METHOD OF SYNTHESIS OF N-(4- MORPHOLINO- 6-PROPYL -1,3,5- TRIAZINE-2-YL)- ACETAMIDES OR -BENZAMIDES OR THEIR NONTOXIC PHARMACEUTICALLY ACCEPTABLE ACID SALTS

摘要

the essence of the u0438u0437u043eu0431u0440u0435u0442u0435u043du0438u00a0: product n - (4 - morpholino - 6 - propyl - 1,3,5 - u0442u0440u0438u0430u0437u0438u043d - 2 - yl) - acetamide or u0431u0435u043du0437u0430u043cu0438u0434 s - lu 1, where ri is the h, ci - Gj - u0430u043bu043au0438u043b; RZ - c1 - c4 - u0430u043bu043au0438u043b, u0444u0435u043du0438u043b, ben u0437u0438u043bu0440u0430u0434u0438u043au0430u043b. agent 1: 2 - amino - 4 - u043cu043eu0440u0444u043eu043bu0438 - but - 6 - propyl - 1,3,5 - u0442u0440u0438u0430u0437u0438u043d. agent 2: hal - COR2. u0443u0441u043bu043eu0432u0438u00a0 reaction: u044du043au0432u0438u043cu043eu043bu00a0u0440u043du043eu0435 ratio of reactants. u0441u043eu0435u0434u0438u043du0435u043du0438u00a0 provide stimulus to the holy u043du0435u0440u0433u0438u0447u0435u0441u043au0443u044e system. table 6.s la 1 0 - tfrb cr CHjCH - j (l c