Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64875생성일: 2026년 10월 24일
1-(3-(Trifluoromethyl)phenyl)piperazine → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-trifluoromethylphenyl)piperazine hydrochloride
https://huagongshe.com/ko/reaction/64875
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(3-(Trifluoromethyl)phenyl)piperazine | HCID 4296 | — |
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazole | HCID 10910880 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-trifluoromethylphenyl)piperazine hydrochloride | HCID 13520737 | 35.8% |
반응 단계
A mixture of 6.5 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 5.8 g of N-(α,α,α-trifluoro-m-tolyl)piperazine, 7.0 g of potassium carbonate and a few crystals potassium iodide in 80 ml of dimethylformamide was stirred at 70°-75° C. for seven hrs. The reaction mixture was cooled, filtered and concentrated to an oil, which was stirred with water and extracted with ether-ethyl acetate. The organic extracts were washed with water (2×), saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture was filtered and concentrated to an oil, which was converted to a salt by treatment with ethereal hydrogen chloride. The salt was recrystallized from ethyl acetate/methanol to give 4 g (35%) of product mp, 208°-209° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04610988 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-c2676640fd80454395df9609f6d257ce |
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| 출처 메모 | uspto-grants-1986_09 |
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