HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → N-Phenyl-4-[(3R)-piperidin-3-ylmethyl]piperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl (3S)-3-{[4-(anilinocarbonyl)piperazin-1-yl]methyl}piperidine-1-carboxylate | HCID 57656784 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Phenyl-4-[(3R)-piperidin-3-ylmethyl]piperazine-1-carboxamide | HCID 57656757 | — |
Reaction Steps
tert-Butyl (3S)-3-{[4-(anilinocarbonyl)piperazin-1-yl]methyl}piperidine-1-carboxylate (4.0 g) was added to a mixture of dichloromethane (20 ml) and TFA (20 ml) and the reaction mixture stirred for 2 h. The solvent was removed in-vacuo and the residue dissolved in dichloromethane (20 ml) and subsequently poured into hydrochloric acid solution (1N, 20 ml). The aqueous layer was basified using potassium carbonate and extracted with dichloromethane (3×15 ml). The organic layer was dried using a phase separation cartridge and the solvent removed under reduced pressure to afford the desired compound as a white foam white (2.0 g), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710224B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-fed8536070314919bf2a48f7a7558081 |
| Source note | uspto-grants-2014_04 |