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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484758생성일: 2026년 10월 25일

Methanol → N2 [(1,1-Dimethylethoxy)carbonyl]-N6-[(phenylmethoxy)carbonyl]-L-lysine, methyl ester

https://huagongshe.com/reaction/484758

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Methyl iodideHCID 6328—
반응물Cesium carbonateHCID 10796—
반응물N2 [(1,1-dimethylethoxy)carbonyl]-N6-[(phenylmethoxy)carbonyl]-L-lysineHCID 86742311—
용매Ethyl AcetateHCID 8857—
생성물N2 [(1,1-Dimethylethoxy)carbonyl]-N6-[(phenylmethoxy)carbonyl]-L-lysine, methyl esterHCID 131714291—

반응 단계

Cesium carbonate (2.14 g., 6.55 mmole) is added to a mixture of N2 -[(1,1-dimethylethoxy)carbonyl]-N6 -[(phenylmethoxy)carbonyl]-L-lysine (5.0 g., 13.10 mmole) and 20% aqueous methanol (30 ml.). The solution becomes homogeneous after 5 minutes, the methanol is stripped, and the residual water is removed azetropically with acetonitrile (twice). The resulting oil is taken up in dry methylene chloride (10 ml.) and treated with methyl iodide (1.6 ml., 2.0 eq.) at 25° in an argon atmosphere. After 4 hours the reaction mixture is taken up in ethyl acetate and washed successively with water, saturated sodium bicarbonate and brine, dried (MgSO4), and evaporated. The residue (4.7 g.) is chromatographed on silica (160 g.) eluting with hexane/ethyl acetate (3:1) to give 4.0 g. of N2 -[(1,1-dimethylethoxy)carbonyl]-N6 -[(phenylmethoxy)carbonyl]-L-lysine, methyl ester as an oil after evaporation. TLC (hexane/ethyl acetate; 2:1) major spot at Rf =0.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533661
출처 데이터셋uspto-grants-1985_08
ORD IDord-07fbc4c8362c439f8c44466c7c1c52f8
출처 메모uspto-grants-1985_08