反应详情

4-(2-Fluoro-4-nitrophenyl)dihydro-2H-1,2-thiazin-3(4H)-one 1,1-dioxide (2.43 g, 8.44 mmol) and sodium borohydride (3.83 g, 101.3 mmol) are placed under nitrogen and dry THF (70 ml) added. To the ice cooled suspension is added trifluoroacetic acid (7.8 ml, 101.3 mmol) over 5 min. After stirring for 16 hr additional trifluoroacetic acid (20.0 ml, 260 mmol) is added followed by methanol (20 ml). The solution is evaporated and the residue dissolved in ethyl acetate (150 ml) and washed with sodium bicarbonate solution (3×100 ml) and brine (50 ml). Evaporation gives a yellow gum which is chromatographed over silica gel (90 g) eluting with 1-3% methanol-chloroform. The title compound is obtained as a gum (1.99 g, 86%): Calcd for C10H11FN2O4S: C, 43.79; H, 4.04; N, 10.21. Found: C, 43.72; H, 4.07; N, 10.11.

1. additionis added
2. customThe solution is evaporated
3. dissolutionthe residue dissolved in ethyl acetate (150 ml)
4. washwashed with sodium bicarbonate solution (3×100 ml) and brine (50 ml)
5. customEvaporation
6. customgives a yellow gum which
7. customis chromatographed over silica gel (90 g)
8. washeluting with 1-3% methanol-chloroform