Реакция #1653
ord-560dc193ecc34b789acc357ab3f450a5
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1КонцентрированиеThe reaction was then concentrated to about 10 mL
- 2workup.ADDITIONdiluted with ethyl acetate (100 mL)
- 3Сушкаdried (MgSO4)
- 4Другоеthe solvents were removed in vacuo
- 5workup.DISSOLUTIONThe residue was dissolved in dioxane (40 mL)
- 6Температураthe solution was heated at 80° C. for 30 min under nitrogen
- 7ДругоеThe solvent was evaporated in vacuo
- 8Другоеthe residual oil was chromatographed on silica gel
Методика
To a solution of 2-acetamido-6-diphenylcarbamoyl-9-[2-(phenylselenyl)ethoxymethyl]purine (4.92 g, 8.16 mmol) in dioxane (80 mL) was added 30% H2O2 (4 mL, 35 mmol) and sodium bicarbonate (2.1 g, 24.5 mmol). The mixture was heated at 60° C. for 20 min. The reaction was then concentrated to about 10 mL, diluted with ethyl acetate (100 mL), dried (MgSO4) and the solvents were removed in vacuo. The residue was dissolved in dioxane (40 mL), diisopropylethylamine (1.27 g, 10 mmol) was added and the solution was heated at 80° C. for 30 min under nitrogen. The solvent was evaporated in vacuo and the residual oil was chromatographed on silica gel using CH2Cl2 -ethyl acetate (1:1) as eluent to give the title compound as a yellowish powder: yield 2.3 g (65%).