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HRID 357045생성일: 2026년 10월 24일

Butanal → 5-Butylidene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione

https://huagongshe.com/ko/reaction/357045

반응식

참여 물질

역할이름HCID투입량
반응물ButanalHCID 261—
반응물PiperidineHCID 8082—
반응물3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dioneHCID 18936736—
용매EthanolHCID 702—
생성물5-Butylidene-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dioneHCID 57017637—

반응 단계

To a solution of 3.66 g (12 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione and 1.08 ml (12 mmol) of n-butyraldehyde in 50 ml of ethanol, 0.12 ml (1.2 mmol) of piperidine was added, followed by refluxing for 16 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in chloroform, washed with saturated aqueous sodium hydrogen carbonate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, hexane/ethyl acetate=2/1→1/2) to yield 1.05 g (24.3%, light yellow oily substance) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840732
출처 데이터셋uspto-grants-1998_11
ORD IDord-5bbba87ab58646e1a013c834c8d9bd22
출처 메모uspto-grants-1998_11