戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2197673作成日:2026年10月25日

Ethylenediamine diacetate → 3-{5-[1-[5-(4-Isobutyl-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/2197673

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylenediamine diacetateHCID 10154317—
反応物3-(4-Oxo-2-thioxo-thiazolidin-3-yl)-cyclohexanecarboxylic acidHCID 59446225—
反応物HCID 59446226HCID 59446226—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
生成物3-{5-[1-[5-(4-Isobutyl-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}-cyclohexanecarboxylic acidHCID 8664429572%

反応手順

A mixture of 3-(4-oxo-2-thioxo-thiazolidin-3-yl)-cyclohexanecarboxylic acid (0.075 g, 0.29 mmol), 5-(4-isobutyl-phenyl)-furan-2-carbaldehyde (0.069 g, 0.30 mmol) and ethylenediamine diacetate (0.057 g, 0.32 mmol) in anhydrous ethanol (12 mL) was stirred 30 h at ambient temperature. The reaction mixture was diluted with ethyl acetate (250 mL) and extracted with 0.6 N aq. sodium hydrogensulfite (2×50 mL). The organic layer was separated, dried over sodium sulfate and concentrated. The residue was triturated with hot acetonitrile (5 mL) and allowed to cool to room temperature. The product was filtered off, washed on the funnel with acetonitrile (0.5 mL) and dried in a vacuum oven at 60° C. for 17 h to afford 3-{5-[1-[5-(4-isobutyl-phenyl)-furan-2-yl]-methylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}-cyclohexanecarboxylic acid (98 mg, 72%) as a solid. 1H NMR (400 MHz, DMSO-d6): δ 0.88 (6H, d, J=6.4 Hz), 1.16-1.45 (2H, m), 1.68 (1H, m), 1.84-1.92 (4H, m), 2.25-2.54 (3H, m), 4.98 (1H, m), 7.27 (1H, d, J=3.6 Hz), 7.36 (2H, m), 7.36 (1H, d, J=3.6 Hz), 7.58 (1H, s), 7.77 (2H, m), 12.22 (1H, s). LC/MS: APCI 469.51, HPLC 100%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08338465B2
出典データセットuspto-grants-2012_12
ORD IDord-578468d40da141f28f3d10ed92b038b6
出典メモuspto-grants-2012_12