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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721102Generated: November 1, 2026

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

https://huagongshe.com/reaction/721102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
Reactant3-(3-Fluorophenoxy)propan-1-OLHCID 15086014—
Reactant4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2,3-dimethylanilineHCID 21890452—
ReactantToluene triethylamineHCID 22504574—
SolventDichloromethaneHCID 6344—
Product3-(3-Fluorophenoxy)propyl N-{4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-2,3-dimethylphenyl}carbamateHCID 2189009162.4%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2,3-di-methylaniline (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-(3-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 (68 mg, yield 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-b438c00c0c4e4dd8802b834f0354108b
Source noteuspto-grants-2006_11