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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410508Generated: November 1, 2026

Morpholine → 2-(2,6-Difluorophenyl)-5-(4-(morpholine-4-carbonyl)phenylamino)oxazole-4-carbonitrile

https://huagongshe.com/reaction/1410508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant4-(4-Cyano-2-(2,6-difluorophenyl)oxazol-5-ylamino)benzoic acidHCID 59587492—
SolventEthyl AcetateHCID 8857—
Product2-(2,6-Difluorophenyl)-5-(4-(morpholine-4-carbonyl)phenylamino)oxazole-4-carbonitrileHCID 5958755737.3%

Reaction Steps

To a solution of 4-(4-cyano-2-(2,6-difluorophenyl)oxazol-5-ylamino)benzoic acid (0.020 g, 0.059 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.022 g, 0.059 mmol), and diisopropylethylamine (0.020 mL, 0.117 mmol) in N,N-dimethylformide (2 mL) was added morpholine (0.005 mL, 0.059 mmol) and the reaction mixture stirred at room temperature for 16 hours. The reaction was then diluted with EtOAc washed with 1M HCl, water and brine. The organic phase was dried over MgSO4 and the solvent removed in vacuo. The residue was purified by preparative HPLC to afford 2-(2,6-difluorophenyl)-5-(4-(morpholine-4-carbonyl)phenylamino)oxazole-4-carbonitrile (0.009 g, 0.022 mmol, 37%) as a yellow solid. LCMS (2) Rt: 2.38 min; m/z (ES+) 411.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921544B2
Source datasetuspto-grants-2014_12
ORD IDord-4ce505bd641f4c4e8fc0dcd5b4ff3b72
Source noteuspto-grants-2014_12