HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 58625163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | HCID 58625066 | HCID 58625066 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58625163 | HCID 58625163 | — |
Reaction Steps
A mixture of N-[3-(4-amino-3-propylaminomethyl-phenoxy)-phenyl]-benzenesulfonamide (0.0044 mol) in ethanol (50 mL) was stirred at room temperature and cyanogen bromide (0.0064 mol) was added, then the reaction mixture was stirred and refluxed for 4 hours. After cooling, the precipitate was filtered off and was stirred in boiling CH3CN with CH3OH. The resulting solids were filtered off, washed with diisopropyl ether and dried to yield the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383637B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-0c8ad2e30e9a41f8ae624719e98d474e |
| Source note | uspto-grants-2013_02 |