참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Acetamidine monohydrochloride | HCID 67170 | — |
| 반응물 | Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate | HCID 54012347 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 6-(5-Chloro-2-methoxyphenyl)-2-methylpyrimidin-4-ol | HCID 136341888 | 68% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07419984B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-5314391f367944da93370148cb759c3c |
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| 출처 메모 | uspto-grants-2008_09 |
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