HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22474239, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | HCID 22473879 | HCID 22473879 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22474239 | HCID 22474239 | 85.7% |
Reaction Steps
A mixture of 2-bromo-1-(4-methylbenzo[b]thiophen-2-yl)propan-1-one (0.27 g), 2-imidazolidinethione (0.1 g), acetic acid (2 ml) and ethanol (4 ml) was heated under reflux for 3 hours, then cooled to ambient temperature. The solvents were removed in vacuo and the residue was triturated with ether (2×1 ml). The resulting solid was collected by filtration, washed with ethanol (2 ml) and dried in vacuo at 60° C. for 2 hours to give 2-methyl-3-(4-methylbenzo[b]thiophen-2-yl)-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide (0.3 g) as a cream solid, m.p. 201-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900216B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-ba79f3cb39544003ab4dd827f218eb3e |
| Source note | uspto-grants-2005_05 |