反应详情

温度

70 °C

1-(2-hydroxyethyl)-5-(4-methylthiophen-2-yl)pyrazin-2(1H)-one (98.2 mg, 416 μmol), 4-chloro-7-methoxyquinoline (93.1 mg, 481 μmol), cesium carbonate (162 mg, 497 μmol), and palladium(II) acetate (23 mg, 102 μmol) were suspended in PhMe (2.8 mL) and racemic-2-(di-t-butylphosphino)-1,1′-binaphthyl (50 mg, 125 μmol) was added. The reaction was placed in a preheated oil bath (70° C.) and stirred under argon for 2.5 hours. The reaction was then cooled to room temperature and filtered through ˜0.5 inches of silica gel with 5:1 CH2Cl2/(2 N ammonia in MeOH). The filtrate was concentrated, and washed with Et2O and MeOH. The MeOH washings were combined with the solid, concentrated, and purified on HPLC (10%->95% MeCN/water with 0.1% TFA over 30 minutes) to afford the desired product (86.5 mg, 0.220 mmol, 53% yield). MS (ESI pos. ion) m/z (MH+): 394. Calc'd exact mass for C21H19N3O3S: 393. 1H NMR (400 MHz, CDCl3): 8.95 (d, J=7.0 Hz, 1H), 8.29 (s, 1H), 8.10 (d, J=9.0 Hz, 1H), 7.71 (d, J=3.0 Hz, 1H), 7.59 (s, 1H), 7.30 (dd, J=9 Hz, 3 Hz, 1H), 7.20 (s, 1H), 7.03 (d, J=7.0 Hz, 1H), 6.92 (s, 1H), 4.80 (t, J=5.0 Hz, 2H), 4.57 (t, J=5.0 Hz, 2H), 4.02 (s, H), 2.30 (s, 3H).

1. customThe reaction was placed in a preheated oil bath
2. temperatureThe reaction was then cooled to room temperature
3. filtrationfiltered through ˜0.5 inches of silica gel with 5:1 CH2Cl2/(2 N ammonia in MeOH)
4. concentrationThe filtrate was concentrated
5. washwashed with Et2O and MeOH
6. concentrationconcentrated
7. custompurified on HPLC (10%->95% MeCN/water with 0.1% TFA over 30 minutes)