Реакция #10195
ord-61f22df1abf941a0bb796b93e209b430
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1Другое(reaction becomes dark red)
- 2ДругоеThe reaction was quenched with NaHSO3 and water (pH 2.5)
- 3Экстракцияthen extracted with ethyl acetate (4×30 mL)
- 4СушкаAfter drying (Na2SO4)
- 5Фильтрацияthe solution was filtered
- 6Концентрированиеconcentrated to a yellow oil which
- 7Другоеwas chromatographed on Silica gel
- 8Другоеto provide a yellow oil
- 9Другоеabove yielded 5 g, 67%)
Методика
1-(4-Amino-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone (500 mg, 1.85 mmol) was dissolved in H2O (5 mL) and concentrated H2SO4 solution (0.5 mL) then cooled to 0° C. and treated with a solution of sodium nitrite (NaNO2) (140 mg, 2.04 mmol) in H2O (2 mL) dropwise. Potassium iodide (460 mg, 2.78 mmol) in 1N H2SO4 solution (0.5 mL) was added over 10 minutes (reaction becomes dark red). The resulting solution was warmed to room temperature and stirred 18 hours. The reaction was quenched with NaHSO3 and water (pH 2.5) then extracted with ethyl acetate (4×30 mL). After drying (Na2SO4), the solution was filtered and concentrated to a yellow oil which was chromatographed on Silica gel to provide a yellow oil. (260 mg, 37%). (TLC 30% ethyl acetate/hexanes Rf 0.70). (A 5.4 g scale performed as above yielded 5 g, 67%).