HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075274Generated: October 31, 2026
Sodium → Methyl 4-aminopyrimidine-2-carboxylate
https://huagongshe.com/reaction/1075274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-Ethoxycarbonylformamidine hydrobromide | HCID 23316851 | — |
| Reactant | Ethyl 3-ethoxyacrylimidate hydrochloride | HCID 86737728 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-aminopyrimidine-2-carboxylate | HCID 13060221 | 39% |
Reaction Steps
To a solution of ethyl 3-ethoxyacrylimidate hydrochloride (4.0 g) and 1-ethoxycarbonylformamidine hydrobromide (4.4 g) in methanol (110 ml) was added dropwise a solution of sodium metal (1 g) in methanol (110 ml) at 0° C. The reaction mixture was stirred for an hour at 0° to 5° C. and for additional 4 hours at ambient temperature. The solution was evaporated to dryness and the residue was dissolved in a mixture of ethyl acetate and an aqueous solution of sodium chloride. The organic layer was separated out and the aqueous layer was extracted with ethyl acetate five times. All organic layers were combined, dried over anhydrous magnesium sulfate and evaporated to dryness. The residue was triturated with diethylether to give methyl 4-aminopyrimidine-2-carboxylate (1.33 g), which was recrystallized from ethyl acetate, mp. 140°-142.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04395411 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-4a85533222bf44bc8f533d8887f71f67 |
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| Source note | uspto-grants-1983_07 |
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