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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363162Generated: November 3, 2026

1,2-Dimethoxyethane → HCID 67238563, compound

https://huagongshe.com/reaction/2363162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantCesium carbonateHCID 10796—
Reactant(3-Phenylphenyl)boronic acidHCID 2734315—
Reactant2-Chloro-oxazole-4-carboxylic acid [1-(3,5-difluoro-4-methanesulfonylamino-phenyl)-ethyl]-amideHCID 67110887—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 67238563HCID 6723856354.1%

Reaction Steps

In a 5 ml glass tube were placed 2-chloro-oxazole-4-carboxylic acid [1-(3,5-difluoro-4-methanesulfonylamino-phenyl)-ethyl]-amide (100 mg, 0.26 mmol), 3-biphenyl boronic acid (104 mg, 0.53 mmol), Cs2CO3 (257 mg, 0.79 mmol), Pd(PPh3)2Cl2 (15 mg, 0.021 mmol), DME (0.8 mL), ethanol (0.2 mL), and a magnetic stir bar. The vial was sealed with septum and placed into the Microwave cavity. The vial was irradiated in a Microwave synthesizer at 140° C. for 20 min. The mixture was diluted with EtOAc and washed with 1N HCl and water. The organic layer was dried over anhydrous MgSO4 and concentrated under reduced pressure. The crude residue was purified by column chromatography (gradient 12% to 100% EtOAc in n-hexane) to give title compound (70 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691855B2
Source datasetuspto-grants-2014_04
ORD IDord-46a5fe6033ba47e790e80158bd4c4cb0
Source noteuspto-grants-2014_04