反应详情

温度

60 °C

THF (40 ml) was added to methyl 3-[3-bromo-4-(indan-2-yloxy)-5-nitrophenyl]propionate (14.00 g, prepared according to the method of International Patent Publication No. WO 03/70686), 1-methyl-1H-indazol-5-boronic acid (7.62 g, prepared according to the method of International Patent Publication No. WO 03/70686), palladium acetate (75 mg, Wako Pure Chemical Industries, Ltd.) and triphenylphosphine (0.17 g, Wako Pure Chemical Industries, Ltd.), and the mixture solution was stirred. Then, a solution having tripotassium phosphate (16.97 g, Wako Pure Chemical Industries, Ltd.) dissolved in water (27 ml) was added to the above mixture, and the mixture solution was purged with nitrogen. Then, this mixture solution was stirred for 4 hours at 60° C. to react. After confirming the completion of the reaction, the reaction solution was partitioned to obtain the upper layer. The upper layer was cooled to room temperature, ethyl acetate (40 ml) and activated carbon (2.8 g, Japan Envirochemicals, Ltd.) were added thereto, and the mixture solution was further stirred for 1 hour at room temperature. The suspension was filtered to obtain a filtrate, and the residue was washed on the filter with ethyl acetate (20 ml) to obtain the wash solution. The filtrate and the wash solution were combined and concentrated under reduced pressure to obtain a concentrate (44 g). Then, acetone (140 ml) was added to the concentrate. The mixture solution was stirred and water (140 ml) was added thereto over 1 hour while stirring. The mixture solution was further stirred for another 1 hour at room temperature. Then, this mixture solution was filtered, the solids were washed on the filter with water (70 ml), and wet solids were obtained. These wet solids were dried under reduced pressure at 50° C. to obtain crystals of the title compound (15.7 g).

1. customprepared
2. additionwas added to the above mixture
3. customthe mixture solution was purged with nitrogen
4. customto react
5. customthe completion of the reaction
6. customthe reaction solution was partitioned
7. customto obtain the upper layer
8. temperatureThe upper layer was cooled to room temperature
9. stirringthe mixture solution was further stirred for 1 hour at room temperature
10. filtrationThe suspension was filtered
11. customto obtain a filtrate
12. washthe residue was washed on the
13. filtrationfilter with ethyl acetate (20 ml)
14. customto obtain the wash solution
15. concentrationconcentrated under reduced pressure
16. customto obtain
17. concentrationa concentrate (44 g)
18. additionThen, acetone (140 ml) was added to the concentrate
19. stirringThe mixture solution was stirred
20. additionwater (140 ml) was added
21. stirringover 1 hour while stirring
22. stirringThe mixture solution was further stirred for another 1 hour at room temperature
23. filtrationThen, this mixture solution was filtered
24. washthe solids were washed on the
25. filtrationfilter with water (70 ml)
26. customwet solids were obtained
27. customThese wet solids were dried under reduced pressure at 50° C.