Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | HCID 22474187 | HCID 22474187 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22474262 | HCID 22474262 | 94.7% |
Reaction Steps
A mixture of 2-bromo-1-(4-fluorobenzo[b]thiophen-2-yl)propan-1-one (0.67 g), 2-imidazolidinethione (0.24 g), acetic acid (10 ml) and ethanol (5 ml) was heated under reflux for 2 hours then cooled to 20° C. The mixture was concentrated in vacuo and the resulting solid was collected by filtration, washed with ethanol (5 ml) and dried in vacuo at 60° C. for 2 hours to give 3-(4-fluorobenzo[b]thiophen-2-yl)-2-methyl-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide (0.82 g) as beige solid, m.p. 224-226° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900216B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-49c4aa1e0c0849b6aa10aeee0d63116b |
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| Source note | uspto-grants-2005_05 |
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