HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 3-Amino-2-cyano-6-iodopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 3-Amino-6-chloropyridine-2-carbonitrile | HCID 592750 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 3-Amino-2-cyano-6-iodopyridine | HCID 19040785 | — |
Reaction Steps
A stirred suspension of 12.0 grams (0.08 mole) of 3-amino-6-chloro-2-cyanopyridine [prepared by the method of Colbry, Elslager, and Werbel; previously cited] and 26.9 grams (0.18 mole) of sodium iodide in 300 mL of n-butanone is heated at reflux for about 3 days. After this time, the reaction mixture is concentrated under reduced pressure to a residue. The residue is then stirred with about 50 mL of water. The resultant solid is collected by filtration and washed with water. The solid is dried, yielding 3-amino-2-cyano-6-iodopyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532367 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-c130eeca075547f0963bc0c91f27bf05 |
| Source note | uspto-grants-1996_07 |