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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1297179생성일: 2026년 10월 27일

p-Toluenesulfonic acid → N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamide

https://huagongshe.com/reaction/1297179

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-Bromo-2-chlorobenzoic acidHCID 108829—
반응물5-Bromo-2-thiophenesulfonamideHCID 1241304—
용매DichloromethaneHCID 6344—
생성물N-[4-bromo-2-chlorobenzoyl]-5-bromothiophene-2-sulfonamideHCID 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 reduced pressure to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07250430B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-580c9d00c6cd47ceb84475476bc6b7b8
출처 메모uspto-grants-2007_07