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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357205생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/357205

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3-(2-Methoxyphenyl)propanalHCID 266744—
반응물3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 18936694—
용매EthanolHCID 702—
생성물5-[3-(2-Methoxyphenyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dioneHCID 56983096—

반응 단계

To a solution of 964 mg (3.0 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione and 657 mg (4.0 mmol) of 3-(2-methoxyphenyl)-1-propanal in 20 ml of ethanol, 26 mg (0.3 mmol) of piperidine was added, followed by refluxing for 3.5 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 1.40 g (quant., 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-072143bf38ba468a9b2eb4f0804a645c
출처 메모uspto-grants-1998_11