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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721554Erstellt: 26. Oktober 2026

1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[2-(diisopropylamino)ethyl]urea

https://huagongshe.com/reaction/721554

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
EduktTriethylamineHCID 8471—
EduktTriphosgeneHCID 94429—
Edukt2-Chloro-4-((6,7-dimethoxyquinazolin-4-yl)oxy)anilineHCID 21889899—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
ProduktN-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-[2-(diisopropylamino)ethyl]ureaHCID 2188992343%

Reaktionsschritte

2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-aniline (100 mg) was dissolved in chloroform (10 ml) and triethylamine (1 ml) to prepare a solution. A solution of triphosgene (134 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 (65 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 (64 mg, yield 43%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-a7d2937793e145159f0cb275d2a99639
Quellennotizuspto-grants-2006_11