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HRID 583111作成日:2026年10月26日

N-benzyloxycarbonyl-3-[3-(4-formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamine → 3-(3-(4-Formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamine

https://huagongshe.com/reaction/583111

反応式

関与物質

役割名称HCID仕込み量
反応物N-benzyloxycarbonyl-3-[3-(4-formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamineHCID 21584186—
触媒HCID 178418390HCID 178418390—
溶媒EthanolHCID 702—
生成物3-(3-(4-Formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamineHCID 1968942485%

反応条件

温度60 °C

反応手順

A mixture comprising 30.4 g of N-benzyloxycarbonyl-3-[3-(4-formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamine, 3.1 g of 5% palladium carbon and 300 ml of ethanol, was stirred at 60° C. for 9 hours under a hydrogen atmosphere. Palladium carbon was filtered off, and then the filtrate was distilled off under reduced pressure to obtain 17.99 g of the above-identified compound as slightly brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05929074
出典データセットuspto-grants-1999_07
ORD IDord-d982800720d6455987588f91bb211934
出典メモuspto-grants-1999_07