Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,3,6-Trifluorobenzyl bromide | HCID 519061 | — |
| Reactant | Ethyl 8-hydroxy-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate | HCID 86717883 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86717935 | HCID 86717935 | — |
Reaction Steps
3.00 g (12.81 mmol) of ethyl 8-hydroxy-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate Example 17A, 3.27 g (14.1 mmol) of 2-(bromomethyl)-1,3,4-trifluorobenzene and 9.18 g (28.17 mmol) of caesium carbonate were initially charged in 183 ml of dry DMF and heated for 30 min in an oil bath warmed to 60° C. About 1.8 l of water were added to the reaction mi×ture, the mixture was stirred for 30 min and the solid was filtered off, washed with water and dried under reduced pressure. This gave 5.07 g of the title compound (99% of theory; purity about 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796305B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-d25f00bde7874ed190b7444f9f8e3e68 |
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| Source note | uspto-grants-2014_08 |
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