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HRID 628792作成日:2026年10月24日

Indole-5-carbonitrile → 3-(4-hydroxybutanoyl)-1H-indole-5-carbonitrile

https://huagongshe.com/ja/reaction/628792

反応式

関与物質

役割名称HCID仕込み量
反応物Indole-5-carbonitrileHCID 27513—
反応物4-Chlorobutyryl chlorideHCID 78370—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物3-(4-Hydroxybutyl)-1H-indole-5-carbonitrileHCID 12150985—
生成物3-(4-hydroxybutanoyl)-1H-indole-5-carbonitrileHCID 72710223—

反応手順

The present inventors have further surprisingly and unexpectedly found that 3-(4-hydroxybutyl)-1H-indole-5-carbonitrile intermediate can be prepared, in high purity and with high yield, by reacting 5-cyanoindole with 4-chlorobutyryl chloride in the presence of aluminium chloride to produce an intermediate compound, followed by reacting the compound with an aqueous alcohol to produce 3-(4-hydroxybutyryl)-1H-indole-5-carbonitrile, which is then reduced with sodium cyanoborohydride in the presence of hydrochloric acid and water in acetonitrile solvent to produce 3-(4-hydroxybutyl)-1H-indole-5-carbonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315456B2
出典データセットuspto-grants-2016_04
ORD IDord-710fbf00b52a4cb6b7e7a7fd84c93967
出典メモuspto-grants-2016_04