HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[4-([1-(4-nitro-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide → N-[4-([1-(4-Amino-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[4-([1-(4-nitro-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide | HCID 19992415 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-([1-(4-Amino-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide | HCID 19992427 | 92.5% |
Reaction Steps
A solution of N-[4-([1-(4-nitro-2-pyridyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide (see Preparation 5) (140 mg) in ethanol (50 ml) was hydrogenated at room temperature and 3.5 bar in the presence of 5% palladium on carbon until the required amount of hydrogen had been absorbed. The catalyst was filtered off and the filtrate was evaporated to give the product (120 mg), m.p. 213°-214° (from ethyl acetate/methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05057528 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-fc52c9c135ce4bacbf73adfbb7d451e5 |
| Source note | uspto-grants-1991_10 |