反应详情

温度

110 °C

Compound 73 (160 mg, 0.252 mmol) obtained in Example 73 was dissolved in chloroform (2.5 mL), and heat-stirred at 110° C. for 30 minutes with a microwave reactor after adding 3-(dimethylamino)propyl 4-nitrophenyl carbonate hydrochloride (115 mg, 0.379 mmol) synthesized according to the method described in Journal of American Chemical Society (J. Am. Chem. Soc.), 1981, Vol. 103, p. 4194-4199, and triethylamine (0.141 mL, 1.01 mmol). 3-(Dimethylamino)propyl 4-nitrophenyl carbonate hydrochloride (38.4 mg, 0.126 mmol) was added to the reaction mixture, and heat-stirred at 110° C. for 30 minutes with a microwave reactor. After being diluted with chloroform, the reaction mixture was washed with a 1 mol/L sodium hydroxide aqueous solution three times and then with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure after filtration. The resulting residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 95/5) to give compound 116 (42.6 mg, 22.1%).

1. customsynthesized
2. stirringheat-stirred at 110° C. for 30 minutes with a microwave reactor
3. washthe reaction mixture was washed with a 1 mol/L sodium hydroxide aqueous solution three times
4. dry with materialwith saturated brine, dried over anhydrous magnesium sulfate
5. concentrationconcentrated under reduced pressure
6. filtrationafter filtration
7. customThe resulting residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 95/5)