HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28555Generated: October 26, 2026
Potassium Carbonate → 6-(5-Chloro-2-methoxyphenyl)-2-methylpyrimidin-4-ol
https://huagongshe.com/reaction/28555
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate | HCID 54012347 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-(5-Chloro-2-methoxyphenyl)-2-methylpyrimidin-4-ol | HCID 136341888 | 68% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07419984B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-5314391f367944da93370148cb759c3c |
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| Source note | uspto-grants-2008_09 |
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