돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537849생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/537849

반응식

참여 물질

역할이름HCID투입량
반응물N-(3-Aminophenyl)-1-phenylmethanesulfonamideHCID 16772451—
반응물4-(2-Chlorooxazol-5-yl)benzonitrileHCID 68443558—
용매IsopropanolHCID 3776—
생성물N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamideHCID 71060644—

반응 조건

온도80 °C

반응 단계

A mixture of 4-(2-chlorooxazol-5-yl)benzonitrile 2 (0.20 g, 0.98 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 4 (0.256 g, 0.98 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, a white solid precipitated out which was filtered off, washed with 2-propanol, and dried. This was then triturated with ether and filtered to yield the title product, a white solid, as the hydrochloride salt of 5 (0.15 g, 36%). Free amine containing filtrate was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide 5 (0.15 g, 36% yield) as pale yellow solid. MS (ES) m/z 431 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865709B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-2c17b9bee21e4cc08df6e108e92c2e04
출처 메모uspto-grants-2014_10