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HRID 17642作成日:2026年10月25日

tert-Butyl 4-formylpiperidine-1-carboxylate → tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate

https://huagongshe.com/reaction/17642

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
反応物2-Butylamino-4,6-di(3-diethylaminopropoxy)anilineHCID 66977544—
溶媒EthanolHCID 702—
生成物tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylateHCID 6697750669%

反応手順

A solution of 1-(t-butyloxycarbonyl)piperdine-4-carboxaldehyde (235 mg; 1.1 mmol) and 2-butylamino-4,6-di(3-diethylaminopropoxy)aniline (synthesized via General Procedures J1 and J2 and I) (424 mg; 1 mmol) in ethanol (5 mL) was subjected to General Procedure K. The crude product was purified by silica gel column chromatography using 10% MeOH in DCM with a gradual increment of triethylamine (0.2 to 1.0%) as eluent to afford 425 mg of tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737285B2
出典データセットuspto-grants-2010_06
ORD IDord-64ef82b016524b0e990e1594c8b1277f
出典メモuspto-grants-2010_06