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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

반응식

참여 물질

역할이름HCID투입량
반응물4-(Thiophen-2-yl)benzene-1-sulfonyl chlorideHCID 18387759—
반응물3-(cis-3,5-Dimethyl-1-piperazinyl)-4-(methyloxy)anilineHCID 59007045—
용매DichloromethaneHCID 6344—
용매Pyridine methylene chlorideHCID 21875418—
생성물N-[3-(cis-3,5-Dimethyl-1-piperazinyl)-4-(methyloxy)phenyl]-4-(2-thienyl)benzenesulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-c605a5a7a06b49218e76290c326b7258
출처 메모uspto-grants-2008_06