反应详情

A solution of 1.0 M aqueous HCl (2.76 mL) was added slowly to a solution of (2R)-4-[4-(4-fluorophenyl)-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide (257 mg, 0.55 mmol) in 2-propanol (15 mL) at room temperature. The reaction was allowed to stir at room temperature overnight. After 18 hours the reaction was concentrated to afford a brown solid. Crude material was triturated in ethyl acetate (50 mL) for 1 hour; the solid was collected via filtration and washed with hexanes (20 mL). The solid was allowed to dry on the filter under high vacuum to afford an off-white solid. Yield 153 mg, 73%. MS (APCI) m/z 383.6 (M+H), 1H NMR (400 MHz, DMSO-d6) δ ppm 1.55 (s, 3 H) 2.08-2.19 (m, 1 H) 2.34-2.44 (m, 1 H) 3.08 (s, 3 H) 3.64-3.80 (m, 1 H) 4.04-4.13 (m, 1 H) 6.62 (dd, J=7.02, 2.15 Hz, 1 H) 6.67 (d, J=1.95 Hz, 1 H) 7.20-7.41 (m, 2 H) 7.64-7.84 (m, 3 H) 11.12 (br. s., 1 H)

1. concentrationAfter 18 hours the reaction was concentrated
2. customto afford a brown solid
3. customCrude material was triturated in ethyl acetate (50 mL) for 1 hour
4. filtrationthe solid was collected via filtration
5. washwashed with hexanes (20 mL)
6. customto dry on the
7. filtrationfilter under high vacuum
8. customto afford an off-white solid