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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721555Erstellt: 25. Oktober 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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
EduktTriethylamineHCID 8471—
EduktTriphosgeneHCID 94429—
Edukt4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-nitroanilineHCID 21890730—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
ProduktN-[2-(Diisopropylamino)ethyl]-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2-nitrophenyl}ureaHCID 2189039570%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-2ed5e4946b954909a33a62e6cee1d9b7
Quellennotizuspto-grants-2006_11