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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-IodosuccinimideHCID 120273—
Reactant6-(2,4-Difluorophenyl)imidazo[2,1-b]oxazoleHCID 59457870—
SolventDimethylformamideHCID 6228—
Product6-(2,4-Difluorophenyl)-5-iodoimidazo[2,1-b]oxazoleHCID 5945780695%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790741B2
Source datasetuspto-grants-2010_09
ORD IDord-5e5bd099109d4d0b83ce15e97a2af504
Source noteuspto-grants-2010_09