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HRID 353作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/353

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Bis(3,5-bis(trifluoromethyl)phenyl)(3,6-dimethoxy-2',4',6'-tri(propan-2-yl)(1,1'-biphenyl)-2-yl)phosphaneHCID 44597232—
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), bis(3,5-bis(trifluoromethyl)phenyl)(2',4',6'-triisopropyl-3,6-dimethoxybiphenyl-2-yl)phosphine (80 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 switch in regioselectivity again with respect to the bidentate ligand Xantphos, with the other isomer becoming the major product in 28% yield based on internal standard (note: this is a rough estimate as the U.V absorbance may be significantly different to the other regioisomer). None of the other regioisomer observed. Conclusion: Switch in regioselectivty with the change in ligand may be worth pursuing, this reaction is _apparently_ completely selective for the 4-regioisomer. Note: Necessary to isolate product to confirm.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-f5babb1245424d42a4fc7bc229425c40
出典メモ750 AstraZeneca ELN dataset