戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2120195作成日:2026年10月27日

Piperidine → 3-(4-Methoxy-3-thiophen-2-yl-benzylidene)-6-pyridin-3-yl-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/2120195

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物6-Pyridin-3-yl-1,3-dihydro-indol-2-oneHCID 21915579—
反応物4-Methoxy-3-(thiophen-2-yl)benzaldehydeHCID 21981024—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物3-(4-Methoxy-3-thiophen-2-yl-benzylidene)-6-pyridin-3-yl-1,3-dihydroindol-2-oneHCID 6988369615%

反応手順

A mixture of 6-pyridin-3-yl-1,3-dihydro-indol-2-one (100 mg, 0.5 mmol), 4-methoxy-3-thiophen-2-yl-benzaldehyde (110 mg, 0.5 mmol) and piperidine (0.23 mL) in ethanol (4 mL) was heated to reflux and stirred overnight. The reaction mixture was then cooled and diluted with ether to afford a precipitate which removed by filtration. Thefiltrate was column chromatographed (eluant—isopropanol/dichloromethane) to give 30 mg (15%) of 3-(4-methoxy-3-thiophen-2-yl-benzylidene)-6-pyridin-3-yl-1,3-dihydroindol-2-one as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06689806B1
出典データセットuspto-grants-2004_02
ORD IDord-109e72eee4dd4152a9a69a299f59271f
出典メモuspto-grants-2004_02