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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1731972생성일: 2026년 10월 25일

Water → Nepsilon-tert.butoxycarbonyl-L-lysyl-L-proline isobutylamide

https://huagongshe.com/reaction/1731972

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzyl chloroformateHCID 10387—
반응물Potassium BicarbonateHCID 516893—
반응물2-(Adamantan-1-yl)acetaldehydeHCID 5086084—
반응물Nalpha-benzyloxycarbonyl-Nepsilon-tert.butoxycarbonyl-L-lysyl-L-proline isobutylamideHCID 131714979—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매Diethyl EtherHCID 3283—
용매Ethyl acetate hexaneHCID 21226206—
생성물Nepsilon-tert.butoxycarbonyl-L-lysyl-L-proline isobutylamideHCID 131714978—

반응 단계

A solution of 6.3 g (0.012 mol) of Nα -benzyloxycarbonyl-Nε -tert.butoxycarbonyl-L-lysyl-L-proline isobutylamide in 100 ml of methanol was hydrogenated for 3 hours in the presence of 0.6 g of 5% palladium/carbon. A solution of 2.2 g (0.012 mol) of adamantane acetaldehyde in 5 ml of methanol was added via a septum cap and the hydrogenation was continued for 16 hours. The catalyst was removed by filtration and the filtrate was evaporated. A solution of the residue in 70 ml of diethyl ether was treated with 60 ml of water containing 2.5 g (0.025 mol) of potassium bicarbonate. 1.85 ml (0.023 mol) of benzyl chloroformate were added and the mixture was stirred vigorously for 1 hour. The organic solution was separated washed with 5% citric acid solution, water, 5% sodium bicarbonate solution and brine, dried over magnesium sulphate and evaporated to give a foam. Chromatography on 150 g of silica gel using n-hexane/ethyl acetate (2:1) yielded 4.4 g (53%) of Nα -(1-adamantylethyl)-Nα -benzyloxycarbonyl)-Nε -tert.butoxycarbonyl-L-lysyl-L-proline isobutylamide as a foam; Rf-value [n-hexane/ethyl acetate (2:1)]: 0.49.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04623639
출처 데이터셋uspto-grants-1986_11
ORD IDord-7638ecf506864237bda42bc09cddc02d
출처 메모uspto-grants-1986_11