HRID1371440

反应详情

EQUATION

反应方程式

HRID 1371440 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

4-Fluoro-N-methylaniline (0.007 ml) was added to a solution of Intermediate 10 (0.025 g) in anhydrous pyridine (1 ml). The mixture was heated at 110° C. in a thick walled glass vial (Reactivial) for 20 h. The mixture was evaporated to remove the pyridine, and partitioned between ethyl acetate (10 ml) and saturated aqueous sodium bicarbonate solution (10 ml). The organic layer was washed with further sodium bicarbonate (10 ml×5), brine (10 ml), dried (MgSO4), concentrated in vacuo. The residue was purified by chromatography on silica gel (Trikonex flash tube 2002, 2 g), eluting with 70% ethyl acetate in cyclohexane to give the title compound as a pale yellow gum 0.014 g. LCMS (system A) Rt 2.52 min, Mass Spectrum m/z 426 [MH+].

WORKUP

后处理

  1. customThe mixture was evaporated
  2. customto remove the pyridine
  3. custompartitioned between ethyl acetate (10 ml) and saturated aqueous sodium bicarbonate solution (10 ml)
  4. washThe organic layer was washed with further sodium bicarbonate (10 ml×5), brine (10 ml)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by chromatography on silica gel (Trikonex flash tube 2002, 2 g)
  8. washeluting with 70% ethyl acetate in cyclohexane