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
6-Bromo-7-chloro-4H-pyrido[3,2-b][1,4]oxazin-3-one (22 g, 83.7 mmole) and trans-2-phenylvinylboronic acid (17.33 g, 117 mmole) were dissolved in 1,4-dioxane (300 mL) and the solution was degassed with argon. (Ph3P)4Pd (1.9 g, 2 mole %) was added, followed by a solution of potassium hydrogen carbonate (21 g, 210 mmole) in H2O (100 mL). The reaction was heated at reflux under argon overnight, then was cooled to room temperature and diluted with ethyl acetate (1 L). The solution was washed sequentially with H2O and brine, dried (Na2SO4), and concentrated in vacuo. The residue was slurried with chloroform (120 mL), then diluted with diethyl ether (100 mL). The precipitated product was collected by filtration and washed with ether to provide the product (16.4 g, 68%) as an off-white solid.
WORKUP
后处理
- customthe solution was degassed with argon
- addition(Ph3P)4Pd (1.9 g, 2 mole %) was added
- temperatureThe reaction was heated
- temperatureat reflux under argon overnight
- washThe solution was washed sequentially with H2O and brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
- additiondiluted with diethyl ether (100 mL)
- filtrationThe precipitated product was collected by filtration
- washwashed with ether