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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030775Erstellt: 26. Oktober 2026

Acetonitrile → 5'-O-acetyl-2',3'-dideoxyadenosine

https://huagongshe.com/reaction/1030775

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
Edukt1,1'-Diheptyl-4,4'-bipyridinium dibromideHCID 80262—
Edukt9-(2,5-di-O-acetyl-3-bromo-3-deoxy-beta-D-xylofuranosyl)adenineHCID 10982560—
EduktHCID 178418361HCID 178418361—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelTriethylamineHCID 8471—
Produkt((2S,5R)-5-(6-Amino-9H-purin-9-yl)-2,5-dihydrofuran-2-yl)methyl acetateHCID 11022122—
Produkt5'-O-acetyl-2',3'-dideoxyadenosineHCID 1498946711%
Produkt2',5'-di-O-acetyl-3'-deoxyadenosineHCID 149894683%

Reaktionsschritte

To 120 ml of acetonitrile were added 1.50 g (3.62 mmols) of 9-(2,5-di-O-acetyl-3-bromo-3-deoxy-β-D-xylofuranosyl) adenine, 946 mg (1.84 mmol) of N,N'-diheptyl-4,4'-bipyridinium dibromide, 1.13 g of 10% palladium-carbon (water content, 50%) and 2.5 ml of triethylamine. The mixture was stirred for 2 hours at room temperature in a hydrogen atmosphere. The analysis by HPLC reveals that the raw material disappeared and 5'-O-acetyl-2',3'-didehydro-2',3'-dideoxyadenosine (85), 5'-O-acetyl-2',3'-dideoxyadenosine (11%) and 2',5'-di-O-acetyl-3'-deoxyadenosine (3%) were formed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05106962
Quelldatensatzuspto-grants-1992_04
ORD IDord-ae99ac58e91b4559a1428c60995f923b
Quellennotizuspto-grants-1992_04