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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737137Generated: October 30, 2026

Methyl iodide → 1-Methyl-2-phenyl-4-(2'-chloro-5'-methyl-biphenyl-4-ylmethyl)-piperazine

https://huagongshe.com/reaction/737137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57849521HCID 57849521—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product1-Methyl-2-phenyl-4-(2'-chloro-5'-methyl-biphenyl-4-ylmethyl)-piperazineHCID 57849650—

Reaction Conditions

Temperature80 °C

Reaction Steps

This compound could be made the following manner: 100 mg of 3-benzyl-1-(2′-chloro-5′-methyl-biphenyl-4-ylmethyl)-piperazine would be dissolved in acetonitrile, 3 equiv. of N,N-diisopropylethylamine would be added followed by 1.1 equiv. of iodomethane. The reaction would be stirred at 80° C. overnight. The reaction would be diluted with dichloromethane and washed with 1N aqueous NaOH solution. The organic layer would be dried over Na2SO4, filtered and concentrated in vacuo. The crude residue would be purified by column chromatography to afford 1-methyl-2-phenyl-4-(2′-chloro-5′-methyl-biphenyl-4-ylmethyl)-piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-c0c205d68ac345f886eea1d2f4e8253d
Source noteuspto-grants-2009_09