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HRID 1268683作成日:2026年10月27日

Diisopropylethylamine → N-[4-(8-Methyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-3-piperidin-1-yl-propionamide

https://huagongshe.com/reaction/1268683

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-Piperidinepropanoic acidHCID 117782—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-{8-Methylimidazo[1,2-a]pyridin-2-yl}anilineHCID 2771077—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(8-Methyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-3-piperidin-1-yl-propionamideHCID 2201560723.9%

反応手順

To a mixture of the product of Step B (330 mg) and N,N-diisopropylethylamine (0.28 mL) in dichloromethane (3 mL) and N,N-dimethylformamide(1 mL), was added 1-piperidinepropionic acid (256 mg), WSC.HCl (1-Ethyl-3-(3′dimethylaminopropyl)-carbodiimide.HCl) (312 mg), and 1-hydroxybenzotriazole hydrate (220 mg). The solution was stirred at ambient temperature for approximately 18 hours. The mixture was poured into a separatory funnel and washed sequentially with an equal volume of 1 N sodium hydroxide and water. The organic phase was dried over sodium sulfate, decanted and evaporated. The residue was purified via silica gel chromatography (methanol/dichloromethane) to yield the title compound (128 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07199117B2
出典データセットuspto-grants-2007_04
ORD IDord-43f11231d0114f229c069af685acd277
出典メモuspto-grants-2007_04