反应详情

温度

50 °C

A solution of 1.15 mL (10.2 mmol) of 4-fluorobenzyl alcohol in 35 mL of dry DMF was treated with 0.48 g (12 mmol) of sodium hydride (60% oil dispersion), and the mixture was stirred at 50° C. for 30 minutes. A solution of 1.15 g (3.64 mmol) of (7R,8aS)-7-methanesulfonyloxy-2-(5-fluoropyrimidin-2-yl)-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazine (Preparation 7) in 35 mL of dry DMF was added and the solution stirred at 100° C. for 18 hours. The solution was cooled, diluted with water, and extracted with diethyl ether (2×). The combined organic phase was dried (magnesium sulfate), filtered and evaporated. Purification by flash silica gel chromatography with ethyl acetate gave 0.25 g (20%) of the title compound. Mp (.D-(−)-tartrate) 76-81° C. 13C NMR (base, CDCl3): δ 36.3, 43.6, 48.8, 51.3, 60.2, 61.9, 70.4, 76.6, 115.0, 115.3, 129.43, 129.53, 134.0, 144.9, 145.2, 149.9, 153.2, 158.9, 160.6, 163.9. HRMS calc'd for C18H20F2N4O (MH+): 347.1683, found: 347.1706.

1. stirringthe solution stirred at 100° C. for 18 hours
2. temperatureThe solution was cooled
3. extractionextracted with diethyl ether (2×)
4. dry with materialThe combined organic phase was dried (magnesium sulfate)
5. filtrationfiltered
6. customevaporated
7. customPurification by flash silica gel chromatography with ethyl acetate