Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657357Generated: November 2, 2026

Acetic Anhydride → HCID 54726179, compound

https://huagongshe.com/reaction/1657357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPyrazofurinHCID 135413551—
SolventMethanolHCID 887—
ProductHCID 54726179HCID 54726179—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1.0 g. of 4-hydroxy-3-β-D-ribofuranosylpyrazole-5-carboxamide in 20 cc. of anhydrous methyl alcohol was stirred and cooled to 0°C. To the cold stirred solution was added 5 cc. of acetic anhydride dropwise over about 10 minutes. The reaction mixture was stirred for about 1 hour while the temperature was allowed to increase to about 25°C. The solvent was removed under reduced pressure to provide an oily residue which was dissolved in 25 cc. of 50 percent methanol-toluene. Again the solvent was removed under reduced pressure. This procedure was repeated three times to insure complete removal of any excess acylating agent. After the final solvents were totally removed, 4-hydroxy-3β-D-ribofuranosyl-N1 -acetylpyrazole-5-carboxamide remained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03960836
Source datasetuspto-grants-1976_06
ORD IDord-702965488f124ff09070e24035941d64
Source noteuspto-grants-1976_06