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HRID 1878442作成日:2026年10月26日

Acetonitrile → N-phenyl-6-(pyrid-3-yl)imidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/1878442

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Sodium CarbonateHCID 10340—
反応物3-Pyridinylboronic acidHCID 2734378—
反応物6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771673—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物N-phenyl-6-(pyrid-3-yl)imidazo[1,2-a]pyridine-2-carboxamideHCID 4413763348.9%

反応手順

150 mg of 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 1), 0.237 g of pyridine-3-boronic acid, 45 mg of tetrakis(triphenylphosphine)palladium, 2 mL of aqueous 2M sodium carbonate solution, 4 mL of acetonitrile and 4 mL of toluene are placed in a microwave tube. The mixture is heated for 20 minutes in a microwave machine set at 150° C., and then cooled and filtered, the insoluble matter being washed with a mixture of methanol and dichloromethane. The combined filtrates are concentrated to dryness under reduced pressure. The residue is concreted with aqueous methanol to give 73 mg of N-phenyl-6-(pyrid-3-yl)imidazo[1,2-a]pyridine-2-carboxamide in the form of an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08314109B2
出典データセットuspto-grants-2012_11
ORD IDord-4b02cd74bd674f53bf290ff6610a4748
出典メモuspto-grants-2012_11