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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537864생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/537864

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-Aminophenyl)methanesulfamideHCID 2734262—
반응물2-Chloro-5-(4-(trifluoromethyl)phenyl)oxazoleHCID 71060395—
용매IsopropanolHCID 3776—
생성물N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl) methane sulfonamideHCID 7106044241%

반응 조건

온도80 °C

반응 단계

A mixture of 2-chloro-5-(4-(trifluoromethyl)phenyl)oxazole 31 (0.599 g, 2.42 mmol) and commercially available N-(3-aminophenyl)methanesulfonamide 6 (0.451 g, 2.42 mmol) in 2-propanol (20 mL) was heated to 80° C. for 14 h with stirring. Upon cooling, solvent was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide N-(3-((5-(4-(trifluoromethyl)phenyl)oxazol-2-yl)amino)phenyl) methane sulfonamide 33 (0.393 g, 41% yield) as a solid. MS (ES) m/z 398 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865709B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-168bbfb1619c43dfbb3c7a38f0e41240
출처 메모uspto-grants-2014_10