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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1835696Erstellt: 25. Oktober 2026

Water → (R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine

https://huagongshe.com/reaction/1835696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktParaxanthineHCID 4687—
EduktSodium hydrideHCID 24758—
Edukt(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
Produkt(R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthineHCID 54338253120,5%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a stirring solution of 1,7-dimethylxanthine (0.30 g, 1.67 mmol) in dimethylsulfoxide (20 ml) was added sodium hydride (42 mmg, 1.75 mmol) in one portion. After stirring for 30 minutes, (R)-5-acetoxy-1-bromohexane (0.31 g, 1.75 mmol) was added neat. (R)-5-Acetoxy-1-bromohexane was prepared according to methods described in U.S. patent application Ser. No. 09/002,345, which is incorporated herein by reference. After heating at 80° C. for 18 hours, water (25 ml) was added and the aqueous solution was extracted with dichloromethane (3×20 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (50 ml), dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica eluting with ethyl acetate to give (R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine (0.34 g, 64% yield) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06774130B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-38e733cee3844851a04ddd5dfa6c63b5
Quellennotizuspto-grants-2004_08