HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 6,7-Dihydropyrazolo[1,5-a]pyrimidine-4(5H)-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4H,5H,6H,7H-pyrazolo(1,5-a)pyrimidine | HCID 135627629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6,7-Dihydropyrazolo[1,5-a]pyrimidine-4(5H)-carbaldehyde | HCID 15077742 | — |
Reaction Steps
To acetic anhydride (0.153 ml) was added formic acid (0.077 ml) at 15-20° C. The mixture was stirred at ambient temperature for 30 minutes. To this solution was added 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (100 mg) under ice-cooling and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was added to a mixture of dichloromethane and aqueous sodium bicarbonate solution. The separated organic layer was dried over magnesium sulfate and evaporated in vacuo to give 4-formyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (79.9 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05173485 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-67ca3f84fc8f4cc28f0e1d1d5876d3e7 |
| Source note | uspto-grants-1992_12 |