HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-(2-(4-aminophenoxy)pyridin-3-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone → 1-(4-(2-(4-Aminophenoxy)pyridin-3-yl)piperidin-1-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-(2-(4-aminophenoxy)pyridin-3-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone | HCID 59373928 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-(2-(4-Aminophenoxy)pyridin-3-yl)piperidin-1-yl)ethanone | HCID 59373939 | — |
Reaction Steps
A solution of 1-(4-(2-(4-aminophenoxy)pyridin-3-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone (0.98 g, 3.17 mmol) in ethanol (16 mL) was added palladium, 10 wt. % on carbon (0.1 g, 0.094 mmol) and hydrogenated (double-walled balloon pressure) at room temperature for 18 h. The reaction mixture was filtered via a pad of Celite, and the filtrate was concentrated in vacuo and chromatographed via flash column chromatography (20% to 80% EtOAc/Hexanes) to give 1-(4-(2-(4-aminophenoxy)pyridin-3-yl)piperidin-1-yl)ethanone as a light tan solid. MS (ESI, pos. ion) m/z: 312.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637500B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-b56748327584449c8830bebfd4b38b7b |
| Source note | uspto-grants-2014_01 |