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HRID 466876作成日:2026年10月25日

1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide → Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/466876

反応式

関与物質

役割名称HCID仕込み量
反応物1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamideHCID 19031938—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylateHCID 406301358.8%

反応手順

1.1 g of 1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide were dissolved in 40 ml of ethanol. 0.1 g of 10% palladium-on-carbon was added and the mixture was hydrogenated at room temperature and under atmospheric pressure for 2 hours. The catalyst was filtered off. The filtrate was evaporated to give 0.74 g of crude product which was purified by flash chromatography on silica gel using 5% methanol in dichloromethane for the elution. After evaporation of the solvents there was obtained 0.44 g of 4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide as an oil; MS: m/e 286 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05157041
出典データセットuspto-grants-1992_10
ORD IDord-f5b0257492ef4b688059ae3c703070be
出典メモuspto-grants-1992_10