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HRID 476896Erstellt: 24. Oktober 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/de/reaction/476896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt2-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]ethyl chlorideHCID 11809153—
EduktN-methyl-N-(4,6-dimethyl-2-pyridyl)benzimidazole-2-carboxamideHCID 14371319—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktN-Methyl-N-(4,6-dimethyl-2-pyridyl)-1-[2-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamideHCID 980999579,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04886803
Quelldatensatzuspto-grants-1989_12
ORD IDord-f6323285af62467588d63c16ce98f4cc
Quellennotizuspto-grants-1989_12