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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)aniline | HCID 59007063 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07381728B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-5f4f9e09ca37412db2a3eae206990843 |
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| 출처 메모 | uspto-grants-2008_06 |
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