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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237362생성일: 2026년 10월 23일

Hydrochloric Acid → N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide

https://huagongshe.com/ko/reaction/237362

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물2,3-DichloroquinoxalineHCID 16659—
반응물Benzenesulfonamide, 3-nitro-HCID 67138—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 5007601—

반응 조건

온도150 °C

반응 단계

2,3-Dichloroquinoxaline (26.1 g, 131.1 mmol), m-Nitrobenzene sulfonamide (26.5 g, 131.1 mmol) and potassium carbonate (18.1 g, 131.1) were dissolved in anhydrous DMSO (500 mL). The reaction was heated to 150° C. for 2 h. The reaction mixture was poured into water (400 mL), followed by addition of 2M HCl (60 mL). The product was extracted with EtOAc (3×500 mL). The organic layers were combined and washed water (2×500 mL) and brine (2×500 mL). The product was then dried with sodium sulfate to give N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) for C14H9ClN4O4S: 364.94, 366.97 (MH+)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642584B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-c2d2f7f0d90d43d5b762d39a4c2ce1a8
출처 메모uspto-grants-2014_02