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HRID 49088作成日:2026年10月24日

Piperidine → 2-Oxo-3-[5-(2-pyrrolidin-1-yl-ethoxy)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-sulfonic acid amide

https://huagongshe.com/ja/reaction/49088

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物2-Oxoindoline-5-sulfonamideHCID 10198232—
反応物5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehydeHCID 22042092—
溶媒EthanolHCID 702—
生成物2-Oxo-3-[5-(2-pyrrolidin-1-yl-ethoxy)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-sulfonic acid amideHCID 6934408380%

反応条件

温度90 °C

反応手順

A mixture of 2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide (28 mg, 0.13 mmol), 5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde (34 mg, 0.13 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated at 90° C. for 2 hours. The reaction was cooled at 0° C. for overnight. The precipitate was collected by vacuum filtration, washed with cold ethanol and dried to give 47 mg (80%) of the title compound as an orange solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706709B2
出典データセットuspto-grants-2004_03
ORD IDord-22473575d84e496bb2a3edaf31178be3
出典メモuspto-grants-2004_03