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HRID 476896作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Ammonium ChlorideHCID 25517—
反応物2-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]ethyl chlorideHCID 11809153—
反応物N-methyl-N-(4,6-dimethyl-2-pyridyl)benzimidazole-2-carboxamideHCID 14371319—
溶媒Dimethyl SulfoxideHCID 679—
生成物N-Methyl-N-(4,6-dimethyl-2-pyridyl)-1-[2-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamideHCID 980999579.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04886803
出典データセットuspto-grants-1989_12
ORD IDord-f6323285af62467588d63c16ce98f4cc
出典メモuspto-grants-1989_12