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HRID 17656作成日:2026年10月23日

Dimethylformamide → 4-(4-{2-butyl-1-[4-(4-fluoro-3-trifluoromethyl-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-1-methyl-piperidine

https://huagongshe.com/ja/reaction/17656

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Phenacyl bromideHCID 6259—
反応物4-[4-Fluoro-3-(trifluoromethyl)phenoxy]anilineHCID 66977344—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物4-(4-{2-butyl-1-[4-(4-fluoro-3-trifluoromethyl-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-1-methyl-piperidineHCID 59699365—

反応手順

To a stirred solution of 4-(4-fluoro-3-trifluoromethyl-phenoxy)-aniline (1.64 mmol) in anhydrous DMF (30 mL) DIEA (3 eq) was added, followed by slow addition of the alpha-bromoacetophenone described above (2 eq), according to General Procedure R2. The reaction mixture was stirred under nitrogen at rt until completion, as indicated by TLC and HPLC. The reaction mixture was then diluted with cold H2O and the product was isolated in Et2O. The combined organic layers were washed with brine and dried over sodium sulfate. Evaporation of solvent in vacuuo afforded the desired product. The crude alkylated aniline was purified by chromatography on silica gel (elution with 5-20% EtOAc/Hexane).

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-a3c4b57671024732b848cf03e61f3468
出典メモuspto-grants-2010_06