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HRID 1972727作成日:2026年10月23日

2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamide → N-methyl-2-piperazin-1-ylacetamide

https://huagongshe.com/ja/reaction/1972727

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamideHCID 36845230—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物N-methyl-2-piperazin-1-ylacetamideHCID 496207598.9%

反応手順

10% Palladium on carbon (115 mg, 10% by wt.) was placed under an inert atmosphere and suspended in EtOH (5 mL). A solution of 2-(4-benzyl-piperazin-1-yl)-N-methyl-acetamide (1.15 g, 4.65 mmol) dissolved in EtOH (18 mL) was added. The reaction mixture was placed under H2 atmosphere (1 Atm pressure) and stirred overnight. The resulting mixture was filtered through a pad of Celite® and the solvent was concentrated in vacuo to give 723 mg (98.9%) of the title compound as a white solid. 1H-NMR (300 MHz, DMSO-d6) 7.61 (broad s, 1H), 2.80 (s, 2H), 2.68 (t, 4H), 2.59 (d, 3H), 2.31 to 2.26 (m, 4H); ES-MS m/z 158.0 [M+H]+, RT (min) 1.13.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08431695B2
出典データセットuspto-grants-2013_04
ORD IDord-831faa8a6f864fac96be13c9251261ac
出典メモuspto-grants-2013_04