反应详情

To a solution of (3-chloro-pyrazin-2-ylmethyl)-thiocarbamic acid S-methyl ester (3.05 g, 0.0140 mol) in MeCN (70 mL) were added DMF (4.3 mL, 0.056 mol) and POCl3 (5.2 mL, 0.056 mol) at 0° C. under nitrogen. The reaction mixture was slowly warmed to rt and stirred overnight. The solvent was evaporated under reduced pressure and the residue was cooled at 0° C. and diluted with EtOAc (250 mL), then quenched with sat. aq. NaHCO3 (100 mL). The mixture was washed with brine (50 mL), and dried over anhydrous sodium sulfate. The crude material was purified by silica gel chromatography (Hex:EtOAc=80:20→70:30) to give the title compound as a light-yellow solid; LC-MS (ES, Pos.): 200/202 (3/1) [MH+]; 1H NMR (CDCl3, 400 MHz) δ 2.71 (s, 3H), 7.40 (d, J=5.1 Hz, 1H), 7.74 (dd, J=5.1, 1.0 Hz, 1H), 7.90 (s, 1H).

1. customThe solvent was evaporated under reduced pressure
2. temperaturethe residue was cooled at 0° C.
3. additiondiluted with EtOAc (250 mL)
4. customquenched with sat. aq. NaHCO3 (100 mL)
5. washThe mixture was washed with brine (50 mL)
6. dry with materialdried over anhydrous sodium sulfate
7. customThe crude material was purified by silica gel chromatography (Hex:EtOAc=80:20→70:30)