HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038969Generated: November 1, 2026
Hydrochloric Acid → 6-Oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1038969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanimidamide, hydrochloride (1:1) | HCID 10313058 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester | HCID 96347 | — |
Reaction Steps
A mixture of formamidine hydrochloride (4.02 g, 49.9 mmol) and diethyl ethoxymethylenemalonate (5 ml, 24.95 mmol) in ethanol (4.99 ml) was heated to 120° C. (by microwave irradiation) for 15 h. After the reaction mixture was cooled to room temperature, ethyl acetate, hydrochloric acid (1M), and water were added. The aqueous layer was washed with ethyl acetate and then extracted with 3:1 chloroform:isopropanol. The combined organic extracts were dried over magnesium sulfate and concentrated under reduced pressure to afford ethyl 6-oxo-1,6-dihydropyrimidine-5-carboxylate as an orange solid. LRMS (ESI) calc'd for (C7H9N2O3) [M+H]+, 169.1; found 169.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552019B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-c927a47ce03d44228d7563403e097ce6 |
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| Source note | uspto-grants-2013_10 |
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