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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-Hexanesulfonyl chloride | HCID 84504 | — |
| 반응물 | [4-(6-Aminopyridin-3-YL)piperazin-1-YL]-(2-trifluoromethylphenyl)methanone | HCID 67419145 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Hexane-1-sulfonic acid {5-[4-(2-trifluoromethylbenzoyl)piperazin-1-YL]pyridin-2-YL}amide | HCID 11294961 | 8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08383628B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-e33776045e6c44e9acbd26e6e6c5ac00 |
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| 출처 메모 | uspto-grants-2013_02 |
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