HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Morpholin-3-ylmethyl 4-(2,4-difluorophenyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 3-[4-(2,4-Difluoro-phenyl)-piperazine-1-carbonyloxymethyl]-morpholine-4-carboxylic acid tert-butyl ester | HCID 66934537 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Morpholin-3-ylmethyl 4-(2,4-difluorophenyl)piperazine-1-carboxylate | HCID 42634521 | 79% |
Reaction Steps
To 3-[4-(2,4-difluoro-phenyl)-piperazine-1-carbonyloxymethyl]-morpholine-4-carboxylic acid tert-butyl ester (170 mg, 0.39 mmol) in DCM (5 mL) at 0° C. was added TFA (1 mL in 5 mL DCM). The reaction mixture was allowed to warm to room temperature and stirred overnight. The solvent was removed in vacuo and the residue suspended between sat aq NaHCO3 (10 mL) and DCM (10 mL). The aqueous phase was extracted with DCM (2×10 mL). The combined organic layers were dried (MgSO4) and the solvent removed in vacuo to give morpholin-3-ylmethyl 4-(2,4-difluorophenyl)piperazine-1-carboxylate (104 mg, 79%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851471B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ea3aa07249104d4b9ae9a0a7e629e8ca |
| Source note | uspto-grants-2010_12 |