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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893494생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-[(7-fluoroimidazo[1,2-a]quinoxalin-4-yl)amino]propyl (2R)-2-[(tert-butoxycarbonyl)amino]propanoate

https://huagongshe.com/reaction/1893494

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물3-[(7-Fluoroimidazo[1,2-a]quinoxalin-4-yl)amino]propan-1-olHCID 4329362—
반응물N-[(1,1-Dimethylethoxy)carbonyl]-D-alanine 2,5-dioxo-1-pyrrolidinyl esterHCID 11580086—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-[(7-fluoroimidazo[1,2-a]quinoxalin-4-yl)amino]propyl (2R)-2-[(tert-butoxycarbonyl)amino]propanoateHCID 5933331412%

반응 조건

온도60 °C

반응 단계

To a solution of commercially available (Peakdale) 3-[(7-fluoroimidazo[1,2-a]quinoxalin-4-yl)amino]propan-1-ol (20 mg, 0.08 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (12 μL, 0.08 mmol) in anhydrous dimethylformamide (600 μL) under argon was added dropwise a solution of tert-butyl {(1R)-2-[(2,5-dioxopyrrolidin-1-yl)oxy]-1-methyl-2-oxoethyl}carbamate (22 mg, 0.08 mmol) in anhydrous dimethylformamide (200 μL). The mixture was stirred at 60° C. for 65 h, then diluted with cold water and extracted four times with chloroform and once with chloroform/isopropanol (5:1). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and evaporated. The crude product was purified by preparative TLC (silica, dichloromethane/methanol 20/1) to afford the title compound as a colorless oil (4 mg, 12%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513250B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-84aa437415f64c03aef66361a8453af1
출처 메모uspto-grants-2013_08