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Ethyl bromopyruvate → Ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl bromopyruvate | HCID 66144 | — |
| 反応物 | 4-Ethylpyridin-2-amine | HCID 118425 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate | HCID 20072849 | 18.6% |
反応手順
A mixture of 2-amino-4-ethylpyridine (3.8 g), ethyl 3-bromo-2-oxopropionate (6.84 g) and ethanol (30 ml) was refluxed for 6 hours. After the reaction mixture was concentrated, water (30 ml) and ehtyl acetate (30 ml) were added to the residue. The mixture was made basic with an aqueous solution of potassium carbonate, and the separated organic layer was washed with brine and dried over magnesium sulfate. The solvent was evaporated and the residue was subjected to a column chromatography on silica gel (150 g) and eluted with 15% solution of ethyl acetate in chloroform. The fractions containing the object compound were combined and concentrated to give ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate (1.26 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04988698 |
| 出典データセット | uspto-grants-1991_01 |
| ORD ID | ord-813225852fa145a39cf7ab9cac993ee1 |
| 出典メモ | uspto-grants-1991_01 |