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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333083Generated: October 29, 2026

Oxalyl chloride → (E)-N-[2-[(2,6-Dimethyl-4-pyridyl)amino]propyl]-4,4,4-trifluoro-but-2-enamide

https://huagongshe.com/reaction/333083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4,4-Trifluorocrotonic acidHCID 5709614—
ReactantN2-(2,6-dimethyl-4-pyridyl)propane-1,2-diamineHCID 66835421—
CatalystDichloromethaneHCID 6344—
SolventDimethylformamideHCID 6228—
Product(E)-N-[2-[(2,6-Dimethyl-4-pyridyl)amino]propyl]-4,4,4-trifluoro-but-2-enamideHCID 86691170—

Reaction Steps

(E)-4,4,4-Trifluorobut-2-enoic acid (15.4 mg, 0.11 mmol) was dissolved in DCM (0.75 ml containing one drop of dimethyl formamide), oxalyl chloride was added (14 mg, 0.11 mmol) and the solution was stirred at room temperature for 15 minutes. This solution was added to a solution of N2-(2,6-dimethyl-4-pyridyl)propane-1,2-diamine (21.6 mg, 0.1 mmol) and diisopropylethylamine (44 μl, 0.25 mmol) dissolved in dimethylformamide (1 ml) and the resulting mixture was stirred at room temperature overnight. The volatiles were removed under reduced pressure and the residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 10.7 mg (0.035 mmol, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877934B2
Source datasetuspto-grants-2014_11
ORD IDord-0f7dd4447c064d1cab251fe9a2dbeb5b
Source noteuspto-grants-2014_11