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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 249571생성일: 2026년 10월 23일

4-Methylmorpholine → Nalpha [S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteinyl]-Nepsilon-t-butoxycarbonyl-L-lysine methyl ester

https://huagongshe.com/ko/reaction/249571

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(S)-Methyl 2-amino-6-((tert-butoxycarbonyl)amino)hexanoateHCID 7018776—
반응물S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteineHCID 14969990—
용매BenzeneHCID 241—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Nalpha [S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteinyl]-Nepsilon-t-butoxycarbonyl-L-lysine methyl esterHCID 8674687761.1%

반응 단계

To a stirred solution of S-benzyl-N-(3-benzylthio-2,2-dimethylpropionyl)-L-cysteine (4.01 g), Nε -t-butoxycarbonyl-L-lysine methyl ester (2.08 g) and NMM (1.1 ml) in DMF (20 ml), HOBt (2.16 g) and then a solution of DCC (1.82 g) in DMF (10 ml) were added slowly under ice cooling. The mixture was stirred for 1 hr. under ice cooling and for 18 hr. at room temperature. After an addition of a mixture of ethyl acetate and benzene (2:1, 500 ml), the mixture was washed with 10% citric acid solution, water, saturated sodium bicarbonate solution, water and then saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The oily residue was purified by a silica gel column chromatography to give 3.22 g (61%) of the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05214181
출처 데이터셋uspto-grants-1993_05
ORD IDord-16f92afb86334198936b5dba7e08f801
출처 메모uspto-grants-1993_05