Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707509Generated: November 2, 2026

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

https://huagongshe.com/reaction/707509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Benzhydrylazetidin-3-yl)-4-methylpiperazineHCID 2225915689.4%

Reaction Steps

To a mixed solution of a commercially available product of 1-(diphenylmethyl)azetidin-3-one (1.00 g, 4.21 mmol), THF (20 mL) and acetic acid (1.00 mL) was added methylpiperazine (561 μL, 5.05 mmol) at room temperature. The resultant mixture was stirred at room temperature for 15 minutes. To the reaction mixture was added sodium triacetoxyborohydride (1.79 g, 8.42 mmol) at room temperature, and the resultant mixture was stirred at room temperature for 2 hours and 15 minutes. Sodium hydrogen carbonate and water were added to the reaction mixture, and the resultant mixture was extracted with ethyl acetate. An organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate, and then filtrated. The solvent was evaporated under a reduced pressure, and the resultant residue was purified by silica gel column chromatography (ethyl acetate-methanol) and then further purified by NH silica gel column chromatography (heptane:ethyl acetate=1:1) to give the title compound (1.21 g, yield: 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174998B2
Source datasetuspto-grants-2015_11
ORD IDord-fdea08d0274e477a83d868d3f09f6acc
Source noteuspto-grants-2015_11