HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10103331, compound → 1478883-60-1
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10103331 | HCID 10103331 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ammonia methanol | HCID 21705897 | — |
| Product | 1478883-60-1 | HCID 51723276 | 38% |
Reaction Steps
To a solution of (1R,5S)-8-methyl-8-azabicyclo[3.2.1]octane-3-carbonitrile (J. Org. Chem., 1977, 3114) (83 mg, 0.55 mmol) in NH3/MeOH (0.5%) (10 mL) was added Raney Ni (ca. 50 mg). The reaction mixture was hydrogenated at atmospheric pressure for 16 hours. After filtration, the solvents were evaporated and the oil was purified by ion exchange on SCX-II acidic resin (2 g) eluting with methanol, then 2M ammonia-methanol. The basic fractions were combined and the solvent was removed in vacuo to give ((1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)methanamine as colourless oil (32 mg, 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058045B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-788673cdb603429b91592e27e35714d2 |
| Source note | uspto-grants-2011_11 |