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
5-(Benzoxazol-2-yl)-2-fluoronitrobenzene (see Working Example 15-2) (0.55 g, 2.13 mmol), triethylamine (0.26 g, 2.57 mmol), and aminotetrahydropyran (0.24 g, 2.34 mmol) were added to ethanol (10 mL), and this reaction mixture liquid was heated to reflux with stirring for 2 hours. The reaction mixture was cooled to room temperature and was concentrated under reduced pressure, and 0.1N aqueous hydrochloric acid solution (50 mL) was added to the residue obtained, this was successively extracted with ethyl acetate (approx. 50 mL, 4 times), washed with water (30 mL), and dried over anhydrous sodium sulfate, and the solvent was distilled off at reduced pressure. The residue obtained was purified by silica gel column chromatography to yield the title compound (440 mg, 60.9% yield) as light brown crystals.
WORKUP
后处理
- temperaturethis reaction mixture liquid was heated
- temperatureto reflux
- concentrationwas concentrated under reduced pressure, and 0.1N aqueous hydrochloric acid solution (50 mL)
- additionwas added to the residue
- customobtained
- extractionthis was successively extracted with ethyl acetate (approx. 50 mL, 4 times)
- washwashed with water (30 mL)
- dry with materialdried over anhydrous sodium sulfate
- distillationthe solvent was distilled off at reduced pressure
- customThe residue obtained
- customwas purified by silica gel column chromatography