HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21837262, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 21837258 | HCID 21837258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21837262 | HCID 21837262 | — |
Reaction Steps
To a solution of 1-(4-(4-piperidinyloxy)-2-(trifluoromethoxy)phenylacetyl)-2-carbamoyl-4-(2-methylphenyl)piperazine hydrochloride (0.30 g, 0.5 mmol) from Example 33 in CH2Cl2 (50 mL) was added acetic anhydride (0.10 mL, 1.0 mmol) and DIEA (0.17 mL, 1.0 mmol). The solution was stirred at ambient temperature for 1 h and the solvent was removed under reduced pressure. The residue was dissolved in EtOAc (100 mL) and washed with 0.25 M aqueous citric acid (50 mL), H2O (25 mL), and saturated aqueous NaHCO3 (75 mL). The organic phase was dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give the title compound as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968938 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-7ee2d06a9c6f491d84724a16cc003af8 |
| Source note | uspto-grants-1999_10 |