HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanoic acid, 2-ethyl-3-oxo-, ethyl ester → 2-(5-chloro-2-thienyl)-5-ethyl-4-methyl-1H-pyrimidin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanoic acid, 2-ethyl-3-oxo-, ethyl ester | HCID 79065 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-Chlorothiophene-2-carboximidamide hydrochloride | HCID 45791998 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(5-chloro-2-thienyl)-5-ethyl-4-methyl-1H-pyrimidin-6-one | HCID 135996612 | 47% |
Reaction Steps
A 100-mL round bottomed flask was charged with 5-chlorothiophene-2-carboxamidine HCl salt (394 mg, 2 mmol, 1 eq.), ethyl 2-ethyl-3-oxo-butanoate (950 mg, 6 mmol, 3 eq.), and ethanol (10 ml). To the mixture was added sodium methoxide (25 w % in methanol, 1.73 g, 8 mmol, 3 eq.). The resulting mixture was stirred under reflux for 7 hr. After cooling to room temperature, the mixture was evaporated under reduced pressure to dryness and the residue was treated with 2N HCl (4.5 ml). Solid was collected by filtration and washed with water followed by hexane. The product thus obtained was forwarded to the next step without any further purification (240 mg, 47% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221843B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-eacd980f7b4749ea8236cabfba37d7fc |
| Source note | uspto-grants-2015_12 |