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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889079Generated: October 25, 2026

Triethyloxonium tetrafluoroborate → HCID 66598910, compound

https://huagongshe.com/reaction/1889079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant5-FluoropicolinohydrazideHCID 55280967—
Reactant4-[(2,4-Dichloro-3-fluorophenyl)carbonyl]-2-piperazinoneHCID 66599361—
SolventDichloromethaneHCID 6344—
ProductHCID 66598910HCID 66598910—

Reaction Steps

To a solution of 4-[(2,4-dichloro-3-fluorophenyl)carbonyl]-2-piperazinone (I37) (0.146 g, 0.5 mmol) in Dichloromethane (DCM) (3 mL) was added triethyloxonium tetrafluoroborate (0.100 g, 0.525 mmol). The solution was then stirred, under argon, for 10 minutes before 5-fluoro-2-pyridinecarbohydrazide (I24) (0.093 g, 0.600 mmol) was added. The solution was then stirred for a further hour before the solvent was concentrated and n-butanol (3.00 mL) was added. The solution was then stirred, under argon and reflux, for 3 hours before being cooled to room temperature. The solvent was then evaporated in vacuo and the remaining residue was purified by flash chromatography (Biotage SP4, 25M cartridge) with a gradient of 0-10% 2M NH3/MeOH in DCM. TLC confirmed product location and the solvent from the combined fractions was evaporated in vacuo. The remaining residue was then further purified by mass-direct automated HPLC, and the solvent evaporated in vacuo. The remaining solid was then triturated with ether and dried in a vac-oven to yield the product in 0.045 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-825fc682cea94cc295592bac89d03ba1
Source noteuspto-grants-2013_08