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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182291Generated: 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/2182291

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 numberUS06897221B2
Source datasetuspto-grants-2005_05
ORD IDord-76f0c314823a43e4878978c0916bebc5
Source noteuspto-grants-2005_05