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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130441생성일: 2026년 10월 24일

p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamide

https://huagongshe.com/ko/reaction/130441

반응식

참여 물질

역할이름HCID투입량
반응물p-Bromobenzenesulfonyl chlorideHCID 7396—
반응물4-MethylmorpholineHCID 7972—
반응물5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)anilineHCID 59007063—
용매DichloromethaneHCID 6344—
생성물4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamideHCID 44452776—

반응 단계

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)aniline (D4) (1.20 g, 5.1 mmol) in dichloromethane (35 ml) was treated with morpholinomethyl-polystyrene HL resin (2.45 g, 4.2 mmol/g loading, 10.29 mmol) followed by 4-bromobenzenesulfonyl chloride (2.60 g, 10.2 mmol). The resulting solution was stirred at room temperature overnight (˜24hours)and then the resin filtered off with methanol and the solvent evaporated in vacuo. The residue was passed through an SCX column eluting first with methanol followed by 2M ammonia in methanol. The relevant fractions were collected, combined and the solvent evaporated in vacuo. The crude product was purified by Flashmaster causing an elution gradient of 0 to 10% methanol in dichloromethane. The relevant fractions were collected, combined and the solvent evaporated to afford the title compound (E106). MS (ES+) m/e 454/456 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-5f4f9e09ca37412db2a3eae206990843
출처 메모uspto-grants-2008_06