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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276773생성일: 2026년 10월 24일

Potassium Iodide → 1-{5-[5-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazine

https://huagongshe.com/ko/reaction/276773

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1-(2-Methylpropyl)piperazineHCID 2052052—
반응물2-chloro-5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridine dihydrochlorideHCID 178478573—
용매WaterHCID 962—
용매CyclohexaneHCID 8078—
생성물1-{5-[5-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazineHCID 986733479.6%

반응 단계

A suspension of 2-chloro-5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridine dihydrochloride (1.07 g, 2.6 mmol), N-isobutylpiperazine (0.95 g, 6.72 mmol), potassium carbonate (0.5 g, 3.62 mmol), and potassium iodide (0.5 g, 0.54 mmol) in xylenes (5 mL) was heated to reflux under a nitrogen atmosphere for 24 hours. The reaction mixture was then cooled to ambient temperature and a solution of potassium carbonate (19) in water (10 mL) and cyclohexane (10 mL) were added. The mixture was stirred vigorously for 15 min, and the precipitate was collected by filtration. The filter cake was washed with water (10 mL) and triturated with methyl tert-butyl ether (4 mL) to provide 1-{5-[5(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazine (2.07 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355635B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-f5a3b30afdc447b988dd4d805b8e252d
출처 메모uspto-grants-2002_03