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HRID 397516作成日:2026年10月25日

1H-1,2,4-Triazole → 3-[1,2,4]Triazol-1-yl-pyridine-2-carbonitrile

https://huagongshe.com/reaction/397516

反応式

関与物質

役割名称HCID仕込み量
反応物1H-1,2,4-TriazoleHCID 9257—
反応物Cesium carbonateHCID 10796—
反応物2-Cyano-3-fluoropyridineHCID 7060408—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-[1,2,4]Triazol-1-yl-pyridine-2-carbonitrileHCID 21866301—

反応条件

温度65 °C

反応手順

To a solution of 2-cyano-3-fluoro-pyridine (2.99 g, 24.49 mmol) in DMF (30 ml) is added cesium carbonate (2.03 g, 29.39 mmol) and 1,2,4-triazole (2.03 g, 29.39 mmol) and the reaction mixture is stirred at 65° C. for 4 h. After cooling to room temperature, the mixture is diluted with water and extracted with EtOAc 3 times. The aqueous layer is saturated with LiCl and further extracted with EtOAc. The combined organic layer is dried on sodium sulfate, concentrated in vacuo. The crude product is purified by flash chromatography (silica gel, 2% MeOH containing 10% NH4OH in CH2Cl2 to 6%) to give 3-[1,2,4]Triazol-1-yl-pyridine-2-carbonitrile. 1H NMR (CDCl3, 400 MHz) δ8.95 (s, 1H); 8.8 (d, J=4 Hz, 1H); 8.24 (s, 1H); 8.22 (d, J=8.5 Hz, 1H); 7.75 (dd, J=4, 8.5 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610701B2
出典データセットuspto-grants-2003_08
ORD IDord-f16af703873c4c6dba395327c641ea2f
出典メモuspto-grants-2003_08