HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64409Generated: October 25, 2026
Bromoacetone → HCID 86713417, compound
https://huagongshe.com/reaction/64409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetone | HCID 11715 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate | HCID 86713416 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86713417 | HCID 86713417 | — |
Reaction Steps
To a suspension of 2.15 g of methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate in 43 ml of ethanol was added 1.09 ml of bromoacetone, followed by stirring at 80° C. for 4 hours. To the reaction mixture was added 1.09 ml of bromoacetone, followed by stirring at 80° C. for 4 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and the solvent was evaporated under reduced pressure, followed by extracting with ethyl acetate and washing with saturated brine. After drying over anhydrous magnesium sulfate and then filtering, the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 1.39 g of methyl 8-[(2-fluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-6-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447090B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-2d92678427e44e14afb990b87d1e5427 |
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| Source note | uspto-grants-2016_09 |
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