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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476896생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물2-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]ethyl chlorideHCID 11809153—
반응물N-methyl-N-(4,6-dimethyl-2-pyridyl)benzimidazole-2-carboxamideHCID 14371319—
용매Dimethyl SulfoxideHCID 679—
생성물N-Methyl-N-(4,6-dimethyl-2-pyridyl)-1-[2-(4-(3,4-dimethoxybenzoyl)-1-piperazinyl)ethyl]benzimidazole-2-carboxamideHCID 980999579.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04886803
출처 데이터셋uspto-grants-1989_12
ORD IDord-f6323285af62467588d63c16ce98f4cc
출처 메모uspto-grants-1989_12