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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1038433생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-Aminophenyl)-1-phenylmethanesulfonamideHCID 16772451—
반응물2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazoleHCID 71060395—
용매IsopropanolHCID 3776—
생성물1-phenyl-N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl)methane sulfonamideHCID 71060466—

반응 조건

온도80 °C

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08551992B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-a8ab3eb49e8045ffb5fd057807149178
출처 메모uspto-grants-2013_10