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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383109Generated: November 2, 2026

Phenyl isocyanate → HCID 57545296, compound

https://huagongshe.com/reaction/2383109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantHCID 67051023HCID 67051023—
SolventPyridineHCID 1049—
ProductHCID 57545296HCID 5754529630.1%

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 N-{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 numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-c046460a024a44be900de3d16ed90e08
Source noteuspto-grants-2012_09