戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 32429作成日:2026年10月25日

2-Chloroethanol → 3-Chloro-N-[1-(2-chlorophenyl)-2-[1-(2-hydroxyethyl)-piperidin-4-ylmethoxy]ethyl]-1H-indole-6-carboxamide

https://huagongshe.com/reaction/32429

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChloroethanolHCID 34—
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物3-chloro-N-[1-(2-chlorophenyl)-2-(piperidin-4-ylmethoxy)ethyl]-1H-indole-6-carboxamideHCID 69307888—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物3-Chloro-N-[1-(2-chlorophenyl)-2-[1-(2-hydroxyethyl)-piperidin-4-ylmethoxy]ethyl]-1H-indole-6-carboxamideHCID 6931055932%

反応手順

To a solution of 3-chloro-N-[1-(2-chlorophenyl)-2-(piperidin-4-ylmethoxy)ethyl]-1H-indole-6-carboxamide (200 mg, 0.45 mmol) in 5 mL of EtOH was added potassium carbonate (247 mg, 1.8 mmol), potassium iodide (224 mg, 1.4 mmol) and 2-chloroethanol (0.09 mL, 1.4 mmol). The reaction was allowed to stir at room temperature overnight after which time water was added and the resulting precipitate was isolated by filtration. Purification of the filtrate (SiO2: 10:0.5 EtOAc:isopropylamine) provided 70 mg (32%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427632B2
出典データセットuspto-grants-2008_09
ORD IDord-820aeae5bdb84ba49a24b28cd989f7d3
出典メモuspto-grants-2008_09