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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389768Generated: October 30, 2026

Sodium Carbonate → 2-(2,6-Difluorophenyl)-5-(4-hydroxyphenyl)oxazole-4-carboxamide

https://huagongshe.com/reaction/389768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Hydroxyphenylboronic acidHCID 2734360—
Reactant5-Bromo-2-(2,6-difluorophenyl)oxazole-4-carboxamideHCID 59587599—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-(2,6-Difluorophenyl)-5-(4-hydroxyphenyl)oxazole-4-carboxamideHCID 5958757880%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a mixture of 5-bromo-2-(2,6-difluorophenyl)oxazole-4-carboxamide (0.060 g, 0.20 mmol), 4-hydroxyphenylboronic acid (0.055 g, 0.40 mmol) and 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride (0.008 g, 0.01 mmol) in MeCN (4 ml) was added 1M aqueous Na2CO3 (0.4 ml, 0.4 mmol). The reaction was heated via microwave irradiation to 150° C. and held at this temperature for 15 minutes. The reaction was then diluted with EtOAc and washed with 2M HCl. The organic layer was dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by silica gel flash chromatography using 5-70% EtOAc in hexane as eluant to furnish 2-(2,6-difluorophenyl)-5-(4-hydroxyphenyl)oxazole-4-carboxamide (0.050 g, 0.16 mmol, 80%) as an off white powder. LCMS (1) 1.73 min; m/z (ES−) 315.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-59784cd9d8334c8395ac3b6d1d15010a
Source noteuspto-grants-2013_02