HRID2193183

反应详情

EQUATION

反应方程式

HRID 2193183 的结构方程式

PROCEDURE

实验过程

0.29 g of tert-butyl(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(7-methoxy-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate was added to 10 mL of 4 mol/L hydrogen chloride/ethyl acetate solution, and stirred at room temperature for 22 hours. The solvent was removed under reduced pressure, 2-propanol was added to the residue obtained and the resulting solid was filtered to afford 0.20 g of 1-(2-(4-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxyquinolin-2(1H)one hydrochloride as a pale yellowish white solid.

WORKUP

后处理

  1. customThe solvent was removed under reduced pressure, 2-propanol
  2. additionwas added to the residue
  3. customobtained
  4. filtrationthe resulting solid was filtered