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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721555Generated: October 25, 2026

1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → N-[2-(Diisopropylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}urea

https://huagongshe.com/reaction/721555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroanilineHCID 21890730—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-[2-(Diisopropylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}ureaHCID 2189039570%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroaniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (131 mg) in chloroform was then added to the solution, and the mixture was stirred at room temperature for 10 min. Next, N1,N1-diisopropyl-1,2-ethanediamine (63 mg) was added thereto, and the mixture was further stirred at room temperature for one hr. Water was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by concentration. The residue was purified on a column using chloroform/methanol to give the title compound (103 mg, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135466B2
Source datasetuspto-grants-2006_11
ORD IDord-2ed5e4946b954909a33a62e6cee1d9b7
Source noteuspto-grants-2006_11