反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
To a flask containing (6-chloropyridin-3-yl)methanamine 33-2 (642 mg, 4.50 mmol), 2-fluoropyridin-4-ylboronic acid 38-1 (634 mg, 4.50 mmol), Pd(OAc)2 (51 mg, 0.23 mmol), S-Phos (186 mg, 0.45 mmol) and potassium phosphate (2.85 g, 13.50 mmol) under argon was added 2-butanol (5 mL). The mixture was stirred at 100° C. for 10 hours. After cooling to room temperature, the mixture was filtered through celite cake. The filtrate was diluted with ethyl acetate, washed with H2O and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 5% methanol containing ˜7N ammonia in dichloromethane to give (2′-fluoro-2,4′-bipyridin-5-yl)methanamine 38-2 as yellow solid. MS m/z 204.1 (M+1)
WORKUP
后处理
- temperatureAfter cooling to room temperature
- filtrationthe mixture was filtered through celite cake
- additionThe filtrate was diluted with ethyl acetate
- washwashed with H2O and brine
- dry with materialdried over Na2SO4
- concentrationconcentrated to dryness by rotary evaporation
- customThe crude product was purified by silica gel flash chromatography
- washeluted with 5% methanol containing ˜7N ammonia in dichloromethane