反应详情

To a yellow solution of 5-bromo-2-chloro-N-cycloheptylpyrimidin-4-amine (18.1 g, 55.5 mmol) in THF (200 mL) were added propargyl alcohol (4.5 mL, 1.4 equiv) and a solution of tetrabutylammonium fluoride in THF (1M, 130 mL, 2.3 equiv) and the resulting brown mixture was treated with a stream of nitrogen for 15 min (bubble in the solution). The mixture was then treated with bis(triphenylphosphine)palladium(II) chloride (2.09 g, 0.054 equiv) and heated to reflux for 5 h. After cooling, the reaction mixture was filtered through a pad of celite (rinsed with EtOAc ˜350 mL). The filtrate was concentrated to remove THF, further diluted with EtOAc (total volume 250 mL), washed with sat. NaHCO3 (2×150 mL) and water (150 mL), dried over Na2SO4, filtered and concentrated. Titration of the residue in acetone and CH2Cl2 provided 3-(2-chloro-4-(cycloheptylamino)pyrimidin-5-yl)prop-2-yn-1-ol (8.65 g) in 56% yield. 1H NMR (400 MHz, CD3OD) δ 7.98 (s, 1H), 4.45 (s, 2H), 4.19 (septet, J=4.5 Hz, 1H), 1.95 (m, 2H), 1.77-1.52 (m, 10Hz); MS m/z 280.4 (M+H)+

1. custombubble in the solution)
2. temperatureheated
3. temperatureto reflux for 5 h
4. temperatureAfter cooling
5. filtrationthe reaction mixture was filtered through a pad of celite (rinsed with EtOAc ˜350 mL)
6. concentrationThe filtrate was concentrated
7. customto remove THF
8. additionfurther diluted with EtOAc (total volume 250 mL)
9. washwashed with sat. NaHCO3 (2×150 mL) and water (150 mL)
10. dry with materialdried over Na2SO4
11. filtrationfiltered
12. concentrationconcentrated