2,4-Dichloropyridine → Ethyl 2-[(4-chloro-2-pyridinyl)amino]-1,3-oxazole-4-carboxylate

温度

140 °C

Pd2(dba)3 (22.89 mg, 0.025 mmol), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (43.4 mg, 0.075 mmol), 2,4-dichloropyridine (148 mg, 1.00 mmol), cesium carbonate (651 mg, 2.00 mmol),ethyl 2-aminooxazole-4-carboxylate (156 mg, 1.00 mmol) were added to an oven dried microwave vial, the vial was capped and placed under an inert atmosphere, dioxane (4 mL) was added and the resulting mixture was heated to 140 °C for 1 h by microwave irradiation under a nitrogen atmosphere. The crude product was purified by reverse-phase flash chromatography, elution gradient 0 to 100% MeCN in water. Pure fractions were evaporated to dryness to afford ethyl 2-(4-chloropyridin-2-ylamino)oxazole-4-carboxylate (99 mg, 37.0 %) as a pale yellow solid. Conclusion: Yield produced under microwave conditions is essentially identical to overnight reaction with conventional heating. Therefore screening of other aminooxazoles can be carried out under microwave conditions in the interest of time. .

ORDレコード

ord-731adccc0a564281bbf0c68982fd70e6

出典データセット

750 AstraZeneca ELN dataset

元リンク

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