HRID1644443

反应详情

EQUATION

反应方程式

HRID 1644443 的结构方程式

PROCEDURE

实验过程

1-[2-(4-Aminopiperidin-1-yl)ethyl]-6,7-difluoro quinoxalin-2(1H)-one (Intermediate 150, 190 mg, 0.62 mmol), 3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde (WO 2004/058144) (110 mg, 0.62 mmol), and sodium triacetoxy borohydride (390 mg, 1.90 mmol) were reacted as described according to Example 69 to give 180 mg (62%) of the free base of the product as a colorless solid.