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HRID 576作成日:2026年10月23日

2-Chloropyridine → N-pyridin-2-yl-1,3-oxazol-2-amine

https://huagongshe.com/ja/reaction/576

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChloropyridineHCID 7977—
反応物2-AminooxazoleHCID 558521—
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N-pyridin-2-yl-1,3-oxazol-2-amineHCID 676367270%

反応条件

温度100 °C

反応手順

Palladium(II) acetate (4.49 mg, 0.02 mmol) and 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.017 g, 0.03 mmol) were mixed together in a reaction vessel and evacuated and purged with nitrogen 3 times. Dioxane (1 mL) was added and the resulting mixture was heated to to 50°C for 30 minutes. oxazol-2-amine (0.101 g, 1.20 mmol) together with 2-chloropyridine (0.094 mL, 1.00 mmol) and cesium carbonate (0.456 g, 1.40 mmol) were placed in a second vessel, evacuated and purged with nitrogen 3 times and dioxane (3 mL) was added. The catalyst solution was added and the resulting mixture heated at 100 °C for 16 hours. **No oxazol-2-amine present in proton NMR of crude reaction mixture.** The starting material is decomposing under the reaction conditions, could be the route of the very low productivity in the C-N couplings using these substrates. Only chloropyridine observed in the proton NMR and LCMS of the crude reaction mixture. Conclusion: Experiment abandoned, none of the desired product isolated. .

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-cdacdc2f62e2433897c344ea48603986
出典メモ750 AstraZeneca ELN dataset