HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 5-[[7-[(5-Ethyl-2-pyridinyl)methoxy]quinolin-3-yl]methyl]-2-imino-1,3-thiazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Methyl 2-bromo-3-[7-(5-ethyl-2-pyridylmethoxy)-3-quinolyl]propionate | HCID 21469288 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[[7-[(5-Ethyl-2-pyridinyl)methoxy]quinolin-3-yl]methyl]-2-imino-1,3-thiazolidin-4-one | HCID 141576964 | — |
Reaction Steps
In ethanol (20 mL) was dissolved the crude residue (790 mg) of methyl 2-bromo-3-[7-(5-ethyl-2-pyridylmethoxy)-3-quinolyl]propionate. The solution was heated under reflux for 15 hours after addition of thiourea (140 mg, 1.84 mmol.) and sodium acetate (150 mg, 1.84 mmol.). After the completion of reaction was confirmed, ethanol was distilled off. To the residue were added ethyl acetate and aqueous sodium hydrogen carbonate. The organic portion was recovered, washed with water, and dried over sodium sulfate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693651 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-b4c2325227fb431a821ce6554d1a385d |
| Source note | uspto-grants-1997_12 |