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
N-(4-(6-Chloropyrimidin-4-yloxy)phenyl)-N′-phenylurea (68.0 mg, 0.200 mmol) and 3,4,5-trimethoxyaniline (183 mg, 1.00 mmol) were heated and stirred in 1-methylpyrrolidone (1 ml) at 150° C. for 2 hours. The reaction solution was distributed between ethyl acetate and water, the organic layer was washed with saturated aqueous sodium bicarbonate, water and saturated saline and dried over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (eluent-ethyl acetate:hexane=3:1), the fraction containing the target substance was concentrated, converted to a hydrochloride with 1N hydrochloric acid and suspended in methanol, the suspension was diluted with ethyl acetate and the crystals were filtered out, washed with ethyl acetate and blow-dried to obtain the title compound (50.0 mg, 0.095 mmol, 48%) as light green crystals.
WORKUP
后处理
- washthe organic layer was washed with saturated aqueous sodium bicarbonate, water and saturated saline
- dry with materialdried over anhydrous magnesium sulfate
- filtrationthe drying agent was filtered off
- distillationthe filtrate was distilled off under reduced pressure
- customThe obtained crude product
- additionthe fraction containing the target substance
- concentrationwas concentrated
- additionthe suspension was diluted with ethyl acetate
- filtrationthe crystals were filtered out
- washwashed with ethyl acetate
- customblow-dried