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HRID 721579作成日:2026年10月26日

Triethylamine → N-[2-(Dibutylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}urea

https://huagongshe.com/reaction/721579

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N,N-DibutylethylenediamineHCID 77062—
反応物TriphosgeneHCID 94429—
反応物4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物N-[2-(Dibutylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}ureaHCID 2189080343.1%

反応手順

4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (151 mg) in chloroform was then added to the solution, and the mixture was stirred at room temperature for 10 min. Next, N1,N1-dibutyl-1,2-ethanediamine (88 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 (72 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-bfee4618b2194ed7ace30b129b2ecf10
出典メモuspto-grants-2006_11