HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-Chloro-3-iodopyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Boc-Amino-3-iodo-4-chloropyridine | HCID 59852886 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-3-iodopyridin-2-amine | HCID 22936596 | 90.4% |
Reaction Steps
A solution of aqueous HBr (48%, 10 mL, 13.26 mmol) was added to tert-butyl (4-chloro-3-iodopyridin-2-yl)carbamate (4.7 g, 13.26 mmol) and the suspension was stirred at RT for 3 h. The reaction mixture was diluted with water (40 ml), basified with 2N NaOH and the resultant suspension was filtered, washed with water (4×1 mL) and dried to afford 4-chloro-3-iodopyridin-2-amine as white solid (3.05 g, 90% yield). MS (ESI) m/z: 254.9 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569319B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-399d47f5fba5491899c37c1490d9db8f |
| Source note | uspto-grants-2013_10 |