HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2-Amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | {2-Oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-carbamic acid tert-butyl ester | HCID 59559599 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone | HCID 59559629 | 126.5% |
Reaction Steps
TFA (13 mL) was added drop wise to {2-Oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-carbamic acid tert-butyl ester (2.6 g, 6.27 mmol) in DCM (15 mL) at 0° C. The resulting mixture was stirred at room temperature for 2 hours. Concentrating the mixture afforded a crude product, which was recrystallized from hexane to afford 2.5 g (93% yield) of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone as TFA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07842696B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-bb02afe912cf494093109cd497dfdd1a |
| Source note | uspto-grants-2010_11 |