HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967061Generated: October 27, 2026
Phenol → 1-(2-Phenoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine
https://huagongshe.com/reaction/967061
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)ethanol | HCID 11356628 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-Phenoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 10236539 | — |
Reaction Steps
2-(4-Amino-1H-imidazo[4,5-c]quinolin-1-yl)ethanol (25 mg, 0.108 mmol) and N,N-dimethylformamide (1 mL) were combined. Phenol (12 mg, 0.130 mmol) and triphenylphosphine (34 mg, 0.130 mmol) were added and the resulting slurry was sonicated for about 1 minute. Diethyl azodicarboxylate (23 mg, 0.130 mmol) was added and the reaction mixture was shaken at ambient temperature for 24 hours. Analysis by LC-MS showed that a major amount of starting material remained. An additional equivalent each of phenol, triphenylphosphine and diethyl azodicarboxylate were added. The reaction mixture was sonicated for 30 minutes. After 1 hour analysis by LC-MS showed product. The solvent was removed and the residue was purified by semi-preparative HPLC using Method A. Mass Measurement: TM=304, NM[M+H]+1=305.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953804B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-982b05d59fcc47b99d20d9d3f99e8762 |
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| Source note | uspto-grants-2005_10 |
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