HRID1822849

反应详情

EQUATION

反应方程式

HRID 1822849 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of 4-chloro-6,7-dimethoxy-3-quinolinecarboxamide (0.046 g, 0.17 mmol), 2-aminobenzamide (0.029 g, 0.21 mmol) and acetic acid (40 μl) in DMF (0.8 ml) was heated at 100° C. for 6 h. After cooling the reaction mixture was evaporated. The residue was dissolved in a mixture of MeCN and water (1:3) containing 0.1% trifluoroacetic acid and the turbid solution was filtered through a plug of glass wool. Preparative HPLC using a gradient (containing 0.1% trifluoroacetic acid) of 10→40% MeCN in water as eluent gave, after evaporation, the title compound as the trifluoroacetic acid salt. The product was suspended in saturated aqueous NaHCO3 an absorbed on a short SPE column [ISOLUTE™ C18 (EC)] pre-conditioned subsequently with methanol and then water. The column was washed extensively with water until the pH of the eluent was neutral. The product was then eluted with methanol. After evaporation, the residue was crystallized from ethanol to give the title compound (26 mg, 41%).

WORKUP

后处理

  1. temperatureAfter cooling the reaction mixture
  2. customwas evaporated
  3. dissolutionThe residue was dissolved in a mixture of MeCN and water (1:3)
  4. additioncontaining 0.1% trifluoroacetic acid
  5. filtrationthe turbid solution was filtered through a plug of glass wool
  6. additiona gradient (containing 0.1% trifluoroacetic acid) of 10→40% MeCN in water as eluent
  7. customgave
  8. customafter evaporation
  9. customan absorbed on a short SPE column [ISOLUTE™ C18 (EC)] pre-conditioned subsequently with methanol
  10. washThe column was washed extensively with water until the pH of the eluent
  11. washThe product was then eluted with methanol
  12. customAfter evaporation
  13. customthe residue was crystallized from ethanol