HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(Benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide dihydrate
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 dihydrate | HCID 68779021 | — |
Reaction Steps
A mixture of 3-(2-bromoacetyl)benzo[b]thiophen (2.39 g), 2-imidazolidinethione (0.78 g), ethanol (60 ml) and acetic acid (40 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The resulting solid was collected by filtration, washed with ether (2×50 ml), and dried in vacuo at ambient temperature to give 3-(benzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1 -b]thiazole monohydrobromide dihydrate as a white solid (2.96 g), m.p. 239°-240° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869492 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-fd09965459ef41efa16387e585faa295 |
| Source note | uspto-grants-1999_02 |