HRID562469

反应详情

EQUATION

反应方程式

HRID 562469 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

100 mg (0.3 mmol) of the compound from Example 13A, 63 mg (0.4 mmol) of 4,4-difluoropiperidine hydrochloride and 116 μl (86 mg, 0.7 mmol) of N-ethyl-N-(propan-2-yl)propane-2-amine are initially charged in 2 ml of tetrahydrofuran and reacted in a single mode microwave (Emrys Optimizer) at 120° C. for 2.5 h. After concentration under reduced pressure, the residue is taken up in acetonitrile/water and purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient). Yield: 82 mg (71% of theory)

WORKUP

后处理

  1. customreacted in a single mode microwave (Emrys Optimizer) at 120° C. for 2.5 h
  2. concentrationAfter concentration under reduced pressure
  3. custompurified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient)