HRID877523

反应详情

EQUATION

反应方程式

HRID 877523 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

5-[5-Fluoro-2-oxo-1,2-dihydro-indol-(3Z)-ylidenemethyl]-2, 4-dimethyl-1H-pyrrole-3-carboxylic acid (100 g) and dimethylformamide (500mL) were stirred and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (221 g), 1-(2-aminoethyl)pyrrolidine (45.6 g) and triethylamine (93 mL) were added. The mixture was stirred for 2 hours at ambient temperature. The solid product was collected by vacuum filtration and washed with ethanol. The solids were slurry-washed by stirring in ethanol (500 mL) for one hour at 64° C. and cooled to room temperature. The solids were collected by vacuum filtration, washed with ethanol, and dried under vacuum to give 5-[5-fluoro-2-oxo-1, 2-dihydro-indol-(3Z)-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-pyrrolidin-1-yl-ethyl)-amide (101.5 g, 77% yield).

WORKUP

后处理

  1. filtrationThe solid product was collected by vacuum filtration
  2. washwashed with ethanol
  3. washThe solids were slurry-washed
  4. stirringby stirring in ethanol (500 mL) for one hour at 64° C.
  5. temperaturecooled to room temperature
  6. filtrationThe solids were collected by vacuum filtration
  7. washwashed with ethanol
  8. customdried under vacuum