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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 517612Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/517612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktPiperidineHCID 8082—
Edukt3-(2-Aminoethyl)-5-(4-ethoxybenzyl)thiazolidine-2,4-dioneHCID 71697071—
Edukt3-(2-(Tritylamino)ethyl)thiazolidine-2,4-dioneHCID 71697168—
LösungsmittelEthanolHCID 702—
Produkt3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dioneHCID 155124448,1%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09115122B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-1c0a01a673f2498fba074e97cbe46588
Quellennotizuspto-grants-2015_08