Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469388Generated: October 25, 2026

Sodium Carbonate → 2-[2-(4-Fluorophenyl)-1,3-oxazol-4-yl]pyrimidine

https://huagongshe.com/reaction/1469388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-BromopyrimidineHCID 78345—
ReactantSodium AcetateHCID 517045—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant2-(4-Fluorophenyl)oxazol-4-yl trifluoromethanesulfonateHCID 11659599—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-[2-(4-Fluorophenyl)-1,3-oxazol-4-yl]pyrimidineHCID 89485723—

Reaction Steps

A stirred solution of 2-(4-fluorophenyl)-1,3-oxazol-4-yl trifluoromethanesulfonate (3.8 g, 12.21 mmol), Fe(dppf)2 (0.338 g, 0.611 mmol), Pd(dppf)Cl2 (0.447 g, 0.611 mmol), sodium acetate and bis(pinacolato)diboron (4.03 g, 15.87 mmol) in 50 ml of dioxane was heated at 100° C. for 3 h. Then 2-bromopyrimidine (2.91 g, 18.32 mmol), Pd(PPh3)2Cl2 (0.857 g, 1.221 mmol) and sodium carbonate (12.2 ml, 2 M, 2.42 mmol) were added. The resultant mixture was then heated at 95° C. overnight, diluted with H2O and extracted with EtOAc. The organic extract was washed with brine, dried over MgSO4, filtered, and the filtrate was concentrated. The resulting residue was purified by flash chromatography (silica gel column, EtOAc/hexane) to give the title compound. LC-MS m/z 241.11 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006268B2
Source datasetuspto-grants-2015_04
ORD IDord-b15224f715f344bcb1747f3dd9317aa9
Source noteuspto-grants-2015_04