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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1966427생성일: 2026년 10월 26일

Water → [4-[3-(Benzylamino)-4-nitrophenyl]piperazin-1-yl]-phenylmethanone

https://huagongshe.com/reaction/1966427

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-BenzoylpiperazineHCID 762654—
반응물N-benzyl-5-bromo-2-nitroanilineHCID 24902978—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물[4-[3-(Benzylamino)-4-nitrophenyl]piperazin-1-yl]-phenylmethanoneHCID 29063151,362.5%

반응 단계

A solution of N-benzyl-5-bromo-2-nitrobenzenamine (50 mg, 0.16 mmol) and phenyl(piperazin-1-yl)methanone (93 mg, 0.48 mmol) in NMP (1 mL) was heated to 110° C. for 16 h. The solution was cooled to room temperature to which was slowly added H2O (5 mL). The resulting yellow precipitate was filtered, washed with 2 mL of water, dried (high vacuum, 14 h) to furnish (4-(3-(benzylamino)-4-nitrophenyl)piperazin-1-yl)(phenyl)methanone (520 mg, 2.18 mmol), 92% yield. 1H NMR (500 MHz, CDCl3) d (ppm) 8.85 (m, 1H), 8.14 (d, J=9.5 Hz, 1H), 7.51-7.3 (m, 10H), 6.24 (dd, J=2.5 Hz, 10 Hz, 1H), 5.88 (d, J=2.5 Hz, 1H), 4.55 (d, J=5 Hz, 2H) 3.9-3.2 (m, 8H).+ESI HRMS (calcd for C24H24N4O3Na, M+Na) 439.1746, found 439.1741

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08420640B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-6a1dff251f6342e4a63d7807772b5687
출처 메모uspto-grants-2013_04