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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547255Erstellt: 24. Oktober 2026

2-Fluorothiophenol → HCID 10434433, Verbindung

https://huagongshe.com/de/reaction/547255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-FluorothiophenolHCID 520216—
Edukt2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]-purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diolHCID 67189486—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelSodium HydroxideHCID 14798—
ProduktHCID 10434433HCID 1043443385,4%

Reaktionsschritte

To a solution of 2-fluorothiophenol (38 mL, 406 mmol) in 2N sodium hydroxide (100 mL) was added 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol (15.0 g, 40.6 mmol) in N,N-dimethylformamide (120 mL). The mixture was warmed to 100 C for 4 hours, following the progress of the reaction by TLC. The N,N-dimethylformamide was removed under reduced pressure, and the remaining mixture was diluted with water (200 mL), neutralized with acetic acid, extracted with ethyl acetate (3×125 mL), and the combined organic layers were dried over MgSO4. After removing the solvent under reduced pressure the residue was triturated with diethyl ether and filtered, to afford 16 grams of 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-[(2-fluorophenylthio)methyl]oxolane-3,4-diol as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07939509B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-4d3b175681e0492eac47b52da4c361c7
Quellennotizuspto-grants-2011_05