反应详情

To 1.20 g of 5-fluoro-1,2,3,4-tetrahydroquinoxalin-2-one (EXAMPLE 24), 1.26 ml of diisopropylethylamine, and 15 ml of THF at 0° is added 6.0 ml of 1.2 M phosgene in toluene. The ice bath is removed and the reaction is stirred for 2 h, at which time an additional 0.2 ml of diisopropylethylamine and 1.0 ml of phosgene solution are added. After an hour, 1.26 ml of diisopropylethylamine and 0.60 ml of pyrrolidine are added and the reaction is stored in the freezer over the weekend. The reaction is then partitioned between ethyl acetate and aq. sodium bicarbonate and saline. The organic layers are dried over magnesium sulfate and concentrated and the crude product is chromatographed on silica gel (250 ml) using ethyl acetate/dichloromethane (30/70) to give 1.47 g of product. Recrystallization from ethyl acetate/ethyl ether/hexane gives product in two crops; mp 186.5°-187.5°; MS (m/z) at 263; IR (mineral oil) 1692, 1658, 1407, 1604, 1623 cm-1 ; NMR (CDCl3) 1.85, 3.28, 4.27, 6.68, 6.82, 7.04, 8.41 δ.

1. customThe ice bath is removed
2. additionare added
3. waitAfter an hour
4. addition1.26 ml of diisopropylethylamine and 0.60 ml of pyrrolidine are added
5. customThe reaction is then partitioned between ethyl acetate and aq. sodium bicarbonate and saline
6. dry with materialThe organic layers are dried over magnesium sulfate
7. concentrationconcentrated
8. customthe crude product is chromatographed on silica gel (250 ml)