HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 178509224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 5-Bromo-2-chloronicotinonitrile | HCID 21948269 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 178509224 | HCID 178509224 | — |
Reaction Steps
(Step 7-i) To a solution of 5-bromo-2-chloropyridine-3-carbonitrile (2 g, 9.22 mmol) in 30 mL n-butanol was added 2 mL anhydrous hydrazine. The reaction mixture was heated under reflux for 14 hrs and allowed to cool to room temperature. The solvent was removed by evaporation and the residue was poured into a saturated NaHCO3 solution. The resulting precipitate was collected and washed with water. After drying in vacuo, the product, 5-bromo-1H-pyrazolo[3,4-b]pyridin-3-amine, can be used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481538B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-711450a1f81645fea6423bbc0b429397 |
| Source note | uspto-grants-2013_07 |