HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229444Generated: October 30, 2026
Guanidine Hydrochloride → Ethyl 2-amino-4-(trifluoromethyl)-5-pyrimidinecarboxylate
https://huagongshe.com/reaction/229444
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 74965881 | HCID 74965881 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-amino-4-(trifluoromethyl)-5-pyrimidinecarboxylate | HCID 2737153 | 62% |
Reaction Steps
Sodium ethoxide (2 eq, 83.8 mmol, 5.7 g) was added in one portion to a solution of guanidine hydrochloride (4 g, 41.9 mmol) in absolute ethanol (100 ml) and the resulting mixture was stirred at ambient temperature for 1 hour. A dichloromethane solution of 3-methoxy-2-(2,2,2-trifluoro-acetyl)-acrylic acid ethyl ester was then added and the mixture was stirred at ambient temperature for an additional 20 hours. The solvent was then removed by evaporation, water was added to the residue, and the mixture was stirred vigorously for 2 hours then allowed to stand at room temperature. The resulting solid was isolated by filtration, washed with water then dried in vacuo to afford 6.10 g (62% yield) of 2-amino-4-trifluoromethyl-pyrimidine-5-carboxylic acid ethyl ester. m/z (M+H)=236.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07563797B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-4d486094f329406db59a7cb40a1ef281 |
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| Source note | uspto-grants-2009_07 |
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