戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1038433作成日:2026年10月26日

N-(3-Aminophenyl)-1-phenylmethanesulfonamide → 1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide

https://huagongshe.com/reaction/1038433

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3-Aminophenyl)-1-phenylmethanesulfonamideHCID 16772451—
反応物2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazoleHCID 71060395—
溶媒IsopropanolHCID 3776—
生成物1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamideHCID 71060466—

反応条件

温度80 °C

反応手順

A mixture of 2-chloro-5-(4-(trifluoromethyl)phenyl)oxazole 31 (0.651 g, 2.63 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 26 (0.69 g, 2.63 mmol) in 2-propanol (50 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide 1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamide. 34 (0.407 g, 33% yield) as a solid. MS (ES) m/z 474 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08551992B2
出典データセットuspto-grants-2013_10
ORD IDord-a8ab3eb49e8045ffb5fd057807149178
出典メモuspto-grants-2013_10