反应详情

5-Bromo-4-(2,2-dimethyl-propylamino)-pyrimidine-2-carbonitrile (7.58 mmol) and ethynyl-trimethyl-silane (22.74 mmol) in DMF (20 ml) are treated with triethylamine (38.0 mmol), copper (I) iodide (0.76 mmol), and dichlorobis(triphenylphosphine)palladium(II) (0.38 mmol) at room temperature. The mixture is stirred for 1.5 h at room temperature, poured into an ice water and extracted with AcOEt. The organic layer is washed with brine, dried over magnesium sulfate and concentrated. The crude product is dissolved in methanol (60 ml)—water (10 ml) and cesium fluoride (4.2 mmol) is added at room temperature and the mixture is stirred at room temperature for 5 min. The reaction mixture is evaporated, then water and CH2Cl2 are added. The organic layer is washed with brine, dried over magnesium sulfate and concentrated. The crude product is purified by silica gel column chromatography to give the product in 76% yield. Rf=0.67 (n-hexane:AcOEt=2:1)

1. extractionextracted with AcOEt
2. washThe organic layer is washed with brine
3. dry with materialdried over magnesium sulfate
4. concentrationconcentrated
5. additionis added at room temperature
6. stirringthe mixture is stirred at room temperature for 5 min
7. customThe reaction mixture is evaporated
8. additionwater and CH2Cl2 are added
9. washThe organic layer is washed with brine
10. dry with materialdried over magnesium sulfate
11. concentrationconcentrated
12. customThe crude product is purified by silica gel column chromatography
13. customto give the product in 76% yield