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HRID 75541作成日:2026年10月25日
Isothiocyanatotrimethylsilane → 6-(2,6-Dimethoxypyridin-3-yl)-1-(2-hydroxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
https://huagongshe.com/reaction/75541
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Isothiocyanatotrimethylsilane | HCID 75297 | — |
| 反応物 | HCID 86684678 | HCID 86684678 | — |
| 溶媒 | 2-Methyltetrahydrofuran | HCID 7301 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 6-(2,6-Dimethoxypyridin-3-yl)-1-(2-hydroxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one | HCID 86684679 | 16% |
反応手順
To a solution of (Z)-ethyl 3-(2,6-dimethoxypyridin-3-yl)-3-((2-hydroxyethyl)amino)acrylate (100 mg, 0.34 mmol) in 2-MeTHF (1.0 mL) was added (trimethylsilyl)isothiocyanate (0.30 mL, 2.0 mmol) and the reaction mixture was heated at 80° C. for 4 hours. The cooled reaction mixture was diluted with EtOAc and washed with a saturated aqueous sodium bicarbonate solution. The layers were separated and the organic layer was concentrated in vacuo. The residue was triturated with MeOH and the resulting solids were collected by vacuum filtration to give the title compound (16 mg, 16%) as a white solid.
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-57d982c63b564ccf8f14e28d8af23c19 |
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| 出典メモ | uspto-grants-2014_09 |
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