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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721555생성일: 2026년 10월 26일

1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → N-[2-(Diisopropylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}urea

https://huagongshe.com/reaction/721555

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroanilineHCID 21890730—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물N-[2-(Diisopropylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}ureaHCID 2189039570%

반응 단계

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroaniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (131 mg) in chloroform was then added to the solution, and the mixture was stirred at room temperature for 10 min. Next, N1,N1-diisopropyl-1,2-ethanediamine (63 mg) was added thereto, and the mixture was further stirred at room temperature for one hr. Water was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by concentration. The residue was purified on a column using chloroform/methanol to give the title compound (103 mg, yield 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-2ed5e4946b954909a33a62e6cee1d9b7
출처 메모uspto-grants-2006_11