HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → 2-(4-Benzyl-piperidin-1-yl)-N-(4-methoxy-phenyl)-2-oxo-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | (4-Benzylpiperidin-1-yl)oxoacetic acid | HCID 16110264 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Benzyl-piperidin-1-yl)-N-(4-methoxy-phenyl)-2-oxo-acetamide | HCID 44892038 | — |
Reaction Steps
The title compound is prepared from (4-benzyl-piperidin-1-yl)-oxo-acetic acid (Example 5b) and 4-methoxyaniline (Aldrich) according to the method described in Example 1c. Melting Point: 144-146° C. (diethylether)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435744B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-641a35960eb34fd084672cf00899ad69 |
| Source note | uspto-grants-2008_10 |