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HRID 44706作成日:2026年10月23日

Triethylamine → 1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclobutanol

https://huagongshe.com/ja/reaction/44706

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Chloro-3-nitroquinolineHCID 11275808—
反応物1-(Aminomethyl)cyclobutan-1-olHCID 28260009—
溶媒DichloromethaneHCID 6344—
生成物1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclobutanolHCID 57457811—

反応手順

To a solution of 1-(aminomethyl)cyclobutanol (62.5 mmol) in dichloromethane (312 mL) was added triethylamine (8.71 mL, 62.5 mmol) and 4-chloro-3-nitroquinoline (13.04 g, 62.5 mmol). More triethylamine (3 mL) was added almost immediately. The reaction was stirred under N2 for 10 d at rt, then was diluted with dichloromethane and washed with 1 M aqueous NaOH. A solid formed and was isolated by filtration. The organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated to a solid that was crystallized from isopropanol. The resulting crystals were combined with the solid that was isolated from the extraction and the mixture was triturated with hot isopropanol. The solid was isolated by filtration, washed with diethyl ether, and air dried to yield 1-{[(3-nitroquinolin-4-yl)amino]methyl}cyclobutanol as yellow crystals. (12.83 g, 75%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541438B2
出典データセットuspto-grants-2013_09
ORD IDord-220d0047b7ff4594bc9afa7e60146efa
出典メモuspto-grants-2013_09