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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31537생성일: 2026년 10월 26일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-(tert-Butoxycarbonyl-{4-[tert-butoxycarbonyl-(2-octadec-8-enyloxycarbonyl-ethyl)-amino]-butyl}-amino)-propionic acid octadec-8-enyl ester

https://huagongshe.com/reaction/31537

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물2-DimethylaminopyridineHCID 21885—
반응물Oleyl AlcoholHCID 5284499—
반응물N,N'-Bis-(2-carbethoxyethyl)-N,N'-bis-(tert-butoxycarbonyl)-1,4-diaminobutaneHCID 86618851—
용매DichloromethaneHCID 6344—
생성물3-(tert-Butoxycarbonyl-{4-[tert-butoxycarbonyl-(2-octadec-8-enyloxycarbonyl-ethyl)-amino]-butyl}-amino)-propionic acid octadec-8-enyl esterHCID 8661885099.5%

반응 단계

To a solution of the N-protected amino acid 4 (n=4; 15.2 g, 35.1 mmol), dimethylaminopyridine (1.70 g, 14.0 mmol) and oleyl alcohol (18.4 g, 68.4 mmol) in dichloromethane (200 mL) was added a solution of EDCI (13.1 g, 68.4 mmol), in dichloromethane (50 mL) at 0° C. The resulting mixture was allowed to warm to room temperature and then stirred under N2 for 18 h. Dichloromethane (250 mL) was added and the mixture was washed with brine (4×200 mL), dried (Na2SO4) and concentrated in vacuo to leave an oil which was purified by column chromatography eluting with a solvent gradient of CH2Cl2 (50-90%) in hexane to afford the ester 5 as a colourless oil (13.0 g, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425645B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-4f0683b1699744fda12b8eda8e175f72
출처 메모uspto-grants-2008_09