HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610252Generated: October 31, 2026
HCID 22121270, compound → HCID 22121260, compound
https://huagongshe.com/reaction/610252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22121270 | HCID 22121270 | — |
| Reactant | Ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate | HCID 54402571 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22121260 | HCID 22121260 | 45.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05998436 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-350817fd9e2a431a9fe896baa5dcecf0 |
|---|
| Source note | uspto-grants-1999_12 |
|---|