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HRID 1243437作成日:2026年10月26日

Piperidine → 3-[4-Methyl-5-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrol-3-yl]-propionic acid

https://huagongshe.com/reaction/1243437

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物5-Methylindolin-2-oneHCID 5325716—
反応物3-(5-formyl-4-methyl-1H-pyrrol-3-yl)propanoic acidHCID 15160752—
溶媒EthanolHCID 702—
生成物3-[4-Methyl-5-(5-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrol-3-yl]-propionic acidHCID 5367751742.2%

反応手順

4-(2-Carboxyethyl)-2-formyl-3-methylpyrrole (90 mg), 74 mg 5-methyl-2-oxindole and 75 μL piperidine in 2 mL of ethanol were heated at 95° C. for 5 hours. The reaction mixture was cooled and concentrated. The residue was suspended in 6 N aqueous hydrochloric acid. The precipitate was filtered, washed with water to pH 6 and dried in a vacuum oven to give 65 mg (42%) of the title compound as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119090B2
出典データセットuspto-grants-2006_10
ORD IDord-757fc7a727d24fed9fbc5ff0b4120422
出典メモuspto-grants-2006_10