HRID1177452

反应详情

EQUATION

反应方程式

HRID 1177452 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A mixture of 2-(4-(1,3-dioxan-2-yl)-3,5-dimethylphenyl)-5-(1-phenyl-cyclopropyl)thiazolo[5,4-b]pyridine (96.0 mg, 217 μmol) and hydrochloric acid (5.0M, aq; 1.5 mL, 7500 μmol) in THF (3.0 mL) was heated at 60° C. in a sealed flask under argon. After 2 h, the reaction mixture was allowed to cool to 25° C. The resulting mixture was diluted with EtOAc (50 mL) and water (20 mL), neutralized with 5.0N NaOH (1.5 mL), and saturated aqueous sodium bicarbonate (10 mL) was added. The organic layer was then separated, sequentially washed with water (20 mL) and brine (15 mL), dried over sodium sulfate, filtered, and concentrated in vacuo to provide 2,6-dimethyl-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]-pyridine-2-yl)benzaldehyde as a yellow-orange solid. MS (ESI) m/z: Calculated: 384.1; Observed: 385.1 (M++1).

WORKUP

后处理

  1. temperatureto cool to 25° C
  2. additionwas added
  3. customThe organic layer was then separated
  4. washsequentially washed with water (20 mL) and brine (15 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo