HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S)-1-(1-(Diphenylmethyl)azetidin-3-yl)-2,4-dimethylpiperazine → (2S)-1-(azetidin-3-yl)-2,4-dimethylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S)-1-(1-(Diphenylmethyl)azetidin-3-yl)-2,4-dimethylpiperazine | HCID 118162470 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2S)-1-(azetidin-3-yl)-2,4-dimethylpiperazine | HCID 118162468 | 162.4% |
Reaction Steps
To a mixed solution of (2S)-1-(1-(diphenylmethyl)azetidin-3-yl)-2,4-dimethylpiperazine (321 mg, 0.957 mmol) described in Production Example 6-2 and methanol (7.0 mL) was added palladium hydroxide-carbon (150 mg) at room temperature. The resultant mixture was stirred under a hydrogen atmosphere at room temperature and at 0.35 MPa to 0.40 MPa for 5 hours. The reaction mixture was purged with a nitrogen atmosphere and then filtrated using Celite. A filtrate was concentrated under a reduced pressure to give a mixture (263 mg) of the title compound and benzylbenzene. The product was used in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174998B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-71649c2afee24cc489d6810e341511be |
| Source note | uspto-grants-2015_11 |