戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 9502作成日:2026年10月24日

Ethoxyacetyl chloride → 1-[2-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-3-(2-methylethyl)urea

https://huagongshe.com/ja/reaction/9502

反応式

関与物質

役割名称HCID仕込み量
反応物Ethoxyacetyl chlorideHCID 84189—
反応物1-[2-(3-Amino-7-bromoquinolin-4-ylamino)ethyl]-3-(2-methylethyl)ureaHCID 21984426—
溶媒PyridineHCID 1049—
生成物1-[2-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-3-(2-methylethyl)ureaHCID 21984285—

反応条件

温度80 °C

反応手順

To a stirred solution of 1-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]-3-(2-methylethyl)urea (27.2 g, 0.0743 mol) in 600 mL pyridine was slowly added ethoxyacetyl chloride (1.1 equivalents). After 1.5 hours the mixture was yellow and turbid. The reaction mixture was then heated at 80° C. for 12 hours and then concentrated under reduced pressure. The residue was dissolved in water and saturated aqueous potassium carbonate and stirred vigorously for three hours. A precipitate was present, was isolated by filtration, and air-dried for 48 hours to provide 32 g of 1-[2-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-3-(2-methylethyl)urea.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091214B2
出典データセットuspto-grants-2006_08
ORD IDord-9312b9100a3448fd880c4a1e4f95c690
出典メモuspto-grants-2006_08