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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1368127Erstellt: 26. Oktober 2026

Propyl Isothiocyanate → N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthiourea

https://huagongshe.com/reaction/1368127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropyl IsothiocyanateHCID 69403—
Edukt1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 12148992—
LösungsmittelPyridineHCID 1049—
LösungsmittelChloroformHCID 6212—
ProduktN-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthioureaHCID 99545256,6%

Reaktionsschritte

A solution of propyl isothiocyanate (0.78 g, 7.72 mmol) in chloroform (5 mL) was added at ambient temperature to a solution of 1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amine (0.256 g, 7.72 mmol) in a mixture of chloroform (25 mL) and pyridine (5 mL). The reaction mixture was maintained at ambient temperature over the weekend. The reaction was quenched with ethanol and then concentrated under vacuum to provide a pale orange syrup. This material was purified by flash chromatography (silica gel, eluting with 10% methanol in dichloromethane). The pure fractions were combined and concentrated under vacuum to provide 0.22 g of N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N′-propylthiourea as a white solid, m.p. 113-116° C. Mass spec M+1=433.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06573273B1
Quelldatensatzuspto-grants-2003_06
ORD IDord-243255be496c483981037bfc8186b1ce
Quellennotizuspto-grants-2003_06