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HRID 2391275作成日:2026年10月26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/reaction/2391275

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US08273741B2
出典データセットuspto-grants-2012_09
ORD IDord-bb0344d669744857a7803d339af9601e
出典メモuspto-grants-2012_09