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HRID 1533901作成日:2026年10月25日

N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide → N-[4-(1-Piperazinyl)phenyl]acetamide

https://huagongshe.com/reaction/1533901

反応式

関与物質

役割名称HCID仕込み量
反応物N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamideHCID 960610—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物N-[4-(1-Piperazinyl)phenyl]acetamideHCID 1563176156.5%

反応手順

This compound was prepared by the hydrogenation of 7.7 g (0.025 mol) of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]acetamide in 100 mL of methanol using palladium on carbon as the catalyst. The solution was filtered and the filtrate concentrated under reduced pressure to give an oil which crystallized. The solid was dissolved in a minimum amount of a methylene chloride/10% methanol solution and passed through a 100 g Florisil column. The desired fractions were concentrated to an oil under reduced pressure which crystallized to give 3.1 g (56%) of crude product. A 0.5 g portion was recrystallized from methanol/petroleum ether to give a cream colored solid, mp 191°-193° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05086055
出典データセットuspto-grants-1992_02
ORD IDord-8caf3478076c484ba7009e19d11347c5
出典メモuspto-grants-1992_02