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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511042Generated: November 4, 2026

Sodium hydride → HCID 67485570, compound

https://huagongshe.com/reaction/1511042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-3-nitropyridine-2-carbonitrileHCID 2769698—
Reactant2-Ethylpyridin-3-olHCID 3837232—
ReactantHCID 178418616HCID 178418616—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67485570HCID 6748557058%

Reaction Steps

To a solution of 2-ethylpyridin-3-ol (2.5 g, 20.3 mmol) in DMF (20 ml) at 0° C. was added sodium hydride (0.512 g, 21.3 mmol). After 15 minutes, 5-bromo-3-nitropicolinonitrile (4.63 g, 20.3 mmol) was added and the mixture was allows to warm slowly to ambient temperature and stirred for 2 hours. Pridine-2-thiol (0.804 g, 7.23 mmol) was added followed by sodium hydride (0.182 g, 7.60 mmol) and the mixture was stirred at ambient temperature overnight. Water (200 ml) was added and the mixture was extracted with diethyl ether (3×100 mL), washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified over silica gel (25 to 75% EtOAc in Hexanes) to afford 3-(2-ethylpyridin-3-yloxy)-5-(pyridin-2-ylthio)picolinonitrile (1.4 g, 4.19 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212045B2
Source datasetuspto-grants-2012_07
ORD IDord-10f083994ec64f1db97d7d6e72f74cb2
Source noteuspto-grants-2012_07