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HRID 539492作成日:2026年10月25日

Toluene → 8-Methoxyphenanthridin-6-amine

https://huagongshe.com/reaction/539492

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734652—
反応物2-Bromo-5-methoxybenzonitrileHCID 21784096—
反応物Potassium phosphate, tribasic, monohydrateHCID 22031701—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
生成物8-Methoxyphenanthridin-6-amineHCID 7065435268%

反応手順

2-Bromo-5-methoxybenzonitrile (1.32 g, 6.23 mmol), 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (1.36 g, 6.23 mmol), bis(triphenylphosphine)palladiumdichloride (0.437 g, 0.623 mmol) and potassium phosphate monohydrate (4.30 g, 18.68 mmol) were added to toluene (30 mL) and water (3 mL). The reaction mixture was degassed with bubbled nitrogen gas for 30 minutes before being refluxed under nitrogen for 15 h. After cooling, the reaction mixture was filtered through Celite® and the organic layer was extracted with ethyl acetate. After removal of the solvents, the crude material was triturated with 40 mL of DCM followed by 50 mL of hexanes to give 8-methoxyphenanthridin-6-amine (0.95 g, 68%) as a light yellow solid. The product was confirmed by GC/MS and NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871361B2
出典データセットuspto-grants-2014_10
ORD IDord-64e2c143a486468fb1914509aa94df46
出典メモuspto-grants-2014_10