HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-amino-4-phenylthiophene-3-carboxylate → Thieno(2,3-d)pyrimidin-4(1H)-one, 5-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-amino-4-phenylthiophene-3-carboxylate | HCID 73242 | — |
| Reactant | Formamidine acetate | HCID 160693 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Thieno(2,3-d)pyrimidin-4(1H)-one, 5-phenyl- | HCID 215639 | — |
Reaction Steps
A stirred mixture of 2-amino-4-phenylthiophene-3-carboxylic acid ethyl ester (350.43 g, 1.535 mol), formamidine acetate (799.13 g, 7.7 mol) and ethanol (1500 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The resulting solid was collected by filtration, washed with a little cold ethanol, then crystallised from ethanol to give 5-Phenyl-3H-thieno[2,3-d]pyrimidin-4-one as a yellow solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022076B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-6e912309763f44a5a8a3d8b62049b509 |
| Source note | uspto-grants-2011_09 |