反应详情

Ethyl [2-(7-methoxy-5-{[6-(methylsulfonyl)pyridin-3-yl]oxy}-1H-indol-2-yl)-4,5-dihydro-1,3-thiazol-5-yl]acetate (11.06 g) was dissolved in a mixture of tetrahydrofuran (100 mL) and ethanol (100 mL). To the mixture was added 1M aqueous sodium hydroxide solution (37 mL) and the mixture was stirred at room temperature for 1 h. The mixture was concentrated under reduced pressure. The residue was dissolved in water and 1M hydrochloric acid (37 mL) was added to the mixture. The resulting yellow suspension was filtered to collect a yellow solid. The solid was dissolved in ethyl acetate-tetrahydrofuran. The solution was dried over magnesium sulfate, filtered and concentrated. The residual solid was washed with diethyl ether to give the title compound (9.65 g, 93%) as a yellow solid. MS 462 (MH+).

1. concentrationThe mixture was concentrated under reduced pressure
2. dissolutionThe residue was dissolved in water
3. addition1M hydrochloric acid (37 mL) was added to the mixture
4. filtrationThe resulting yellow suspension was filtered
5. customto collect a yellow solid
6. dissolutionThe solid was dissolved in ethyl acetate-tetrahydrofuran
7. dry with materialThe solution was dried over magnesium sulfate
8. filtrationfiltered
9. concentrationconcentrated
10. washThe residual solid was washed with diethyl ether