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HRID 24481作成日:2026年10月24日

Piperidine → HCID 53888754、化合物

https://huagongshe.com/ja/reaction/24481

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2-Oxo-2,3-dihydro-1H-indole-5-sulfonic acid dimethylamideHCID 9816185—
溶媒EthanolHCID 702—
生成物HCID 53888754HCID 5388875457%

反応手順

A mixture of 5-dimethylaminosulfonyl-2-oxindole (96 mg), 3-methylindole-2-carbaldehyde (56 mg) (prepared according to Synthetic Communications, 1986, 16, 1799) 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 76 mg (57% yield) of 3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid dimethylamide (mixture of isomers).

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-c2dc38cd3e5f41908283bfed9b702586
出典メモuspto-grants-2005_02