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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 361Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-DichloropyridineHCID 33515—
Edukt2-AminooxazoleHCID 558521—
ReagenzPotassium Phosphate, TribasicHCID 62657—
Katalysator1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amineHCID 1300162600%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

Objective: Will increased catalyst loading lead to increased isolated yield of the desired product? 2,4-dichloropyridine (0.109 mL, 1.01 mmol), oxazol-2-amine (102 mg, 1.22 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (186 mg, 0.20 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (352 mg, 0.61 mmol) (Xantphos) and potassium phosphate (430 mg, 2.03 mmol) were added to a microwave vail and the vial was purged with nitrogen. Degassed dioxane (4mL) was then added and the reaction mixture was heated to 160 °C for 6 h under microwave irradiation. Dichloromethane (10 mL) was added to the crude reaction mixture and the mixture was adsorbed onto silica gel. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in heptane. Unfortunately and somewhat surprisingly, none of the desired product was isolated, although only a trace of required product was observed in the LCMS of the crude reaction mixture. Conclusion: It appears that under this higher catalyst loading the reaction is less efficent, potentially a concentration effect?

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-4973899cb35d49cd8a53a56048cd33f7
Quellennotiz750 AstraZeneca ELN dataset