戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 912864作成日:2026年10月25日

Sodium Carbonate → 6-(3,4-difluorophenyl)-2-(4-(3-(trifluoromethyl)pyridin-2-yl)-piperazin-1-yl)-1H-benzo[d]imidazole

https://huagongshe.com/reaction/912864

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Lithium ChlorideHCID 433294—
反応物3,4-Difluorobenzeneboronic acidHCID 2734337—
反応物6-Bromo-2-[4-(3-trifluoromethylpyridin-2-yl)piperazin-1-yl]-1H-benzoimidazoleHCID 11597064—
触媒HCID 178418397HCID 178418397—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Ethyl AcetateHCID 8857—
生成物6-(3,4-difluorophenyl)-2-(4-(3-(trifluoromethyl)pyridin-2-yl)-piperazin-1-yl)-1H-benzo[d]imidazoleHCID 10434329—

反応条件

温度80 °C

反応手順

To a mixture of 3,4-difluorophenylboronic acid (111 mg, 0.7 mmol, Aldrich) and 6-bromo-2-[4-(3-trifluoromethylpyridin-2-yl)piperazin-1-yl]-1H-benzoimidazole (213 mg, 0.5 mmol, Example 23c) in ethylene glycol dimethyl ether (2 mL) were added lithium chloride (63 mg, 1.5 mmol, Aldrich) and 2M aqueous sodium carbonate (0.75 mL, 1.5 mmol). Nitrogen gas was bubbled through the mixture for 10 min and tetrakis(triphenylphosphine)palladium (58 mg, 0.05 mmol, Aldrich) was added. The reaction mixture was stirred at 80° C. under nitrogen atmosphere for 16 h, cooled to room temperature, diluted with EtOAc (50 mL) and filtered through Celite® pad. The filtrate was washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (55% EtOAc/hexane) to give the title compound as a white solid. MS (ESI, pos. ion) m/z: 460.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08026241B2
出典データセットuspto-grants-2011_09
ORD IDord-d96781883e2a4d4d94b742d712ef20dc
出典メモuspto-grants-2011_09