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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822763Generated: October 26, 2026

1,3-Dimethylimidazolium Iodide → HCID 22170183, compound

https://huagongshe.com/reaction/1822763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethylimidazolium IodideHCID 20334—
ReactantSodium hydrideHCID 24758—
Reactant4-Dimethylamino-1-naphthaldehydeHCID 608052—
Reactant1-Bromo-6,7-dimethoxyisoquinoline-4-carbonitrileHCID 22048350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 22170183HCID 2217018344.3%

Reaction Steps

Sodium hydride (11 mg, 0.26 mmol) was added to a stirred mixture of 1-bromo-6,7-dimethoxy-isoquinoline-4-carbonitrile (see example 1) (50 mg, 0.17 mmol), 4-dimethylamino-1-naphthaldehyde (51.8 mg, 0.26 mmol), 1,3-dimethylimidazolium iodide (16 mg, 0.26 mmol) in DMF (2 mL). The reaction mixture became dark color. After 1 h, water (4 mL) was added to the above mixture, and extracted with chloroform (6 mL). The extract was washed with water (4 mL), dried over sodium sulfate, filtered and concentrated in vacuo to afford a solid. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 0–40% EtOAc in methylenechloride in 30 min) afforded 1-(4-dimethylamino-naphthalene-1-carbonyl)-6,7-dimethoxy-isoquinoline-4-carbonitrile (31 mg, 41%) as a white solid. LC-MS m/e calcd for C21H18N2O5 (MH+) 379. found 379.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037924B2
Source datasetuspto-grants-2006_05
ORD IDord-fcca407dfd3841d3b02d1970cbe6cff9
Source noteuspto-grants-2006_05