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HRID 476897作成日:2026年10月26日

Sodium hydride → N-(2-Pyridyl)-1-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamide

https://huagongshe.com/reaction/476897

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1-(2-Chloroethyl)-4-(2-methoxyphenyl)piperazineHCID 595673—
反応物1H-Benzimidazole-2-carboxamide, N-2-pyridinyl-HCID 3087291—
溶媒Dimethyl SulfoxideHCID 679—
生成物N-(2-Pyridyl)-1-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamideHCID 1437129252.1%

反応手順

In an argon atmosphere, N-(2-pyridyl)benzimidazole-2-carboxamide (1.55 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-(2-methoxyphenyl)-1-piperazinyl]ethyl chloride (1.65 g) in DMSO was added dropwise and stirred at room temperature overnight. The reaction solution was poured into an aqueous solution of ammonium chloride and extracted with chloroform, and the chloroform layer was dired. The residue obtained by distilling off the solvent was purified by column chromatography on silica gel to give the title compound (1.54 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-035fea96d86f4eb0a1425042ebd72572
出典メモuspto-grants-1989_12