戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 8365作成日:2026年10月23日

2-Amino-4-methylpyridine → 2-(4'-Chloropropoxy-2'fluorophenyl)-7-methylimidazo[1,2-a]pyridine

https://huagongshe.com/ja/reaction/8365

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-methylpyridineHCID 1533—
反応物alpha-Bromo-2'-fluoro-4'-chloropropoxyacetophenoneHCID 22015593—
溶媒EthanolHCID 702—
生成物2-(4'-Chloropropoxy-2'fluorophenyl)-7-methylimidazo[1,2-a]pyridineHCID 22015617—

反応手順

A solution of the product of Step B (1.0 g) and 2-amino-4-picoline (0.357 g) in ethanol (4 mL) was heated at 73° C. for 18 hours. The reaction mixture was cooled to ambient temperature and the solvent evaporated in vacuo. A portion of the residue was purified via silica gel chromatography (ethyl acetate/hexane) directly. The remainder of the residue was dissolved in methanol/dichloromethane and treated with Dowex® 550A basic resin (Aldrich, Milwaukee, Wis.) for 10 minutes. The resin was removed via filtration and the filtrate evaporated prior to silica gel chromatography (ethyl acetate/hexane). The combined material (0.42 g) containing the title compound was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087757B2
出典データセットuspto-grants-2006_08
ORD IDord-95e42f03238643bf8dd17789479a8a05
出典メモuspto-grants-2006_08