関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Maleic Anhydride | HCID 7923 | — |
| 反応物 | Hydrochloride methanol | HCID 21893726 | — |
| 反応物 | trimethylsilyldiazomethane Et2O | HCID 23159941 | — |
| 反応物 | Methyl 3-(5-ethoxy-1,3-oxazol-2-yl)propanoate | HCID 59179423 | — |
| 生成物 | Dimethyl 5-hydroxy-2-(3-methoxy-3-oxopropyl)pyridine-3,4-dicarboxylate | HCID 59179398 | 30% |
反応手順
A mixture of methyl 3-(5-ethoxy-1,3-oxazol-2-yl)propanoate (7.00 g, 35.1 mmol) and maleic anhydride (3.44 g, 35.1 mmol) was stirred at room temperature for 2 hr, 10% hydrochloric acid-methanol solution (100 mL) was added, and the mixture was heated under reflux for 15 hr. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→70/30). The purified product was dissolved in methanol, 2M trimethylsilyldiazomethane/diethyl ether solution (34 mL, 68 mmol) was added at room temperature, and the mixture was stirred for 30 min. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=25/75→50/50) to give the title compound (3.10 g, yield 30%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08273761B2 |
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| 出典データセット | uspto-grants-2012_09 |
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| ORD ID | ord-d42a55341dc3431886b22fc9a9422f29 |
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| 出典メモ | uspto-grants-2012_09 |
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