HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl thiooxamate → Ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl thiooxamate | HCID 2733398 | — |
| Reactant | 3-Bromo-4-(3-bromophenyl)butan-2-one | HCID 62393918 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate | HCID 86711480 | 42.1% |
Reaction Steps
A mixture of 3-bromo-4-(3-bromophenyl)butan-2-one (1.8 g, 5.9 mmol) and ethyl 2-amino-2-thioxoacetate (745 mg, 5.6 mmol) in EtOH (20 mL) was refluxed overnight. The solvent was removed and the residue was purified by silica gel column chromatography (EtOAc:Petroleum ether=1:5) to afford ethyl 5-(3-bromobenzyl)-4-methylthiazole-2-carboxylate as a light yellow solid (800 mg, 42.1%). MS (ES+) C14H14BrNO2S requires: 339, 341 found: 340[M+H]+, 342 [M+2+H]+(1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115120B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-b9e1a5fcec0d4727a7ff2f29d26f66be |
| Source note | uspto-grants-2015_08 |