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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877517Generated: October 25, 2026

Water → 2-Cyano-5-fluoro-3-(2-pyridin-2-ylethylamino)pyridine

https://huagongshe.com/reaction/1877517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-PyridineethanamineHCID 75919—
Reactant2-Cyano-3,5-difluoropyridineHCID 2783253—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product2-Cyano-5-fluoro-3-(2-pyridin-2-ylethylamino)pyridineHCID 6701684437.8%

Reaction Conditions

Temperature115 °C

Reaction Steps

841 mg of 2-cyano-3,5-difluoropyridine, 880 mg of 2-(2-aminoethyl)pyridine and 1.658 g of potassium carbonate in 12.5 ml of dimethyl sulphoxide are introduced into a 20 ml microwave tube reactor. The mixture is then heated in a microwave for 1 and a half hours at 115° C. The reaction medium is run into 100 ml of water and 100 ml of ethyl acetate. The aqueous phase is re-extracted twice with 50 ml of ethyl acetate. The combined organic phases are washed with water and then with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. After purification by flash chromatography on 70 g of silica gel, elution being carried out with a mixture of ethyl acetate and cyclohexane (40/60 by volume), and the first eluted product being recovered, 549 mg of 2-cyano-5-fluoro-3-(2-pyridin-2-ylethylamino)pyridine are thus obtained in the form of a beige powder, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309721B2
Source datasetuspto-grants-2012_11
ORD IDord-785175c821a54b1e9c196bb17eb8d556
Source noteuspto-grants-2012_11