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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598282Generated: October 30, 2026

Phenyl isocyanate → HCID 57545296, compound

https://huagongshe.com/reaction/598282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantHCID 67051023HCID 67051023—
SolventPyridineHCID 1049—
ProductHCID 57545296HCID 57545296—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of 2-(4-aminobutyl)-7-benzyloxy-1-(2-phenoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.40 g, 0.83 mmol) and pyridine (10 mL) was cooled to 0° C., and phenyl isocyanate (91 μL, 0.84 mmol) was added. The reaction was stirred for one hour and additional phenyl isocyanate (10 μL) was added. The reaction was stirred for one hour and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluting with 95:5-chloroform:methanol), recrystallized from toluene, and dried in a vacuum oven to provide 150 mg of TV-{4-[4-amino-7-benzyloxy-1-(2-phenoxyethyl)-1H-imidazo[4,5-c]quinolin-2-yl]butyl}-N′-phenylurea as a white crystalline solid, mp 186.3-186.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-02cba73cd943431da9376f60e2170704
Source noteuspto-grants-2011_03