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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389978생성일: 2026년 10월 25일

1-Hexanesulfonyl chloride → Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amide

https://huagongshe.com/reaction/389978

반응식

참여 물질

역할이름HCID투입량
반응물1-Hexanesulfonyl chlorideHCID 84504—
반응물[4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanoneHCID 67419145—
용매PyridineHCID 1049—
용매Ethyl AcetateHCID 8857—
생성물Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amideHCID 112949618%

반응 조건

온도60 °C

반응 단계

To a solution of [4-(6-aminopyridin-3-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)-methanone (0.035 g, 0.10 mmol) in pyridine (3 mL) was added hexanesulfonyl chloride (0.022 mL, 0.12 mmol). After heating at 60° C. for 20 h, the mixture was diluted with ethyl acetate (100 mL), washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. Purification by preparative thin layer chromatography afforded the title compound as a white solid (3.8 mg, 8% yield). 1H NMR (300 MHz, CDCl3) δ 7.66, 7.29, 4.08, 3.91, 3.38, 3.27, 3.08, 1.84, 1.35, 1.27, 0.87. MS (ES+) m/z 499.4 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383628B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-e33776045e6c44e9acbd26e6e6c5ac00
출처 메모uspto-grants-2013_02