Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | HCID 86702821 | HCID 86702821 | — |
| Product | HCID 86702822 | HCID 86702822 | — |
Reaction Steps
1,3-Dichloroacetone (0.252 g, 2 mmol) was added to a solution of (E)-ethyl 3-(2-aminothiazol-5-yl)acrylate (0.199 g, 1 mmol) in EtOH (5 mL). The solution was heated at 80° C. overnight in a closed vial. The reaction mixture was then evaporated and the residue was treated with a saturated NaHCO3 solution (20 mL). It was extracted with EtOAc (30 mL). The organic layer was separated, dried over Na2SO4, filtered and evaporated. The crude was purified by silica gel column chromatography (50-100% gradient of EtOAc in Hexanes) to provide pure (E)-ethyl 3-(6-(ethoxymethyl)imidazo[2,1-b]thiazol-2-yl)acrylate (0.080 g) as a tan solid. ES+(M+H)+281.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957066B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-29982206fc754ff9bb83a36936ddcff6 |
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| Source note | uspto-grants-2015_02 |
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