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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433981Generated: October 27, 2026

Phenol → 1-(2-Phenoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine

https://huagongshe.com/reaction/433981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)ethanolHCID 11356628—
SolventDimethylformamideHCID 6228—
Product1-(2-Phenoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670372B2
Source datasetuspto-grants-2003_12
ORD IDord-9cb88b8aa8c742619805b062e08b4f23
Source noteuspto-grants-2003_12