Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775332Generated: October 31, 2026

Oxalyl chloride → (E)-4,4-Difluoro-N-[(3S)-1-(5-methyl-3-pyridyl)pyrrolidin-3-yl]pent-2-enamide

https://huagongshe.com/reaction/1775332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant(E)-4,4-Difluoropent-2-enoic acidHCID 75530053—
Reactant(3S)-1-(4-methyl-2-pyridyl)pyrrolidin-3-amine trihydrochlorideHCID 131734734—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(E)-4,4-Difluoro-N-[(3S)-1-(5-methyl-3-pyridyl)pyrrolidin-3-yl]pent-2-enamideHCID 7176532167%

Reaction Steps

(E)-4,4-Difluoropent-2-enoic acid (22 mg, 0.16 mmol) was dissolved in dichloromethane (1 ml), oxalyl chloride (14 μl, 0.16 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 (3S)-1-(4-methyl-2-pyridyl)pyrrolidin-3-amine trihydrochloride (29 mg, 0.1 mmol) in DCM (2 ml). Ethyl-N,N-diisopropylamine (DIPEA, 70 μl, 0.4 mmol) was added and the resulting mixture was stirred at room temperature overnight. The mixture was concentrated 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 20 mg of a solid (0.067 mmol, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-786d5b9bc954410bbbb9899b4d1be446
Source noteuspto-grants-2016_02