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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 126780생성일: 2026년 10월 25일

Potassium Iodide → 2-[3-[4-[3-(Trifluoromethyl)phenyl]-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one

https://huagongshe.com/reaction/126780

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물1,2,4-Triazolo(4,3-a)pyridin-3(2H)-oneHCID 81431—
반응물Piperazine, 1-(3-chloropropyl)-4-(3-(trifluoromethyl)phenyl)-HCID 3060362—
반응물SodiumHCID 5360545—
용매AcetonitrileHCID 6342—
용매Potassium HydroxideHCID 14797—
생성물2-[3-[4-[3-(Trifluoromethyl)phenyl]-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-oneHCID 20287986—

반응 단계

The hydrochloride salt of 1-(3-chloropropyl)-4-[3-(trifluoromethyl)phenyl]piperazine, 6.41 g. (0.0187 mole) is dissolved in dilute KOH solution and the free base which is formed is extracted into ether. The ether solution is washed with water and brine, dried over magnesium sulfate, and concentrated under reduced pressure to afford the desired free base. A suspension of 2.61 g. (0.0166 mole) of the sodium salt of 1,2,4-triazolo[4,3-a]pyridin-3(2H)-one and 5.09 g (0.0166 mole) of 1-(3-chloropropyl)-4-[3-(trifluoromethyl)phenyl]piperazine in 100 ml. of acetonitrile is treated with approximately 50 mg. of potassium iodide, and refluxed for 24 hrs. The mixture is then cooled and filtered, and the filtrate concentrated to an oil under reduced pressure. The residual oil solidifies when triturated with ether. This solid is recrystallized twice from ethanol to give 4.34 g. (58%) of product, m.p. 207.5°-209.5°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254124
출처 데이터셋uspto-grants-1981_03
ORD IDord-0393b0cf2b554452a7bc58ad18c28ff1
출처 메모uspto-grants-1981_03