反应 #41923
ord-20c47747d4944f5c96f2dc4f1765c73b
反应方程式
反应物
反应条件
后处理
- 1其他the tube was sealed
- 2温度After cooling
- 3过滤the mixture was filtered
- 4洗涤washed with methylene chloride (50 ml)
- 5洗涤The filtrate was washed with deionized water (3×50 ml)
- 6干燥with brine (50 ml), dried over magnesium sulfate
- 7浓缩then concentrated
- 8其他dried in vacuo
- 9其他Flash column chromatography (Silica gel, 0-100% methylene chloride in hexane) gave a solid which
- 10洗涤washed with diethyl ether
- 11过滤filtered
- 12其他dried in vacuo
实验过程
Ethyl 2-(4-hydroxy-6-iodo-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate (0.200 g, 0.46 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.048 g, 0.087 mmol), Copper cyamide (0.194 g, 2.2 mmol) and Tris(dibenzylideneacetone)dipalladium (0.020 g, 0.022 mmol) in 1,4-dioxane (2 ml) were combined in a 10 ml tube. Tetraethylammonium cyamide (0.085 g, 0.54 mmol) and 1,4-dioxane (1 ml) were added and the tube was sealed and heated to 145° C. for 15 min under Argon in a microwave (Personal Chemistry 300 W). After cooling, the mixture was filtered and washed with methylene chloride (50 ml). The filtrate was washed with deionized water (3×50 ml), then with brine (50 ml), dried over magnesium sulfate then concentrated and dried in vacuo. Flash column chromatography (Silica gel, 0-100% methylene chloride in hexane) gave a solid which washed with diethyl ether, filtered and dried in vacuo to give ethyl 2-(6-cyano-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetate (0.135 g, 90% yield).