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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44204생성일: 2026년 10월 24일

Nitrogen → 4-Chloro-N-(3-chloro-quinoxalin-2-yl)-benzenesulfonamide

https://huagongshe.com/ko/reaction/44204

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium CarbonateHCID 11430—
반응물2,3-DichloroquinoxalineHCID 16659—
반응물4-ChlorobenzenesulfonamideHCID 66824—
용매DimethylformamideHCID 6228—
생성물4-Chloro-N-(3-chloro-quinoxalin-2-yl)-benzenesulfonamideHCID 2366510—

반응 단계

To a solution of 4-Chlorobenzenesulfonamide (1.92 g, 10 mmol) in anhydrous DMF (50 mL) was added solid potassium carbonate (1.38 g, 10 mmol) in one portion. The reaction mixture was stirred for 10 minutes, followed by the addition of 2,3-dichloroquinoxaline (1.99 g, 10 mmol). Heating the resultant mixture under refux conditions in an atmosphere of N2 for 2.5 h gave the desired product. The progress of the reaction was monitored by TLC using, hexanes/EtOAc 3:1. After cooling the reaction mixture is slowly added to a vigorously stirred aqueous solution of AcOH (1%, 500 mL). The desired product precipitates as grey crystals, which are filtered and dried overnight in desiccator. Yield 2.32 g, 66%; Rf=0.7 (hexanes/EtOAc 1:1); HPLC/MS: [M+H]+ m/z 354. 1H NMR: (DMSO-d6, 600 MHz) 7.68 (t, J=7.8 Hz, 1H), 7.72 (d, J=8.4 Hz, 2H), 7.78 (td, J=7.8 Hz, J=1.2 Hz, 1H), 7.89 (d, J=8.4 Hz, 2H), 8.19 (d, J=8.4 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541415B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-668aa4d5580442bc9eb04a23c849f206
출처 메모uspto-grants-2013_09