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HRID 15339作成日:2026年10月27日

Ammonium Bicarbonate → (cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxamide

https://huagongshe.com/reaction/15339

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium BicarbonateHCID 14013—
反応物HOAtHCID 181649—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物(cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxylic acid sodium saltHCID 131728173—
溶媒DimethylformamideHCID 6228—
生成物(cis)-4-Hydroxy-1-(phenylmethyl)-3-piperidinecarboxamideHCID 68684194109.6%

反応手順

To a solution of (cis)-4-hydroxy-1-(phenylmethyl)-3-piperidinecarboxylic acid sodium salt (17 g) and 1-hydroxy-7-azabenzotriazole (5 g, 37 mmol) in N,N-dimethylformamide was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (14.1 g, 73.4 mmol), followed by ammonium bicarbonate (21 g, 26.6 mmol). The reaction mixture was stirred at room temperature for 18 h. The solvent was then removed under reduced pressure and the residue was treated with aqueous sodium bicarbonate solution. The aqueous phase was extracted with 9:1 dichloromethane:methanol mixture. The organic layer was dried (MgSO4) and the solvent was removed under reduced pressure. The residue was subjected to column chromatography on silica gel using a methanol and dichloromethane gradient (0-20% methanol/dichloromethane). This provided the desired compound (9.5 g, 62%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732461B2
出典データセットuspto-grants-2010_06
ORD IDord-52297c47cb074e87971b38222413d726
出典メモuspto-grants-2010_06