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HRID 874347作成日:2026年10月26日
Methyl 2-aminopyridine-4-carboxylate → Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylate
https://huagongshe.com/reaction/874347
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl 2-aminopyridine-4-carboxylate | HCID 236984 | — |
| 反応物 | 2-Bromo-1-(2,5-difluorophenyl)ethanone | HCID 2778264 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylate | HCID 90383269 | 135.9% |
反応手順
2-Bromo-1-(2,5-difluorophenyl)ethanone (1.5 g) was added to an ethanol (8.2 ml) solution of methyl 2-aminoisonicotinate (1.0 g), and the obtained mixture was then stirred in a nitrogen atmosphere at 60° C. for 18 hours. Thereafter, 2-bromo-1-(2,5-difluorophenyl)ethanone (0.77 g) was added to the reaction solution, and the obtained mixture was then stirred for 6 hours at the same temperature as described above. Thereafter, the reaction solution was concentrated under reduced pressure, and ethyl acetate (10 ml) was then added to the obtained residue. The precipitated solid was collected by filtration, and it was washed with ethyl acetate (15 ml) and heptane (6 ml) and was then dried, so as to obtain the title compound (2.5 g) in the form of a pink solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08980888B2 |
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| 出典データセット | uspto-grants-2015_03 |
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| ORD ID | ord-b35c6db733204e129668dc195af0bff4 |
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| 出典メモ | uspto-grants-2015_03 |
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