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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707518Generated: October 31, 2026

(2R)-4-(1-(Diphenylmethyl)azetidin-3-yl)-1,2-dimethylpiperazine → (R)-4-(Azetidin-3-YL)-1,2-dimethylpiperazine

https://huagongshe.com/reaction/707518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-4-(1-(Diphenylmethyl)azetidin-3-yl)-1,2-dimethylpiperazineHCID 118162432—
CatalystHCID 178502593HCID 178502593—
SolventMethanolHCID 887—
Product(R)-4-(Azetidin-3-YL)-1,2-dimethylpiperazineHCID 118162417166.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174998B2
Source datasetuspto-grants-2015_11
ORD IDord-22568a4e58624ec8883ce825e30d5d99
Source noteuspto-grants-2015_11