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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230431생성일: 2026년 10월 25일

Sodium hydride → 5,6-Dichloro-1-(2-fluoro-benzyl)-2-(2,2,2-trifluoro-ethyl)-1H-benzoimidazole

https://huagongshe.com/reaction/230431

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물alpha-Bromo-o-fluorotolueneHCID 67968—
반응물5,6-Dichloro-2-(2,2,2-trifluoro-ethyl)-1H-indoleHCID 66968833—
반응물dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzoimidazoleHCID 66968977—
용매DimethylformamideHCID 6228—
생성물5,6-Dichloro-1-(2-fluoro-benzyl)-2-(2,2,2-trifluoro-ethyl)-1H-benzoimidazoleHCID 44430143—

반응 조건

온도0 °C

반응 단계

NaH (60%) (60 mg, 1.5 mmol) was added into a solution of dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzoimidazole. 5,6-Dichloro-2-(2,2,2-trifluoro-ethyl)-1H-indole (269 mg, 1 mmol) in DMF (5 ml) at 0° C. The resulting mixture was stirred at 0° C. for half hour. 2-fluorobenzyl bromide (283.5 mg, 1.5 mmol) was then added to the reaction mixture at 0° C. The reaction temperature was raised to 25° C. and then the reaction mixture was stirred for 18 hours. NH4Cl (aq.) was added and extracted with EtOAc. The organic layer was washed with brine, then dried over anhydrous MgSO4. The solvent was distilled out under reduced pressure. Column chromatography (silica gel, EtOAc/hexanes (0% to 60%) yielded the title compound as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566733B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-8ff1b88d73314a1984ea3ea4e01925da
출처 메모uspto-grants-2009_07