HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → Ethyl 2-amino-5-benzyl-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl 3-bromo-2-oxo-4-phenylbutanoate | HCID 10755525 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-amino-5-benzyl-1,3-thiazole-4-carboxylate | HCID 12603729 | 15.1% |
Reaction Steps
Ethyl 3-bromo-2-oxo-4-phenylbutanoate (5.8 g) was dissolved in EtOH (110 ml), and then thiourea (3.1 g) was added to the solution. The reaction mixture was refluxed for 2 hours under N2 atmosphere. The cooled reaction mixture was evaporated in vacuo. The residual solid was suspended (pH=8) in saturated NaHCO3 and water. The solid was collected by filtration, and purified by flash column chromatography over silica gel with CHCl3/MeOH (10:1) as an eluent to give ethyl 2-amino-5-benzyl-1,3-thiazole-4-carboxylate (808.2 mg) as a yellow wax.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125901B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-500a526f3be64f21868c112588ea11d7 |
| Source note | uspto-grants-2006_10 |