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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098303Generated: November 1, 2026

Imidazole → 7-imidazol-1-yl-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one

https://huagongshe.com/reaction/1098303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant7-iodo-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 23156803—
CatalystCopper iodideHCID 83717—
Solvent1,4-DioxaneHCID 31275—
Product7-imidazol-1-yl-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 2315677993.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

10.4 mg (0.025 mmol) of the 7-iodo-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one obtained in Step A, 0.48 mg (0.0025 mmol) of copper iodide (I), 2.0 mg (0.03 mmol) of imidazole, and 11.1 mg (0.0525 mmol) of potassium phosphate were suspended in 0.25 ml of 1,4-dioxane. Then, 2.6 μl of N,N′-dimethylethylenediamine was added to the suspension, and the obtained mixture was then stirred at 110° C. overnight. Thereafter, the reaction solution was cooled to a room temperature, and a saturated ammonium chloride aqueous solution was then added to the reaction solution, followed by extraction with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and was then concentrated. The obtained residue was purified by silica gel column chromatography (methylene chloride:methanol=25:1 to 20:1), so as to obtain 8.3 mg (93%) of 7-imidazol-1-yl-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one in the form of a colorless viscous oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143274B2
Source datasetuspto-grants-2012_03
ORD IDord-67b4d56095544fbb9f9ec40df47c0987
Source noteuspto-grants-2012_03