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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | 1,2,4-Triazolo(4,3-a)pyridin-3(2H)-one | HCID 81431 | — |
| 반응물 | Piperazine, 1-(3-chloropropyl)-4-(3-(trifluoromethyl)phenyl)- | HCID 3060362 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Potassium Hydroxide | HCID 14797 | — |
| 생성물 | 2-[3-[4-[3-(Trifluoromethyl)phenyl]-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04254124 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-0393b0cf2b554452a7bc58ad18c28ff1 |
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| 출처 메모 | uspto-grants-1981_03 |
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