HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 70284500, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethylenethiourea | HCID 2723650 | — |
| Reactant | HCID 57175247 | HCID 57175247 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 70284500 | HCID 70284500 | 57.4% |
Reaction Steps
A mixture of the crude 3-(2-bromoacetyl)-5-chlorobenzo[b]thiophen (4.2 g), 2-imidazolidinethione (1 g), ethanol (15 ml) and acetic acid (10 ml) was heated under reflux under nitrogen for 18 hours, then allowed to cool to ambient temperature. The resulting solid was collected by filtration, washed with ethanol (15 ml), and dried in vacuo to give 3-(5-chlorobenzo[b]thiophen-3-yl)-5,6-dihydroimidazo[2,1-b]thiazole monohydrobromide as a white solid (2.1 g), m.p. 286°-288° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869492 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-018a43fac15a4943bd2445c6946d8fdc |
| Source note | uspto-grants-1999_02 |