HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-amino-4-phenylthiophene-3-carboxylate → HCID 67382085, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-amino-4-phenylthiophene-3-carboxylate | HCID 73242 | — |
| Reactant | Trifluoroacetamidine | HCID 2776882 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67382085 | HCID 67382085 | 49.9% |
Reaction Steps
Ethyl 2-amino-4-phenyl-thiophene-3-carboxylate (2 g, 8.087 mmol) and trifluoroacetamidine (4.531 g, 40.44 mmol) were combined in ethanol (20 mL) and heated to reflux overnight. Further trifluoroacetamidine (4.531 g, 40.44 mmol) was added and the reaction heated to reflux for a further 18 hours. The reaction mixture was allowed to cool to room temperature. The resulting precipitate was filtered off, washed with ethanol (5 mL) and dried in vacuo at 40° C. to afford 5-phenyl-2-(trifluoromethyl)-3H-thieno[2,3-d]pyrimidin-4-one (1.195 g). LCMS: purity 99%, RT=4.11 min, M+1=297.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290511B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-635d39ab66754a58aac72a2ce5a53af1 |
| Source note | uspto-grants-2016_03 |