反应详情

Under argon gas, 4-methoxy-5-methyl-2-methylthio-7H-pyrrolo[2,3-d]pyrimidine (4.18 g) was dissolved in anhydrous DME (120 ml). Then, with ice-cooling and stirring, 60% sodium hydride-oil (0.88 g) was added in 3 installments. After completion of addition, the mixture was stirred for 30 minutes, at the end of which time a solution of 4-(4-fluorobenzoyl)benzyl bromide (6.74 g) in anhydrous DME (20 ml) was added. Then, at room temperature, the mixture was stirred for 2 hours. The solvent was distilled off under reduced pressure and the residue was dissolved in ethyl acetate, washed with saturated aqueous NaCl solution, and dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure, whereupon colorless needles separated out. These crystals were collected by filtration, rinsed with ethyl acetate, and dried to provide the title compound (7.07 g). 1H-NMR (CDCl3) 5: 2.33(3H,d,J=1.2Hz), 2.61(3H,s), 4.09(3H,s), 5.37(2H,s), 6.58(1H,d,J=1.2Hz), 7.15(2H,t,J=8.6Hz), 7.29(2H,d,J=8.4Hz), 7.71(2H,d,J=8.4Hz), 7.82(2H,dd,J=5.4&8.8Hz).

1. temperatureThen, with ice-cooling
2. additionAfter completion of addition
3. additionwas added
4. stirringThen, at room temperature, the mixture was stirred for 2 hours
5. distillationThe solvent was distilled off under reduced pressure
6. dissolutionthe residue was dissolved in ethyl acetate
7. washwashed with saturated aqueous NaCl solution
8. dry with materialdried over anhydrous sodium sulfate
9. distillationThe solvent was then distilled off under reduced pressure, whereupon colorless needles
10. customseparated out
11. filtrationThese crystals were collected by filtration
12. washrinsed with ethyl acetate
13. customdried