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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1008401Erstellt: 24. Oktober 2026

Pentylamine → N-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-pentylurea

https://huagongshe.com/de/reaction/1008401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentylamineHCID 8060—
EduktTriphosgeneHCID 94429—
EduktSodium BicarbonateHCID 516892—
Edukt2-Chloro-4-((6,7-dimethoxyquinazolin-4-yl)oxy)anilineHCID 21889899—
LösungsmittelChloroformHCID 6212—
LösungsmittelTriethylamineHCID 8471—
ProduktN-{2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]phenyl}-N'-pentylureaHCID 2266709449%

Reaktionsschritte

2-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-aniline (50 mg) was dissolved in chloroform (5 ml) and triethylamine (1 ml), and a solution of triphosgene (45 mg) in chloroform was then added to the solution. The mixture was stirred at room temperature for 30 min. Next, amylamine (26 μl) was added to the reaction solution, and the mixture was stirred at room temperature for additional 30 min. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by HPLC by development with chloroform/methanol to give 33 mg (yield 49%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06797823B1
Quelldatensatzuspto-grants-2004_09
ORD IDord-95a4d538c7f6408d9e9ed6b6da4153bb
Quellennotizuspto-grants-2004_09