HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21258456, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | HCID 21258424 | HCID 21258424 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21258456 | HCID 21258456 | 31.2% |
Reaction Steps
A mixture of 2-bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]-2-phenylethanone (3.8 g), imidazolidine-2-thione (0.97 g), ethanol (70 ml) and acetic acid (40 ml) was heated under reflux for 20 hours then allowed to cool to ambient temperature. The solvents were removed in vacuo and the residue was crystallised from ethanol. The resulting product was collected by filtration, washed with ethanol (10 ml) and dried in vacuo at 100° C. to give 3-[1-(3,4-dichlorophenyl)cyclobutyl]-2-phenyl-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide as a pale brown solid (1.43 g), m.p. 280° C. (decomposes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187802B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-013baa0ec7cd4033952dc5f03b94c054 |
| Source note | uspto-grants-2001_02 |