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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 587135생성일: 2026년 10월 25일

Water → 3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamide

https://huagongshe.com/reaction/587135

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2,4-Dichloro-1,3,5-triazineHCID 17810—
반응물Sodium BicarbonateHCID 516892—
반응물(3-Aminophenyl)methanesulfonamideHCID 13266255—
용매DimethylformamideHCID 6228—
생성물3-[(4-Chloro-1,3,5-triazin-2-yl)amino]benzenemethanesulfonamideHCID 86679822—

반응 조건

온도0 °C

반응 단계

To a solution of 2,4-dichloro-1,3,5-triazine (1.0 eq) in dry DMF (0.7 M) at 0° C. under N2 atmosphere was added a solution of (3-aminophenyl)-methanesulfonamide (1.0 eq) in dry DMF (0.7 M). The reaction mixture was stirred for 2.5 h at 0° C. Then water was added and the aqueous solution was neutralized with sat. aq. NaHCO3 solution. The aqueous layer was extracted with EtOAc and the combined organic layers were dried over Na2SO4. Evaporation of solvent gave A1 as a white solid which was used in the next step without further purification. 1H NMR (400 MHz, d6-DMSO, 300K) δ 4.26 (s, 2H), 6.89 (s, 2H), 7.15 (d, J=7.4 Hz, 1H), 7.36 (d, J=7.4 Hz, 1H), 7.66 (d, J=7.4 Hz, 1H), 8.64 (s, 1H), 9.75 (br. s, 1H), 10.83 (s, 1H). MS (ES) C10H10ClN5O2S requires: 299. found: 300 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09226929B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-4c537d3662694d899423edc50d09fd9b
출처 메모uspto-grants-2016_01