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HRID 397992Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → (2r,3r,4s,5s)-2-{6-(2,2-Diphenyl-ethylamino)-2-[2-(1-methyl-1h-imidazol-4-yl)-ethylamino]-purin-9-yl}-5-(3-propyl-[1,2,4]oxadiazol-5-yl)-tetrahydro-furan-3,4-diol formate

https://huagongshe.com/reaction/397992

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
Edukt1-MethylhistamineHCID 3614—
EduktHCID 56624011HCID 56624011—
LösungsmittelDiisopropylethylamineHCID 81531—
Produkt(2r,3r,4s,5s)-2-{6-(2,2-Diphenyl-ethylamino)-2-[2-(1-methyl-1h-imidazol-4-yl)-ethylamino]-purin-9-yl}-5-(3-propyl-[1,2,4]oxadiazol-5-yl)-tetrahydro-furan-3,4-diol formateHCID 70020694—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of Intermediate 23 (0.075 g, 0.135 mmol), and 2-(1-methyl-1H-imidazol-4-yl)ethylamine (0.085 g, 0.677 mmol) in diisopropylethylamine (0.04 ml) and DMSO (0.04 ml), in a sealed vial (e.g. Reacti-vial™) was heated at 85° C. for 40 h. A further portion of 2-(1-methyl-1H-imidazol-4-yl)ethylamine (0.085 g, 0.677 mmol) was added after the first 20 h. Purification by Autoprep. HPLC afforded the title compound after freeze drying as a cream solid (0.037 g). LC/MS system B Rt=2.71 mins, m/z=651 MH+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610665B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-6a2cee94268749dc8854975ee901a27a
Quellennotizuspto-grants-2003_08