HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4H,5H,6H,7H-pyrazolo(1,5-a)pyrimidine | HCID 135627629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine | HCID 15077743 | — |
Reaction Steps
To a suspension of 62% sodium hydride (1.41 g) in N,N-dimethylformamide (30 ml) was added 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (4.5 g) under ice-cooling. To this solution was added dropwise methyl iodide (2.27 ml) under ice-cooling, and the mixture was stirred at the same temperature for 1.5 hours. The reaction mixture was poured into ethyl acetate (50 ml), and the resulting precipitate was filtered off. The filtrate was evaporated to give 4-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (5.05 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05366970 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-27438b75cbf948a0ae7430f12ffc8ab0 |
| Source note | uspto-grants-1994_11 |