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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17728생성일: 2026년 10월 25일

Dimethylformamide → [3-(4-{2-butyl-1-[4-(4-chloro-2-cyclohexyl-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amine

https://huagongshe.com/reaction/17728

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물4-(4-Chloro-2-cyclohexylphenoxy)anilineHCID 68684533—
반응물2-Bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanoneHCID 86591969—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물[3-(4-{2-butyl-1-[4-(4-chloro-2-cyclohexyl-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amineHCID 59699407—

반응 단계

To a stirred solution of 4-(4-chloro-2-cyclohexylphenoxy)aniline (1.2 eq., 2.5 mmol) in anhydrous DMF (5 mL) DIEA (3 eq. 6 mmol) was added, followed by slow addition of the 2-bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone described above (2.4 mmol), according to General Procedure R2. The reaction mixture was stirred under nitrogen at rt until completion, as indicated by TLC or HPLC. The reaction mixture was then diluted with cold H2O and the product was isolated in EtOAc. 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 (Silica gel). Pure product obtained from 2-4% MeOH/DCM (yield˜50-60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737285B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5cbd554d65364d76aa89d6fe80581cea
출처 메모uspto-grants-2010_06