medicinal agent of group of drugs used for control of gastric acid secretion. Invention describes method of synthesis of 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]sulfinyl-1H-benzimidazole (omeprazole) of the formula: . Method involves interaction of 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridyl)-methyl] thio] benzimidazole with 3-chloroperoxybenzoic acid and indicated interaction is carried out in ethyl acetate medium at temperature between -10 C and 5 C. Synthesized product is purified by its dissolving in methylamine aqueous solution, precipitated by addition of hydrochloric acid and compound is isolated in pure form. Invention provides the development of the improved method of synthesis of omeprazole of high purity degree. EFFECT: improved method of synthesis. 2 ex
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