HRID1644438

反应详情

EQUATION

反应方程式

HRID 1644438 的结构方程式

PROCEDURE

实验过程

1-[2-(4-Aminopiperidin-1-yl)ethyl]-7-methoxyquinoxalin-2(1H)-one (Intermediate 146, 60 mg crude, 0.20 mmol), 3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde (WO 2004/058144) (36 mg, 0.20 mmol), and sodium triacetoxy borohydride (130 mg, 0.60 mmol) were reacted as described according to Example 69 to give the free base of the product, which was crystallized from dichloromethane/ethyl acetate to give 45 mg (50%) as a colorless solid.

WORKUP

后处理

  1. customto give the free base of the product, which
  2. customwas crystallized from dichloromethane/ethyl acetate
  3. customto give 45 mg (50%) as a colorless solid