HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1-Phenethyl-piperidin-3-ylmethyl)-N-phenyl-propionamide → (R)-N-(1-Phenethyl-piperidin-3-ylmethyl)-N-phenyl-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1-Phenethyl-piperidin-3-ylmethyl)-N-phenyl-propionamide | HCID 9950309 | — |
| Reactant | (R)-N-(1-Boc-piperidin-3-ylmethyl)-aniline | HCID 20598046 | — |
| Reactant | (R)-N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl-propionamide | HCID 20598047 | — |
| Product | (R)-N-(1-Phenethyl-piperidin-3-ylmethyl)-N-phenyl-propionamide | HCID 9906423 | — |
Reaction Steps
Following a procedure similar to that described in Examples 4 and 5, (R)-N-(1-Boc-piperidin-3-ylmethyl)-aniline 28 was converted first to (R)-N-(1-Boc-piperidin-3-ylmethyl)-N-phenyl-propionamide 29, and then to (R) N-(1-Phenethyl-piperidin-3-ylmethyl)-N-phenyl-propionamide 30 (LRMS 350).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06645980B1 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-03018e75825746518ea5b14a835862c5 |
| Source note | uspto-grants-2003_11 |