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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730702생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/730702

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물2-chloro-6-(trifluoromethyl)-1H-benzimidazoleHCID 337905—
반응물1-(2,6-Dichlorophenyl)piperazineHCID 11492345—
용매Dimethyl SulfoxideHCID 679—
생성물2-[4-(2,6-Dichlorophenyl)piperazin-1-yl]-6-trifluoromethyl-1H-benzoimidazoleHCID 10047447—

반응 단계

A mixture of the benzoimidazole from step (c) above (75 mg, 0.34 mmol), the piperazine from step (a) above (90 mg, 0.39 mmol) and N,N-diisopropylethylamine (0.1 mL, 0.58 mmol, Aldrich) in DMSO (2 mL) was stirred at 80° C. for 24 h. The mixture was cooled to room temperature, water (10 mL) was added and the mixture was extracted with EtOAc (2×20 mL). The combined organic phases were washed with water (2×10 mL) and brine (5 mL), dried over Na2SO4, and filtered. The solvent was removed in vacuo and the residue was purified by silica gel chromatography, eluting with 20% EtOAc/hexane to give the title compound as a white solid. M.p. 263-265° C. MS (ESI, pos. ion) m/z: 415 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582761B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-18db05cfa2954c4b856ff9818bcadebf
출처 메모uspto-grants-2009_09