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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2404993Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → 4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butanal

https://huagongshe.com/reaction/2404993

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butan-1-olHCID 68996527—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butanalHCID 86626643100,1%

Reaktionsschritte

Under a nitrogen atmosphere, dimethylsulfoxide (3.6 mL, 1.5 eq.) and oxalyl chloride (3.5 mL, 1.1 eq.) were sequentially added dropwise to chilled (dry ice/acetone bath) dichloromethane (100 mL). A solution of 4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butan-1-ol (10 g, 37 mmol, 1 eq.) in dichloromethane was added dropwise. Triethylamine (15.5 mL, 3 eq.) was added. The ice bath was removed and the reaction mixture was allowed to warm to ambient temperature. After about 2 hours analysis by TLC indicated that the reaction was complete. The reaction mixture was diluted with dichloromethane (175 mL) and water (200 mL) and made basic (pH 10) with aqueous 5% sodium carbonate. The organic layer was washed sequentially with water (2×200 mL) and brine (150 mL) and then concentrated under reduced pressure to provide 9.9 g of 4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butanal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08802853B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-a7310def4c1848dea55c9d98d05de177
Quellennotizuspto-grants-2014_08