HRID1180835

反应详情

EQUATION

反应方程式

HRID 1180835 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of N-phenyl-N′-{4-[1-(2-propen-1-yl)-4-(1H-pyrrolo[2,3-b]pyridin-4-yl)-1H-pyrazol-3-yl]phenyl}urea (0.18 mmol) in 5:1 acetone:water (1.2 mL) was added N-methylmorpholine N-oxide (0.276 mmol) followed by a 2.5% solution of osmium tetroxide in t-butanol (93.5 mg). The reaction mixture was stirred at room temperature for 18 h. The reaction was quenched with saturated aqueous sodium sulfate (1 mL), filtered through a pad of celite (rinsing with ethyl acetate) and concentrated in vacuo. The residue was purified by Gilson reverse phase HPLC to afford the title compound as a white solid (14%). ESMS [M+H]+: 469.2

WORKUP

后处理

  1. customThe reaction was quenched with saturated aqueous sodium sulfate (1 mL)
  2. filtrationfiltered through a pad of celite (rinsing with ethyl acetate)
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by Gilson reverse phase HPLC