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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730220생성일: 2026년 10월 24일

6-Methoxy-m-toluenesulfonyl chloride → Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide

https://huagongshe.com/ko/reaction/730220

반응식

참여 물질

역할이름HCID투입량
반응물6-Methoxy-m-toluenesulfonyl chlorideHCID 145149—
반응물Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amideHCID 1151877679.8%

반응 단계

To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)-amide (1 mmol, prepared as in Example 1) in DCM (2 mL) and pyridine (2 mL), 2-methoxy-5-methylbenzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight. The reaction mixture was then diluted with DCM (10 mL). The organic phase was washed with 10% aqueous HCl (10 mL), water (10 mL) and brine (10 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 obtain 390 mg of benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide. LC: Tr 1.25 min; MS: 489.1 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582673B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-a1631ad6ce614e76885649047060fa4d
출처 메모uspto-grants-2009_09