関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Acetamidine monohydrochloride | HCID 67170 | — |
| 反応物 | Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate | HCID 54012347 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-(5-Chloro-2-methoxyphenyl)-2-methylpyrimidin-4-ol | HCID 136341888 | 68% |
反応手順
A mixture of 3-(5-chloro-2-methoxy-phenyl)-3-oxopropionic acid ethyl ester (0.9 g, 3.2 mmol), acetamidine hydrochloride (448 mg, 4.7 mmol) and potassium carbonate (1.3 g, 9.6 mmol) in ethanol (15 ml) was stirred at 100° C. in thick wall tube for 60 hours. After cooling to room temperature, the mixture was poured into ice cold water. The solid was collected by filtration, washed with water and ether and dried under vacuum to provide 6-(5-chloro-2-methoxy-phenyl)-2-methyl-3H-pyrimidin-4-one (530 mg, 68% yield) as a white powder. 1H NMR (DMSO-d6) δ 2.32 (s, 3H, CH3), 3.85 (s, 3H, CH3), 6.77 (s, 1H, CH, Ar), 7.15 (d, 1H, J=8.8 Hz, Ar), 7.45 (dd, 1H, J=8.8 Hz, J=2.9 Hz, Ar), 7.90 (d, 1H, J=2.9 Hz, Ar), 12.42 (s, 1H, NH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07419984B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-5314391f367944da93370148cb759c3c |
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| 出典メモ | uspto-grants-2008_09 |
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