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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 529217생성일: 2026년 10월 26일

Diisopropylethylamine → N-{N-[(5-tert-butoxycarbonylthiophen-2-yl)methyl]-N-methyl-L-leucyl}-L-aspartic acid dimethyl ester

https://huagongshe.com/reaction/529217

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물L-Aspartic acid, 1,4-dimethyl ester, hydrochloride (1:1)HCID 2734892—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물N-[(5-tert-butoxycarbonylthiophen-2-yl)methyl]-N-methyl-L-leucine lithium saltHCID 90107093—
용매DichloromethaneHCID 6344—
생성물N-{N-[(5-tert-butoxycarbonylthiophen-2-yl)methyl]-N-methyl-L-leucyl}-L-aspartic acid dimethyl esterHCID 8671469953.4%

반응 단계

The compound (0.20 g, 0.58 mmol) obtained in step 2, aspartic acid dimethyl ester hydrochloride (0.12 g, 0.58 mmol), WSC hydrochloride (0.17 g, 0.87 mmol), 1-hydroxybenzotriazole monohydrate (0.090 g, 0.58 mmol), and N,N-diisopropylethylamine (0.39 mL, 2.8 mmol) were dissolved in dichloromethane (5 mL), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, and ethyl acetate was added. The mixture was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (0.15 g, 0.31 mmol, 53%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346821B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-980ce20558f64a81a5fdc025a3bf6337
출처 메모uspto-grants-2016_05