反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a stirred solution of 3-bromo-7-(2-fluorophenyl)pyrazolo[1,5-d][1,2,4]triazin-2-ol (0.2073 g, 0.671 mmol) in anhydrous DMF (10 ml) under nitrogen was added cesium carbonate (0.8731 g, 2.680 mmol), then solid 3-chloromethyl-2-methyl-2H-[1,2,4]triazole hydrochloride (0.1703 g, 1.014 mmol). The mixture was stirred at room temperature for 22.5 h, then at 60° C. for 2.33 h. This was then partitioned between water (40 ml) and ethyl acetate (40 ml). The aqueous layer was further extracted with ethyl acetate (2×40 ml), and the combined organic extracts were dried (Na2SO4) and evaporated in vacuo. The residue was purified by flash chromatography (silica gel, EtOAc) to give 0.2299 g (85%) of the title compound as a white solid: mp=215-219° C. (CH2Cl2-EtOAc-isohexane); 1H NMR (360 MHz, CDCl3) δ 3.87 (3H, s), 5.52 (2H, s), 7.28 (1H, m), 7.39 (1H, t, J=7.5 Hz), 7.65 (1H, m), 7.77 (1H, t, J=7.5 Hz), 7.87 (1H, s), 9.22 (1H, s); MS (ES+) m/e 404/406 [MH]+. Anal. Found C, 44.41; H, 2.53; N, 24.04%. C15H11BrFN7O requires C, 44.57; H, 2.74; N, 24.26%.
WORKUP
后处理
- waitat 60° C. for 2.33 h
- customThis was then partitioned between water (40 ml) and ethyl acetate (40 ml)
- extractionThe aqueous layer was further extracted with ethyl acetate (2×40 ml)
- dry with materialthe combined organic extracts were dried (Na2SO4)
- customevaporated in vacuo
- customThe residue was purified by flash chromatography (silica gel, EtOAc)