関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Cyanoacetamide | HCID 7898 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | CID 275522 | HCID 275522 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | Ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate | HCID 275523 | 65.8% |
反応手順
To a stirred solution of ethyl 4-ethoxy-2-oxopent-3-enoate (22.5 g, 121 mmol) and 2-cyanoacetamide (9.0 g, 107 mmol) in acetone (250 mL) was added potassium carbonate (15.8 g, 114 mmol). The reaction was refluxed (85° C. oil bath) for 10 hr (the reaction formed a thick ppt. in a deep red solution). The slurry was added to cold 1 N HCl (230 mL) in ice. After stirring for 30 min. the suspension was filtered, washed with water and dried under vacuum to give the product ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate (14.51 g, 70.4 mmol, 65.7% yield) as a light pink solid. 1H NMR (400 MHz, DMSO-d6) δ12.60 (br. s., 1H), 7.05 (br. s., 1H), 4.34 (q, J=7.1 Hz, 2H), 2.45 (s, 3H), 1.32 (t, J=7.1 Hz, 3H). MS(ES)+ m/e 206.8 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09446041B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-575b23db65c8470daead26cfe841190b |
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| 出典メモ | uspto-grants-2016_09 |
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