関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromoacetone | HCID 11715 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate | HCID 86713416 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 86713417 | HCID 86713417 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09447090B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-2d92678427e44e14afb990b87d1e5427 |
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| 出典メモ | uspto-grants-2016_09 |
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