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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1250000Erstellt: 26. Oktober 2026

Borane → 2'-o-Phthalimidoethyl-5-methyluridine

https://huagongshe.com/reaction/1250000

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoraneHCID 6331—
EduktN-(2-Hydroxyethyl)phthalimideHCID 77499—
Edukt2,2'-Anhydro-1-beta-arabinofuranosylthymineHCID 168045—
EduktSodium BicarbonateHCID 516892—
EduktHCID 178418361HCID 178418361—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2'-o-Phthalimidoethyl-5-methyluridineHCID 1000283990%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

N-(2-Hydroxyethyl)phthalimide (277 g, 1.45 mol) was slowly added to a solution of borane in tetrahydrofuran (1 M, 600 mL) with stirring. Hydrogen gas evolved as the solid dissolved. Once the rate of bubbling subsided, the solution was placed in a 2 L stainless steel bomb. 2,2′-anhydro-5-methyluridine (60 g, 0.25 mol) and sodium bicarbonate (120 mg) were added and the bomb was sealed. After 30 minutes, the bomb was vented for the last time and then placed in an oil bath and heated to 150° C. internal temperature for 24 hours. The bomb was cooled to room temperature and opened. TLC revealed all the starting material was gone. The crude solution was concentrated and the residue was columned on silica gel starting with straight ethyl acetate to remove the excess phthalimide reagent followed by ethyl acetate-methanol 95/5 to elute the product to give 22.2 g (20.6%) of ca 90% pure product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06335437B1
Quelldatensatzuspto-grants-2002_01
ORD IDord-d9c4b76605064fd0b929d8fdbe98ba41
Quellennotizuspto-grants-2002_01