HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(Benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | 1-(1-Benzothiophen-3-yl)-2-bromoethan-1-one | HCID 2776341 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(Benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide | HCID 51071984 | 87.3% |
Reaction Steps
A mixture of 3-(2-bromoacetyl)benzo[b]thiophen (10.0 g), 2-imidazolidinethione (4.0 g), ethanol (120 ml) and acetic acid (80 ml) was heated under reflux for 24 hours then allowed to cool to ambient temperature. The resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 3-(benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide 1.8 hydrate as a white solid (11.6 g), m.p. 227°-229° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869492 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-4f580d759c6347298f2ae97b8ee1ba13 |
| Source note | uspto-grants-1999_02 |