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HRID 248874作成日:2026年10月26日

2-(N-Benzyl-N-methylamino)-1-(N-piperidinyl)ethane → Methyl(2-(piperidin-1-yl)ethyl)amine

https://huagongshe.com/reaction/248874

反応式

関与物質

役割名称HCID仕込み量
反応物2-(N-Benzyl-N-methylamino)-1-(N-piperidinyl)ethaneHCID 23208436—
触媒Palladium hydroxideHCID 9942167—
溶媒EthanolHCID 702—
生成物Methyl(2-(piperidin-1-yl)ethyl)amineHCID 3157473—

反応手順

A solution of the title compound of Step 11 (1.85 g, 7.96mmol) and 20% Pd(OH)2 on carbon in EtOH (50 mL) was placed under a hydrogen atmosphere (60 psi) at room temperature for 17 hours. The mixture was filtered and concentrated to give the title compound as a clear, yellow liquid (1.02 g, 90% crude yield). The proton spectral data were consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212185
出典データセットuspto-grants-1993_05
ORD IDord-24f9471b682b46ea902a3d42b6b01974
出典メモuspto-grants-1993_05