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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490186생성일: 2026년 10월 26일

Formaldehyde → N-{[4-(2-pyridinyl)-1-piperazinyl]methyl}cyclohexanecarboxamide

https://huagongshe.com/reaction/490186

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Potassium CarbonateHCID 11430—
반응물CyclohexanecarboxamideHCID 14283—
반응물1-(2-Pyridyl)piperazineHCID 94459—
용매EthanolHCID 702—
생성물N-{[4-(2-pyridinyl)-1-piperazinyl]methyl}cyclohexanecarboxamideHCID 1047019799.2%

반응 단계

A mixture of 1-pyridin-2-ylpiperazine (16 mg, 0.1 mmol, Aldrich), paraformaldehyde (30 mg, 1 mmol), cyclohexanecarboxylic acid amide (64 mg, 0.5 mmol, Aldrich), and 42 mg of potassium carbonate (0.3 mmol) in 2 mL absolute ethyl alcohol was heated to reflux under nitrogen overnight. The mixture was cooled to room temperature, filtered, and the solvent was removed under reduced pressure. The residue was purified by flash column chromatography on silica gel (10% methanol:ethyl acetate) to give 30 mg (66%) pure compound. 1H NMR (500 MHz, DMSO-d6) δ 1.05-1.40 (m, 5H), 1.59-1.68 (m, 5H), 2.15 (m, 1H), 2.48 (m, 4H), 3.45 (t, J=4 Hz, 4H), 3.95 (d, J=5 Hz, 1H), 6.62 (t, J=6 Hz, 1H), 6.81 (d, J=6 Hz, 1H), 7.53 (t, J=6 Hz, 1H), 8.01 (t, J=5 Hz, 1H), 8.10 (d, J=5 Hz, 1H); MS (ESI/APCI−) m/e 301 (M−H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528134B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-7ff2b7dec02241dd9e4288b00af3a76a
출처 메모uspto-grants-2009_05