HRID1375420
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
A mixture of 0.96 g (2.8 mmol) of 5-amino-2-[[4-[2-(diethylamino)-ethoxy]phenyl]amino]-4-(ethylamino)pyrimidine pyrimidine, 0.83 g (35 mmol) of ethyl 2-(3,5-dimethoxyphenyl)-2-oxoacetate (from Example 4(2)), and 1 mL of acetic acid in 25 mL EtOH is heated under reflux for 14 hours, and the solvent is removed under vacuum. The residue is then dissolved in water and washed with EtOAc. The aqueous layer is made basic with aqueous ammonia, and the crude product is extracted into fresh EtOAc. Chromatography on alumina, eluting with hexane/EtOAc (1:1), then gives 0.81 g (56%) of the title compound (Compound 14): mp (MeOH) 154–155° C.
WORKUP
后处理
- temperatureis heated
- temperatureunder reflux for 14 hours
- customthe solvent is removed under vacuum
- dissolutionThe residue is then dissolved in water
- washwashed with EtOAc
- extractionthe crude product is extracted into fresh EtOAc
- washChromatography on alumina, eluting with hexane/EtOAc (1:1)