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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1108889생성일: 2026년 10월 26일

Cyclohexene → tert-butyl N-[2-(pyridin-2-ylamino)ethyl]carbamate

https://huagongshe.com/reaction/1108889

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexeneHCID 8079—
반응물HCID 178453672HCID 178453672—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물tert-butyl N-[2-(pyridin-2-ylamino)ethyl]carbamateHCID 18419519200%

반응 단계

10% Pd/C (106.4 mg, 0.10 mmole) was added to a solution of 2-[[2-(Boc-amino)ethyl]amino]pyridine-N-oxide (126.7 mg, 0.5 mmole) and cyclohexene (0.25 mL, 0.25 mmole) in absolute EtOH (5 mL), and the mixture was heated to reflux. After 16 hr, the reaction was filtered through celite® and the filtrate was concentrated. The residue was combined with the residue obtained from a separate preparation (0.5 mmole scale), and the combined materials were purified by silica gel chromatography (5% MeOH/CHCl3). The title compound (148.4 mg, 63% based on 1 mmole of 2-[[2-(Boc-amnino)ethyl]amino]pyridine-N-oxide) was obtained as a yellow oil: TLC (5% MeOH/CHCl3) Rf 0.43; 1H NMR (400, CDCl3) δ 8.05-8.12 (m, 1 H), 7.37-7.46 (m, 1H), 6.53-6.61 (m, 1 H), 6.41 (d, J=8.3 Hz, 1 H), 5.12 (br s, 1 H), 4.86 (br s, 1 H), 3.26-3.51 (m, 4 H), 1.44 (s, 9 H); MS (ES) m/e 238 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06069158
출처 데이터셋uspto-grants-2000_05
ORD IDord-bb591e82c526416d811a2745ca06cc68
출처 메모uspto-grants-2000_05