HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711784Generated: November 1, 2026
Water → 6-(2,4-Difluorophenyl)-5-iodoimidazo[2,1-b]oxazole
https://huagongshe.com/reaction/1711784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 6-(2,4-Difluorophenyl)imidazo[2,1-b]oxazole | HCID 59457870 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(2,4-Difluorophenyl)-5-iodoimidazo[2,1-b]oxazole | HCID 59457806 | 95% |
Reaction Steps
Into a round bottom flask charged with 6-(2,4-difluorophenyl)-imidazo[2,1-b]oxazole (5.0 g, 23 mmol; prepared using A from 6-(2,4-difluorophenyl)-imidazo[2,1-b]oxazole [prepared according to WO2004110990A2, Example 1, Steps 1-3 using 2-bromo-1-(2,4-difluorophenyl)-ethanone in place of 2-bromo-1-(4-fluorophenyl)-ethanone]) and DMF (100 mL) was added a solution of NIS (5.4 g, 24 mmol) in DMF (20 mL) at ambient temperature. The reaction was allowed to stir at ambient temperature for about 1 h upon which time it was poured into water (800 mL). The resulting precipitate was filtered, washed with water (2×20 mL), and dried in a vacuum oven for about 16 h to provide the title compound (7.5 g, 95%) as a light yellow solid: LC/MS (Table 1, Method a) Rt=2.04 min; MS m/z/z: 347.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790741B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5e5bd099109d4d0b83ce15e97a2af504 |
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| Source note | uspto-grants-2010_09 |
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