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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901647생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/901647

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Phenacyl bromideHCID 6259—
반응물4-[4-Fluoro-3-(trifluoromethyl)phenoxy]anilineHCID 66977344—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물4-(4-{2-butyl-1-[4-(4-fluoro-3-trifluoromethyl-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-1-methyl-piperidineHCID 59699365—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361678B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-baf314a250104332a8a57cae2acddab2
출처 메모uspto-grants-2008_04