HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 2-Hydrazinyl-5-iodopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Chloro-5-iodopyridine | HCID 4397176 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Hydrazinyl-5-iodopyridine | HCID 22397188 | — |
Reaction Steps
A mixture of 2-chloro-5-iodopyridine (1.918 g, 8.01 mmol), anhydrous hydrazine (1.26 mL, 40.05 mmol) and pyridine (30 mL) was warmed at reflux for 18 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was partitioned between dichloromethane and 1N aqueous sodium hydroxide solution. The organic layer was separated, dried (magnesium sulfate) and concentrated under reduced pressure. The residue was triturated with hexanes, and the resultant precipitate was collected and dried in vacuo to afford the title compound as off-white crystals. LC/MS 235.8 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157490B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-bea3ef6a301e4f3685fe133979457d6b |
| Source note | uspto-grants-2007_01 |