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HRID 338189作成日:2026年10月26日

Cesium carbonate → 9-Fluoro-6-phenanthridinamine

https://huagongshe.com/reaction/338189

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Amantadine HydrochlorideHCID 64150—
反応物2-Chloro-4-fluorobenzonitrileHCID 109000—
反応物2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734652—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物9-Fluoro-6-phenanthridinamineHCID 112528283,082.6%

反応手順

To a solution of 2-chloro-4-fluorobenzonitrile (1.0 g, 6.42 mmol), 2-aminophenylboronic acid pinacol ester (1.6 g, 7.1 mmol), palladium(II) acetate (0.07 g, 0.32 mmol), amantadine hydrochloride (0.24 g, 1.3 mmol) and cesium carbonate (4.6 g, 14.1 mmol) were added to dioxane previously deaerated with nitrogen and heated to reflux for 17 hours. After cooling, both distilled water and methylene chloride (50 mL) were added to the reaction mixture. The solvent layer was separated and concentrated to give a crude oil that was purified by column chromatography by first using 1:1 ethyl acetate and hexanes ratio followed by 4:1 ethyl acetate/hexanes as the eluants. The pure product was collected to give 9-fluoro-6-phenanthridinamine (42 g, 32% Yield) whose NMR spectrum is consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889864B2
出典データセットuspto-grants-2014_11
ORD IDord-f33504768f854612ad3dd57118648f0e
出典メモuspto-grants-2014_11