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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1320생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1320

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Cesium carbonateHCID 10796—
반응물Methanol--water (1/1)HCID 22242641—
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 (4.28 g., 13.1 moles) was added to a mixture of N2 -[(1,1-dimethylethoxy)carbonyl]-N6 -[(phenylmethoxy)carbonyl]-L-lysine (10 g., 26.3 moles) and 20% water-methanol (60 ml.). The solution became homogeneous within 5 minutes so the solvent was stripped and the residual water removed azeotropically with acetonitrile (3×). The resulting oil was dried in vacuo, dissolved in dry dimethyl-formamide and treated with methyl iodide (3.2 ml., 2.0 eq.). The reaction mixture was stirred at room temperature for 1.5 hours under argon, diluted with ethyl acetate (200 ml.) and washed successively with water (2×25 ml.), saturated sodium bicarbonate (25 ml.) and brine (25 ml.). The organic phase was dried (anhydrous magnesium sulfate), filtered, evaporated to dryness and dried in vacuo to give 10.11 g., of product as a light yellow syrup; Rf =0.30 (ethyl acetate:hexanes, 1:2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723602
출처 데이터셋uspto-grants-1998_03
ORD IDord-a5a96d1b986849b2b488b84cd2b4e308
출처 메모uspto-grants-1998_03