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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419783Generated: October 29, 2026

5-Nitro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone → 5-Nitro-1-beta-D-ribofuranosylpyridin-2(1H)-one

https://huagongshe.com/reaction/419783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinoneHCID 11273267—
SolventAmmoniaHCID 222—
Product5-Nitro-1-beta-D-ribofuranosylpyridin-2(1H)-oneHCID 66649608—

Reaction Steps

A mixture of 5-nitro-1-(2′,3′,5′-tri-O-benzoyl-β-ribofuranosyl)-2-pyridone (10, R=Bz, Y=H, Z=CH; 100 mg, 0.17 mmol) and saturated methanolic ammonia (10 mL) was stirred at room temperature for 12 h. The mixture was concentrated to dryness, and the residue triturated with EtOH to precipitate 10 (R=Y=H, Z=CH), which was collected and recrystallized from water (37 mg, 81%) as a white solid. 1H NMR (DMSO-d6+D2O) δ 3.64 (m, 1H), 3.90 (m, 1H), 4.01 (m, 3H), 5.89 (s, 1H), 6.48 (d, J=10.4 Hz, 1H), 8.12 (dd, J=3.2, 10 Hz, 1H), 9.65 (d, J=3.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093380B2
Source datasetuspto-grants-2012_01
ORD IDord-e0e00f1c933d466e893aa2689309f616
Source noteuspto-grants-2012_01