HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 178526495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Nitroindazole | HCID 21501 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178526495 | HCID 178526495 | 97.2% |
Reaction Steps
To a solution of 5-nitro-1H-indazole (10.0 g, 62.3 mmol) in DMF (120 ml) was added potassium hydroxide (12.9 g, 230.4 mmol) followed by iodine (31.1 g, 122.6 mmol) portion wise over 5 minutes. The resulting mixture was stirred at room temperature for 14 hours and then poured onto 10% sodium metabisulfite (100 ml) and extracted into ethyl acetate (3×50 ml). The combined organic extracts were washed with brine (50 ml), dried (Na2SO4) and concentrated in vacuo to afford the title compounds as a pale orange solid (17.5 g). 1H NMR (400 MHz, DMSO-d6) δ 7.77 (1H, d), 8.26 (1H, d), 8.34 (1H, s), 14.15 (1H, s). MS (ES+) m/e=290.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041687B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-f99c06c08d824ccca6cd8934e9048600 |
| Source note | uspto-grants-2006_05 |