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HRID 341229作成日:2026年10月25日

Potassium Carbonate → 7-(4-Fluoro-phenyl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/341229

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-Fluorophenylboronic acidHCID 285645—
反応物7-Chloroimidazo(1,2-a)pyridineHCID 19695901—
溶媒Toluene-methanol ethanol waterHCID 68594318—
生成物7-(4-Fluoro-phenyl)-imidazo[1,2-a]pyridineHCID 5932079983%

反応条件

温度80 °C

反応手順

A mixture of 7-chloro-imidazo[1,2-a]pyridine (15.0 g, 98.6 mmol), 4-fluorophenylboronic acid (16.55 g, 118.3 mmol), potassium carbonate (81.5 g, 590 mmol) in toluene-methanol-ethanol-water (1:1:1:1, 800 mL) was degassed with N2 and then bis(tri-tert-butylphosphine)palladium(0) (400 mg) added. The mixture was degassed and then heated to 80° C. for 18 h. The mixture was cooled to ambient, transferred to a separating funnel and the layers separated. The organic portion was reduced under reduced pressure and the residue extracted with dichloromethane. The dichloromethane extracts were washed with water, dried (MgSO4), filtered and concentrated under reduced pressure to afford 17.3 g (83%) of the title compound. 1H NMR (400 MHz, CDCl3) δ 8.22 (1H, d), 7.87 (1H, s), 7.71 (1H, s), 7.69-7.58 (3H, m), 7.20 (2H, t), 7.11 (1H, d).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895745B2
出典データセットuspto-grants-2014_11
ORD IDord-965f4eff0732487dbdf7d17a47502445
出典メモuspto-grants-2014_11