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HRID 1725545作成日:2026年10月26日

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

https://huagongshe.com/reaction/1725545

反応式

関与物質

役割名称HCID仕込み量
反応物8-AminoquinolineHCID 11359—
反応物5-acetyl-2-ethyl-4-nitro-6-(3-chlorophenyl)pyridazin-3(2H)-oneHCID 10519832—
溶媒EthanolHCID 702—
生成物5-Acetyl-6-(3-chlorophenyl)-2-ethyl-4-(quinolin-8-ylamino)pyridazin-3(2H)-oneHCID 6848615850%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07491722B2
出典データセットuspto-grants-2009_02
ORD IDord-fe70117417d8446b864d13c0c5052126
出典メモuspto-grants-2009_02