An Efficient CuI-Catalyzed C–S Cross-Coupling Reaction under Microwave Irradiation in DMF

Rakhi Katla; Ramesh Katla; Nelson L. C. Domingues

doi:10.1055/s-0040-1720029

Synthesis, Inhaltsverzeichnis

Synthesis 2022; 54(20): 4608-4614
DOI: 10.1055/s-0040-1720029

paper

An Efficient CuI-Catalyzed C–S Cross-Coupling Reaction under Microwave Irradiation in DMF

Rakhi Katla‡

^aOrganic Catalysis and Biocatalysis Laboratory - LACOB, Federal University of Grande Dourados-UFGD, Dourados/MS, Brazil

,

Ramesh Katla ‡

^bForeign Visiting Professor, Organic Chemistry Laboratory-4, School of Chemistry and Food, Federal University of Rio Grande-FURG, Rio Grande, RS-Brazil

,

Nelson L. C. Domingues ∗

^aOrganic Catalysis and Biocatalysis Laboratory - LACOB, Federal University of Grande Dourados-UFGD, Dourados/MS, Brazil

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Abstract

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Abstract

Microwave irradiated C–S cross-coupling reaction to synthesize 5-aryllthiobenzo-2,1,3-thiadiazole derivatives from a variety of benzene thiols with 5-bromo-2,1,3-benzothiadiazole, catalyzed by Cu(I) iodide and potassium carbonate as a cost-effective base in DMF, was conducted, affording excellent yields of the desired products. Microwave conditions assisted in the development of C–S cross-coupling reaction with higher yields.

Key words

CuI - 5-bromo-2,1,3-benzothiadiazole - thiophenols - MW irradiation - DMF

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Referenzen

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