HRID1511316
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
A 50 mL RB flask was charged with 3-(azidomethyl)-6-phenyl-[1,2,4]triazolo[4,3-b][1,2,4]triazine (0.3492 g, 1.38 mmol) and THF (14.0 ml, 171 mmol), resulting in a dark brown solution. Triphenylphosphine (0.545 g, 2.08 mmol) and water (0.0998 ml, 5.54 mmol) were added, and the flask was placed in a 65° C. oil bath for 2 hours. The reaction mixture was concentrated to give a thick brown oil, which was purified by column chromatography using an 80 g ISCO column, eluting with a gradient of 5% MeOH (containing NH4OH)/DCM to 10% MeOH (containing NH4OH)/DCM over 40 minutes. (6-phenyl-[1,2,4]triazolo[4,3-b][1,2,4]triazin-3-yl)methanamine was isolated as a yellow solid.
WORKUP
后处理
- customresulting in a dark brown solution
- customwas placed in a 65° C.
- customfor 2 hours
- concentrationThe reaction mixture was concentrated
- customto give a thick brown oil, which
- customwas purified by column chromatography
- washeluting with a gradient of 5% MeOH (containing NH4OH)/DCM to 10% MeOH (containing NH4OH)/DCM over 40 minutes