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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantDichloromethaneHCID 6344—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 74965881HCID 74965881—
SolventEthanolHCID 702—
ProductEthyl 2-amino-4-(trifluoromethyl)-5-pyrimidinecarboxylateHCID 273715362%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563797B2
Source datasetuspto-grants-2009_07
ORD IDord-4d486094f329406db59a7cb40a1ef281
Source noteuspto-grants-2009_07