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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371309Generated: October 25, 2026

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

https://huagongshe.com/reaction/1371309

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 numberUS07157453B2
Source datasetuspto-grants-2007_01
ORD IDord-9c77339e09194ecba97e92c4317ed771
Source noteuspto-grants-2007_01