HRID1951411
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
The title compound is prepared in analogy to example 10 from 50 mg (0.13 mmol) of 3-acetyl-2-methyl-4-(2-methyl-4-oxo-4H-chromen-8-yl)-4,6-dihydro-1,6-naphthyridin-5(1H)-one and 22 mg (0.15 mmol) of cyclopropanesulfonyl chloride. 54 mg (84% of theory) of the product are obtained as a pale yellow solid.
WORKUP
后处理
- custom54 mg (84% of theory) of the product are obtained as a pale yellow solid