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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339564생성일: 2026년 10월 24일

Triethylamine → 4-(methylamino)-N-[4-(6-methylimidazo[1,2-a]pyridin-2-yl)phenyl]benzamide

https://huagongshe.com/ko/reaction/339564

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(Methylamino)benzoic acidHCID 66345—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물4-(6-Methylimidazo[1,2-a]pyridin-2-yl)anilineHCID 821084—
용매DimethylformamideHCID 6228—
생성물4-(methylamino)-N-[4-(6-methylimidazo[1,2-a]pyridin-2-yl)phenyl]benzamideHCID 5834207733.2%

반응 단계

To a stirred solution of 4-(6-methylimidazo[1,2-a]pyridin-2-yl)aniline (0.10 g, 0.448 mmol), 1-hydroxybenzotriazole (0.06 g, 0.448 mmol), 4-methylaminobenzoic acid (0.068 g, 0.448 mmol) and triethylamine (62 μl, 0.045 g, 0.448 mmol) in dry DMF (5 ml) at 0° C. was added 1-ethyl-3-[3-(dimethylaminopropyl]-carbodiimide hydrochloride (0.086 g, 0.448 mmol) under an atmosphere or argon. After 10 min the cooling bath was removed and the reaction mixture was stirred at room temperature for 4 d. The reaction mixture was then added to water (150 ml) with stirring and the precipitate was collected by filtration. Purification by flash chromatography (25:1 DCM/MeOH) gave the title compound (0.053 g, 33%) as an almost colourless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895313B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-7e9a0e0620404989977747eea8dccf69
출처 메모uspto-grants-2014_11