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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 721554생성일: 2026년 10월 26일

1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[2-(diisopropylamino)ethyl]urea

https://huagongshe.com/reaction/721554

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
반응물TriethylamineHCID 8471—
반응물TriphosgeneHCID 94429—
반응물2-Chloro-4-((6,7-dimethoxyquinazolin-4-yl)oxy)anilineHCID 21889899—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[2-(diisopropylamino)ethyl]ureaHCID 2188992343%

반응 단계

2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-aniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (134 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 (65 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 (64 mg, yield 43%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135466B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-a7d2937793e145159f0cb275d2a99639
출처 메모uspto-grants-2006_11