Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130434생성일: 2026년 10월 26일
4-(Thiophen-2-yl)benzene-1-sulfonyl chloride → N-[3-(cis-3,5-Dimethyl-1-piperazinyl)-4-(methyloxy)phenyl]-4-(2-thienyl)benzenesulfonamide
https://huagongshe.com/reaction/130434
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-(Thiophen-2-yl)benzene-1-sulfonyl chloride | HCID 18387759 | — |
| 반응물 | 3-(cis-3,5-Dimethyl-1-piperazinyl)-4-(methyloxy)aniline | HCID 59007045 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Pyridine methylene chloride | HCID 21875418 | — |
| 생성물 | N-[3-(cis-3,5-Dimethyl-1-piperazinyl)-4-(methyloxy)phenyl]-4-(2-thienyl)benzenesulfonamide | HCID 11518200 | — |
반응 단계
A solution of 3-(cis-3,5-dimethyl-1-piperazinyl)-4-(methyloxy)aniline (D2) (117 mg, 0.5 mmol) in pyridine:dichloromethane (1:1, 4 ml) was treated with a solution 4-(2-thienyl)benzenesulfonyl chloride (WO 9827069) (143 mg, 0.55 mmol) in dichloromethane (2 ml). The solution was stirred at room temperature for 24 hours, quenched with methanol (2 ml) and concentrated in vacuo. The residue was dissolved in dichloromethane and washed with water (×3). The organic phase 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 (dichloromethane to 1:4 2M ammonia in methanol:dichloromethane) to afford the title product (E11). MS (ES+) m/e 458 [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-c605a5a7a06b49218e76290c326b7258 |
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| 출처 메모 | uspto-grants-2008_06 |
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