反应详情

Acetonitrile (240 ml), methanol (150 ml) and 28% sodium methoxide (15.24 g, 78.97 mmol) were added to ethyl 4-methyl-5-(4-nitrophenyl)-2-(3-phenylureido)thiophene-3-carboxylate (30.00 g, 70.51 mmol), and the mixture was stirred for 1 hour while refluxing under heating. 2,6-difluorobenzyl bromide (17.52 g, 84.61 mmol) was dissolved in acetonitrile (60 ml), and the solution was added to the previous reaction mixture under refluxing. After refluxing under heating for 5 hours, 28% sodium methoxide (1.36 g, 7.05 mmol) was added thereto under reflux, and the mixture was stirred for 1 hour. The reaction mixture was cooled to room temperature, water (150 ml) was added dropwise, which was stirred at room temperature for 1 hour. The crystals were filtered and washed with water (240 ml) and diisopropyl ether/ethanol=9/1 (240 ml). The resulting crystals were suspended in ethyl acetate (600 ml), and the suspension was stirred for 1 hour under reflux. The mixture was cooled to room temperature and, after stirred for 1 hour, the crystals were filtered, washed with ethyl acetate (60 ml) and dried under vacuum at 60° C. to give 1-(2,6-difluorobenzyl)-5-methyl-6-(4-nitrophenyl)-3-phenylthieno[2,3-d]pyrimidine-2,4(1H, 3H)-dione (31.4 g, 62.12 mmol, 88.1%).

1. temperaturewhile refluxing
2. temperatureunder heating
3. additionthe solution was added to the previous reaction mixture
4. temperatureunder refluxing
5. temperatureAfter refluxing
6. temperatureunder heating for 5 hours
7. temperatureunder reflux
8. stirringthe mixture was stirred for 1 hour
9. stirringwhich was stirred at room temperature for 1 hour
10. filtrationThe crystals were filtered
11. washwashed with water (240 ml) and diisopropyl ether/ethanol=9/1 (240 ml)
12. stirringthe suspension was stirred for 1 hour
13. temperatureunder reflux
14. temperatureThe mixture was cooled to room temperature
15. stirringafter stirred for 1 hour
16. filtrationthe crystals were filtered
17. washwashed with ethyl acetate (60 ml)
18. customdried under vacuum at 60° C.