참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Maleic Anhydride | HCID 7923 | — |
| 반응물 | Hydrochloride methanol | HCID 21893726 | — |
| 반응물 | trimethylsilyldiazomethane Et2O | HCID 23159941 | — |
| 반응물 | Methyl 3-(5-ethoxy-1,3-oxazol-2-yl)propanoate | HCID 59179423 | — |
| 생성물 | Dimethyl 5-hydroxy-2-(3-methoxy-3-oxopropyl)pyridine-3,4-dicarboxylate | HCID 59179398 | 30% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08273761B2 |
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| 출처 데이터셋 | uspto-grants-2012_09 |
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| ORD ID | ord-d42a55341dc3431886b22fc9a9422f29 |
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| 출처 메모 | uspto-grants-2012_09 |
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