HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-Chloro-4-[4-(4-fluorophenyl)sulfonylpiperazin-1-yl]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | 7-Chloro-4-(piperazin-1-yl)quinoline | HCID 738389 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Chloro-4-[4-(4-fluorophenyl)sulfonylpiperazin-1-yl]quinoline | HCID 1506751 | — |
Reaction Steps
7-Chloro-4-(piperazin-1-yl)quinoline (0.25 g, 1.0 mmol), 4-fluorobenzenesulfonyl chloride (0.23 g, 1.2 mmol), and triethylamine (349 μL, 2.5 mmol) are stirred at room temp. for 15 h. The reaction mixture is diluted with EtOAc, washed with water, dried (MgSO4), and concentrated. The residue is purified by column chromatography with hexane-EtOAc yielding the title 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-19767460b63c495daa8cf38ebc504508 |
| Source note | uspto-grants-2007_05 |