反应详情

To a solution of the carboxamide (0.304 mmol) of step 1 above in dichloromethane (5 mL) in a 25 ml round bottom flask was added pyridine (0.304 mmol) and benzenesulfonyl chloride (0.304 mmol). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was then diluted with hydrochloric acid (2N) and extracted with dichloromethane (2×15 mL). The combined organic extracts were washed with a saturated aqueous solution of sodium bicarbonate (2×10 mL). The organic layers were then dried with magnesium sulfate, filtered, and concentrated under reduced pressure to yield a brown oil. The oil was further purified by silica gel chromatography using 5% ethyl acetate in bexanes as the mobile phase to yield ′3-[(phenylsulfonyl)amino]-N-(2,4,6-trimethyl-3-pyrrolidin-1-ylphenyl)thiophene-2-carboxamide as a white to yellow solid.

1. extractionextracted with dichloromethane (2×15 mL)
2. washThe combined organic extracts were washed with a saturated aqueous solution of sodium bicarbonate (2×10 mL)
3. dry with materialThe organic layers were then dried with magnesium sulfate
4. filtrationfiltered
5. concentrationconcentrated under reduced pressure
6. customto yield a brown oil
7. customThe oil was further purified by silica gel chromatography