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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357093생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/357093

반응식

참여 물질

역할이름HCID투입량
반응물BenzenepropanalHCID 7707—
반응물PyrrolidineHCID 31268—
반응물3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dioneHCID 18936736—
용매EthanolHCID 702—
생성물5-(3-Phenylpropylidene)-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dioneHCID 57260764—

반응 조건

온도60 °C

반응 단계

1.53 g (5 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione and 20 ml of ethanol were placed in a reaction flask, followed by stirring at 60° C. for 20 minutes, to dissolve the starting materials. After this mixture was kept standing to 50° C., an ethanol solution of 0.05 ml (0.5 mmol) of pyrrolidine was added. Next, an ethanol solution of 0.66 ml (5 mmol) of 3-phenylpropionaldehyde was added, followed by refluxing for 19 hours. Six hours later, 0.66 ml (5 mmol) of 3-phenylpropionaldehyde and 0.05 ml (0.5 mmol) of pyrrolidine were added. After the reaction mixture was cooled, the solvent was distilled off, followed by extraction with dichloromethane and water. After the organic layer was dried with sodium sulfate, the solvent was distilled off. The residue was eluted by column chromatography (eluent, hexane/ethyl acetate=1/1) to yield 26 mg (1.2%, 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-dcae2e9c56c2411b9f4c9ab2d1acd2d0
출처 메모uspto-grants-1998_11