Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Pyrazofurin | HCID 135413551 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54726179 | HCID 54726179 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03960836 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-702965488f124ff09070e24035941d64 |
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| Source note | uspto-grants-1976_06 |
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