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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610252Generated: October 31, 2026

HCID 22121270, compound → HCID 22121260, compound

https://huagongshe.com/reaction/610252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22121270HCID 22121270—
ReactantEthyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylateHCID 54402571—
SolventEthanolHCID 702—
ProductHCID 22121260HCID 2212126045.4%

Reaction Steps

A solution of 300 mg of unpurified 2-amino-6-t-butylamino-3-cyano-5-fluoropyridine in 2 ml ethanol was added dropwise to a solution of 420 mg of ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate in 2 ml ethanol at room temperature, and the mixture was stirred overnight. The solvent was distilled off the reaction solution, and to the residue were added 3 ml of N,N-dimethylformamide and 210 mg of potassium carbonate, and the mixture was stirred at room temperature for 90 minutes and 80° C. for 2 hours. The reaction solution was extracted by adding water and ethyl acetate, and the organic layer was collected and dried over magnesium sulfate. The solvent was distilled off, and the residue was collected by filtration using ethanol and washed with diethylether to obtain 280 mg of the title compound as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998436
Source datasetuspto-grants-1999_12
ORD IDord-350817fd9e2a431a9fe896baa5dcecf0
Source noteuspto-grants-1999_12