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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130424생성일: 2026년 10월 24일

5-Bromothiophene-2-sulfonyl chloride → 5-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]-2-thiophenesulfonamide

https://huagongshe.com/ko/reaction/130424

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
반응물5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroanilineHCID 59007078—
용매Pyridine methylene chlorideHCID 21875418—
생성물5-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]-2-thiophenesulfonamideHCID 59007109—

반응 단계

A solution of 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroaniline (D34) (100 mg, 0.42 mmol) in pyridine:dichloromethane (1:1, 4 ml) was treated with 5-bromo-2-thiophenesulfonyl chloride (132 mg, 0.51 mmol). The solution was stirred at room temperature for 2 hours, quenched with methanol and concentrated in vacuo. The residue was applied to a SCX cartridge (Varian bond-elute, 5 g) and washed with methanol and 2M ammonia in methanol. The combined basic fractions were concentrated in vacuo and the resulting residue was purified by column chromatography (FlashMaster) (gradient of dichloromethane to 4% metlianol:dichloromethane) to afford the title product (D36). MS (ES+) m/e 464/466/468 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-b25f89cab3aa45d48fefb505f715d870
출처 메모uspto-grants-2008_06