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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725545생성일: 2026년 10월 25일

8-Aminoquinoline → 5-Acetyl-6-(3-chlorophenyl)-2-ethyl-4-(quinolin-8-ylamino)pyridazin-3(2H)-one

https://huagongshe.com/reaction/1725545

반응식

참여 물질

역할이름HCID투입량
반응물8-AminoquinolineHCID 11359—
반응물5-acetyl-2-ethyl-4-nitro-6-(3-chlorophenyl)pyridazin-3(2H)-oneHCID 10519832—
용매EthanolHCID 702—
생성물5-Acetyl-6-(3-chlorophenyl)-2-ethyl-4-(quinolin-8-ylamino)pyridazin-3(2H)-oneHCID 6848615850%

반응 단계

To a stirred solution of 100 mg (0.311 mmol) of 5-acetyl-2-ethyl-4-nitro-6-(3-chlorophenyl)pyridazin-3(2H)-one (Dal Piaz, V et al, J. Med. Chem. 1997, 40, 1417) in ethanol (4 mL), 8-aminoquinoline (67 mg, 0.467 mmol) was added. The resulting mixture was stirred at room temperature for two hours. The solvent was evaporated and the residue purified by column chromatography (silica gel, hexane/ethyl acetate 2:1) to yield the title compound (65 mg, 50% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07491722B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-fe70117417d8446b864d13c0c5052126
출처 메모uspto-grants-2009_02