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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1892539Erstellt: 25. Oktober 2026

Ethyl Acetate → N-(4-{2-[4-(2-sulfanylethyl)phenyl]ethyl}-1,3-thiazol-2-yl)acetamide

https://huagongshe.com/reaction/1892539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAcetylthioureaHCID 2723593—
EduktN-(4-{2-[4-(2-bromoethyl)phenyl]ethyl}thiazol-2-yl)acetamideHCID 86227322—
LösungsmittelEthanolHCID 702—
ProduktN-(4-{2-[4-(2-sulfanylethyl)phenyl]ethyl}-1,3-thiazol-2-yl)acetamideHCID 8665004468,7%

Reaktionsschritte

To a suspension of N-(4-{2-[4-(2-bromoethyl)phenyl]ethyl}-1,3-thiazol-2-yl)acetamide (353.3 mg, 1.000 mmol) in ethanol (4 ml) was added 1-acetyl-2-thiourea (177.4 mg, 1.501 mmol), and the mixture was heated under reflux for 7 hr. 1-Acetyl-2-thiourea (176.6 mg, 1.495 mmol) was added, and the mixture was heated under reflux for 17 hr. The mixture was cooled to room temperature, ethyl acetate (10 ml) was added, and the precipitated solid was filtered off. The filtrate was concentrated under reduced pressure, and purified twice by silica gel column chromatography (FUJI SILYSIA CHEMICAL LTD. DM-2035 21 g, ethyl acetate:hexane=2:3→1:1) to give N-(4-{2-[4-(2-sulfanylethyl)phenyl]ethyl}-1,3-thiazol-2-yl)acetamide (210.4 mg, 0.687 mmol, 68.7%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08507690B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-6b5dc05936ed4c9bab2805d7f41537d1
Quellennotizuspto-grants-2013_08