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HRID 24489作成日:2026年10月24日

Indole-2-carboxaldehyde → 6-chloro-3-(1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one

https://huagongshe.com/ja/reaction/24489

反応式

関与物質

役割名称HCID仕込み量
反応物Indole-2-carboxaldehydeHCID 96389—
反応物6-Chloro-1,3-dihydroindol-2-oneHCID 736344—
触媒PiperidineHCID 8082—
溶媒EthanolHCID 702—
生成物6-chloro-3-(1H-indol-2-ylmethylene)-1,3-dihydroindol-2-oneHCID 5455349987%

反応手順

A mixture of 6-chloro-2-oxindole (41 mg) (commercially available), indole-2-carbaldehyde (42 mg) (prepared according to Synthetic Communications, 1993, 23, 3109) and piperidine (1 drop) in ethanol (3 mL) was held in a sealed tube at 95° C. for 3 hours. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in vacuum oven to give 62 mg (87% yield) of 6-chloro-3-(1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one as a shiny orange solid.

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-1e89f92e0b244e2aaec6e141d1a75b76
出典メモuspto-grants-2005_02