反应详情

温度

-78 °C

To a solution of 6-methoxypyridin-3-amine (61.4 mg, 0.494 mmol) in THF (5 mL) cooled to −78° C., lithium bis(trimethylsilyl)amide (1M in THF, 0.494 mL, 0.494 mmol) was added dropwise under nitrogen. After the reaction was stirred at −78° C. for 10 minutes, a solution of 4′-(cyclopropylmethyl)-N-methyl-2-(methylsulfinyl)-4,5′-bipyrimidin-2′-amine (5-1) (30 mg, 0.099 mmol) in THF (1 mL) was added to the reaction at −78° C. The reaction was slowly warmed up to rt, then the reaction was allowed to stir for 1 hour. The reaction was quenched with saturated ammonium chloride solution, then concentrated in vacuo. The reaction was taken up in acetonitrile, purified by reverse-phase HPLC [10-90% organic phase over 15 minutes], then further purified by Biotage™ silica gel chromatography [10 g SNAP column, 100% DCM to 7% MeOH/DCM] to afford the title compound as a white solid (19.49 mg, 46.0% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 0.04 (br. s., 2H) 0.34 (d, J=7.58 Hz, 2H) 1.01 (br. s., 1H) 2.77 (d, J=6.57 Hz, 2H) 2.86 (d, J=4.55 Hz, 3H) 3.74-3.86 (m, 3H) 6.78 (d, J=9.09 Hz, 1H) 6.97 (d, J=5.05 Hz, 1H) 7.36 (d, J=4.04 Hz, 1H) 7.99 (dd, J=8.59, 2.53 Hz, 1H) 8.35-8.50 (m, 3H) 9.46 (s, 1H). HRMS (ES+) for C19H21N7O.H+ [MH+]: calcd, 364.1886; found, 364.1891. UV-LC: 94.60/100% UV purity at 254/214 nm; tR=5.08 minutes over 7.75 minutes.

1. temperatureThe reaction was slowly warmed up to rt
2. stirringto stir for 1 hour
3. customThe reaction was quenched with saturated ammonium chloride solution
4. concentrationconcentrated in vacuo
5. custompurified by reverse-phase HPLC [10-90% organic phase over 15 minutes]
6. customfurther purified by Biotage™ silica gel chromatography [10 g SNAP column, 100% DCM to 7% MeOH/DCM]