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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182292Generated: October 30, 2026

3-Pyridyl isothiocyanate → HCID 9890753, compound

https://huagongshe.com/reaction/2182292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridyl isothiocyanateHCID 2737242—
Reactant1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 12148992—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
ProductHCID 9890753HCID 989075342.8%

Reaction Steps

A solution of pyridine-3-isothiocyanate (0.136 g, 1.0 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 (0.331 g, 1.0 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 an off-white solid. 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 0.2 g of N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N′-(3-pyridyl)thiourea as a white solid, m.p. 118-120° C. Mass spec M+1=468.3. Analysis: Calculated for C26H25N7S: % C, 66.79; % H, 5.39; % N, 20.97. Found: % C, 64.29; % H, 5.46; % N, 20.06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897221B2
Source datasetuspto-grants-2005_05
ORD IDord-f2575848166540078355d2e55fc1b5be
Source noteuspto-grants-2005_05