Facile N9-Alkylation of Xanthine Derivatives and Their Use as Precursors for -Heterocyclic Carbene Complexes.

Molecules

Faculty of Mathematics and Natural Sciences, Inorganic Chemistry, Bergische University Wuppertal, 42119 Wuppertal, Germany.

Published: June 2021

The xanthine-derivatives 1,3,7-trimethylxanthine, 1,3-dimethyl-7-benzylxanthine and 1,3-dimethyl-7-(4-chlorobenzyl)xanthine are readily ethylated at N9 using the cheap alkylating agents ethyl tosylate or diethyl sulfate. The resulting xanthinium tosylate or ethyl sulfate salts can be converted into the corresponding PF and chloride salts. The reaction of these xanthinium salts with silver(I) oxide results in the formation of different silver(I) carbene-complexes. In the presence of ammonia, ammine complexes [Ag(NHC)(NH)]PF are formed, whilst with EtNH, the bis(carbene) salts [Ag(NHC)]PF were isolated. Using the xanthinium chloride salts neutral silver(I) carbenes [Ag(NHC)Cl] were prepared. These silver complexes were used in a variety of transmetallation reactions to give the corresponding gold(I), ruthenium(II) as well as rhodium(I) and rhodium(III) complexes. The compounds were characterized by various spectroscopic methods as well as X-ray diffraction.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234118PMC
http://dx.doi.org/10.3390/molecules26123705DOI Listing

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