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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368127Generated: October 26, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl IsothiocyanateHCID 69403—
Reactant1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 12148992—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
ProductN-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthioureaHCID 99545256.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573273B1
Source datasetuspto-grants-2003_06
ORD IDord-243255be496c483981037bfc8186b1ce
Source noteuspto-grants-2003_06