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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986315생성일: 2026년 10월 26일

Nalpha-benzyloxycarbonyl-Nepsilon-tert.-butoxycarbonyl-L-lysine-3-{2-[2-(2,6-dichlorophenylamino)-phenyl]-acetylamino}-2-hydroxypropylamide → Nepsilon-tert.-butoxycarbonyl-L-lysine-3-{2-[2-(2,6-dichlorophenylamino)-phenyl]-acetylamino}-2hydroxypropylamide

https://huagongshe.com/reaction/986315

반응식

참여 물질

역할이름HCID투입량
반응물Nalpha-benzyloxycarbonyl-Nepsilon-tert.-butoxycarbonyl-L-lysine-3-{2-[2-(2,6-dichlorophenylamino)-phenyl]-acetylamino}-2-hydroxypropylamideHCID 13772485—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매dimethoxyethane N,N-dimethylformamideHCID 18463208—
생성물Nepsilon-tert.-butoxycarbonyl-L-lysine-3-{2-[2-(2,6-dichlorophenylamino)-phenyl]-acetylamino}-2hydroxypropylamideHCID 13772487—

반응 단계

1.80 g (2.46 mmol) of Nα -benzyloxycarbonyl-Nε -tert.-butoxycarbonyl-L-lysine-3-{2-[2-(2,6-dichlorophenylamino)-phenyl]-acetylamino}-2-hydroxypropylamide are dissolved in 100 ml of 1,2-dimethoxyethane/dimethylformamide (9:1) and after the addition of 0.40 g of palladium-on-carbon (10%) the whole is treated for 11/4 hours with hydrogen. The catalyst is filtered off, the filtrate is concentrated by evaporation at 30° in a rotary evaporator and the residue is lyophilised after being taken up in 100 ml of dioxan/water (7:3). Nε -tert.-butoxycarbonyl-L-lysine-3-{2-[2-(2,6-dichlorophenylamino)-phenyl]-acetylamino}-2hydroxypropylamide is obtained in the form of a colourless powder which is immediately processed further; Rf =0.52 (acetonitrile:water=3:1), Rf =0.66 (ethyl acetate:n-butanol:pyridine:acetic acid:water=42:21:21:6:10).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04711879
출처 데이터셋uspto-grants-1987_12
ORD IDord-87e05433a8e54a0186dcfb21f9f5cae6
출처 메모uspto-grants-1987_12