HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-(1H-benzimidazol-2-yl)[1,4]diazepane hydriodic acid salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 1-ethoxycarbonyl-4-(1H-benzimidazol-2-yl)[1,4]diazepane | HCID 18465091 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(1H-benzimidazol-2-yl)[1,4]diazepane hydriodic acid salt | HCID 86583889 | — |
Reaction Steps
Combine 1-ethoxycarbonyl-4-(1H-benzimidazol-2-yl)[1,4]diazepane (16.7 g, 58 mmol) and aqueous 48% hydrobromic acid solution (80 mL). Heat to reflux. After 3 hours, cool to ambient temperature, add to ethanol (700 mL), and cool to 0° C. to give a solid. Combine the solid with aqueous 48% hydriodic acid (80 mL) and water (150 mL). Heat on a steam bath. After about 1 hour, cool to ambient temperature, dilute with ethanol (500 mL), and add to diethyl ether (8 L) to give a solid. Collect solid by filtration and dry in vacuo to give the title compound: mp; >290° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06423704B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-6170ab396df84d739dfbe721a9388d74 |
| Source note | uspto-grants-2002_07 |