돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730704생성일: 2026년 10월 25일

Water → 2-[4-(2,6-Dichlorobenzyl)piperazin-1-yl]-6-trifluoromethyl-1H-benzoimidazole

https://huagongshe.com/reaction/730704

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
반응물Sodium BicarbonateHCID 516892—
반응물2-Piperazin-1-yl-6-trifluoromethyl-1H-benzoimidazoleHCID 11666201—
용매DimethylformamideHCID 6228—
생성물2-[4-(2,6-Dichlorobenzyl)piperazin-1-yl]-6-trifluoromethyl-1H-benzoimidazoleHCID 57835114—

반응 단계

A mixture of the benzoimidazole from step (a) above (96 mg, 0.36 mmol), 2,6-dichlorobenzyl bromide (86 mg, 0.36 mmol, Aldrich) and NaHCO3 (151 mg, 1.8 mmol) in DMF (2 mL) was stirred at room temperature for 16 h. Water (10 mL) was then added and the mixture was extracted with EtOAc (2×20 mL). The combined organic phases were washed with water (5 mL) and brine (5 mL) then dried over Na2SO4 and filtered. The solvent was removed in vacuo and the residue purified by silica gel chromatography, eluting with 40% EtOAc/hexane. The material was recrystallized from EtOAc/hexanes to give the title compound as a white solid. M.p. 254-256° C. MS (ESI, pos. ion) m/z: 429 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582761B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-af1eb4f0e7624a048bf98ab324ed4cea
출처 메모uspto-grants-2009_09