HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 57157975, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Benzyl-3-azabicyclo[3.3.1]nonan-9-one | HCID 15639123 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57157975 | HCID 57157975 | — |
Reaction Steps
A mixture of 3-benzyl-3-azabicyclo[3.3.1]nonan-9-one (0.72 g, 3.14 mmol), methanol (25 ml), piperazine(2.71 g, 31.4 mmol), several 3A molecular sieves, and NaBH3CN (0.39 g, 6.28 mmol) was refluxed for 60 hr, cooled, and concentrated. The residue was taken up in 1N HCl (50 ml), washed with ethyl acetate, the pH adjusted to 12 with 1N NaOH aqueous solution, and extracted with dichloromethane. The extract was dried over Na2SO4 and concentrated to afford 0.72 g (72% crude) of an oil, which was used directly in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859011 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-aec35423f4ba45a99abee71cf1956101 |
| Source note | uspto-grants-1999_01 |