HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 21101963, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Chloro-4-(piperazin-1-yl)quinoline | HCID 738389 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21101963 | HCID 21101963 | — |
Reaction Steps
A suspension of 7-Chloro-4-(piperazin-1-yl)quinoline (496 mg, 2.0 mmol) and NaHCO3 (504 mg, 6.0 mmol) in EtOH is treated with cyanogen bromide (5 M in MeCN, 440 μL, 2.2 mmol) and stirred at room temp. for 2 h. The solvent is removed, and the residue suspended in CH2Cl2 and filtered. The filtrate is concentrated, and the residue is purified by column chromatography with hexane-EtOAc giving 221 mg of the product as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-bf21191589a6460e93b4d78500ec55e5 |
| Source note | uspto-grants-2007_05 |