戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 730702作成日:2026年10月25日

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

https://huagongshe.com/reaction/730702

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DiisopropylethylamineHCID 81531—
反応物2-chloro-6-(trifluoromethyl)-1H-benzimidazoleHCID 337905—
反応物1-(2,6-Dichlorophenyl)piperazineHCID 11492345—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-[4-(2,6-Dichlorophenyl)piperazin-1-yl]-6-trifluoromethyl-1H-benzoimidazoleHCID 10047447—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582761B2
出典データセットuspto-grants-2009_09
ORD IDord-18db05cfa2954c4b856ff9818bcadebf
出典メモuspto-grants-2009_09