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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1197513생성일: 2026년 10월 24일

Toluene → 1-[2-(Bis-(4-fluorophenyl)-methoxy)-ethyl]-4-(3-phenyloxadiazol-5-yl-methyl)piperazine

https://huagongshe.com/ko/reaction/1197513

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물5-(Chloromethyl)-3-phenyl-1,2,4-oxadiazoleHCID 966714—
반응물1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]piperazineHCID 9974013—
용매WaterHCID 962—
생성물1-[2-(Bis-(4-fluorophenyl)-methoxy)-ethyl]-4-(3-phenyloxadiazol-5-yl-methyl)piperazineHCID 19106740—

반응 단계

1.08 g (3.3 mM) of 1-[2-(bis-(4-fluorophenyl)-methoxy)ethyl]piperazine and 0.97 g of 3-phenyl-5-chloromethyl-1,2,4-oxadiazole (prepared according to Chem.Ber. 105 (1972)2825) were dissolved in 5 ml of dry dimethylformamide. 1.4 g of potassium carbonate were added and the mixture was stirred at room temperature overnight. Toluene and water were added, the aqueous phase extracted with toluene, the combined organic phases washed three times with water, treated with charcoal and evaporated in vacuo. The residue was dissolved in 10 ml of ethanol and 0.69 g of maleic acid were added. The precipitate was isolated by filtration and recrystallized from hot acetonitrile to obtain the dimaleate salt of the title compound as colourless crystals melting at 142°-143°. Analytical data were in accordance with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05276035
출처 데이터셋uspto-grants-1994_01
ORD IDord-a9aa31526e9e43b3be5fba1f02c9e189
출처 메모uspto-grants-1994_01