HRID730238
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
The nitro intermediate (0.5 mmol) above was dissolved in EtOH (10 mL) and was treated with tin(II) chloride (2.5 mmol). The reaction mixture was heated to reflux for 12 h. The contents were cooled to RT and treated with 1 M aqueous NaOH until the pH of the reaction mixture was between 8-9 which resulted in formation of a precipate. The precipitate was then filtered, washed with methanol (10 mL) and DCM (10 mL). The combined filtrate was concentrated in vacuo and the residue obtained was purified by column chromatography eluting with DCM/ethyl acetate as eluant to give 115 mg of 5-bromo-N-(4-fluoro-2-aminophenyl)-2-methoxybenzenesulfonamide.
WORKUP
后处理
- temperatureThe reaction mixture was heated
- temperatureto reflux for 12 h
- customresulted in formation of a precipate
- filtrationThe precipitate was then filtered
- washwashed with methanol (10 mL) and DCM (10 mL)
- concentrationThe combined filtrate was concentrated in vacuo
- customthe residue obtained
- customwas purified by column chromatography
- washeluting with DCM/ethyl acetate as eluant