3,4,5-SUBSTITUTED PYRAZOLES EHXIBITING ANTIFUNGAL ACTIVITY

摘要

the use of u0438u0437u043eu0431u0440u0435u0442u0435u043du0438u00a0: as u0430u043du0442u0438u0433u0440u0438u0431u043au043eu0432u044bu0445 tools in medicine. the essence of the u0438u0437u043eu0431u0440u0435u0442u0435u043du0438u00a0: product v 3,4,5 - replaced u0449u0435u043du043du044bu0435 u043fu0438u0440u0430u0437u043eu043bu044b sn (u0441u043du0437) u043cu043cu043du0441 (u0441u043du0437) CCH2CH2SR indicated compound, r, resource, exit,%, u0442.u043fu043b., & deg; c, or u0442.u043au0438u043f.: la, 4 f u0441u0431u043d4, Ci3Hi5FN2S, 69.69-70; 16, u0441u0437u043d , CioHi8N2S, 43, 180 - 183 & deg; c / 3 mm u0440u0442.u0441u0442; 1b, u04414u043d9, CnH2oN2S, 82, 196 200 & deg; c / 1 mm u0440u0442.u0441u0442., u0441u043eu0435u0434u0438u043du0435u043du0438u00a0 moderately toxic reagent i: 3,5 - dimethyl - (4 - (2 - bromoethane) pyrazole reagent 2. 4 - u0444u0442u043eu0440u0442u0438u043eu0444u0435u043du043eu043b. u0443u0441u043bu043eu0432u0438u00a0 u0440u0435u0430u043au0446u0438u0438u0438: environment u043fu0440u043eu043fu0438u043bu043eu0432u043eu0433u043e alcohol with 80 & deg;. table 1