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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853913Generated: October 29, 2026

1-Methylpiperazine → 1-Methyl-4-({(2S)-1-[(4-methylphenyl)sulfonyl]pyrrolidin-2-yl}methyl)piperazine

https://huagongshe.com/reaction/853913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant{(2S)-1-[(4-methylphenyl)sulfonyl]pyrrolidin-2-yl}methyl 4-methylbenzenesulfonateHCID 10905672—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product1-Methyl-4-({(2S)-1-[(4-methylphenyl)sulfonyl]pyrrolidin-2-yl}methyl)piperazineHCID 5893255855%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of {(2S)-1-[(4-methylphenyl)sulfonyl]pyrrolidin-2-yl}methyl 4-methylbenzenesulfonate (9.427 g, 23.13 mmol) (Tetrahedron, 43(14), 3289, 1987) in toluene (150 mL), was added n-methyl-piperazine (12.8 mL, 115.65 mmol) and DBU (0.352 g, 2.313 mmol) and the solution was stirred at 140° C. overnight. The reaction was then diluted with ether and washed with brine. The organic layer was dried over Na2SO4, filtered, concentrated and purified on Biotage flash 40M cartridge silica gel eluting with CH2Cl2/CH3OH/NH4OH (95.5/3/1.5) to give an off white solid (2.570 g, 55% ). NMR (400 Mz, DMSO-d6): consistent. MS (ES+) m/z 338.1 [M+H]. m.p.: 96.5-97.7° C. Reference: (Tetrahedron, 43(14), 3289, 1987).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256198B2
Source datasetuspto-grants-2007_08
ORD IDord-fef5cb0c18be48b29be5920d6bae3773
Source noteuspto-grants-2007_08