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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088989Generated: October 25, 2026

Diisopropylethylamine → 2-Chloro-6-(3,3-difluoroazetidin-1-yl)-4-iodopyridine

https://huagongshe.com/reaction/2088989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,3-Difluoroazetidine hydrochlorideHCID 2758247—
Reactant2,6-Dichloro-4-iodopyridineHCID 11737393—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-6-(3,3-difluoroazetidin-1-yl)-4-iodopyridineHCID 8664986849.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of 2,6-dichloro-4-iodopyridine (1 g, 3.65 mmol) and 3,3-difluoroazetidine hydrochloric acid salt (0.497 g, 3.83 mmol) in 25 mL tetrahydrofuran was added diisopropylethylamine (0.797 ml, 4.56 mmol). The reaction mixture was heated at 90° C. for 16 hours. Further addition of another equivalent of amine and base was performed, and the suspension was heated at 100° C. for several hours, and then cooled, diluted with ethyl acetate, washed with water, brine, dried over MgSO4, filtered, and concentrated. The residue was purified on silica gel using flash chromatography (5% to 20% ethyl acetate/hexane) to afford 0.6 g of the title compound. MS (DCI+) m/z 331.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435980B2
Source datasetuspto-grants-2013_05
ORD IDord-04b73413fc8f47f59614d0371babcbdc
Source noteuspto-grants-2013_05