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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2283815생성일: 2026년 10월 27일

Sodium Iodide → 2-ethyl-1-[4-(4-pyridin-2-ylpiperazin-1-yl)butyl]-2H-pyrazolo[3,4-c]quinolin-4-amine monohydrate

https://huagongshe.com/reaction/2283815

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물1-(2-Pyridyl)piperazineHCID 94459—
반응물1-(4-chlorobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 57717514—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-ethyl-1-[4-(4-pyridin-2-ylpiperazin-1-yl)butyl]-2H-pyrazolo[3,4-c]quinolin-4-amine monohydrateHCID 6695856294.8%

반응 조건

온도60 °C

반응 단계

A mixture of 1-(4-chlorobutyl)-2-ethyl-2H-pyrazolo[3,4-c]quinoline-4-amine (prepared as described in Example 19, 1.0 g, 3.3 mmol), 1-(2-pyridyl)piperazine (0.752 mL, 4.95 mmol), potassium carbonate (1.8 g, 13.2 mmol), and sodium iodide (123 mg, 0.825 mmol) in DMF (6 mL) was heated at 60° C. for 1 hour, then at 90° C. for 2 hours. The reaction was allowed to cool to ambient temperature and white solid formed. Water (100 mL) was added to the mixture. The mixture was stirred for 30 min and the solid was isolated by filtration and dried to yield 1.4 g of 2-ethyl-1-[4-(4-pyridin-2-ylpiperazin-1-yl)butyl]-2H-pyrazolo[3,4-c]quinolin-4-amine monohydrate as a white solid, mp 183-184° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09145410B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-0cd4046f2dcf46278e4aca9f2020ea0e
출처 메모uspto-grants-2015_09