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HRID 267147作成日:2026年10月24日

Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylate → 1-Piperazinecarboxamide

https://huagongshe.com/ja/reaction/267147

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylateHCID 4063013—
反応物(2S,3S)-1,2-Epoxy-3-(Cbz-amino)-4-phenylbutaneHCID 9861019—
溶媒IsopropanolHCID 3776—
生成物1-PiperazinecarboxamideHCID 258192—

反応手順

0.395 g of 4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamide was dissolved in 50 ml of dry isopropanol and treated with 0.413 g of 3(S)-(benzyloxyformamido)-1,2(S)-epoxy-4-phenylbutane. The mixture was stirred at room temperature for 72 hours. The solvent was removed by evaporation to give a brown semi-solid material which was purified by flash chromatography on silica gel using 5% methanol in dichloromethane for the elution. There was obtained 0.234 g of 1-[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4-(tert.butoxycarbonyl)-N-tert.butyl-2(R or S)-piperazinecarboxamide as a mixture of diastereomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05652369
出典データセットuspto-grants-1997_07
ORD IDord-96f3d5b06688444f9955b08e0f63c379
出典メモuspto-grants-1997_07