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HRID 60792作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Ammonium cerium-nitrateHCID 57418452—
反応物rac-cis-N-((1-(4-methoxybenzyl)-3-methylpiperidin-2-yl)methyl)quinoline-8-carboxamideHCID 131737121—
反応物rac-cis-N-((3-methylpiperidin-2-yl)methyl)quinoline-8-carboxamide 4-methoxybenzaldehydeHCID 131737122—
溶媒Propan-2-one--water (1/1)HCID 18366337—
生成物rac-cis-N-((3-Methylpiperidin-2-yl)methyl)quinoline-8-carboxamideHCID 131737120—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440982B2
出典データセットuspto-grants-2016_09
ORD IDord-3f372c9674ec4a14ba051a8feaf2fcad
出典メモuspto-grants-2016_09