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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542211생성일: 2026년 10월 26일

Chloroform → 4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline

https://huagongshe.com/reaction/542211

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물4-Amino-6,7-dimethoxy-2-(4-benzylpiperazin-1-yl)quinolineHCID 13359991—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물4-Amino-6,7-dimethoxy-2-(piperazin-1-yl)quinolineHCID 1406899851.2%

반응 단계

4-Amino-6,7-dimethoxy-2-(4-benzylpiperazin-1-yl)quinoline (6.2 g) in ethanol (300 ml) with 5% Pd/C catalyst was stirred at 50° under an atmosphere of hydrogen (50 p.s.i.) for 20 hours. The mixture was cooled, chloroform (100 ml) added and the solution filtered through "Solkafloc". The solid was washed with chloroform-methanol (1:1, 4×100 ml) and the combined filtrates evaporated in vacuo. The residue was partitioned between chloroform-sodium carbonate solution (10%), the organic layer removed, the aqueous phase saturated with salt and further extracted with chloroform. The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated in vacuo to yield 4-amino-6,7-dimethoxy-2-(piperazin-1-yl)quinoline (2.42 g). Spectroscopy showed this product to be the same as that of Example 32.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04656174
출처 데이터셋uspto-grants-1987_04
ORD IDord-6479889b16bc45df8345a373e0507f3d
출처 메모uspto-grants-1987_04