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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| 반응물 | Methyl 2-[(2-aminophenyl)sulfanyl]benzoate | HCID 614949 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Methyl 2-{[2-({[4-(acetylamino)phenyl]sulfonyl}amino)phenyl]thio}benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07393873B2 |
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| 출처 데이터셋 | uspto-grants-2008_07 |
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| ORD ID | ord-02c64c4ec5bc4132bdd771d93dd44e68 |
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| 출처 메모 | uspto-grants-2008_07 |
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