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 1N 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 | US09242962B2 |
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| 出典データセット | uspto-grants-2016_01 |
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| ORD ID | ord-952798e87ea34fe590227fa907cd7ca1 |
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| 出典メモ | uspto-grants-2016_01 |
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