HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598282Generated: October 30, 2026
Phenyl isocyanate → HCID 57545296, compound
https://huagongshe.com/reaction/598282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | HCID 67051023 | HCID 67051023 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57545296 | HCID 57545296 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897597B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-02cba73cd943431da9376f60e2170704 |
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| Source note | uspto-grants-2011_03 |
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