反应详情

To a solution of 2-(2-aminopyridin-3-yl)-5,6-dihydrothieno[2,3-c]pyridin-7(4H)-one (250 mg, 1.02 mmol) in DMF (3 ml) was added NBS (199 mg, 1.12 mmol). The reaction was stirred at room temperature for 1 h, then concentrated and taken up in DCM (10 mL). The organic solution was washed with a sat. aq. Na2S2O3, then dried over Na2SO4, and concentrated to give 2-(2-amino-5-bromopyridin-3-yl)-5,6-dihydrothieno[2,3-c]pyridin-7(4H)-one (320 mg, 97% yield) as an orange solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.06 (d, J=2.0 Hz, 1H), 7.73 (br. s., 1H), 7.66 (d, J=1.8 Hz, 1H), 7.29 (s, 1H), 6.23 (br. s., 2H), 3.40-3.50 (m, 2H), 2.83 (t, J=6.9 Hz, 2H); MS (EI) m/z=325.2 [M+1]+.

1. concentrationconcentrated
2. washThe organic solution was washed with a sat. aq. Na2S2O3
3. dry with materialdried over Na2SO4
4. concentrationconcentrated