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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476896Generated: October 26, 2026

Sodium hydride → N-Methyl-N-(4,6-dimethyl-2-pyridyl)-1-[2-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamide

https://huagongshe.com/reaction/476896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]ethyl chlorideHCID 11809153—
ReactantN-methyl-N-(4,6-dimethyl-2-pyridyl)benzimidazole-2-carboxamideHCID 14371319—
SolventDimethyl SulfoxideHCID 679—
ProductN-Methyl-N-(4,6-dimethyl-2-pyridyl)-1-[2-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamideHCID 980999579.2%

Reaction Steps

In an argon atmosphere, N-methyl-N-(4,6-dimethyl-2-pyridyl)benzimidazole-2-carboxamide (2.00 g) was dissolved in DMSO (15 ml), and 60% sodium hydride (0.33 g) was added and stirred at room temperature for 1 hr. A solution (7 ml) of 2-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]ethyl chloride (2.20 g) in DMSO was added dropwise and allowed to react overnight at room temperature under agitation. The reaction solution was added to an aqueous solution of ammonium chloride and extracted with chloroform, the chloroform layer was dried over Na2SO4, and the solvent was distilled off. Purification of the residue by column chromatography gave the title compound (3.10 g) as amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886803
Source datasetuspto-grants-1989_12
ORD IDord-f6323285af62467588d63c16ce98f4cc
Source noteuspto-grants-1989_12