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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 910249생성일: 2026년 10월 25일

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/reaction/910249

반응식

참여 물질

역할이름HCID투입량
반응물Bis(2-pyridylmethyl)amineHCID 73759—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-[3-(4-Imidazo[1,2-a]pyridin-2-ylphenyl)-1H-1-pyrazolyl]acetic acidHCID 67405489—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물N1,N1-Di(2-pyridylmethyl)-2-[3-(4-imidazo[1,2-a]pyridin-2-ylphenyl)-1H-1-pyrazolyl]acetamideHCID 6740446472.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08022075B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-f9236efd8d384e90a53a9a1fa0931a3f
출처 메모uspto-grants-2011_09