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HRID 1294587作成日:2026年10月25日

Methyl vinyl ketone → 2-(2-(Imidazo[1,2-a]pyridin-2-yl)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1294587

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl vinyl ketoneHCID 6570—
反応物PhthalimideHCID 6809—
反応物2-AminopyridineHCID 10439—
反応物2-(4-Bromo-3-oxobutyl)-1H-isoindole-1,3(2H)-dioneHCID 3759744—
溶媒EthanolHCID 702—
生成物2-(2-(Imidazo[1,2-a]pyridin-2-yl)ethyl)isoindoline-1,3-dioneHCID 153126996.6%
生成物2-(4-Bromo-3-oxobutyl)-1H-isoindole-1,3(2H)-dioneHCID 3759744—

反応手順

2-(4-Bromo-3-oxo-butyl)-isoindole-1,3-dione is prepared by condensation of but-1-en-3-one with phthalimide followed by bromination according to known procedures (J. Med. Chem., 35:3239, 1992. A solution of 2-(4-bromo-3-oxo-butyl)-isoindole-1,3-dione (8.9 g, 30.06 mmol) and 2-aminopyridine (2.8 g, 29.75 mmol) in ethanol is heated at reflux for 4 hours. The mixture is cooled to room temperature and concentrated. The residue is purified by chromatography (silica gel, dichloromethane/ethanol 95:5); to give 4.23 g of 2-[2-(imidazo[1,2-a]pyridin-2-yl)ethyl]-isoindole-1,3-dione (49%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07241772B2
出典データセットuspto-grants-2007_07
ORD IDord-f7efda1210db48a0993d6c3ee16e7592
出典メモuspto-grants-2007_07