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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1796453생성일: 2026년 10월 27일

N-(2-aminoethyl)acetamide → 4-{[2-(acetylamino)ethyl]amino}-N,N-diethyl-3-nitrobenzamide

https://huagongshe.com/reaction/1796453

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참여 물질

역할이름HCID투입량
반응물N-(2-aminoethyl)acetamideHCID 66082—
반응물N,N-diethyl-4-fluoro-3-nitrobenzamideHCID 22181444—
용매EthanolHCID 702—
생성물4-{[2-(acetylamino)ethyl]amino}-N,N-diethyl-3-nitrobenzamideHCID 2218131463%

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온도90 °C

반응 단계

Following general procedure 2B: A mixture of N,N-diethyl-4-fluoro-3-nitrobenzamide (0.200 g, 0.833 mmol), N-(2-aminoethyl)acetamide (0.077 g, 0.757 mmol) in 80% aq. EtOH (5 mL) was heated at 90° C. overnight. After work-up, the crude product was purified by silica gel column chromatography (100% EtOAc to 5% MeOH/EtOAc) to provide the title compound (0.152 g, 63%) as a bright yellow solid. 1H-NMR (CDCl3): δ 8.27 (d overlapping with br s, J=2.0 Hz, 2H), 7.55 (dd, J=8.4 Hz, J=2.0 Hz, 1H), 6.99 (d, J=9.2 Hz, 1H), 6.06 (br s, 1H), 3.58–3.50 (m, 4H), 3.44 (br s, 4H), 2.02 (s, 3H), 1.22 (t, J=7.2 Hz, 6H). MS (ESI) (M+H)+=323.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07030139B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-1ba8569fe2ba49c0bf05eb58a3ede7ed
출처 메모uspto-grants-2006_04