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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245648Generated: October 25, 2026

1,3-Dibromobenzene → 2-(3-Bromo-phenyl)-6-dimethylamino-2H-isoquinolin-1-one

https://huagongshe.com/reaction/2245648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromobenzeneHCID 7927—
ReactantPotassium CarbonateHCID 11430—
Reactant6-(Dimethylamino)-1,2-dihydroisoquinolin-1-oneHCID 57424142—
SolventDimethyl SulfoxideHCID 679—
Product2-(3-Bromo-phenyl)-6-dimethylamino-2H-isoquinolin-1-oneHCID 5921643061.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

6-Dimethylamino-2H-isoquinolin-1-one (39 mg, 0.21 mmol), cuprous iodide (8.0 mg, 0.041 mmol), and potassium carbonate (29 mg, 0.21 mmol) were deposited in sealed vessel. 3 mL DMSO and 1,3-dibromobenzene (98 mg, 0.42 mmol) were added. Argon was bubbled through the mixture for 2 minutes and the lid was tightly closed. This was heated at 150° C. for 5 hours. The resulting mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, concentrated in vacuo, and purified by flash chromatography (25% ethyl acetate/hexanes) to yield 2-(3-Bromo-phenyl)-6-dimethylamino-2H-isoquinolin-1-one (45 mg, 0.13 mmol). MS (ESI) 345.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683064B2
Source datasetuspto-grants-2010_03
ORD IDord-7c0a4889c3a74eefa4c0c46212eb65cd
Source noteuspto-grants-2010_03