HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-piperidin-4-yl-3H-imidazo[4,5-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tert-butyl 4-[(4-nitro-1-oxidopyridin-3-yl)amino]piperidine-1-carboxylate | HCID 57935996 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 3-piperidin-4-yl-3H-imidazo[4,5-c]pyridine | HCID 57935985 | — |
Reaction Steps
To a solution of tert-butyl 4-[(4-nitro-1-oxidopyridin-3-yl)amino]piperidine-1-carboxylate (4 g) in methanol (100 ml) was added 10% palladium on carbon (50 mg) and the mixture was placed under a hydrogen atmosphere (60 psi) for 48 hours. The mixture was filtered through Celite and evaporated to dryness to give the title compound as a solid, which was used without further purification. Yield 3.21 g. MS 293 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07615555B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-7477aa79154742518fa27c30b5e345b6 |
| Source note | uspto-grants-2009_11 |