HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2H-Pyrazolo[4,3-b]pyridine, 7-bromo-2-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Bromo-1H-pyrazolo[4,3-b]pyridine | HCID 67470457 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2H-Pyrazolo[4,3-b]pyridine, 7-bromo-2-methyl- | HCID 67469527 | — |
Reaction Steps
A solution of 7-bromo-1H-pyrazolo[4,3-b]pyridine (100 mg, 0.505 mmol) and sodium hydride (24.24 mg, 0.606 mmol) in THF (2.0 mL) was stirred at 0° C. for 15 minutes. Iodomethane (71.7 mg, 0.505 mmol) was added, and the reaction was warmed to room temperature for 1 hour. The reaction was quenched with water, extracted with EtOAc, dried over MgSO4, and evaporated to dryness to give 7-bromo-2-methyl-2H-pyrazolo[4,3-b]pyridine which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073918B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-c8af38c32b404e4aac0eaf59cf76df9d |
| Source note | uspto-grants-2015_07 |