HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2R)-4-(1-(Diphenylmethyl)azetidin-3-yl)-1,2-dimethylpiperazine → (R)-4-(Azetidin-3-YL)-1,2-dimethylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2R)-4-(1-(Diphenylmethyl)azetidin-3-yl)-1,2-dimethylpiperazine | HCID 118162432 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-4-(Azetidin-3-YL)-1,2-dimethylpiperazine | HCID 118162417 | 166.2% |
Reaction Steps
To a mixed solution of (2R)-4-(1-(diphenylmethyl)azetidin-3-yl)-1,2-dimethylpiperazine (342 mg, 1.02 mmol) described in Production Example 5-2 and methanol (10 mL) was added palladium hydroxide-carbon (200 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 (287 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-22568a4e58624ec8883ce825e30d5d99 |
| Source note | uspto-grants-2015_11 |