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HRID 75557作成日:2026年10月25日
Isothiocyanatotrimethylsilane → Ethyl 2-(6-(2,4-dimethoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetate
https://huagongshe.com/reaction/75557
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isothiocyanatotrimethylsilane | HCID 75297 | — |
| 反応物 | Ethylacetate heptane | HCID 21899848 | — |
| 反応物 | (Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate | HCID 86684695 | — |
| 溶媒 | 2-Methyltetrahydrofuran | HCID 7301 | — |
| 生成物 | Ethyl 2-(6-(2,4-dimethoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetate | HCID 86684696 | — |
反応手順
To a solution of (Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate (4.68 g, 15.1 mmol) in 2-methyltetrahydrofuran (38 mL) was added (trimethylsilyl)isothiocyanate (12.9 mL, 90.8 mmol). The resulting solution was purged with nitrogen gas for 3 times, and the mixture was heated at 110° C. for 18 hours. The mixture was cooled down to room temperature and the solvent was removed under reduced pressure to give a red solid. This residue was suspended in a mixture of 3:1 heptane/EtOAc (200 mL), and it was stirred at room temperature for 1 hour. The solid was filtered, and triturated with CH2Cl2 (100 mL), concentrated under reduced pressure and dried under vacuum the title compound (4.42 g, 87%) as a pink solid. This material was used without further purification in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835449B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-5356724165aa47ea97f6a12f0ced82f0 |
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| 出典メモ | uspto-grants-2014_09 |
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