HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(1-(4-fluorobenzyl)-1H-benzimidazol-2-yl)[1,4]diazepane hydriodic acid salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 1-t-butoxycarbonyl-4-(1-(4-fluorobenzyl)-1H-benzimidazol-2-yl)[1,4]diazepane | HCID 18464846 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(1-(4-fluorobenzyl)-1H-benzimidazol-2-yl)[1,4]diazepane hydriodic acid salt | HCID 86583901 | — |
Reaction Steps
Combine 1-t-butoxycarbonyl-4-(1-(4-fluorobenzyl)-1H-benzimidazol-2-yl)[1,4]diazepane (1.12 g, 2.64 mmol) and ethanol (15 mL). Add aqueous hydriodic acid (5 mL, 57%). Heat to reflux. After 1 hour, cool to ambient temperature and dilute with diethyl ether (250 mL) and stir to give a solid. Collect the solid by filtration, rinse with diethyl ether, and dry to give the title compound: Rf =0.16 (silica gel, 10% methanol/dichloromethane/0.01% concentrated aqueous ammonia.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05932571 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-f03a8ccb11884589a557f041a8414805 |
| Source note | uspto-grants-1999_08 |