Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | HCID 22473621 | HCID 22473621 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10156218 | HCID 10156218 | 66.8% |
Reaction Steps
A mixture of 2-bromo-1-(4-chlorobenzo[b]thiophen-2-yl]ethan-1-one (2.5 g), 2-imidazolidinethione (0.88 g), acetic acid (25 ml) and ethanol (50 ml) was heated under reflux for 90 minutes, then cooled to 0° C. The resulting solid was collected by filtration and dried in vacuo at 60° C. for 2 hours to give 3-(4-chlorobenzo[b]thiophen-2-yl)-5,6-dihydroimidazo[-2,1-b]thiazole hydrobromide (2.15 g) as colourless solid, m.p. 261-263° 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-070280b63c2b4356969ce4f2c323d685 |
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| Source note | uspto-grants-2005_05 |
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