Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 5-bromoimidazo[1,2-a]pyridine-2-carboxylate | HCID 19701375 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66598454 | HCID 66598454 | 95% |
Reaction Steps
To a suspension of ethyl 5-bromo-imidazo[1,2-a]pyridine-2-carboxylate (1.50 g, 5.6 mmol), Pd(PPh3)4 (322 mg, 0.279 mmol) in a mixture of toluene (17 mL), NaHCO3 1M (6 mL) and MeOH (4 mL) was added phenylboronic acid at room temperature. The resulting reaction mixture was heated at 80° C. for 12 h, cooled, and diluted with water (50 mL). The insoluble matter was filtered off, and the phases were separated. The aqueous phase was extracted with ethyl acetate, the combined organic layers were washed with water and the solvent was removed under reduced pressure. The crude product was purified by chromatography (prepacked 0.25° g silicagel column, DCM/MeOH from 100/0 to 99/1 as eluent) to afford 1.41 g. of ethyl 5-phenyl-imidazo[1,2-a]pyridine-2-carboxylate (Yield: 95%) as a yellowish solid (M.P.=123-123.8° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101637B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-fd28d33e77184874a954ec53d08430eb |
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| Source note | uspto-grants-2012_01 |
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