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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1865713생성일: 2026년 10월 24일

2-Dimethylaminopyridine → N,beta,beta-trimethyl-L-phenylalanyl-N1-((1R,2E)-4-{[4-(benzyloxy)benzyl]oxy}-1-isopropyl-3-methyl-4-oxobut-2-enyl)-N1,3-dimethyl-L-valinamide

https://huagongshe.com/ko/reaction/1865713

반응식

참여 물질

역할이름HCID투입량
반응물2-DimethylaminopyridineHCID 21885—
반응물(4-(Benzyloxy)phenyl)methanolHCID 70043—
반응물N,beta,beta-Trimethyl-L-phenylalanyl-N-((1S,2E)-3-carboxy-1-(1-methylethyl)-2-buten-1-yl)-N,3-dimethyl-L-valinamideHCID 6918637—
용매DichloromethaneHCID 6344—
생성물N,beta,beta-trimethyl-L-phenylalanyl-N1-((1R,2E)-4-{[4-(benzyloxy)benzyl]oxy}-1-isopropyl-3-methyl-4-oxobut-2-enyl)-N1,3-dimethyl-L-valinamideHCID 11671966—

반응 단계

A mixture of N,β,β-trimethyl-L-phenylalanyl-N1-[(1S,2E)-3-carboxy-1-isopropylbut-2-enyl]-N1,3-dimethyl-L-valinamide (287 mg, 0.607 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimine hydrochloride (0.728 mmol), 4-(benzyloxy)benzyl alcohol (137 mg, 0.638 mmol) and dimethylaminopyridine (0.12 mmol) in anhydrous dichloromethane (12 mL) are stirred under a nitrogen atmosphere at room temperature for 20 hours. The solvent is removed, the residue taken up in methanol, and the product purified by reverse phase HPLC (0.01% trifluoroacetic acid in water/acetonitrile) to give the title compound as a white gum, 208 mg, MS: m/z 670.4 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07626023B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-68705f8c46f54ceba22302f2d5bc0406
출처 메모uspto-grants-2009_12