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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2237049생성일: 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/2237049

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 번호US07714013B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-09091a4fc6bb405faadd4fa632138aa0
출처 메모uspto-grants-2010_05