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HRID 2099504作成日:2026年10月27日

Water → 3-(3-Pyridin-2-yl-pyrazol-1-yl)-benzonitrile

https://huagongshe.com/reaction/2099504

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物3-FluorobenzonitrileHCID 67880—
反応物2-(1H-Pyrazol-3-Yl)PyridineHCID 2797657—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-(3-Pyridin-2-yl-pyrazol-1-yl)-benzonitrileHCID 10192768—

反応条件

温度145 °C

反応手順

2-(1H-Pyrazol-3-yl)pyridine (435 mg, 3 mmol), 3-fluorobenzonitrile (0.32 mL, 3 mmol) and K2CO3 (830 mg, 6 mmol) were dissolved in DMF (10 mL) under Ar (g) and heated at 145° C. for 18 h. After cooling to ambient temperature, H2O (40 mL) and EtOAc (40 mL) were added and the reaction mixture shaken, the EtOAc layer was separated and the aqueous layer shaken with EtOAc (2×30 mL). The combined organic layers were washed with brine (3×40 mL), dried over Na2SO4 and concentrated onto silica gel. The crude material was purified by liquid chromatography on silica gel eluting with EtOAc:hexane (1:1) to afford a solid that was recrystallized from EtOAc-hexane to give 3-(3-pyridin-2-yl-1H-pyrazol-1-yl)benzonitrile as a solid. 1H NMR (CD3Cl, 300 MHz) δ 8.68-8.71 (1H, m), 8.18 (1H, m), 8.12-8.15 (1H, m), 8.02-8.06 (2H, m), 7.81 (1H, ddd), 7.60-7.62 (2H, m), 7.30 (1H, ddd), 7.20 (1H, d). MS (ESI) 247 (M+H)+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07569592B2
出典データセットuspto-grants-2009_08
ORD IDord-388019c2f29841dab091fc013b25a4f2
出典メモuspto-grants-2009_08