HRID491782
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
Trans-3-[4-(t-butoxycarbonylamino)cyclohexylcarbonylamino]-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide (10.70 g) obtained in Example 203 is dissolved in dioxane (150 ml), and thereto is added 4N hydrogen chloride in dioxane (150 ml). The mixture is stirred at room temperature for 12 hours, and concentrated under reduced pressure. The residue is crushed in diethyl ether, and collected by filtration to give the title compound (9.80 g).
WORKUP
后处理
- concentrationconcentrated under reduced pressure
- customThe residue is crushed in diethyl ether
- filtrationcollected by filtration