HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxonium, triethyl-, hexafluorophosphate(1-) (1:1) → ethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxonium, triethyl-, hexafluorophosphate(1-) (1:1) | HCID 167684 | — |
| Reactant | (2S)-1-[(4-Fluorophenyl)sulfonyl]-2-piperidinecarboxamide | HCID 8402010 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidate | HCID 57097015 | 92.4% |
Reaction Steps
(2S)-1-[(4-Fluorophenyl)sulfonyl]-2-piperidinecarboxamide (286 mg) [see Preparation 40] was added to a solution of triethyloxonium hexafluorophosphate (304 mg) in dichloromethane (5 ml). The reaction mixture was stirred at room temperature for 18 hours after which time the mixture was diluted with dichloromethane and washed with saturated aqueous sodium hydrogen carbonate solution. The organic layer was separated, dried over magnesium sulphate and the solvent was removed under reduced pressure to afford ethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidate (290 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06610707B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-d61357ce9d34439fa98d3b9052b5191a |
| Source note | uspto-grants-2003_08 |