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HRID 257186作成日:2026年10月27日

Thiazolidinedione → 5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedione

https://huagongshe.com/reaction/257186

反応式

関与物質

役割名称HCID仕込み量
反応物ThiazolidinedioneHCID 5437—
反応物Piperidinium acetateHCID 3014295—
反応物4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]-benzaldehydeHCID 10038089—
溶媒TolueneHCID 1140—
生成物5-(4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedioneHCID 54227469—

反応手順

A solution of 4-[2-(N-methyl-N-(2-pyrimidinyl)amino) ethoxy]benzaldehyde (1.7 g) and 2,4-thiazolidinedione (0.7 g) in toluene (100 ml) containing a catalytic quantity of piperidinium acetate was boiled under reflux in a Dean and Stark apparatus for 2 hours. The mixture was cooled and filtered to give the title compound (mp 189°-90° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260445
出典データセットuspto-grants-1993_11
ORD IDord-bcdcd393a69142229c58293bb4bf9e26
出典メモuspto-grants-1993_11