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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2265182생성일: 2026년 10월 25일

Pyridine → 4-Chloro-2-(quinoxaline-5-sulfonylamino)benzoic acid methyl ester

https://huagongshe.com/reaction/2265182

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물Methyl 4-chloroanthranilateHCID 80001—
반응물Quinoxaline-5-sulfonyl chlorideHCID 16090697—
용매Ethyl AcetateHCID 8857—
생성물4-Chloro-2-(quinoxaline-5-sulfonylamino)benzoic acid methyl esterHCID 6719929290%

반응 단계

A solution of methyl 2-amino-4-chlorobenzoate (0.33 g, 1.8 mmol), quinoxaline-5-sulfonyl chloride (0.40 g, 1.8 mmol), pyridine (0.71 mL, 8.8 mmol), and DCM (10 mL) was stirred at rt for 16 h. EtOAc (75 mL) was added and the solution was washed with satd. aq. NaHCO3 (50 mL), then dried and concentrated. Chromatographic purification of this residue (EtOAc/hexanes) gave the title compound as a white solid (0.60 mg, 90%). MS (ESI+): mass calcd. for C16H12ClN3O4S, 377.0; m/z found, 378 [M+H]+. 1H NMR (400 MHz, CDCl3): 11.44 (s, 1H), 8.97 (d, J=1.8, 1H), 8.95 (d, J=1.8, 1H), 8.61 (dd, J=7.4, 1.4, 1H), 8.33 (dd, J=8.5, 1.4, 1H), 7.89 (dd, J=8.4, 1.0, 1H), 7.84 (d, J=2.0, 1H), 7.77 (d, J=8.6, 1H), 6.89 (dd, J=8.6, 2.0, 1H), 3.90 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07855292B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-249a7dde4624468da5025f0d40e5365e
출처 메모uspto-grants-2010_12