HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 23001045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | HCID 23000976 | HCID 23000976 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 23001045 | HCID 23001045 | 119.8% |
Reaction Steps
To a solution of 4-(3-aminophenyl)-N-hexyl-4-n-propylpiperidine (Preparation 70, 34 mg, 0.11 mmol) in pyridine (0.5 ml) under nitrogen was added ethanesulfonyl chloride (16 ml, 0.17 mmol) and the resultant mixture was stirred overnight. Ice (2 g) was added and, after 15 min, dichloromethane (3 ml) was added and the biphasic mixture was left to stir for 15 min. The layers were separated and the aqueous layer was extracted with dichloromethane (3 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to give the crude product. This was purified by silica (5 g) column chromatography eluting with ethyl acetate:hexane:0.880 ammonia (40:60:1 to 75:25:1) to give the title compound as a pale yellow oil (26 mg, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610711B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-98efeb575e3b4331af759f17f7aa7916 |
| Source note | uspto-grants-2003_08 |