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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357103생성일: 2026년 10월 25일

Piperidine → 5-[3-(3-Pyridyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione

https://huagongshe.com/reaction/357103

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물PyripropanolHCID 72922—
반응물3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 18936694—
용매EthanolHCID 702—
생성물5-[3-(3-Pyridyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 57150425—

반응 단계

To a solution of 1.61 g (5.0 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione and 676 mg (5.0 mmol) of 3-(2-pyridyl)-1-propanol in 20 ml of ethanol, 43 mg (0.5 mmol) of piperidine-was added, followed by refluxing for 4 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in dichloromethane, washed with purified water and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, chloroform/methanol=50/1) to yield 1.56 g (71.1%, 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-26978d1697f54bfe9c6e14b8ac1da42c
출처 메모uspto-grants-1998_11