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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595215Generated: October 30, 2026

Potassium Iodide → 1-(2,4-Dimethoxybenzyl)-4-[(4-iodo-1H-pyrazol-1-yl)methyl]-4-methylpyrrolidin-2-one

https://huagongshe.com/reaction/595215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant4-IodopyrazoleHCID 77022—
Reactant[1-(2,4-Dimethoxybenzyl)-3-methyl-5-oxopyrrolidin-3-yl]methyl methanesulfonateHCID 118208667—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(2,4-Dimethoxybenzyl)-4-[(4-iodo-1H-pyrazol-1-yl)methyl]-4-methylpyrrolidin-2-oneHCID 118208458—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-iodo-1H-pyrazole (270 mg, 1.4 mmol), [1-(2,4-dimethoxybenzyl)-3-methyl-5-oxopyrrolidin-3-yl]methyl methanesulfonate (500 mg, 1.4 mmol), cesium carbonate (910 mg, 2.8 mmol), and potassium iodide (10 mg, 0.05 mmol) in DMF (80 mL) was stirred at 80° C. for 12 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel (ethyl acetate/petroleum ether) to give 1-(2,4-Dimethoxybenzyl)-4-[(4-iodo-1H-pyrazol-1-yl)methyl]-4-methylpyrrolidin-2-one. MS ESI calc'd. for C18H231 N3O3 [M+H]+ 456. found 456. 1H NMR (400 MHz, MeOD): δ 7.49 (s, 1H), 7.44 (s, 1H), 7.05 (d, J=8 Hz, 1H), 6.54 (d, J=2.4 Hz, 1H), 6.49-6.47 (m, 1H), 4.30 (d, J=4 Hz, 2H), 4.06 (d, J=2 Hz, 2H), 3.78 (s, 6H), 3.33-3.29 (m, 1H), 2.91 (d, J=6.4 Hz, 1H), 2.54 (d, J=16.8 Hz, 1H), 2.17 (d, J=16.8 Hz, 1H), 1.01 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-2f0e9168bb694c8abcb1a8599eb89671
Source noteuspto-grants-2016_01