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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901695생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/901695

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물4-(2,4-Dichlorophenoxy)benzenamineHCID 26940—
반응물2-Bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanoneHCID 86591969—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물[3-(4-{2-butyl-1-[4-(2,4-dichloro-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amineHCID 59699284—

반응 단계

To a stirred solution of 4-(2,4-dichloro-phenoxy)aniline described above (1.2 eq., 5.2 mmol) in anhydrous DMF (20 mL) DIEA (3 eq. 15 mmol) was added, followed by slow addition of the 2-bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone described above (4.4 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 ˜5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361678B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-5dccb1a85b994bc1876d0bc079acf50c
출처 메모uspto-grants-2008_04