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HRID 895099Erstellt: 24. Oktober 2026

Diiodomethane → Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl ester

https://huagongshe.com/de/reaction/895099

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiiodomethaneHCID 6346—
EduktPentyl nitriteHCID 10026—
Edukt(2R,3R,4R,5R)-2-(Acetoxymethyl)-5-(2-amino-6-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetateHCID 10788628—
LösungsmittelAcetonitrileHCID 6342—
ProduktAcetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl esterHCID 482588—

Reaktionsschritte

To a solution of (2R,3R,4R,5R)-4-acetyloxy-5-(acetyloxymethyl)-2-(2-amino-6-chloropurin-9-yl)oxolan-3-yl acetate in acetonitrile was added diiodomethane and n-pentyl nitrite. The mixture was heated under nitrogen for 20 hours, then solvent removed under reduced pressure. The residue was purified by chromatography on silica gel, eluting with hexanes to hexanes/ethyl acetate 2:1, to provide (2R,3R,4R,5R)-4-acetyloxy-5-(acetyloxymethyl)-2-(6-chloro-2-iodopurin-9-yl)oxolan-3-yl acetate, which may be recrystallized from ethanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06914053B2
Quelldatensatzuspto-grants-2005_07
ORD IDord-9ba3d757d3e64f63bac5e5f97322b588
Quellennotizuspto-grants-2005_07