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HRID 1172228作成日:2026年10月27日
N-(4-(2,2-Dicyanoethenyl)phenyl)acetamide → N-[4-(6-amino-5-cyano-2-mercapto-2,3-dihydropyrimidin-4-yl)phenyl]acetamide
https://huagongshe.com/reaction/1172228
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-(4-(2,2-Dicyanoethenyl)phenyl)acetamide | HCID 33296 | — |
| 反応物 | Thiourea | HCID 2723790 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | N-[4-(6-amino-5-cyano-2-mercapto-2,3-dihydropyrimidin-4-yl)phenyl]acetamide | HCID 86621820 | 41.8% |
反応手順
To 20 mL of absolute ethanol, 250 mg of metallic sodium was added in small portions. After dissolved completely, 760 mg of thiourea was added to the above solution, and the mixture was stirred at room temperature for 1 hour. To the reaction, 2.11 g of N-[4-(2,2-dicyanovinyl)phenyl]acetamide was added, and the mixture was heated to reflux for 3 hours. Then, the solvent was removed under reduced pressure from the reaction mixture, the residue was dissolved in 30 mL of water. In addition, the mixture was acidified by adding acetic acid in small portions, thereto 30 mL of ethyl acetate was added and then the solution was stirred overnight. Filtration of the precipitated material gave 1.2 g of N-[4-(6-amino-5-cyano-2-mercapto-2,3-dihydropyrimidin-4-yl)phenyl]acetamide as a white powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07834002B2 |
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| 出典データセット | uspto-grants-2010_11 |
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| ORD ID | ord-0d7f92e212674c2f9cf27192a2404cf8 |
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| 出典メモ | uspto-grants-2010_11 |
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