HRID1782712

反应详情

EQUATION

反应方程式

HRID 1782712 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of 2.67 g (7.66 mmol) of 4-(2-aminophenyl)-1,3-dihydro-1-[1-(phenylmethyl)-4-piperidinyl]-2H-imidazol-2-one in 50 ml of chloroform was mixed with 3.0 g of paraformaldehyde and refluxed for 3.5 hours. The residue remaining after evaporation of the solvent was taken up in 100 ml of methanol and acidified with methanolic hydrogen chloride solution. After stirring for one hour at room temperature the mixture was poured into 300 ml of saturated sodium hydrogen carbonate solution. The resulting mixture was extracted thoroughly with ethyl acetate, the combined extracts were dried over sodium sulphate and evaporated down in vacuo. The residue was purified by column chromatography over silica gel using FM4 as eluant. From the appropriate fractions 0.5 g (18.2% of theory) of a colourless, amorphous substance were isolated, Rf=0.24 (FM4).

WORKUP

后处理

  1. temperaturerefluxed for 3.5 hours
  2. customafter evaporation of the solvent
  3. additionwas poured into 300 ml of saturated sodium hydrogen carbonate solution
  4. extractionThe resulting mixture was extracted thoroughly with ethyl acetate
  5. dry with materialthe combined extracts were dried over sodium sulphate
  6. customevaporated down in vacuo
  7. customThe residue was purified by column chromatography over silica gel using FM4 as eluant
  8. customFrom the appropriate fractions 0.5 g (18.2% of theory) of a colourless, amorphous substance were isolated