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HRID 1667964作成日:2026年10月23日

2,5-Dimethyl-2H-pyrazole-3-carbonyl chloride → N-[3-({2-[(N,N-dimethylglycyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/ja/reaction/1667964

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-Dimethyl-2H-pyrazole-3-carbonyl chlorideHCID 2736299—
反応物N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-N2,N2-dimethylglycinamideHCID 57708553—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
溶媒Sodium HydroxideHCID 14798—
生成物N-[3-({2-[(N,N-dimethylglycyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 2476798049%

反応手順

To a solution of N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-N2,N2-dimethylglycinamide (196 mg, 0.6 mmol) in N-methylpyrrolidone (5.0 mL) was added 1,3-dimethylpyrazole-5-carbonyl chloride (270 mg, 1.7 mmol), and the mixture was stirred at room temperature for 5 hr. The reaction mixture was diluted with 1N aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→460/40) and precipitated from ethyl acetate to give the title compound (131 mg, 49%) as a white powder. melting point 210° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044049B2
出典データセットuspto-grants-2011_10
ORD IDord-f148a40e7f6244afb1fbfb9908bc9464
出典メモuspto-grants-2011_10