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
CONDITIONS
反应条件
- 温度
- 25 °C
PROCEDURE
实验过程
To a stirred solution of 5.0 g (16.3 mmoles) of (4-methylthiophenyl)-3-(4-pyridyl)-6,7-dihydro-[5H]-pyrrolo[1,2-a]imidazole of Example 3 dissolved in 75 ml of chloroform, chilled in an ice bath, was added dropwise a solution of 3.30 g (16.3 mmoles) of 85% 3-chloroperbenzoic acid in chloroform. After stirring at 25° C. overnight, the reaction mixture was washed with 5% sodium carbonate, dried over anhydrous potassium carbonate, and stripped in vacuo. The residue was flash chromatographed on silica eluting with 5 to 10% methanol in methylene chloride: 2-propanol (9:1). The solvent was removed in vacuo and the residue recrystallized from ethyl acetate to give the desired titled compound, mp 163.5°-165.5° C. 1H NMR (360 MHz, CDCl3) δ 8.62 (2H,d), 7.68 (2H,d), 7.57 (2H,d), 7.25 (2H,d), 4.05 (2H,t), 3.02 (2H,t), 2.72 (s) superimposed upon 2.69 (m) (5H total). Mass Spec. ##STR25## (M+H) 324 (MW=323).
WORKUP
后处理
- temperaturechilled in an ice bath
- washthe reaction mixture was washed with 5% sodium carbonate
- dry with materialdried over anhydrous potassium carbonate
- customchromatographed on silica eluting with 5 to 10% methanol in methylene chloride: 2-propanol (9:1)
- customThe solvent was removed in vacuo
- customthe residue recrystallized from ethyl acetate