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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60792생성일: 2026년 10월 23일

Sodium Bicarbonate → rac-cis-N-((3-Methylpiperidin-2-yl)methyl)quinoline-8-carboxamide

https://huagongshe.com/ko/reaction/60792

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물Ammonium cerium-nitrateHCID 57418452—
반응물rac-cis-N-((1-(4-methoxybenzyl)-3-methylpiperidin-2-yl)methyl)quinoline-8-carboxamideHCID 131737121—
반응물rac-cis-N-((3-methylpiperidin-2-yl)methyl)quinoline-8-carboxamide 4-methoxybenzaldehydeHCID 131737122—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물rac-cis-N-((3-Methylpiperidin-2-yl)methyl)quinoline-8-carboxamideHCID 131737120—

반응 단계

Cerium ammonium nitrate (1.25 g, 2.28 mmol) was added portionwise to a mixture of rac-cis-N-((1-(4-methoxybenzyl)-3-methylpiperidin-2-yl)methyl)quinoline-8-carboxamide (0.23 g, 0.57 mmol) in acetone/water (10 mL, 9:1 v/v) at 0° C. and allowed to stir at rt for 5 h. Sat. NaHCO3 (aq.) was added and the resulting suspension was stirred at r.t for 10 min, concentrated in vacuo to remove the acetone, then filtered through diatomaceous earth and rinsed with EtOAc. The bi-layer filtrate was extracted with EtOAc and the combined organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo to provide a brown oil as a 1:1 mixture of rac-cis-N-((3-methylpiperidin-2-yl)methyl)quinoline-8-carboxamide/4-methoxybenzaldehyde, which was used as-is without further purification. MS (ESI) 284.13 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440982B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-3f372c9674ec4a14ba051a8feaf2fcad
출처 메모uspto-grants-2016_09