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
2,3-dihydro-1,3-benzothiazole synthesized from 2-aminobenzenethiol (1.25 g) and 37% formalin (0.83 mL) in the same manner as in Example 1 was dissolved in chloroform (7 mL), and triethylamine (1.25 mL) and 3-cyano-5-isopropyl-4-methoxybenzoyl chloride (710 mg) were added to the solution, and then the mixture was stirred at room temperature for 2 hours. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1) to obtain the title compound (1.02 g) as a yellow oily substance.
WORKUP
后处理
- distillationThe solvent was distilled off under reduced pressure and water
- additionwas added
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with 1N hydrochloric acid, 1N sodium hydroxide and saturated brine
- dry with materialdried over anhydrous sodium sulfate
- distillationThe solvent was distilled off under reduced pressure
- customthe obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:1)