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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2116665Erstellt: 25. Oktober 2026

Thioacetamide → 7-bromo-4-(2-methyl-1,3-thiazol-4-yl)-2H-chromen-2-one

https://huagongshe.com/reaction/2116665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThioacetamideHCID 2723949—
Edukt7-bromo-4-(bromoacetyl)-2H-chromen-2-oneHCID 23370239—
LösungsmittelDimethylformamideHCID 6228—
Produkt7-bromo-4-(2-methyl-1,3-thiazol-4-yl)-2H-chromen-2-oneHCID 59814837—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 7-bromo-4-(bromoacetyl)-2H-chromen-2-one (0.605 g, 1.7 mmol) in DMF was added thioacetamide (0.138 g, 1.8 mmol). The mixture was stirred 24 h at rt and at 100° C. overnight. Once cool to rt, it was partitioned between aqueous NH4Cl and EtOAc. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated and the residue swished in hexanes/Et2O to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07439260B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-c33af81955c0450cb8ae90c00e01350a
Quellennotizuspto-grants-2008_10