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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730230생성일: 2026년 10월 24일

2-Methoxy-4-nitrobenzenesulfonyl chloride → Benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-4-nitrobenzenesulfonylamino)phenyl]-amide

https://huagongshe.com/ko/reaction/730230

반응식

참여 물질

역할이름HCID투입량
반응물2-Methoxy-4-nitrobenzenesulfonyl chlorideHCID 309458—
반응물Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물Benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-4-nitrobenzenesulfonylamino)phenyl]-amideHCID 8660504767.9%

반응 단계

To a solution of benzo[b]thiophene-2-sulfonic acid (2-amino-phenyl)-amide (1 mmol, prepared as in Example 1) in DCM (2 mL) and pyridine (2 mL), 2-methoxy-4-nitrobenzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight or until the reaction was complete as determined by TLC or LC-MS. The reaction mixture was then diluted with DCM (20 mL). The organic phase was washed with 10% aqueous HCl (20 mL), water (20 mL), and brine (20 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue obtained was purified by flash column chromatography eluting with DCM/EtOAc to yield 353 mg of benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-4-nitrobenzenesulfonylamino)phenyl]-amide. LC: Tr 1.21 min; MS: 520.7.7 (M+1)+. 1H NMR (CDCl3, 400 MHz): δ 4.24 (s, 3H), 6.72 (bs, 1H), 6.88 (d, 1H), 7.03 (t, 1H), 7.16 (t, 1H), 7.30 (d, 1H), 7.52 (t, 1H), 7.51 (t, 1H), 7.64 (s, 1H), 7.67-7.88 (m, 5H), 7.92 (s, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582673B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-693527df93a5419a8fb649e6eff6b090
출처 메모uspto-grants-2009_09