Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | 2-Bromo-1-[1-(2-naphthyl)cyclobutyl]ethanone | HCID 21258495 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21258509 | HCID 21258509 | — |
Reaction Steps
A mixture of the crude 2-bromo-1-[1-(2-naphthyl)cyclobutyl]ethanone described above, imidazolidine-2-thione (5.1 g), ethanol (60 ml) and acetic acid (40 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The solvents were removed in vacuo and the residue was triturated with a hot mixture of ethyl acetate (100 ml) and acetone (20 ml). The resulting solid was collected by filtration, washed with ethyl acetate (50 ml), dried in vacuo at 60° C., then crystallised from ethanol. The resulting solid was collected by filtration, washed with ethanol (30 ml), and dried in vacuo at 60° C. to give 3-[1-(2-naphthyl)cyclobutyl]-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide as pale yellow prisms (10 g), m.p. 239-241° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187802B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-156e456459d84c7eb20ad2eda81b4488 |
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| Source note | uspto-grants-2001_02 |
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