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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972614Generated: November 2, 2026

Aniline → N-(((2S)-1,4-dibenzyl-2-piperazinyl)methyl)aniline

https://huagongshe.com/reaction/1972614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonateHCID 86670397—
SolventMethanolHCID 887—
ProductN-(((2S)-1,4-dibenzyl-2-piperazinyl)methyl)anilineHCID 6658423073.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

A 20-mL vial was charged ((2R)-1,4-dibenzyl-2-piperazinyl)methyl methanesulfonate (1.01 g, 2.70 mmol, Example 184, Step 1), aniline (1.30 mL, 14.3 mmol, Alfa Aesar, Ward Hill, Mass.) and MeOH (12 mL). The reaction mixture was sealed and heated at 140° C. for 30 min in an Initiator microwave reactor (Biotage AB, Inc., Uppsala, Sweden). The mixture was allowed to cool to room temperature and then concentrated in vacuo. The crude product was purified by column chromatography (50 g of silica gel, (2 M NH3 in MeOH) in CH2Cl2 0 to 5%) to afford N-(((2S)-1,4-dibenzyl-2-piperazinyl)methyl)aniline (0.734 g) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-7c5d0a86eba341358c58c8bc608791cc
Source noteuspto-grants-2013_04