HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1-Benzyl-piperidin-3-yl)-N-phenyl-propionamide → N-phenyl-N-piperidin-3-yl-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1-Benzyl-piperidin-3-yl)-N-phenyl-propionamide | HCID 12741868 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-phenyl-N-piperidin-3-yl-propionamide | HCID 12741869 | 97.2% |
Reaction Steps
A mixture of N-(1-benzyl-piperidin-3-yl)-N-phenyl-propionamide (165) (150 mg) and Pd—C(10%, 50 mg) and MeOH (50 ml) was stirred under H2 (1 atm) for 24 hr. The catalyst was removed by filtration through Celite to give 166 as a colorless oil (105 mg, 97%). 1H-NMR (300 MHz, CDCl3) δ 7.41 (m, 3H), 7.10 (m, 2H), 3.20 (m 1H), 2.90 (m, 1H), 2.40–2.20 (m, 2H), 1.90 (m, 2H), 1.60 (m, 4H), 1.20 (m, 1H), 1.00 (t, 3H) ppm; LRMS (calculated for C14H21N2O) (M+1)+ 233. found 233.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129228B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-06f94b1807d84efb91598db626ad20a9 |
| Source note | uspto-grants-2006_10 |