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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1085078생성일: 2026년 10월 26일

Dicyclohexylcarbodiimide → Nalpha-Benzyloxycarbonyl-Nepsilon-(tert.-butyloxycarbo nylglycyl)-L-lysine

https://huagongshe.com/reaction/1085078

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물N-alpha-Benzyloxycarbonyl-L-lysineHCID 75172—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물N-(tert-butoxycarbonyl)glycineHCID 78288—
용매TriethylamineHCID 8471—
용매tetrahydrofuran N,N-dimethylformamideHCID 21974620—
생성물Nalpha-Benzyloxycarbonyl-Nepsilon-(tert.-butyloxycarbo nylglycyl)-L-lysineHCID 86744723—

반응 단계

9 g of Nα -benzyloxycarbonyl-L-lysine, 5.6 g of tert.-butyloxycarbonylglycine, 3.2 g of triethylamine, 4.9 g of 1-hydroxybenzotriazole and 7.9 g of N,N'-dicyclohexylcarbodiimide are stirred in 100 ml of THF/DMF (7:3) for 1 hour at 0° C. and over night at ambient temperature. After the urea has been filtered off the mixture is concentrated by evaporation, the residue is taken up in ethyl acetate, extracted with saturated KHSO4 solution, washed with water, dried over MgSO4 and concentrated by evaporation in vacuo. The residue is chromatographed over silica gel with methylene chloride/ethyl acetate/methanol (10:1:1). 12.5 g (100% of theory) are obtained in the form of a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05008273
출처 데이터셋uspto-grants-1991_04
ORD IDord-a65e03c9bb7f4545a9f237ad60342ef3
출처 메모uspto-grants-1991_04