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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1294587생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1294587

반응식

참여 물질

역할이름HCID투입량
반응물Methyl vinyl ketoneHCID 6570—
반응물PhthalimideHCID 6809—
반응물2-AminopyridineHCID 10439—
반응물2-(4-Bromo-3-oxobutyl)-1H-isoindole-1,3(2H)-dioneHCID 3759744—
용매EthanolHCID 702—
생성물2-(2-(Imidazo[1,2-a]pyridin-2-yl)ethyl)isoindoline-1,3-dioneHCID 153126996.6%
생성물2-(4-Bromo-3-oxobutyl)-1H-isoindole-1,3(2H)-dioneHCID 3759744—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07241772B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-f7efda1210db48a0993d6c3ee16e7592
출처 메모uspto-grants-2007_07