Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6975생성일: 2026년 10월 25일
p-Toluenesulfonic acid → N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamide
https://huagongshe.com/reaction/6975
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 4-Bromo-2-chlorobenzoic acid | HCID 108829 | — |
| 반응물 | 5-Bromo-2-thiophenesulfonamide | HCID 1241304 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamide | HCID 22019517 | — |
반응 단계
An 8 mL reaction vial is charged with 4-bromo-2-chlorobenzoic acid (0.39 mmol, 1.5 eq) and 2.0 mL of dichloromethane. A stock solution (4.0 mL) containing 5-bromothiophene-2-sulfonamide (0.26 mmol, 1 eq) and N,N-[dimethyl]-4-aminopyridine (48 mg, 0.39 mmol, 1.5 eq) in dichloromethane is added, followed by 0.261 g carbodiimide polystyrene resin (2.0 mmol/g, 0.52 mmol, 2.0 eq, Novabiochem) and the vial is capped and shaken. After 72 hr, 0.77 g sulphonated polystyrene resin (MP-TsOH) is added (1.53 mmol/g, 1.17 mmol, Argonaut). After about 18 hr the reaction mixture is filtered and concentrated under reduced pressure. Chromatography was applied to the residue and fractions containing product were combined and concentrated under reduce pressure to provide the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07084170B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-084376ff6cbd402bbcddd99c0de3c3d7 |
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| 출처 메모 | uspto-grants-2006_08 |
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