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HRID 731140作成日:2026年10月25日

5-fluoro-1,3-dihydro-2H-indol-2-one → 5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid

https://huagongshe.com/reaction/731140

反応式

関与物質

役割名称HCID仕込み量
反応物5-fluoro-1,3-dihydro-2H-indol-2-oneHCID 3731012—
反応物5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic AcidHCID 11073792—
触媒PiperidineHCID 8082—
溶媒EthanolHCID 702—
生成物5-(5-Fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acidHCID 53395102101.4%

反応条件

温度60 °C

反応手順

The reaction mixture of 5-fluorooxindole (100 mg, 0.66 mmol), 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (133 mg, 0.79 mmol), and 10 drops of piperidine in ethanol (3 mL) was stirred at 60° C. overnight and filtered. The solid washed with 1 M of aqueous hydrochloride solution, water, and dried to afford 5-(5-fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (201 mg, quantitative) as a yellow solid. MS m/z (relative intensity, %) 299 ([M−1]+., 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582756B2
出典データセットuspto-grants-2009_09
ORD IDord-2789bc4114c74925a27d432d038a0eb3
出典メモuspto-grants-2009_09