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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactanttert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylateHCID 178452346—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(5-phenyl-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylateHCID 1199290053%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247437B2
Source datasetuspto-grants-2012_08
ORD IDord-ab035be599a8471596c50f2c78cb1f59
Source noteuspto-grants-2012_08