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HRID 598036作成日:2026年10月26日

Triethylamine → 1-{[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanol

https://huagongshe.com/reaction/598036

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-(Aminomethyl)cyclopentan-1-olHCID 13051202—
反応物7-Bromo-4-chloro-3-nitro[1,5]naphthyridineHCID 57457837—
溶媒ChloroformHCID 6212—
生成物1-{[(7-Bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanolHCID 67052453—

反応条件

温度0 °C

反応手順

A suspension of 7-bromo-4-chloro-3-nitro[1,5]naphthyridine (54.42 g, 188.6 mmol) in chloroform (820 mL) was cooled to 0° C., and triethylamine (105 mL, 755 mmol) was added. A solution of 1-(aminomethyl)cyclopentanol (28.25 g, 245.2 mmol) in chloroform (272 mL) was added slowly over a period of 15 minutes. The reaction was allowed to warm to room temperature and stirred for 30 minutes. The solution was washed sequentially with water (500 mL) and saturated aqueous sodium bicarbonate (750 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 1-{[(7-bromo-3-nitro[1,5]naphthyridin-4-yl)amino]methyl}cyclopentanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07897609B2
出典データセットuspto-grants-2011_03
ORD IDord-c3aa6b0b83bb485ca8fb2bfacae7a3f6
出典メモuspto-grants-2011_03