HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 70286678, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | HCID 86753719 | HCID 86753719 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 70286678 | HCID 70286678 | 73.2% |
Reaction Steps
A mixture of 3-(bromoacetyl)benzo[b]thiophen-5-carbonitrile (1.05 g), 2-imidazolidinethione (0.4 g), ethanol (31.5 ml), and acetic acid (21 ml) was heated under reflux under nitrogen for 24 hours, then cooled in ice. The resulting precipitate was collected by filtration, washed with ether, and dried in vacuo at 65° C. to give 3-(5,6-dihydroimidazo[2,1-b]thiazol-3-yl)benzo[b]thiophen-5-carbonitrile monohydrobromide as a white solid (1 g), m.p. 303°-305° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869492 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-523713f3163b4312bf69980ebf091609 |
| Source note | uspto-grants-1999_02 |