HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → HCID 69663205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 69663521 | HCID 69663521 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69663205 | HCID 69663205 | 76% |
Reaction Steps
Benzenesulfonyl chloride (90 μL, 0.7 mmol) was added to a solution of 1-(4-benzenesulfonyl-4-methylpentyl)-3-(methylamino)piperidine (0.22 g, 0.65 mmol) and triethylamine (180 μL, 1.3 mmol) in dichloromethane (5 ml). The reaction was stirred at room temperature for 30 minutes. The mixture was diluted with dichloromethane and washed with water (×2). The organic layer was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with 2–5% methanol/dichloromethane, to give the title compound (220 mg, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101892B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-2f85eae993f4462396a9237234194c49 |
| Source note | uspto-grants-2006_09 |