HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 4-Ethyl-N-hexyl-4-(3-methanesulfonylaminophenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(3-aminophenyl)-4-ethyl-N-hexylpiperidine | HCID 23000925 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ammonia | HCID 222 | — |
| Product | 4-Ethyl-N-hexyl-4-(3-methanesulfonylaminophenyl)piperidine | HCID 23000965 | 62.7% |
Reaction Steps
To 4-(3-aminophenyl)-4-ethyl-N-hexylpiperidine (Preparation 64, 50.0 mg, 0.174 mmol) in anhydrous pyridine (4 ml) under nitrogen at 0° C. was added methanesulfonyl chloride (0.2 ml, 1.18 mmol). The solution was stirred at room temperature for 48 h. Ice (5 g) was added and, after 30 min, the reaction mixture was extracted with dichloromethane (10 ml). The organic extract was dried (Na2SO4), filtered and concentrated in vacuo to give the crude product which was purified by silica (5 g) column chromatography, eluting with ethyl acetate:hexane:0.880 ammonia (40:60:1), then ethyl acetate:0.880 ammonia (100:1) and then methanol:ethyl acetate:0.880 ammonia (10:89:1) to give the title compound as an oil (20 mg, 29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610711B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-bc32e551ea1046af9fec9947b25d66ad |
| Source note | uspto-grants-2003_08 |