反应详情

温度

-20 °C

N-(((3 S,4R,5 S)-3-(2-Fluorophenyl)-4-(hydroxymethyl)-5-(trifluoromethyl)tetrahydrofuran-3-yl)carbamothioyl)benzamide (31.1 g) was dissolved in pyridine (150 mL), and the mixture cooled to −20° C. Trifluoromethanesulfonic anhydride (14.0 mL) was added dropwise over 30 min and the reaction was allowed to warm to 0° C. After stirring for 2 h, the reaction was quenched by the addition of ammonium chloride (sat., aq., 400 mL) and extracted with EtOAc (3×500 mL). The combined organic extracts were dried over MgSO4, concentrated in vacuo and purified by silica gel column chromatography (2% to 30% EtOAc/hex) to obtain the title compound (18.50 g). 1H NMR (400 MHz, CDCl3) δ ppm 2.86 (dd, J=13.9, 3.5 Hz, 1 H), 3.25 (d, J=13.6 Hz, 1 H), 3.61 (br. s., 1 H), 4.00-4.10 (m, 1 H), 4.66 (d, J=8.8 Hz, 1 H), 4.78-4.87 (m, 1 H), 7.12-7.60 (m, 6 H), 7.68-7.73 (m, 1 H), 7.99-8.16 (br. s., 2 H), 8.62-8.66 (m, 1 H)

1. temperatureto warm to 0° C
2. customthe reaction was quenched by the addition of ammonium chloride (sat., aq., 400 mL)
3. extractionextracted with EtOAc (3×500 mL)
4. dry with materialThe combined organic extracts were dried over MgSO4
5. concentrationconcentrated in vacuo
6. custompurified by silica gel column chromatography (2% to 30% EtOAc/hex)