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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707510Generated: October 30, 2026

1-(1-Benzhydrylazetidin-3-yl)-4-methylpiperazine → 1-(Azetidin-3-yl)-4-methylpiperazine

https://huagongshe.com/reaction/707510

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Benzhydrylazetidin-3-yl)-4-methylpiperazineHCID 22259156—
CatalystHCID 178502593HCID 178502593—
SolventMethanolHCID 887—
Product1-(Azetidin-3-yl)-4-methylpiperazineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174998B2
Source datasetuspto-grants-2015_11
ORD IDord-04d896f6073f468eb4c0eebe9daa384d
Source noteuspto-grants-2015_11