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HRID 24477作成日:2026年10月24日

Piperidine → 5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one

https://huagongshe.com/ja/reaction/24477

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物3-Methyl-1H-indole-2-carbaldehydeHCID 277260—
反応物5-Methylindolin-2-oneHCID 5325716—
溶媒EthanolHCID 702—
生成物5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-oneHCID 5375537874%

反応手順

A mixture of 5-methyl-2-oxindole (59 mg), 3-methylindole-2-carbaldehyde (56 mg) and piperidine (30 mg) in ethanol(1 mL) was held in a sealed tube at 90° C. overnight. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in a vacuum oven to give 72 mg (74%) of 5-methyl-3-(3-methyl-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855730B2
出典データセットuspto-grants-2005_02
ORD IDord-6971769eafbc44aa928743994cee0fcd
出典メモuspto-grants-2005_02