HuagongsheHuagongshe Chemistry Print Report · For research reference only
n,n-Dimethyl{2-[4-benzyl-piperazinyl]phenyl}carboxamide → N,N-Dimethyl-2-(1-piperazinyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | n,n-Dimethyl{2-[4-benzyl-piperazinyl]phenyl}carboxamide | HCID 21935201 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N,N-Dimethyl-2-(1-piperazinyl)benzamide | HCID 28749556 | 84.1% |
Reaction Steps
To a round-bottomed flask equipped with stirring was added N,N-dimethyl(2-[4-benzylpiperazinyl]phenyl)carboxamide (Step 2)(420 mg, 1.3 mmol), MeOH (10 mL), 10% Pd/C (Aldrich) (138 mg), and HCO2NH4 (409 mg, 6.5 mmol), and the reaction mixture was heated at reflux for 2 h. The reaction mixture was filtered through Celite®, concentrated in vacuo, and redissolved in CH2Cl2 (20 mL). The reaction mixture was washed with a Na2CO3 (10%, 2×), H2O, brine, dried-over Na2SO4, filtered and concentrated in vacuo yielding N,N-dimethyl(2-piperazinylphenyl)carboxamide (255 mg). MS (ESI, pos. ion) m/z: 234 (M+H). Calc'd for C13H19N3O: 233.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560460B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-7854b3cc273146678812687c84a990b7 |
| Source note | uspto-grants-2009_07 |