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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

반응식

참여 물질

역할이름HCID투입량
반응물4-(piperazin-1-yl)-1H-indoleHCID 594590—
반응물(R)-4-methyl-3-pyridin-2-yl[1,2,3]oxathiazolidine-2,2-dioxideHCID 22863100—
용매AcetonitrileHCID 6342—
생성물(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazineHCID 5395648367.5%

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723464
출처 데이터셋uspto-grants-1998_03
ORD IDord-094501f6e5574d25af8d8557ebfc848e
출처 메모uspto-grants-1998_03