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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1164145Erstellt: 27. Oktober 2026

2(1H)-Pyrimidinone, 4-amino-1-arabinofuranosyl- → N4-nonyloxycarbonyl-1-beta-D-arabinofuranosylcytosine

https://huagongshe.com/reaction/1164145

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2(1H)-Pyrimidinone, 4-amino-1-arabinofuranosyl-HCID 114682—
EduktSodium BicarbonateHCID 516892—
EduktNonyl ChloroformateHCID 544663—
LösungsmittelDimethylacetamideHCID 31374—
ProduktN4-nonyloxycarbonyl-1-beta-D-arabinofuranosylcytosineHCID 1309028337,3%

Reaktionsbedingungen

Temperatur22.5 °C

Reaktionsschritte

In 120 ml of dimethylacetamide, 6.0 g of arabinofuranosylcytosine is dissolved and to the resultant solution are added 4.15 g of sodium hydrogen carbonate and 7.66 g of nonyloxycarbonyl chloride. The mixture is then allowed to react under stirring at 20 to 25° C. for 2 hours. After the reaction, the solvent is removed under reduced pressure and the residue is dissolved in a small amount of ethanol. Water is then added to the resultant solution and the precipitated solids are collected by filtration, followed by drying. The white powders obtained are washed thoroughly with ethyl ether to obtain 3.8 g of N4 -nonyloxycarbonyl-1-β-D-arabinofuranosylcytosine (Yield:37%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04367332
Quelldatensatzuspto-grants-1983_01
ORD IDord-7e063a2917d149f8967e02cab15a0838
Quellennotizuspto-grants-1983_01