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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47113Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → 7,7-Dimethyl-2-phenyl-5-(3-diethylamino-propyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione dihydrochloride

https://huagongshe.com/reaction/47113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktSodium hydrideHCID 24758—
Edukt3-bromo-N,N-diethylpropan-1-amineHCID 415291—
Edukt7,7-Dimethyl-2-phenyl-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione hydrochlorideHCID 70610449—
LösungsmittelWaterHCID 962—
Produkt7,7-Dimethyl-2-phenyl-5-(3-diethylamino-propyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione dihydrochlorideHCID 70610433—

Reaktionsschritte

2.6 gm of a 55% suspension of sodium hydride in oil were added in portions to a mixture of 5.1 gm of 7,7-dimethyl-2-phenyl-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione hydrochloride and 50 ml of dimethyl sulfoxide. After stirring the mixture at room temperature for one hour, 4.8 gm of 3-diethylamino propyl bromide hdyrobromide were added, and the mixture was heated at 50° C. for 3 hours. The reaction mixture was admixed with water and extracted several times with chloroform. The chloroform phases were evaporated and the residue was purified on a silicagel column. The dihydrochloride was precipitated from acetone with ethereal hydrochloric acid and recrystallized from methanol/acetone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04176184
Quelldatensatzuspto-grants-1979_11
ORD IDord-694f1ff6c17349548324165bfe018edb
Quellennotizuspto-grants-1979_11