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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1451056Erstellt: 26. Oktober 2026

Ethanol → 9-(1H-imidazol-1-yl)methyl-4-[(2-phenylethyl)amino]imidazo[5,1-h]pteridin-6(5H)-one

https://huagongshe.com/reaction/1451056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium HydroxideHCID 14798—
Edukt4,6-Dichloro-5-nitropyrimidineHCID 20312—
EduktStannous ChlorideHCID 24479—
EduktN-BenzylphenethylamineHCID 65055—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt2-(1H-imidazol-1-ylmethyl)-1H-imidazoleHCID 19358846—
KatalysatorPalladiumHCID 23938—
Produkt9-(1H-imidazol-1-yl)methyl-4-[(2-phenylethyl)amino]imidazo[5,1-h]pteridin-6(5H)-oneHCID 9908192—

Reaktionsschritte

Prepared by treatment of 4,6-dichloro-5-nitropyrimidine with N-benzylphenylethylamine, followed by reaction with 2-(1H-imidazol-1-yl)methylimidazole, reduction with tin (II) chloride, cyclization with carbonyldiimidazole, and hydrogenation with palladium on carbon in ethanol containing 1.1 eq. NaOH at 50 psi and 50° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05602252
Quelldatensatzuspto-grants-1997_02
ORD IDord-6e6a3bbd5b344200b0d3ad5ef5439664
Quellennotizuspto-grants-1997_02