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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775322Generated: October 31, 2026

Oxalyl chloride → (E)-4,4-Difluoro-1-[4-(5-methyl-1,2,4-oxadiazol-3-yl)piperazin-1-yl]pent-2-en-1-one

https://huagongshe.com/reaction/1775322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-(5-Methyl-1,2,4-oxadiazol-3-yl)piperazine hydrochlorideHCID 86686047—
Reactant(E)-4,4,5,5-tetrafluoropent-2-enoic acidHCID 86691165—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(E)-4,4-Difluoro-1-[4-(5-methyl-1,2,4-oxadiazol-3-yl)piperazin-1-yl]pent-2-en-1-oneHCID 7176525269%

Reaction Steps

(E)-4,4,5,5-Tetrafluoropent-2-enoic acid (31 mg, 0.23 mmol) was dissolved in dichloromethane (1 ml), oxalyl chloride (20 μl, 0.23 mol) and one drop of DMF were added and the resulting solution was stirred at room temperature for 15 minutes. This solution was added to a solution of 5-methyl-3-piperazin-1-yl-1,2,4-oxadiazole hydrochloride (25 mg, 0.122 mmol) in dichloromethane (2 ml) and the resulting mixture was stirred at room temperature for three hours. The solvent was removed under reduced pressure and the resulting residue was purified by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 24.3 mg of a solid (0.083 mmol, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-fd0d4789dd9b4abb8269d7f1bd9a9429
Source noteuspto-grants-2016_02