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HRID 79417作成日:2026年10月24日
N-methyl-2-pyrrolidone → cyano-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide
https://huagongshe.com/ja/reaction/79417
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2,4,6-Trichlorobenzoyl chloride | HCID 2733703 | — |
| 反応物 | 3-ethyl-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-amine | HCID 67259804 | — |
| 反応物 | Lithium 6-cyanoimidazo[1,2-a]pyridine-3-carboxylate | HCID 67260216 | — |
| 生成物 | cyano-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 70814913 | — |
反応手順
Lithium 6-cyanoimidazo[1,2-a]pyridine-3-carboxylate (107 mg, 0.6 mmol) was dissolved in anhydrous NMP (2.8 mL) and 2,4,6-trichlorobenzoyl chloride (94 mL, 0.6 mmol) was added dropwise. The mixture was stirred at ambient temperature for 30 minutes. 3-Ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-amine (137 mg, 0.5 mmol) was added in one portion and the reaction mixture was heated to 80° C. for 6 hours. Saturated sodium bicarbonate solution was added until a precipitate formed and the mixture was allowed to stir at ambient temperature for 1 hour. The precipitate was collected by filtration and dried under high vacuum for 2 hours to give cyano-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide as a beige solid (147 mg). MS m/z 436.3 (M+1, APCI+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08841455B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-270647247a5b43c4aea27b8cc7ddcf68 |
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| 出典メモ | uspto-grants-2014_09 |
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