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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775340Generated: October 29, 2026

Oxalyl chloride → (E)-4,4-Difluoro-1-[(3R)-3-[(4-methyl-2-pyridyl)amino]-1-piperidyl]pent-2-en-1-one

https://huagongshe.com/reaction/1775340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant(E)-4,4-Difluoropent-2-enoic acidHCID 75530053—
Reactant4-Methyl-N-[(3R)-3-piperidyl]pyridin-2-amine dihydrochlorideHCID 89825961—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(E)-4,4-Difluoro-1-[(3R)-3-[(4-methyl-2-pyridyl)amino]-1-piperidyl]pent-2-en-1-oneHCID 11795167848.3%

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 4-methyl-N-[(3R)-3-piperidyl]pyridin-2-amine dihydrochloride (23 mg, 0.087 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 X-bridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 13 mg of a solid (0.042 mmol, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-421c27647cb3436f9b107ee38d8f635e
Source noteuspto-grants-2016_02