反应详情

A mixture of 1-benzenesulfonyl-5-fluoro-2-[1-(4-methanesulfonyl-phenyl)-2-(tetrahydro-pyran-4-yl)-vinyl]-1H-pyrrolo[2,3-b]pyridine (405 mg, 0.75 mmol) and tetrabutylammonium fluoride in tetrahydrofuran (1 M, 15 mL, 15 mmol) was stirred for 12 h at room temperature. The mixture was poured into brine (15 mL), extracted with ethyl acetate (2×50 mL), washed with a saturated aqueous ammonium chloride solution (3×20 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 5-fluoro-2-[(E)-1-(4-methanesulfonyl-phenyl)-2-(tetrahydro-pyran-4-yl)-vinyl]-1H-pyrrolo[2,3-b]pyridine (300 mg, 100%) as a solid: LC/MS m/e calcd for C21H21FN2O3S [M+H]+ 401.48, observed 401.2; 1H NMR (400 MHz, CDCl3) δ ppm 10.24 (br. s., 1H), 7.98 (br. s., 1H), 7.76-7.95 (m, 3H), 7.40-7.56 (m, 2H), 6.54 (s, 1H), 6.17 (d, J=10.1 Hz, 1H), 3.93-4.03 (m, 2H), 3.33-3.48 (m, 2H), 2.95-3.09 (m, 3H), 2.79-2.90 (m, 1H), 1.64-1.83 (m, 4H).

1. extractionextracted with ethyl acetate (2×50 mL)
2. washwashed with a saturated aqueous ammonium chloride solution (3×20 mL)
3. dry with materialdried over anhydrous sodium sulfate
4. concentrationconcentrated in vacuo