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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631796Generated: October 31, 2026

Oxalyl chloride → (E)-N-[2-[(4-Ethoxy-2-pyridyl)amino]ethyl]-4,4-difluoro-pent-2-enamide

https://huagongshe.com/reaction/631796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant(E)-4,4-Difluoropent-2-enoic acidHCID 75530053—
ReactantN-(4-Ethoxy-2-pyridyl)ethane-1,2-diamineHCID 89825952—
CatalystDichloromethaneHCID 6344—
SolventDichloromethaneHCID 6344—
Product(E)-N-[2-[(4-Ethoxy-2-pyridyl)amino]ethyl]-4,4-difluoro-pent-2-enamideHCID 8983242741.7%

Reaction Steps

(E)-4,4-Difluoropent-2-enoic acid (31 mg, 0.23 mmol) was dissolved in dichloromethane (0.5 ml containing one drop of dimethyl formamide), oxalyl chloride was added (20 μl, 0.23 mmol) and the solution was stirred at room temperature for 15 minutes. This solution was added to a solution of N-(4-ethoxy-2-pyridyl)ethane-1,2-diamine (27 mg, 0.15 mmol) and diisopropylethylamine (88 μl, 0.5 mmol) dissolved in DCM (2 ml) and the resulting mixture was stirred at room temperature for three hours. The volatiles were removed under reduced pressure and the residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and 10% to 100% acetonitrile) to yield 18.7 mg of a residue that was purified again by preparative HPLC (gradient of water containing 0.1% trifluoroacetic acid and 10% to 100% acetonitrile). The product obtained was converted to the free base by dissolving in DCM, washing with 1N NaOH solution, water and evaporation to dryness under reduced pressure to yield 13.2 mg of a solid (0.044 mmol, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321724B2
Source datasetuspto-grants-2016_04
ORD IDord-e572b33baf8849f095fc1faea1226258
Source noteuspto-grants-2016_04