HRID573957

反应详情

EQUATION

反应方程式

HRID 573957 的结构方程式

PROCEDURE

实验过程

To (Z)-1-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)-3-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenethyl)urea (F5) (0.40 g, 0.64 mmol) in acetone (30 mL) was added saturated aqueous sodium bicarbonate (3 mL). The reaction was heated to reflux for 12 hours, cooled, and concentrated. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was dried and concentrated. Purification by flash column chromatography using 100-40% A/B, where A=1:1 dichloromethane/hexanes and B=3:1 ethyl acetate/acetone, as eluent provided the title compound as a white solid (0.095 g, 19%).

WORKUP

后处理

  1. temperatureThe reaction was heated
  2. temperatureto reflux for 12 hours
  3. temperaturecooled
  4. concentrationconcentrated
  5. customThe reaction mixture was partitioned between ethyl acetate and water
  6. customThe organic layer was dried
  7. concentrationconcentrated
  8. customPurification by flash column chromatography