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HRID 83538作成日:2026年10月26日

8-Hydroxyquinoline → 3-(2,5-Dimethylpyrrol-1-yl)-1-(2-fluorophenyl)-1H-pyrazole

https://huagongshe.com/reaction/83538

反応式

関与物質

役割名称HCID仕込み量
反応物8-HydroxyquinolineHCID 1923—
反応物Cesium carbonateHCID 10796—
反応物1-Fluoro-2-iodobenzeneHCID 67673—
反応物HCID 178425430HCID 178425430—
触媒HCID 178419072HCID 178419072—
溶媒TolueneHCID 1140—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物3-(2,5-Dimethylpyrrol-1-yl)-1-(2-fluorophenyl)-1H-pyrazoleHCID 86680371—

反応条件

温度110 °C

反応手順

To a solution of 3-(2,5-dimethylpyrrol-1-yl)-1H-pyrazole (1.00 g) prepared according to the same procedures as Preparation 4 in N-methylpyrrolidone (10 ml) were sequentially added 1-fluoro-2-iodobenzene (1.08 ml), copper (I) oxide (89 mg), 8-quinolinol (180 mg) and cesium carbonate (4.04 g) at room temperature, and the mixture was stirred at 110° C. for 3 hours. This reaction mixture was cooled to room temperature, and then toluene was added thereto, and the mixture was filtered through Celite. The filtrate was sequentially washed with a 2N aqueous solution of sodium hydroxide, water and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/0 to 10/1) to give the titled compound (1.19 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846746B2
出典データセットuspto-grants-2014_09
ORD IDord-a21e600cd7d34c8eafc6b8fb94ebf901
出典メモuspto-grants-2014_09