HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluidine → 2-(4-Benzyl-piperidin-1-yl)-N-(4-methyl-phenyl)-2-oxo-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | (4-Benzylpiperidin-1-yl)oxoacetic acid | HCID 16110264 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Benzyl-piperidin-1-yl)-N-(4-methyl-phenyl)-2-oxo-acetamide | HCID 44901907 | — |
Reaction Steps
The title compound is prepared from (4-benzyl-piperidin-1-yl)-oxo-acetic acid (Example 5b) and 4-methyl-aniline (Aldrich) according to the method described in Example 1c. Melting Point: 115-117° C. (diethylether)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435744B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-b75ebf04f5774de8a77fdfc9d5b78ede |
| Source note | uspto-grants-2008_10 |