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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267793Generated: October 25, 2026

Water → Levovirin

https://huagongshe.com/reaction/1267793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantRibavirinHCID 37542—
ReactantMethyl 1-(2,3,5-Tri-O-acetyl-beta-L-ribofuranosyl)-1,2,4-triazole-3-carboxylateHCID 10691464—
SolventAmmonia methanolHCID 21705897—
ProductLevovirinHCID 460516—

Reaction Steps

The substrate (20) (1.1 g) was dissolved in CH3OH/NH3 at 0° C. and placed in a steel bomb. The bomb was closed and stirred at room temperature for 18 h. The steel bomb was cooled, opened and evaporated to dryness. The residue was tried to crystallization with little ethanol. The product crystallized, but on filtration, the crystals re-absorbed water and became a paste. The crystallization repeated several times. Finally it crystallized from Methanol/Ethanol mixture. The colorless crystals was filtered, washed with methanol and dried in vacuo. The filtrate was evaporated again which on standing gave further crystals. Total yield 0.5 g (72%); mp: 177-179° C.; [a]D=+38.33 (c 3 mg/mL H2O); D form of Ribavirin [a]D=−36.0 (c 3.0 mg/mL H2O); 1H NMR (Me2SO-d6) δ 3.46 (m, 1H, C5′H), 3.60 (m, 1H, C5.H), 3.92 (q, 1H, C4′H, 4.12 (q, 1H), 4.34 (q, 1H), 4.88 (t, 1H, C5.OH), 5.20 (d, 1H), 5.58 (d, 1H), 5.80 (d, 1H, C1′H), 7.60 (bs, 1H, NH), 7.82 (bs, 1H, NH), and 8.82 (s, 1H, C3H). Anal. Calc. for C8H12N4O5 (244.20): C, 39.34; H, 4.95; N, 22.94. Found: C, 39.23; H, 4.97; N, 22.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552183B1
Source datasetuspto-grants-2003_04
ORD IDord-65e9935818d5496dbb101cb7d773177c
Source noteuspto-grants-2003_04