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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375530생성일: 2026년 10월 26일

Triethylamine → 4-(1H-Benzimidazol-2-yl)-N-[2-(4-phenyl-1-piperazinyl)ethyl]benzamide

https://huagongshe.com/reaction/375530

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(1h-Benzimidazol-2-yl)benzoic acidHCID 759419—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(4-Phenylpiperazin-1-yl)ethan-1-amineHCID 4742503—
용매DichloromethaneHCID 6344—
생성물AmmoniaHCID 222—
생성물4-(1H-Benzimidazol-2-yl)-N-[2-(4-phenyl-1-piperazinyl)ethyl]benzamideHCID 1899305273.9%

반응 단계

A mixture of 4-(1H-benzimidazol-2-yl)benzoic acid (Example E) (0.50 g), 2-(4-phenylpiperazin-1-yl)ethylamine (0.77 g), 1-(3-dimethylaminopropyl)3-ethylcarbodiimide hydrochloride (0.44 g) and triethylamine (0.29 mL) in dichloromethane (20 mL) is stirred at room temperature for 2 days. The mixture is washed with water (50 mL), dried over MgSO4, filtered and evaporated. The residue is purified by MPLC on silica gel eluting with 100:8:1 dichloromethane: ethanol:0.880 aqueous ammonia to give 0.33 g of the title compound as a beige solid; mp 190°-192° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05486517
출처 데이터셋uspto-grants-1996_01
ORD IDord-fa436fedf31d4580a07fc0fcbdf639d6
출처 메모uspto-grants-1996_01