HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(4-fluorophenyl)-N-[(1S)-1-(4-fluorophenyl)ethyl]piperidine-4-carboxamide;2,2,2-trifluoroacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-(4-fluoro-phenyl)-4-[(S)-1-(4-fluoro-phenyl)-ethylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 66671195 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-fluorophenyl)-N-[(1S)-1-(4-fluorophenyl)ethyl]piperidine-4-carboxamide;2,2,2-trifluoroacetic acid | HCID 86646237 | 128% |
Reaction Steps
To a solution of 4-(4-fluoro-phenyl)-4-[(S)-1-(4-fluoro-phenyl)-ethylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester (735 mg, 1.653 mmol) in dichloromethane (8 mL) at 0° C. was added slowly trifluoroacetic acid (1.78 mL, 23.148 mmol) and stirring continued for 12 h at room temperature. The solvent was removed under reduced pressure. Toluene was added to the residue and evaporated under reduced pressure which was repeated two times. The residue was dried under high vacuum to yield 970 mg 4-(4-fluoro-phenyl)-piperidine-4-carboxylic acid [(S)-1-(4-fluoro-phenyl)-ethyl]-amide; compound with trifluoro-acetic acid. MS ISP (m/e): 345.3 [(M+H)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324250B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-144ca213ab544457ace41645d71840df |
| Source note | uspto-grants-2012_12 |