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HRID 42695作成日:2026年10月25日
Propyl mercaptan → 1,3-Dimethyl-2,4-dioxo-6-(propylthio)-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde
https://huagongshe.com/reaction/42695
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Propyl mercaptan | HCID 7848 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 6-Chloro-5-formyl-1,3-dimethyluracil | HCID 319971 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 1,3-Dimethyl-2,4-dioxo-6-(propylthio)-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde | HCID 86658684 | — |
反応手順
To a stirred solution of propane-1-thiol (2.30 mmol) in dry 1,4-dioxane (4 ml), NaH (2.30 mmol) was added under argon. To the mixture, a solution of 6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (2 mmol) in dry 1,4-dioxane (8 ml) was added at 5-8° C. in one portion. The mixture was stirred at room temperature until the starting material was consumed (monitored by TLC). Then the mixture was poured onto ice water (50 ml) and the aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phases were washed with water and dried over anhydrous MgSO4. The solvent was evaporated in vacuo and the crude product was purified by column chromatography with a mixture of n-hexane:ethyl acetate (1:1) as the eluent.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08536210B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-36c7cc926e514e7ea932e77118df6091 |
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| 出典メモ | uspto-grants-2013_09 |
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