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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 646889생성일: 2026년 10월 24일

1-Methyl-4-(4-nitro-3-(piperidin-1-yl)phenyl)piperazine → 4-(4-Methylpiperazin-1-yl)-2-(piperidin-1-yl)aniline

https://huagongshe.com/ko/reaction/646889

반응식

참여 물질

역할이름HCID투입량
반응물1-Methyl-4-(4-nitro-3-(piperidin-1-yl)phenyl)piperazineHCID 2885704—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물4-(4-Methylpiperazin-1-yl)-2-(piperidin-1-yl)anilineHCID 6867969688.5%

반응 단계

1-(5-Fluoro-2-nitro-phenyl)-piperidine (100 mg, 0.44 mmol) was treated with N-methylpiperizine (3 mL) and heated to 80° C. overnight. The reaction was diluted with EtOAc (10 mL), washed with water (2×10 mL), dried (Na2SO4) and concentrated in vacuo to afford 118 mg (88%) of 1-methyl-4-(4-nitro-3-piperidin-1-yl-phenyl)-piperazine as an oil. The 1-methyl-4-(4-nitro-3-piperidin-1-yl-phenyl)-piperazine (22 mg, 0.07 mmol) was stirred with 13 mg 5% Pd—C in 1 mL of MeOH under H2 for 2 h. The mixture was filtered through SiO2, eluting with 10% MeOH—CHCl3, and the solvent was concentrated in vacuo to give 17 mg (86%) of the title compound as a white solid. Mass spectrum (ESI, m/z): Calcd. for C16H26N4, 275.22 (M+H), found 275.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705042B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-5e116b00b61b4ce28e5987071748db15
출처 메모uspto-grants-2010_04