HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178513792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Pyridinecarbonitrile, 1-oxide | HCID 84684 | — |
| Reactant | 2-Aminopropanediamide | HCID 96457 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178513792 | HCID 178513792 | 90.3% |
Reaction Steps
To a solution of 4-cyanopyridine N-oxide (600 g) in ahydrous methanol (250 ml) was added sodium methoxide (1.35 g), and this solution was stirred for 0.5 hour at room temperature. To this solution were added aminomalonamide (3.51 g) and acetic acid, and this mixture was stirred for 2 hours under reflux. After cooling the reaction mixture to 0°-5° C., the precipitated product was separated by filtration, washed with ethanol, isopropylether and dried under vacuum to give yellow crystal of 4-(4-carbamoyl-5-hydroxyimidazole-2yl)-pyridine-N-oxide (5.96 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04218457 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-d909f152f6744ec59324316f91b5ba83 |
| Source note | uspto-grants-1980_08 |