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HRID 550411Erstellt: 25. Oktober 2026

Dimethylformamide dimethyl acetal → N'-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamide

https://huagongshe.com/reaction/550411

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamide dimethyl acetalHCID 78373—
Edukt5-amino-3-(2-hydroxyethoxy)-1H-pyrazole-4-carbonitrileHCID 16228909—
LösungsmittelAcetonitrileHCID 6342—
ProduktN'-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamideHCID 6702052996%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

5-amino-3-(2-hydroxyethoxy)-1H-pyrazole-4-carbonitrile (prepared as described in Middleton, W. J., J. Am. Chem. Soc., 1958, 80, 2829/3.5 g, 20.8 mmol) and dimethylformamide dimethylacetal (4.15 ml, 31.3 mmol) were dissolved in acetonitrile (30 ml) and the mixture was stirred at 60° C. for 1 hour. The solvent was then removed under vacuum and the residue triturated in diethyl ether to provide a white solid, which was filtered and dried under vacuum to give N′-[4-cyano-3-(2-hydroxyethoxy)-1H-pyrazol-5-yl]-N,N-dimethylimidoformamide (4.45 g, 96%); NMR Spectrum: 2.95 (s, 3H), 3.06 (s, 3H), 3.67 (t, 2H), 4.12 (t, 2H) 8.09 (s, 1H); Mass Spectrum: 238 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947676B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-c914f53d718d4c129c9263204de8b7f5
Quellennotizuspto-grants-2011_05