反应详情

温度

60 °C

A solution of ethyl 4-(1,4-diazepan-1-yl)benzoate (0.621 g, 2.5 mmol), (1-ethoxycyclopropoxy)trimethylsilane (2.51 mL, 12.50 mmol) and acetic acid (0.286 mL, 5.00 mmol) in tetrahydrofuran (50 mL), methanol (5 mL) was treated with sodium cyanoborohydride (0.393 g, 6.25 mmol) at 20° C. The resulting solution was stirred at 60° C. for 18 h. The reaction mixture was cooled, filtered and evaporated to dryness. 1N HCl (40 ml) and water (60 ml) were added and the solution extracted with ethyl acetate (3×50 ml). The aqueous layer was basified to pH 10 with solid potassium carbonate and extracted with ethyl acetate (4×50 ml). The organic extracts washed with saturated NaCl (50 ml) and dried over MgSO4, filtered and evaporated to dryness. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 4-(4-cyclopropyl-1,4-diazepan-1-yl)benzoate (0.849 g, 118%) as a colourless oil.

1. temperatureThe reaction mixture was cooled
2. filtrationfiltered
3. customevaporated to dryness
4. addition1N HCl (40 ml) and water (60 ml) were added
5. extractionthe solution extracted with ethyl acetate (3×50 ml)
6. extractionextracted with ethyl acetate (4×50 ml)
7. washThe organic extracts washed with saturated NaCl (50 ml)
8. dry with materialdried over MgSO4
9. filtrationfiltered
10. customevaporated to dryness
11. customThe crude product was purified by silica column chromatography
12. washeluting with a gradient of 0 to 5% MeOH in DCM
13. customPure fractions were evaporated to dryness