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HRID 910249作成日:2026年10月24日

Bis(2-pyridylmethyl)amine → N1,N1-Di(2-pyridylmethyl)-2-[3-(4-imidazo[1,2-a]pyridin-2-ylphenyl)-1H-1-pyrazolyl]acetamide

https://huagongshe.com/ja/reaction/910249

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-pyridylmethyl)amineHCID 73759—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-[3-(4-Imidazo[1,2-a]pyridin-2-ylphenyl)-1H-1-pyrazolyl]acetic acidHCID 67405489—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物N1,N1-Di(2-pyridylmethyl)-2-[3-(4-imidazo[1,2-a]pyridin-2-ylphenyl)-1H-1-pyrazolyl]acetamideHCID 6740446472.5%

反応手順

2-[3-(4-Imidazo[1,2-a]pyridin-2-ylphenyl)-1H-1-pyrazolyl]acetic acid (51 mg), 2,2′-dipicolylamine (32 mg), and 1-hydroxybenzotriazole (27 mg) were dissolved in N,N-dimethylformamide (1 mL), and triethylamine (56 μL) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (38 mg) were added to the solution, followed by stirring at room temperature for 2 hours. Water was added to the reaction mixture, followed by extraction with chloroform and then drying over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to flash column chromatography. Fractions eluted by dichloromethane-methanol (20:1) were concentrated under reduced pressure, and the solid was recovered through filtration by use of diethyl ether, to thereby yield the title compound (58 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022075B2
出典データセットuspto-grants-2011_09
ORD IDord-f9236efd8d384e90a53a9a1fa0931a3f
出典メモuspto-grants-2011_09