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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichloropyridineHCID 33515—
Reactant2-AminooxazoleHCID 558521—
ReagentSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amineHCID 1300162600%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a vial containing oxazol-2-amine (102 mg, 1.22 mmol), , TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (9.28 mg, 10.14 µmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (9.47 mg, 0.02 mmol) and sodium 2-methylpropan-2-olate (136 mg, 1.42 mmol), was added degassed toluene (4 mL) and 2,4-dichloropyridine (0.109 ml, 1.01 mmol) and the reaction mixture was heated to 100 degrees C for 20 h. None of the desired product was observed by LCMS or in crude proton NMR. **It is of note that although the 2,4-dichloropyridine is present in the crude proton NMR, the oxazole-2-amine is not**. It is possible that under the strongly basic reaction conditions that this starting material decomposed. Product not isolated.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-4ba5714524f04061a19a2e24cddcf117
Source note750 AstraZeneca ELN dataset