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HRID 721554作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
反応物TriethylamineHCID 8471—
反応物TriphosgeneHCID 94429—
反応物2-Chloro-4-((6,7-dimethoxyquinazolin-4-yl)oxy)anilineHCID 21889899—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[2-(diisopropylamino)ethyl]ureaHCID 2188992343%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135466B2
出典データセットuspto-grants-2006_11
ORD IDord-a7d2937793e145159f0cb275d2a99639
出典メモuspto-grants-2006_11