FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to medicine and pharmacy, namely to synthesis of new compounds which may be used in creating therapeutic agents for treating cardiovascular and nervous diseases, more specifically to a method for preparing (S)-2,6-diaminohexane acid 3-methyl-1, 2, 4-triazolyl-5-thioacetate. Preparing an end product is two-staged: the first stage involves preparing an aqueous solution of L-lysine by dissolving L-lysine hydrochloride in water, flowing the solution through a chromatographic column and flowing water to remove L-lysine from an eluate completely, evaporating the eluate to ensure the residual L-lysine content in the concentration of 35-45%; the second stage involves adding the L-lysine with ethanol and 3-methyl-1,2,4-triazolyl-5-thioacetate, and a reaction mixture is boiled at 35-40 minutes while stirring, cooled at 3-5°C, adding activated carbon and boiled for another 20-30 minutes, filtered; 96% ethanol is added to the hot filtrate, cooled to 25-30°C, then to 0 -+5°C; the deposit is filtered, washed in ethanol and dried.
EFFECT: method enables preparing the end product biological activity of which considerably exceeds that of racemate; the end product yield is as high as possible, and the quality meets the Pharmacopoeia requirements.
2 cl, 1 ex
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Authors
Dates
2013-10-20—Published
2012-06-05—Filed