HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 6-Bromo-2-iodopyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 6-Bromopyridin-3-amine | HCID 642811 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Bromo-2-iodopyridin-3-amine | HCID 53401177 | 89.2% |
Reaction Steps
5.0 g 5-Amino-2-bromopyridine were dissolved in 70 ml ethanol. 9.0 g silver sulfate and 7.33 g iodine were added. The reaction mixture was stirred at room temperature overnight. The solvent was removed in vacuo and the residue diluted with 500 ml ethyl acetate and filtered over a celite pad. The filtrate was washed with 200 ml saturated Na2S203 solution and water, dried over MgSO4 and then the solvent was removed in vacuo to obtain 7.7 g 6-Bromo-2-iodo-pyridin-3-ylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946212B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-0e25cf880a41421cb72b4c3519daac3d |
| Source note | uspto-grants-2015_02 |