돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-Nitrophenethyl methanesulfonateHCID 21973884—
반응물7-Fluoro-2-methyl-5-piperazin-1-ylquinolineHCID 57444364—
용매DimethylformamideHCID 6228—
생성물7-Fluoro-2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinolineHCID 5744436688%

반응 조건

온도90 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732600B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9b7d567bdd9f4a2f8c41e6a41934d698
출처 메모uspto-grants-2010_06