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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55869생성일: 2026년 10월 25일

Morpholine → N-(5-Amino-pyridin-2-yl)-2-piperidin-1-yl-acetamide

https://huagongshe.com/reaction/55869

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물Sodium BicarbonateHCID 516892—
반응물Ammonium formateHCID 2723923—
반응물2-chloro-N-(5-nitropyridin-2-yl)acetamideHCID 4066445—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N-(5-Amino-pyridin-2-yl)-2-piperidin-1-yl-acetamideHCID 9035701063%

반응 단계

Compound 20 (3.0 g, 13.9 mmol), was dissolved in THF (100 mL). Morpholine (20 mL, 229 mmol) was added and the mixture stirred at reflux for 1 hour. DCM (200 mL) and saturated aqueous sodium bicarbonate solution (200 mL) were added and the layers separated. The organic phase was dried (MgSO4), filtered and the solvent evaporated in vacuo. The residue was dissolved in EtOH (200 mL) and 10% Pd/C (wet, ˜300 mg) followed by ammonium formate (880 mg, 14.0 mmol) added. The mixture was stirred at reflux for 1 hour. The mixture was cooled to rt, filtered through celite, washing the precipitate with EtOAc. The collected filtrate was diluted with saturated ammonium bicarbonate solution (100 mL) and the layers separated. The organic phase was dried (MgSO4), filtered and the solvent evaporated in vacuo. The residue was triturated with EtOAc-isohexane to afford the title compound as an off-white solid (2.1 g, 63%); (m/z): 237 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09433622B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e5463e04a26a4badb67d0ed2119cd9ca
출처 메모uspto-grants-2016_09