反应 #2320156

反应方程式

pyrrolidine

2-fluoronicotinonitrile

tetrahydrofuran

triethylamine

→

title compound

收率 75.0%

2-pyrrolidin-1-yl-nicotinonitrile

收率 75.0%

溶剂

Water

反应条件

后处理

1. 1
   其他To an oven-dried, N2-purged
2. 2
   workup.ADDITION50-mL flask containing a magnetic stir bar
3. 3
   其他The flask was sealed with a septum
4. 4
   温度to warm to room temperature overnight
5. 5
   其他the mixture was transferred to a separatory funnel
6. 6
   萃取The mixture was extracted with dichloromethane (3×10 mL)
7. 7
   干燥The combined organic extracts were dried over magnesium sulfate
8. 8
   过滤filtered
9. 9
   浓缩concentrated by rotary evaporation to a brown oil
10. 10
    其他The product was recrystallized from ethyl acetate/hexanes

实验过程

To an oven-dried, N2-purged, 50-mL flask containing a magnetic stir bar were added 2-fluoronicotinonitrile (1.22 g, 10.0 mmol), anhydrous tetrahydrofuran (5 mL), and triethylamine (3.04 g, 4.19 mL, 30.0 mmol). The flask was sealed with a septum and cooled to 0° C. in an ice bath. Neat pyrrolidine (1.04 g, 1.24 mmol, 15.0 mmol) was added via syringe. The mixture was stirred at 0° C. for 30 minutes and then allowed to warm to room temperature overnight. Water (10 mL) was added and the mixture was transferred to a separatory funnel. The mixture was extracted with dichloromethane (3×10 mL). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated by rotary evaporation to a brown oil. The product was recrystallized from ethyl acetate/hexanes to give 1.29 g (75%) of the title compound as a tan powder. MS (ESI+) m/z 174.0 (M+H)+; 1H NMR (DMSO-d6) δ 1.91-1.95 (m, 4H), 3.63-3.68 (m, 4H), 6.68 (dd, J=7.6, 4.6 Hz, 1H), 7.91 (dd, J=7.6, 1.9 Hz, 1H), 8.31 (dd, J=4.7, 2.0 Hz, 1H).

来源