反应详情

To the solution of 4-chloro-6-[(2,6-difluorophenyl)amino]-2-(methylthio)-5-pyrimidinecarbonitrile (0.938 g) was added borane.THF complex (1.0 M, 15 mL). The reaction mixture was then heated at reflux for about 4 h until all the starting material disappeared. The solution was cooled to r.t., mixed with HCl solution (6 M, 5 mL), and stirred at room temperature for about 30 minutes. The solution was then mixed with NaOH solution (3 M) to pH 9.0-10.0. The organic phase was separated and the aqueous layer was extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine (50 mL), collected, dried over Na2SO4 and concentrated to afford the title compound 0.97 g (quantative). LC-MS m/z 317 (M+H)+, 1.5 min (ret. time).

1. temperatureThe reaction mixture was then heated
2. temperatureat reflux for about 4 h until all the starting material
3. customThe organic phase was separated
4. extractionthe aqueous layer was extracted with EtOAc (3×30 mL)
5. washThe combined organic layers were washed with brine (50 mL)
6. customcollected
7. dry with materialdried over Na2SO4
8. concentrationconcentrated