HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Phenylpiperidin-4-yl)acetamide → HCID 18930314, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Phenylpiperidin-4-yl)acetamide | HCID 15886675 | — |
| Reactant | HCID 18930293 | HCID 18930293 | — |
| Reactant | HCID 18930304 | HCID 18930304 | — |
| Product | HCID 18930314 | HCID 18930314 | — |
Reaction Steps
5-[(1RS,2SR)-1-acetoxy-2-(3,4-dichlorophenyl)-4-(4-acetamido-4-phenylpiperidino)butyl]-1-phenyl-1,2,3-(1H)-triazole. Using a procedure similar to that described in Example 7, except using 4-acetamido-4-phenylpiperidine as the amine component, and 5-[(1RS,2SR)-1-acetoxy-2-(3,4-dichlorophenyl)-4-oxobutyl]-1-phenyl-1,2,3-(1H)-triazole as the aldehyde component, the coupling product was prepared as a white foam (61%); NMR: 7.75 (s,1), 7.50-7.01 (m,10), 6.79 (d,1), 6.53 (dd,1), 5.94 (d,1), 5.41 (s,H), 3.03 (m,1), 2.65-2.45 (m,2), 2.33 (m,2), 2.16 (s,3), 2.10-1.98 (m,6), 1.97 (s,3), 1.65 (broad m,2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739149 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-9b1c66ae39c04f8c82300746f5ebf1e9 |
| Source note | uspto-grants-1998_04 |