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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715000Generated: November 1, 2026

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

https://huagongshe.com/reaction/715000

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 numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-f1b23cb8175e4db2aad8640fd58950b3
Source noteuspto-grants-2015_11