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HRID 476899作成日:2026年10月26日

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

https://huagongshe.com/reaction/476899

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1H-Benzimidazole-2-carboxamide, N-2-pyridinyl-HCID 3087291—
反応物2-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]ethyl chlorideHCID 11809153—
溶媒Dimethyl SulfoxideHCID 679—
生成物N-(2-pyridyl)-1-[2-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamideHCID 1437129452.9%

反応手順

In an argon atmosphere, N-(2-pyridyl)benzimidazole-2-carboxamide (1.40 g) was dissolved in DMSO (20 ml), and 60% sodium hydride (0.28 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 (1.90 g) in DMSO was added dropwise and allowed to react overnight at room temperature under agitation. The reaction solution was poured into 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 on silica gel gave the title compound (1.60 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-69740c2500544e618dec4d0230f5d979
出典メモuspto-grants-1989_12