HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888179Generated: November 1, 2026
Benzoic Acid → Tert-butyl 4-(5-phenyl-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/888179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | tert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylate | HCID 178452346 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(5-phenyl-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylate | HCID 11992900 | 53% |
Reaction Steps
To a solution of tert-butyl 4-[(hydroxyamino)(imino)methyl]piperazine-1-carboxylate (7 g, 28.6 mmol) in anhydrous DCM (150 mL) was added benzoic acid (3.49 g, 28.6 mmol) followed by diisopropyl carbodiimide (DIC, 3.6 g, 28.6 mmol). The reaction mixture was stirred at RT for 8 hours and filtered. The filtrate was evaporated and the residue obtained was refluxed in pyridine (100 mL) for 3 hours. The solvent was removed under vacuum and the residue was dissolved in DCM. The organic layer was washed with a 10% aqueous solution of sodium bicarbonate, water and brine. The organic layer was dried and the solvent was evaporated. The residue was purified by chromatography using petrol ether/EtOAc (9/1) as eluent to afford 5 g (53%) of the title compound as a solid. TLC-Pet ether/EtOAc (9/1): Rf=0.7). HPLC purity: 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08247437B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-ab035be599a8471596c50f2c78cb1f59 |
|---|
| Source note | uspto-grants-2012_08 |
|---|