Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15883생성일: 2026년 10월 25일
Diisopropylethylamine → 7-Fluoro-2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinoline
https://huagongshe.com/reaction/15883
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 3-Nitrophenethyl methanesulfonate | HCID 21973884 | — |
| 반응물 | 7-Fluoro-2-methyl-5-piperazin-1-ylquinoline | HCID 57444364 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 7-Fluoro-2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinoline | HCID 57444366 | 88% |
반응 단계
N,N-Diisopropylethylamine (0.07 mL; 3 eq) was added to a solution of 2-methyl-5-(1-piperazinyl)-7-fluoro quinoline (0.03 g; 1 eq) and 2-(3-nitrophenyl)ethyl methanesulfonate (D4) (0.033 g; 1.1 eq) in dimethylformamide (1.0 mL). The reaction mixture was heated to 90° C. for 10 hours. The dark solution was cooled to room temperature and concentrated under reduced pressure, diluted with water (3 mL) and brine (1 mL) and extracted into ethyl acetate (3×3 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica, eluting with a gradient from dichloromethane to dichloromethane-MeOH (98:2) affording the title compound in 88% yield (0.04 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07732600B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-9b7d567bdd9f4a2f8c41e6a41934d698 |
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| 출처 메모 | uspto-grants-2010_06 |
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