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HRID 276774作成日:2026年10月26日

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

https://huagongshe.com/reaction/276774

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物IsobutyraldehydeHCID 6561—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物{5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-piperazineHCID 178477952—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium HydroxideHCID 14798—
生成物1-{5-[5-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridin-2-yl}-4-isobutyl-piperazineHCID 9867334—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355635B1
出典データセットuspto-grants-2002_03
ORD IDord-f668ec788e3840d7b5efe71c30b22f9b
出典メモuspto-grants-2002_03