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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595233Generated: October 29, 2026

Sodium hydride → 4-((4-iodo-1H-pyrazol-1-yl)methyl)pyridin-2(1H)-one

https://huagongshe.com/reaction/595233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-IodopyrazoleHCID 77022—
Reactant4-(bromomethyl)pyridin-2(1H)-oneHCID 57281051—
SolventTetrahydrofuranHCID 8028—
Product4-((4-iodo-1H-pyrazol-1-yl)methyl)pyridin-2(1H)-oneHCID 118208509—

Reaction Conditions

Temperature25 °C

Reaction Steps

Sodium hydride (19 mg, 0.48 mmol, 60 wt %) was added to a solution of 4-iodo-1H-pyrazole (47 mg, 0.24 mmol) in THF (2 mL) at 0° C. After 30 minutes, 4-(bromomethyl)pyridin-2(1H)-one (30 mg, 0.16 mmol) was added. The mixture was stirred at 25° C. for 12 hours. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (EtOAc/MeOH) to afford 4-((4-iodo-1H-pyrazol-1-yl)methyl)pyridin-2(1H)-one. MS ESI calc'd. for C9H9IN3O [M+H]+ 302. found 302. 1H NMR (400 MHz, DMSO-d6) δ 11.54 (s, 1H), 8.05 (s, 1H), 7.61 (s, 1H), 7.32 (d, J=6.8 Hz, 1H), 5.93-5.90 (m, 2H), 5.19 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-992745fd4d7d445e90413a99976077be
Source noteuspto-grants-2016_01