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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2069777Erstellt: 26. Oktober 2026

Potassium Carbonate → Acetic acid 2-bromo-6-(6-dimethylamino-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-benzyl ester

https://huagongshe.com/reaction/2069777

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt6-(Dimethylamino)-3,4-dihydroisoquinolin-1(2H)-oneHCID 57424121—
Edukt2,6-Dibromobenzyl acetateHCID 59216413—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktAcetic acid 2-bromo-6-(6-dimethylamino-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-benzyl esterHCID 5921640527,9%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

6-Dimethylamino-3,4-dihydro-2H-isoquinolin-1-one (150 mg, 0.789 mmol), Acetic acid 2,6-dibromo-benzyl ester (487 mg, 1.58 mmol), cuprous iodide (30 mg, 0.16 mmol) and potassium carbonate (109 mg, 0.789 mmol) were deposited in a 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 24 hours. Cuprous iodide (30 mg, 0.l6 mmol) was added and the mixture was heated at 150° C. for an additional 24 hours. This was diluted with dichoromethane and filtered through a pad of celite. The filtrate was partitioned between dichloromethane and 5% aq. ammonium hydroxide. The dichloromethane layer was dried over anhydrous magnesium sulfate, concentrated in vacuo, and purified by flash chromatography (gradient elution 25 to 50% ethyl acetate/hexanes) to yield Acetic acid 2-bromo-6-(6-dimethylamino-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-benzyl ester (93 mg, 0.22 mmol). MS (ESI) 417.1 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08299077B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-6582a227f21a4a4fac0d93991ecfaec7
Quellennotizuspto-grants-2012_10