Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576514생성일: 2026년 10월 26일
Trifluoroacetic acid → 5-allyl-4-[2-(4-fluoro-phenyl)-allyl]-2,4,8-trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole
https://huagongshe.com/reaction/576514
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | N-Allyl-N-p-tolyl-hydrazine | HCID 67328679 | — |
| 반응물 | 3-[2-(4-Fluoro-phenyl)-allyl]-1,3-dimethyl-piperidin-4-one | HCID 67355960 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 5-allyl-4-[2-(4-fluoro-phenyl)-allyl]-2,4,8-trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole | HCID 67356725 | 20.2% |
반응 단계
N-Allyl-N-p-tolyl-hydrazine (600 mg, 3.70 mmol) and 3-[2-(4-fluoro-phenyl)-allyl]-1,3-dimethyl-piperidin-4-one (970 mg, 3.71 mmol) were dissolved in 1,4-dioxane (4 mL). Trifluoroacetic acid (1 mL) was added and the reaction mixture was heated to 100° C. for 3 h. 1,4-Dioxane was removed under reduced pressure, the residue was basified with aqueous sodium bicarbonate, and extracted with EtOAc (2×30 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel (100-200 mesh, eluent as 5% EtOAc in hexane) to obtain 290 mg of 5-allyl-4-[2-(4-fluoro-phenyl)-allyl]-2,4,8-trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09040519B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-a19e3a35ee5c4015bc2ae9aebf57ee06 |
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| 출처 메모 | uspto-grants-2015_05 |
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