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HRID 351作成日:2026年10月23日

2,4-Dichloropyridine → Ethyl 2-[(4-chloro-2-pyridinyl)amino]-1,3-oxazole-5-carboxylate

https://huagongshe.com/ja/reaction/351

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DichloropyridineHCID 33515—
反応物Ethyl 2-amino-1,3-oxazole-5-carboxylateHCID 5260193—
試薬Cesium carbonateHCID 10796—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 2-[(4-chloro-2-pyridinyl)amino]-1,3-oxazole-5-carboxylateHCID 1015844990%

反応条件

温度160 °C

反応手順

Objective: Series of experiments to optimise yield of the above coupled product. Pd2(dba)3 (22.89 mg, 0.025 mmol), di-tert- butyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (42.4 mg, 0.10 mmol), 2,4-dichloropyridine (148 mg, 1.00 mmol), cesium carbonate (651 mg, 2.00 mmol),ethyl 2-aminooxazole-5-carboxylate (156 mg, 1.00 mmol) and 4,4'-di-tert- butylbiphenyl (60 mg, 0.23 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 at 160 °C for 1 h by microwave irradiation under a nitrogen atmosphere. Crude LCMS shows a complete switch in regioselectivity, with the other isomer becoming the major product in 26% yield based on internal standard (note: this is a rough estimate as the U.V absorbance may be significantly different for this regioisomer). The regioisomeric ratio is 2.8:1 and although the product was not formed in synthetically useful yields, it is an interesting result. Conclusion: Switch in regioselectivty with the change in ligand may be worth pursuing.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-0fa704c187644f658d22f391e350db77
出典メモ750 AstraZeneca ELN dataset