HRID562915

反应详情

EQUATION

反应方程式

HRID 562915 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

In 7 ml of DMSO was dissolved 2.22 g of methyl 2-(3-cyano-4-fluorophenyl)isonicotinate, and 2.44 ml of hexamethyleneimine was added thereto, followed by heating at 50° C. for 5 hours. After cooling, the reaction solution was diluted with ethyl acetate and was washed with 1M hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution, and brine, successively. The organic layer was dried and then concentrated under reduced pressure and the resulting residue was dissolved in a mixed solvent of ethyl acetate and diisopropyl ether. Activated carbon was added thereto, followed by stirring for 1 hour. Then, the activated carbon was removed by filtration and washed with ethyl acetate. The resulting filtrate and washing liquid were combined and concentrated to obtain 2.58 g of methyl 2-(4-azepan-1-yl-3-cyanophenyl)isonicotinate. (2) Then, 2.49 g of the compound was dissolved in a mixed solvent of 15 ml of methanol and 30 ml of THF, and 11 ml of a 1M aqueous sodium hydroxide solution was added thereto, followed by heating at 80° C. for 1 hour.

WORKUP

后处理

  1. additionwas added
  2. temperatureAfter cooling
  3. washwas washed with 1M hydrochloric acid
  4. customThe organic layer was dried
  5. concentrationconcentrated under reduced pressure
  6. dissolutionthe resulting residue was dissolved in a mixed solvent of ethyl acetate and diisopropyl ether
  7. additionActivated carbon was added
  8. customThen, the activated carbon was removed by filtration
  9. washwashed with ethyl acetate
  10. washThe resulting filtrate and washing liquid
  11. concentrationconcentrated