関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Magnesium Carbonate | HCID 11029 | — |
| 反応物 | Chloromalonaldehyde | HCID 147646 | — |
| 反応物 | Tert-butyl 3-carbamothioylpyrrolidine-1-carboxylate | HCID 5098610 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | Tert-butyl 3-(5-formylthiazol-2-yl)pyrrolidine-1-carboxylate | HCID 86701991 | — |
反応手順
tert-Butyl 3-carbamothioylpyrrolidine-1-carboxylate (5 g, 21.71 mmol), 2-chloromalonaldehyde (3.70 g, 34.7 mmol) and magnesium carbonate (1.830 g, 21.71 mmol) were combined in dioxane (100 ml). The mixture was heated to 60° C. for 3 hours, stirred overnight at room temperature and then filtered through a pad of diatomaceous earth, rinsing with dichloromethane. The filtrate was concentrated in vacuo and then purified by normal phase chromatography to provide the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09187472B2 |
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| 出典データセット | uspto-grants-2015_11 |
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| ORD ID | ord-e3c4810a0c44440c970a610f7f5f5ced |
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| 出典メモ | uspto-grants-2015_11 |
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