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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130430생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/130430

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
반응물5-(cis-3,5-Dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]anilineHCID 59007092—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물5-Bromo-N-{5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]phenyl]-2-thiophenesulfonamideHCID 59007096—

반응 단계

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-[(phenylmethyl)oxy]aniline (D39) (300 mg, 0.96 mmol) in dichloromethane (5 ml) and pyridine (5 ml) was added 5-bromo-2-thiophenesulfonyl chloride (505 mg, 1.93 mmol) and the mixture stirred at room temperature for 4 hours. The mixture was then reduced in vacuo and the residue purified by SCX (eluting with methanol then ammonia 2M in methanol). The appropriate fractions were combined and reduced and the residue purified by trituaration with methanol to afford the title compound (D42). MS (ES+) m/e 536/538 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-4ecedd6316164cc78f6a55d979f81622
출처 메모uspto-grants-2008_06