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HRID 1663719作成日:2026年10月26日

5-Amino-2-methylphenol → N-[6-(5-amino-2-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1663719

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-2-methylphenolHCID 17818—
反応物Sodium hydrideHCID 24758—
反応物N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)cyclopropanecarboxamideHCID 57386058—
溶媒DimethylformamideHCID 6228—
生成物N-[6-(5-amino-2-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamideHCID 5750548331.2%

反応条件

温度0 °C

反応手順

To a suspension of sodium hydride (56 mg, 1.40 mmol) in N,N-dimethylformamide (2.0 mL) was added a solution of 5-amino-2-methylphenol (173 mg, 1.40 mmol) in N,N-dimethylformamide (1.0 mL), and the mixture was stirred at 0° C. for 30 min. To the reaction mixture was added a solution of N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)cyclopropanecarboxamide (306 mg, 0.933 mmol) in N,N-dimethylformamide (1.5 mL), and the mixture was stirred at 110° C. for 24 hr. The solvent was evaporated under reduced pressure, and ethyl acetate and water were added to the residue. The aqueous layer was extracted three times with ethyl acetate. Combined organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=17/83→90/10) to give the title compound (94 mg, 31%) as a brown powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08034812B2
出典データセットuspto-grants-2011_10
ORD IDord-30c0b424956d40fca0135b0618641151
出典メモuspto-grants-2011_10