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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333980Generated: October 30, 2026

Oxalyl chloride → N-methyl-4-[4-[(E)-4,4,5,5-tetrafluoropent-2-enoyl]piperazin-1-yl]pyridine-2-carboxamide

https://huagongshe.com/reaction/333980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-Methyl-4-piperazin-1-yl-pyridine-2-carboxamide hydrochlorideHCID 66835948—
Reactant(E)-4,4,5,5-tetrafluoropent-2-enoic acidHCID 86691165—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-methyl-4-[4-[(E)-4,4,5,5-tetrafluoropent-2-enoyl]piperazin-1-yl]pyridine-2-carboxamideHCID 56949207—

Reaction Steps

(E)-4,4,5,5-tetrafluoropent-2-enoic acid (19 mg, 0.11 mmol) was dissolved in DCM (1 ml), oxalyl chloride was added (9 μl, 0.11 mmol) followed by a drop of DMF. The mixture was stirred for 10 minutes at room temperature. N-methyl-4-piperazin-1-yl-pyridine-2-carboxamide hydrochloride (25.6 mg, 0.1 mmol) was dissolved in DMF (0.5 ml), the mixtures were combined, diisopropylethylamine (75 μl, 0.4 mmol) was added and the resulting mixture was stirred at room temperature for 1 hour. The mixture was evaporated to dryness under reduced pressure, the residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 20.2 mg (0.054 mmol, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-13210a72890846eb8d8fe909b79d9e75
Source noteuspto-grants-2014_11