HRID403550

反应详情

EQUATION

反应方程式

HRID 403550 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 3.5 g of 1,1-dimethylethyl 4-[6-(benzyloxy)-3-(3,4-dimethoxybenzyl)-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl]piperidine-1-carboxylate obtained in stage 1.5 and 25 ml of TFA in 50 ml of DCM is stirred at AT for 2 h 00. The mixture is neutralized with K2CO3. It is filtered and the filtrate is evaporated under reduced pressure. The residue is taken up in DCM and washed with a saturated NaHCO3 solution and then with an 8% NaOH solution. The solution is dried over Na2SO4 and filtered, and the solvent is evaporated under reduced pressure to give 2.67 g of the expected product.

WORKUP

后处理

  1. filtrationIt is filtered
  2. customthe filtrate is evaporated under reduced pressure
  3. washwashed with a saturated NaHCO3 solution
  4. dry with materialThe solution is dried over Na2SO4
  5. filtrationfiltered
  6. customthe solvent is evaporated under reduced pressure