HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 7-(2-Methoxycarbonylvinyl)imidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | Imidazo(4,3-b)(1,3)thiazole-7-carbaldehyde | HCID 22390357 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-(2-Methoxycarbonylvinyl)imidazo[5,1-b]thiazole | HCID 69930338 | 111.1% |
Reaction Steps
Methyl triphenylphosphoranylideneacetate (500 mg) was added to a solution of 150 mg of 7-formylimidazo[5,1-b]thiazole in 15 ml of methanol. The mixture was stirred at room temperature for 15 min. Ethyl acetate was added thereto. The mixture was washed with water, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (chloroform:methanol=20:1) to give 228 mg of 7-(2-methoxycarbonylvinyl)imidazo[5,1-b]thiazole (a mixture of geometrical isomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458780B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-393498230f3a49aabd605ceb94824974 |
| Source note | uspto-grants-2002_10 |