FIELD: analytical chemistry, more particularly synthesis of biologically active compounds. SUBSTANCE: method comprises reacting 2-thio-4-imino-6-oxopyrimidine or tautomeric form thereof or salt thereof with organic acid selected from HCOOH or CH3COOH at 40-150 C for 5-130 minutes at starting compound to organic acid molar ratio of 1:2.0-50. Method makes it possible to increase yield of the high quality product to 85%. EFFECT: more efficient preparation method. 6 ex, 1 tbl
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