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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466876생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/466876

반응식

참여 물질

역할이름HCID투입량
반응물1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-N-tert.butyl-2-piperazinecarboxamideHCID 19031938—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물Tert-butyl 3-(tert-butylcarbamoyl)piperazine-1-carboxylateHCID 406301358.8%

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05157041
출처 데이터셋uspto-grants-1992_10
ORD IDord-f5b0257492ef4b688059ae3c703070be
출처 메모uspto-grants-1992_10