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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243598생성일: 2026년 10월 25일

Diethylamine → methyl(2S)-3,3-dimethyl-2-{3-[(1-methyl-1H-benzimidazol-2-yl)methyl]-2-oxoimidazolidin-1-yl}butanoate

https://huagongshe.com/reaction/243598

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물Bis(4-nitrophenyl) carbonateHCID 78756—
반응물methyl(2S)-2-[(2-{[(9H-fluoren-9-ylmethoxy)Carbonyl][(1-methyl-1H-benzimidazol-2-yl)methyl]amino}ethyl)amino]-3,3-dimethylbutanoateHCID 66891668—
용매DimethylformamideHCID 6228—
용매1,1-DichloroethaneHCID 6365—
생성물methyl(2S)-3,3-dimethyl-2-{3-[(1-methyl-1H-benzimidazol-2-yl)methyl]-2-oxoimidazolidin-1-yl}butanoateHCID 6689062965.2%

반응 조건

온도25 °C

반응 단계

A solution of the product of Example 148D (0.19 g) in N,N-dimethylformamide (3.5 mL) was treated with diethylamine (0.35 mL), stirred at 25° C. for 1.5 hours and concentrated. A solution of the residue in dichloroethane (7 mL) was treated with bis-(p-nitrophenyl) carbonate (0.128 g, 1.2 equivalents), stirred at 60° C. for 16 hours and concentrated. The residue was chromatographed on silica gel, eluting with ethyl acetate:dichloromethane (3:2) to give 80 mg (64%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653141B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f275c48d35fd4f29a700320587dd4070
출처 메모uspto-grants-2014_02