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HRID 349555Erstellt: 25. Oktober 2026

1,3-Dibromopropane → 4,5,6,7-Tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/reaction/349555

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DibromopropaneHCID 8001—
EduktTriethylamineHCID 8471—
Edukt5-Amino-4-cyanopyrazoleHCID 85515—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4,5,6,7-Tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 135671372—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

To a solution of 5-aminopyrazole-4-carbonitrile (102 g) and triethylamine (316 ml) in 1,4-dioxane (2000 ml) was added 1,3-dibromopropane (115 ml), and the mixture was stirred at 95° C. for 5 days. The insoluble materials were removed by filtration, and the filtrate was concentrated in vacuo. To the residue was added 10% aqueous citric acid solution, and the mixture was extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with 2-propanol and dried in vacuo to give 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile (8.0 g) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179801B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-912c718fea374522827ed71adc7db813
Quellennotizuspto-grants-2007_02