HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[4-([1-(Benzyloxycarbonyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide → N-[4-([Piperidin-4-yl]methoxy)phenyl]methanesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[4-([1-(Benzyloxycarbonyl)piperidin-4-yl]methoxy)phenyl]methanesulphonamide | HCID 19992429 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-([Piperidin-4-yl]methoxy)phenyl]methanesulphonamide | HCID 19992428 | — |
Reaction Steps
A solution of the product of part (iv) (0.15 g) in ethanol was hydrogenated at 50° 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 washed several times with hot ethanol. The combined filtrate and washings were evaporated to give the product, (0.10 g), m.p. 180°-183°, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05057528 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-d1fb43a210fb4816950c0975a54ae9ff |
| Source note | uspto-grants-1991_10 |