HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Methylsulfonamido)aniline → 2-(4-Benzyl-piperidin-1-yl)-N-(4-methanesulfonylamino-phenyl)-2-oxo-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Methylsulfonamido)aniline | HCID 3732577 | — |
| Reactant | (4-Benzylpiperidin-1-yl)oxoacetic acid | HCID 16110264 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Benzyl-piperidin-1-yl)-N-(4-methanesulfonylamino-phenyl)-2-oxo-acetamide | HCID 10273323 | — |
Reaction Steps
The title compound is prepared from (4-benzyl-piperidin-1-yl)-oxo-acetic acid (Example 5b) and N-(4-amino-phenyl)-methanesulfonamide [Tetrahedron, 42, 5739. (1986)] according to the method described in Example 2. Melting Point: 221-225° C. (water)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435744B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-fe52e375ec2e4ce183a9bb892ca26157 |
| Source note | uspto-grants-2008_10 |