HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 23159132, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Benzyl-3-azabicyclo[3.3.1]nonan-9-one | HCID 15639123 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Benzyl-3-azabicyclo[3.3.1]nonan-9-one | HCID 15639123 | — |
| Product | HCID 23159132 | HCID 23159132 | 191.5% |
Reaction Steps
N-benzyl-3-azabicyclo[3.3.1]nonane-9-one (28) was synthesized according to a method described in J. Med. Chem. 1994, 37, 2831-2840. Sodium borohydride (1.49 g) was added into the MeOH (80 ml) solution of (28) (6.75 g) with chilling on ice. After its mixture was stirred for 1 hour with chilling on ice, its solvent was evaporated under reduced pressure. Water was added to its residue, which was then subjected to extraction with methylene chloride, followed by drying its organic layer with anhydrous magnesium sulfate. Its solvent was evaporated under reduced pressure to produce a crude compound (29) (6.52 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101768B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-18adb77f86984444a11c8f3a67f315b9 |
| Source note | uspto-grants-2012_01 |