Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | Imidazo[1,2-a]pyridin-2-ol | HCID 14674030 | — |
| Product | 2-Bromoimidazo[1,2-a]pyridine | HCID 12428957 | 19.9% |
Reaction Steps
To 44.0 g of melted phosphorus oxybromide, 12.0 g of 2-hydroxyimidazo[1,2-a]pyridine is added at 60°-85° C. and stirred for 3 hours at 90° C. The mixture is poured into 300 ml of ice water, neutralized with aqueous ammonia and then extracted with chloroform. The collected chloroform layer is dried over anhydrous sodium sulfate. Chloroform is distilled off and the residue is purified by silica gel chromatography (eluent: chloroform) to obtain 3.5 g of the title compound as a crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05017212 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-3b91fc7bc6524740bf49fea0aaeb9b01 |
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| Source note | uspto-grants-1991_05 |
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