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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Phenyl-4-propylisoxazole-3-carboxylic acid | HCID 54846886 | — |
| Reactant | CID 59604233 | HCID 59604233 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-(5-(5-Phenyl-4-propylisoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)ethanol | HCID 58374091 | 128% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399451B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-7403b3e843c84998a2be617ce93ed932 |
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| Source note | uspto-grants-2013_03 |
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