HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Benzhydrylazetidin-3-yl)-4-methylpiperazine → 1-(Azetidin-3-yl)-4-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Benzhydrylazetidin-3-yl)-4-methylpiperazine | HCID 22259156 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(Azetidin-3-yl)-4-methylpiperazine | HCID 20659800 | — |
Reaction Steps
To a mixed solution of 1-(1-(diphenylmethyl)azetidin-3-yl)-4-methylpiperazine (1.21 g, 3.75 mmol) described in Production Example 3-1 and methanol (20 mL) was added palladium hydroxide-carbon (500 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 4 hours and 45 minutes. The reaction mixture was purged with a nitrogen atmosphere, and then filtrated using Celite. A filtrate was concentrated under a reduced pressure to give the title compound in the form of a mixture (1.00 g) with 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-04d896f6073f468eb4c0eebe9daa384d |
| Source note | uspto-grants-2015_11 |