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HRID 204作成日:2026年10月23日

3-Aminopyridine → 4-chloro-N-pyridin-3-ylpyridin-2-amine

https://huagongshe.com/ja/reaction/204

反応式

関与物質

役割名称HCID仕込み量
反応物3-AminopyridineHCID 10009—
反応物2,4-DichloropyridineHCID 33515—
試薬Cesium carbonateHCID 10796—
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1,4-DioxaneHCID 31275—
生成物4-chloro-N-pyridin-3-ylpyridin-2-amineHCID 10221851251.48%

反応条件

温度100 °C

反応手順

pyridin-3-amine (95 mg, 1.01 mmol), 2,4-dichloropyridine (0.151 mL, 1.01 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (70.4 mg, 0.12 mmol) and cesium carbonate (660 mg, 2.03 mmol) were stirred in dioxane (5 mL). The mixture was purged with nitrogen for 10 minutes. Palladium(II) acetate (22.76 mg, 0.10 mmol) was added and the mixture heated at 100 °C for 2h. The mixture was cooled, filtered and concentrated. The crude product was purified by flash silica chromatography, eluting gradient 5-45% EtOAc in isohexane. Fractions were evaporated to dryness and purified by flash silica chromatography, eluting at 35% EtOAc in isohexane to afford 4-chloro-N-(pyridin-3-yl)pyridin-2-amine (107 mg, 51.5 %) as a cream powder.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-3c36e457f5e64b5b9130db89ea6a541e
出典メモ750 AstraZeneca ELN dataset