HRID869325
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A suspension of 3-(3-Amino-benzyl)-2-(2-amino-pyrimidin-4-yl)-1-methyl-4-oxo-1,4,6,7-tetrahydro-pyrrolo[3,2-c]pyridine-5-carboxylic acid tert-butyl ester (0.030 g, 0.066 mmol) in 4 N HCl in dioxane (2 ml) was stirred at room temperature for 1 h. The solvent was removed under vacuum, affording 3-(3-Amino-benzyl)-2-(2-amino-pyrimidin-4-yl)-1-methyl-1,5,6,7-tetrahydro-pyrrolo[3,2-c]pyridin-4-one hydrochloride (0.028 g, 0.062 mmol, 100%).
WORKUP
后处理
- customThe solvent was removed under vacuum