FIELD: organic chemistry, chemical technology, medicine. SUBSTANCE: invention relates to substituted benzyloxy-carbonylguanidines of the general formula (I) where R(1), R(2) and R(3) mean independently each of other hydrogen atom, (C1-C8)-alkyl, F, Cl, Br, J, OR(25), R(31) SO1- where R(25) means pyridyl, quinolinyl, isoquinolinyl; "I" = 2, R(31) means -(C1-C8)-alkyl; R(1), R(2) and R(3) mean independently each of other +OR(67) or NR(67)R(68) where R(67) and R(68) mean independently each of other alkyl with 1, 2, 3 or 4 C-atoms; R(4) and R(5) mean independently each of other hydrogen atom, F, Cl; R(6) and R(7) mean independently each of other hydrogen atom; X means oxygen atom or NR(72) where R(72) means hydrogen atom or alkyl with 1, 2, 3 or 4 C-atoms. Invention describes a method of their synthesis. Compounds are effective inhibitors of sodium-proton antiport (Na+/H+-exchange) and useful as antiarrhythmic agents. EFFECT: improved method of synthesis, valuable medicinal properties. 6 cl, 1 tbl, 31 ex
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Authors
Dates
2002-08-27—Published
1996-05-15—Filed