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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721107Generated: October 27, 2026

Triphosgene → 3-(4-Fluorophenoxy)propyl N-{4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-2,3-dimethylphenyl}-carbamate

https://huagongshe.com/reaction/721107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
Reactant3-(4-Fluorophenoxy)propan-1-olHCID 13691211—
Reactant4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2,3-dimethylanilineHCID 21890452—
ReactantToluene triethylamineHCID 22504574—
SolventDichloromethaneHCID 6344—
Product3-(4-Fluorophenoxy)propyl N-{4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-2,3-dimethylphenyl}-carbamateHCID 2189104244%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2,3-dimethylaniline (68 mg) was added to toluene/triethylamine=10/1 (7 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (94 mg) in methylene chloride was then added to the solution, and the mixture was heated under reflux for 15 min. Subsequently, 3-(4-fluorophenoxy)-1-propanol (53 mg) was added thereto, and the mixture was further stirred with heating under reflux for 2 hr. After the completion of the reaction, the reaction solution was allowed to cool to room temperature before distilled water was added thereto. The mixture was subjected to separatory extraction with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution and saturated brine. The washed solution was dried over sodium sulfate and was concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (48 mg, yield 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-9305038ad5c74786ad1ecd651ae842cd
Source noteuspto-grants-2006_11