HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-methyl-2-(pyridin-4-yl)-1,3-thiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Pyridinecarbothioamide | HCID 2723788 | — |
| Product | Ethyl 4-methyl-2-(pyridin-4-yl)-1,3-thiazole-5-carboxylate | HCID 619089 | — |
Reaction Steps
2.76 g (20 mmol) of thioisonicotinamide and 3.6 g (22 mmol) of ethyl 2-chloroacetacetate were heated under reflux in 30 ml of ethanol for 20 hours. After the treatment with ethyl acetate as the extraction solvent in an ordinary manner, the obtained crude product was purified by the silica gel column chromatography to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410538B2 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-5341ca442b0a48498b586341c0e7a6e0 |
| Source note | uspto-grants-2002_06 |