HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-Iodo-6-(2,4,5-trifluorophenyl)imidazo[2,1-b]oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 6-(2,4,5-Trifluorophenyl)imidazo[2,1-b]oxazole | HCID 59457851 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Iodo-6-(2,4,5-trifluorophenyl)imidazo[2,1-b]oxazole | HCID 57929886 | 73.3% |
Reaction Steps
To a round bottom flask containing 6-(2,4,5-trifluorophenyl)imidazo[2,1-b]oxazole (11.7 g, 49.1 mmol) and DMF (120 mL) was added NIS (11.4 g, 50.6 mmol). The reaction mixture was stirred at ambient temperature for about 1 h. The reaction mixture was poured into water (300 mL) and the resulting precipitate was collected by vacuum filtration. The solid was dissolved into DCM (500 mL) and the organic suspension was washed sequentially with saturated NaHCO3 solution, 5% sodium thiosulfate solution, and brine. The resulting solution was dried over MgSO4, filtered, and concentrated to dryness under reduced pressure to give the title compound as a pale yellow solid (13.1 g, 73%): LC/MS (Table 1, Method b) Rt=2.17 min; MS m/z 365.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188083B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-1106364313c84c05aaf47a6e42a78aca |
| Source note | uspto-grants-2012_05 |