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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245652Generated: October 25, 2026

Potassium Carbonate → Acetic acid 2-bromo-6-(6-dimethylamino-1-oxo-1H-isoquinolin-2-yl)-benzyl ester

https://huagongshe.com/reaction/2245652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-(Dimethylamino)-1,2-dihydroisoquinolin-1-oneHCID 57424142—
Reactant2,6-Dibromobenzyl acetateHCID 59216413—
SolventDimethyl SulfoxideHCID 679—
ProductAcetic acid 2-bromo-6-(6-dimethylamino-1-oxo-1H-isoquinolin-2-yl)-benzyl esterHCID 5921640344.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

6-Dimethylamino-2H-isoquinolin-1-one (50 mg, 0.27 mmol), Acetic acid 2,6-dibromo-benzyl ester (164 mg, 532 mmol), cuprous iodide (10 mg, 0.053 mmol), and potassium carbonate (37 mg, 0.27 mmol) were deposited in sealed vessel. 3 mL DMSO was 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 (gradient elution 30 to 40% ethylacetate/hexanes) to yield Acetic acid 2-bromo-6-(6-dimethylamino-1-oxo-1H-isoquinolin-2-yl)-benzyl ester (48 mg, 0.12 mmol). MS (ESI) 417.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683064B2
Source datasetuspto-grants-2010_03
ORD IDord-946f619a1fac490f9c5b00aa6cd49107
Source noteuspto-grants-2010_03