Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(4-Fluorophenyl)imidazo[2,1-b][1,3]thiazole-5-carbaldehyde | HCID 2759102 | — |
| Reactant | 3,4-Dimethoxy-2-phenylacetophenone | HCID 12336683 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 51352523 | HCID 51352523 | 75% |
Reaction Steps
To a stirred solution 3,4-dimethoxyphenyl acetophenone (180 mg, 2.7 mmol) and a 6-(4-fluorophenyl)imidazo[2,1-b]thiazol-5-carbaldehyde (246 mg, 2.7 mmol) in ethanol (20 ml) 10% aqueous solution of NaOH was added (5 ml). The reaction mixture was stirred at room temperature 27° C. for 4 h and the reaction was monitored by TLC using ethyl acetate-hexane (3:7) as a solvent system. The solvent was evaporated under vacuum then the residue was dissolved in ethylacetate/water. The organic layer was washed with brine and evaporated. This was further purified by columnchromatography using ethyl acetate:hexane (2:8) as a solvent system to obtain the pure product (8e) as yellow solid (306 mg, 75% yield). Mp: 221-223° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916711B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-33fbfb6d55c44791a90a7d7f4e95cdfc |
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| Source note | uspto-grants-2014_12 |
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