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HRID 573作成日:2026年10月23日

Aniline → N-phenylpyridin-4-amine

https://huagongshe.com/ja/reaction/573

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物4-BromopyridineHCID 14268—
試薬Sodium t-butoxideHCID 23676156—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Palladium (II) acetateHCID 4144353—
溶媒TolueneHCID 1140—
生成物N-phenylpyridin-4-amineHCID 8994520.25%

反応条件

温度100 °C

反応手順

ANILINE (6.85 mL, 75.19 mmol) was added to 4-bromopyridine (9.9 g, 62.66 mmol), PALLADIUM(II) ACETATE (0.281 g, 1.25 mmol), XANTPHOS (2.175 g, 3.76 mmol) and SODIUM TERT-BUTOXIDE (8.43 g, 87.72 mmol) in toluene (500 mL) under nitrogen. The resulting mixture was stirred at 100 °C for 4 hours. The reaction mixture was evaporated to dryness and redissolved in EtOAc (200 mL), and washed sequentially with water (2 x 100 mL) and saturated brine (100 mL). The organic layer was dried over MgSO4, filtered and preadsorbed onto silica. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford N-phenylpyridin-4-amine (2.160 g, 20.25 %) as a pale tan solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-3201a37afe8b4b36ad112c88df6755f7
出典メモ750 AstraZeneca ELN dataset