참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Cyanoacetamide | HCID 7898 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | CID 275522 | HCID 275522 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | Ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate | HCID 275523 | 65.8% |
반응 단계
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]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09242962B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-952798e87ea34fe590227fa907cd7ca1 |
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| 출처 메모 | uspto-grants-2016_01 |
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