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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358Generated: October 24, 2026

2,4-Dichloropyridine → N-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amine

https://huagongshe.com/en/reaction/358

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyridineHCID 33515—
Reactant2-AminooxazoleHCID 558521—
ReagentCesium carbonateHCID 10796—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystBis(3,5-bis(trifluoromethyl)phenyl)(3,6-dimethoxy-2',4',6'-tri(propan-2-yl)(1,1'-biphenyl)-2-yl)phosphaneHCID 44597232—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amineHCID 1300162600%

Reaction Conditions

Temperature140 °C

Reaction Steps

Objective: Reactions using ligands not previously tested under these conditions 2,4-dichloropyridine (0.109 mL, 1.01 mmol), oxazol-2-amine (85 mg, 1.01 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (23.20 mg, 0.03 mmol), bis(3,5-bis(trifluoromethyl)phenyl)(2',4',6'-triisopropyl-3,6-dimethoxybiphenyl-2-yl)phosphine (81 mg, 0.10 mmol) and cesium carbonate (660 mg, 2.03 mmol) were added to an oven-dried microwave vail and the vial was purged with nitrogen. Degassed dioxane (4mL) was then added and the reaction mixture was heated to 140 °C for 1 h under microwave irradiation. Conclusion: None of the desired product was observed in the LCMS of the crude reaction mixture, not progressed.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-de391e2f60334b77bfa7be520f63a36b
Source note750 AstraZeneca ELN dataset