HRID2240606

反应详情

EQUATION

反应方程式

HRID 2240606 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

29 mg of 3-(2-oxo-1,2,5,6-tetrahydro-pyridin-3-yl)-propionic acid (g) was dissolved in 0.5 ml of DMF solution (0.171 mM). 30 mg of BnONH2—HCl (0.188 mM), 0.033 ml of diisopropyl methylamine (0.189 mM), 43 mg of EDC (0.224 mM) and 5 mg of DMAP (0.041 mM) were added thereto and the mixture was stirred for overnight at room temperature. The mixture was diluted with 7 ml of ethyl acetate and washed with 5% HCl (1 ml) and 1 ml of sat. NaHCO3 solution. The organic layer was dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting compound was purified by column chromatography on Silica gel with methanol/chloroform (1:20) solvent mixture as an eluant to give 126 mg of the title compound (h) (yield: 55%).

WORKUP

后处理

  1. washwashed with 5% HCl (1 ml) and 1 ml of sat. NaHCO3 solution
  2. dry with materialThe organic layer was dried over anhydrous MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe resulting compound was purified by column chromatography on Silica gel with methanol/chloroform (1:20) solvent mixture as an eluant