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HRID 4392作成日:2026年10月23日

Thiazolidinedione → 5-{4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene}-2,4-thiazolidinedione

https://huagongshe.com/ja/reaction/4392

反応式

関与物質

役割名称HCID仕込み量
反応物ThiazolidinedioneHCID 5437—
反応物PiperidineHCID 8082—
反応物4-[2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy]benzaldehydeHCID 10757106—
溶媒EthanolHCID 702—
生成物5-{4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene}-2,4-thiazolidinedioneHCID 5448631977.1%

反応手順

A mixture of 4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzaldehyde (5.0 g), 2,4-thiazolidinedione (3.8 g), piperidine (0.32 ml) and ethanol (100 ml) was stirred under reflux for 5 hours. After cooling, the crystals which separated out were collected by filtration to give 5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene}-2,4-thiazolidinedione (5.1 g, 76.8%). Recrystallization from chloroform-ethanol afforded colorless needles, m.p. 213°-214° C. Elemental analysis for C22H18N2O4S, Calcd.: C, 65.01; H, 4.46; N, 6.89. Found: C, 64.81; H, 4.55; N, 6.78.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725610
出典データセットuspto-grants-1988_02
ORD IDord-512f61929c254761a4426dca28886965
出典メモuspto-grants-1988_02