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HRID 126780作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物1,2,4-Triazolo(4,3-a)pyridin-3(2H)-oneHCID 81431—
反応物Piperazine, 1-(3-chloropropyl)-4-(3-(trifluoromethyl)phenyl)-HCID 3060362—
反応物SodiumHCID 5360545—
溶媒AcetonitrileHCID 6342—
溶媒Potassium HydroxideHCID 14797—
生成物2-[3-[4-[3-(Trifluoromethyl)phenyl]-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-oneHCID 20287986—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254124
出典データセットuspto-grants-1981_03
ORD IDord-0393b0cf2b554452a7bc58ad18c28ff1
出典メモuspto-grants-1981_03