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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2296433Erstellt: 25. Oktober 2026

Pyridine → 4-Amino-6-(3,3-dimethylbutyramido)quinazoline

https://huagongshe.com/reaction/2296433

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTripropylamineHCID 7616—
Edukt3,3-Dimethylbutanoyl chlorideHCID 81514—
Edukt4,6-Diaminoquinazoline hydrochlorideHCID 20266086—
LösungsmittelMethanolHCID 887—
LösungsmittelChloroformHCID 6212—
LösungsmittelChloroform methanolHCID 21584188—
Produkt4-Amino-6-(3,3-dimethylbutyramido)quinazolineHCID 1306046064,7%

Reaktionsschritte

To a mixture of 4,6-diaminoquinazoline hydrochloride (10.0 g), tripropylamine (17.61 g) and dry pyridine (100 ml) was added dropwise during 35 minutes 3,3-dimethylbutyryl chloride (10.34 g) under ice-cooling. The reaction mixture was stirred for 2 hours at the same temperature. To the resultant mixture was added ice-water. The mixture was stirred for 5 minutes and then concentrated under reduced pressure. To the residue was added water and sodium hydrogen carbonate (13.0 g) little by little to give precipitates, which were separated by filtration, washed with water and dried. Thus obtained crude crystals were dissolved in a mixture of chloroform and methanol under heating. After insoluble materials were removed by filtration, the filtrate was concentrated under reduced pressure to give a residue, which was suspended in 5% methanol-chloroform solution (70 ml). After stirring under heating, the suspension was filtered to give crystalline 4-amino-6-(3,3-dimethylbutyramido)quinazoline (8.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04429126
Quelldatensatzuspto-grants-1984_01
ORD IDord-1db8f0f1b6f04044b8d10eba5b4e152d
Quellennotizuspto-grants-1984_01