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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631790Generated: October 31, 2026

Oxalyl chloride → (E)-4,4,5,5,5-pentafluoro-N-[2-[(4-methyl-2-pyridyl)amino]ethyl]pent-2-enamide

https://huagongshe.com/reaction/631790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(4-methylpyridin-2-yl)ethane-1,2-diamineHCID 10034794—
Reactant(2E)-4,4,5,5,5-Pentafluoro-2-pentenoic acidHCID 86691160—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(E)-4,4,5,5,5-pentafluoro-N-[2-[(4-methyl-2-pyridyl)amino]ethyl]pent-2-enamideHCID 89832361—

Reaction Steps

(E)-4,4,5,5,5-Pentafluoropent-2-enoic acid (29 mg, 0.15 mmol) was dissolved in DMF (1 ml), oxalyl chloride was added (13 μl, 0.15 mmol) and the solution was stirred at room temperature for 5 minutes. To this solution was added a solution of N′-(4-methyl-2-pyridyl)ethane-1,2-diamine (19 mg, 0.1 mmol) in DMF (0.5 ml) and diisopropylethylamine (51 μl, 0.3 mmol) and the resulting mixture was stirred at room temperature for two hours. The reaction mixture was diluted with ethyl acetate, washed with sat. sodium bicarbonate solution and brine and dried over magnesium sulfate. The volatiles were removed under reduced pressure and the residue obtained was purified by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and 10% to 100% acetonitrile) to yield 18.5 mg (0.057 mmol, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321724B2
Source datasetuspto-grants-2016_04
ORD IDord-8c35979386a74383b5ff2310ce289007
Source noteuspto-grants-2016_04