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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948553Generated: October 27, 2026

Pyridine → 2-(4-(5-(5-Phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethanol

https://huagongshe.com/reaction/1948553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Phenyl-4-propylisoxazole-3-carboxylic acidHCID 54846886—
ReactantCID 59604233HCID 59604233—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-(4-(5-(5-Phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethanolHCID 58374091128%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a mixture of 5-phenyl-4-propylisoxazole-3-carboxylic acid (385 mg, 1.665 mmol) and pyridine (0.135 mL, 1.665 mmol) in DCM (5 mL) was added cyanuric fluoride (0.141 mL, 1.665 mmol). The reaction mixture was stirred for 1 hour. The reaction mixture was diluted with dichloromethane and washed with 1M HCl. The organic layer was dried MgSO4, filtered and concentrated. This crude residue was dissolved in acetonitrile (5.00 mL). (Z)—N′-hydroxy-4-(2-hydroxyethyl)benzimidamide (300 mg, 1.665 mmol) and DIEA (0.582 mL, 3.33 mmol) were added. The reaction mixture was heated at 75° C. overnight. The reaction mixture was diluted with ethyl acetate and washed with sat NaCl. The organic layer was dried MgSO4, filtered, and concentrated to yield 800 mg of 2-(4-(5-(5-phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethanol. MS (m+1)=376. HPLC Peak RT=2.09 minutes. (Analytical Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399451B2
Source datasetuspto-grants-2013_03
ORD IDord-7403b3e843c84998a2be617ce93ed932
Source noteuspto-grants-2013_03