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HRID 721563作成日:2026年10月25日

Triethylamine → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}-N'-[2-(ethyl-3-methylanilino)ethyl]urea

https://huagongshe.com/reaction/721563

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,2-Ethanediamine, N1-ethyl-N1-(3-methylphenyl)-HCID 87984—
反応物TriphosgeneHCID 94429—
反応物4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroanilineHCID 21890730—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}-N'-[2-(ethyl-3-methylanilino)ethyl]ureaHCID 2189076464%

反応手順

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-ethyl-N1-(3-methylphenyl)-1,2-ethanediamine (78 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 (101 mg, yield 64%).

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-fba1e5e55ac34f098ec241ec270dd092
出典メモuspto-grants-2006_11