돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 746741생성일: 2026년 10월 24일

N-Acetylsulfanilyl chloride → Methyl 2-{[2-({[4-(acetylamino)phenyl]sulfonyl}amino)phenyl]thio}benzoate

https://huagongshe.com/ko/reaction/746741

반응식

참여 물질

역할이름HCID투입량
반응물N-Acetylsulfanilyl chlorideHCID 8481—
반응물Methyl 2-[(2-aminophenyl)sulfanyl]benzoateHCID 614949—
용매PyridineHCID 1049—
용매Ethyl AcetateHCID 8857—
생성물Methyl 2-{[2-({[4-(acetylamino)phenyl]sulfonyl}amino)phenyl]thio}benzoateHCID 11442458—

반응 단계

A solution of methyl 2-[(2-aminophenyl)thio]benzoate (0.444 g, 1.71 mmol) and 4-(acetylamino)benzenesulfonyl chloride (0.440 g, 1.88 mmol) in pyridine (1.6 mL) was stirred at room temperature for 1 hr. The reaction mixture was diluted with ethyl acetate and washed with 0.5 N HCl (×2), water (×2), half brine and brine. The organic layer was dried over sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography eluted with 1-5% MeOH in DCM to provide the title compound. MS (ES, M+H+): 457.2. 1H NMR (400 MHz, CD3OD) δ 7.92 (bd, J=8 Hz, 1H), 7.75 (bd, J=8 Hz, 1H), 7.55 (bd, J=9.2 Hz, 2H), 7.50-7.44 (m, 3H), 7.42 (bd, J=8 Hz, 1H), 7.18 (bt, J=7.6 Hz, 1H), 7.14 (bt, J=7.6 Hz, 1H), 7.05 (bt, J=8 Hz, 1H), 6.23 (bd, J=8 Hz, 1H), 3.95 (s, 3H), 2.14 (s, 3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07393873B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-02c64c4ec5bc4132bdd771d93dd44e68
출처 메모uspto-grants-2008_07