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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721564Erstellt: 24. Oktober 2026

Triethylamine → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-nitrophenyl}-N'-[2-(ethyl-3-methylanilino)ethyl]urea

https://huagongshe.com/de/reaction/721564

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1,2-Ethanediamine, N1-ethyl-N1-(3-methylphenyl)-HCID 87984—
EduktTriphosgeneHCID 94429—
Edukt4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-nitroanilineHCID 17755401—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
ProduktN-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-nitrophenyl}-N'-[2-(ethyl-3-methylanilino)ethyl]ureaHCID 2189099769%

Reaktionsschritte

4-[(6,7-Dimethoxy-4-quinazolinyl)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-ethyl-N1-(3-methylphenyl)-1,2-ethanediamine (78 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 (110 mg, yield 69%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-b6bfaefb918846f59e3ec8d06d16a86c
Quellennotizuspto-grants-2006_11