反应详情

A solution of sodium nitrite (0.25 g, 3.6 mmol) dissolved in water (4 ml) was added to 3-(3-hexyl-6-methyl-3-azabicyclo[3.1.0]hex-6-yl)phenylamine (Preparation 12, 0.43 g, 1.6 mmol) dissolved in aqueous hydrochloric acid (2.0 M, 4 ml) at 0° C. After 15 min at 0° C., the reaction mixture was added to potassium iodide (0.61 g, 3.69 mmol) in water (4 ml) at 0° C. with rapid stirring. The reaction mixture was stirred for 30 min at room temperature and was then heated to 90° C. for 5 min. The reaction mixture was cooled to room temperature and then poured cautiously onto solid sodium hydrogen carbonate with cooling. After 12 h, the reaction mixture was extracted with diethyl ether and then ethyl acetate and the combined organic extracts were washed with aqueous sodium thiosulphate solution, dried (MgSO4) and then concentrated in vacuo. The crude residue was purified by chromatography on silica gel eluting with hexane: ethyl acetate (10:1 and then 3:1) to give the title compound (0.18 g, 24%).

1. temperaturewas then heated to 90° C. for 5 min
2. temperatureThe reaction mixture was cooled to room temperature
3. temperaturewith cooling
4. waitAfter 12 h
5. extractionthe reaction mixture was extracted with diethyl ether
6. washethyl acetate and the combined organic extracts were washed with aqueous sodium thiosulphate solution
7. dry with materialdried (MgSO4)
8. concentrationconcentrated in vacuo
9. customThe crude residue was purified by chromatography on silica gel eluting with hexane: ethyl acetate (10:1