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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875217Generated: October 30, 2026

Potassium Iodide → 2-{6-[({[(1,2-dimethyl-1H-imidazol-5-yl)(phenyl)methylene]amino}-oxy)methyl]pyridin-2-yl}-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/875217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant2-(6-Bromomethyl-pyridin-2-YL)-isoindole-1,3-dioneHCID 11232351—
Reactant1-(1,2-dimethyl-1H-imidazol-5-yl)-N-hydroxy-1-phenylmethanimineHCID 86650751—
SolventAcetonitrileHCID 6342—
Product2-{6-[({[(1,2-dimethyl-1H-imidazol-5-yl)(phenyl)methylene]amino}-oxy)methyl]pyridin-2-yl}-1H-isoindole-1,3(2H)-dioneHCID 8665075217.7%

Reaction Steps

To a solution of 1-(1,2-dimethyl-1H-imidazol-5-yl)-N-hydroxy-1-phenylmethanimine (2.29 g, 10.6 mmol) and 2-[6-(bromomethyl)pyridin-2-yl]-1H-isoindole-1,3(2H)-dione (3.71 g, 11.7 mmol) in acetonitrile (100 mL) were added cesium carbonate (7.27 g, 22.3 mmol) and potassium iodide (176 mg, 1.06 mmol). After stirring at room temperature for 31.5 h, the reaction mixture was filtered, the insolubles washed with dichloromethane, and the filtrate concentrated in vacuo. Purification on silica gel afforded 2-{6-[({[(1,2-dimethyl-1H-imidazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}-1H-isoindole-1,3(2H)-dione [848 mg, yield 16%; HPLC/MS: m/z=452 (M+H); log P(HCOOH)=1.84].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981111B2
Source datasetuspto-grants-2015_03
ORD IDord-f53c2665eced4bafa276756da1b1a9ae
Source noteuspto-grants-2015_03