戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 517612作成日:2026年10月26日

Benzaldehyde → 3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/517612

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物PiperidineHCID 8082—
反応物3-(2-Aminoethyl)-5-(4-ethoxybenzyl)thiazolidine-2,4-dioneHCID 71697071—
反応物3-(2-(Tritylamino)ethyl)thiazolidine-2,4-dioneHCID 71697168—
溶媒EthanolHCID 702—
生成物3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dioneHCID 155124448.1%

反応条件

温度75 °C

反応手順

Benzaldehyde (63 μL, 0.62 mmol) and compound 29 (250 mg, 0.62 mmol) were dissolved in 10 mL of anhydrous ethanol at room temperature, and piperidine (7 μL, 0.062 mmol) was added to the reaction solution. The reaction mixture was stirred at 75° C. for 1 day and then allowed to cool down to room temperature until a yellow crystalline precipitate formed, and the solid was collected by filtration, washed with water and ethyl acetate, and dried to afford a white solid. Deprotection following the procedure of compound 6 gave the title compound 30a as a white solid (48.1%, 74 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115122B2
出典データセットuspto-grants-2015_08
ORD IDord-1c0a01a673f2498fba074e97cbe46588
出典メモuspto-grants-2015_08