Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895생성일: 2026년 10월 23일
4-(piperazin-1-yl)-1H-indole → (R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine
https://huagongshe.com/ko/reaction/895
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-(piperazin-1-yl)-1H-indole | HCID 594590 | — |
| 반응물 | (R)-4-methyl-3-pyridin-2-yl[1,2,3]oxathiazolidine-2,2-dioxide | HCID 22863100 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine | HCID 53956483 | 67.5% |
반응 단계
A solution of (R)-4-methyl-3-pyridin-2-yl-[1,2,3]-oxathiazolidine-2,2-dioxide (4.04 g 0.019 moles) and 4-piperazinoindole (3.80 g 0.019 moles) in acetonitrile (200 ml) was heated to 60° C. for 0.5 h then evaporated in vacuo. The residue was taken up into dilute HCl (100 ml), warmed to 60° C. for 0.5 h, cooled, washed with ethyl acetate (2×100 ml), made basic with potassium carbonate, extracted into dichioromethane (3×100 ml), dried (MgSO4) then evaporated in vacuo to give a brown glass. This was purified on a silica column eluting with 10% propan-2-ol in dichloromethane to give (R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine (4.3 g) as a clear glass.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723464 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-094501f6e5574d25af8d8557ebfc848e |
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| 출처 메모 | uspto-grants-1998_03 |
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