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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276774생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/276774

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물IsobutyraldehydeHCID 6561—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물{5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-piperazineHCID 178477952—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Sodium HydroxideHCID 14798—
생성물1-{5-[5-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazineHCID 9867334—

반응 단계

Sodium triacetoxyborohydride (20.2 g) was added to a suspension of 1-{5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-piperazine (23.8 g), acetic acid (5.1 mL), and isobutyraldehyde (6.35 mL) in THF (250 mL). The resultant suspension was stirred at ambient temperature for 18 hours, and then the reaction mixture was diluted with 1 N NaOH (1000 mL) and ethyl acetate (450 mL). The layers were separated, and the organic phase was diluted with hexanes (1000 mL). The resultant precipitate was collected by filtration, and the mother liquors were concentrated to 400 mL. The second crop of precipitate was collected and combined with the first crop to provide 1-{5-[5(3,4,-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazine (22.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355635B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-f668ec788e3840d7b5efe71c30b22f9b
출처 메모uspto-grants-2002_03