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C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase

[Image: see text] A practical C–H functionalization method for the methylation of heteroarenes is presented. Inspiration from Nature’s methylating agent, S-adenosylmethionine (SAM), allowed for the design and development of zinc bis(phenylsulfonylmethanesulfinate), or PSMS. The action of PSMS on a h...

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Detalles Bibliográficos
Autores principales: Gui, Jinghan, Zhou, Qianghui, Pan, Chung-Mao, Yabe, Yuki, Burns, Aaron C., Collins, Michael R., Ornelas, Martha A., Ishihara, Yoshihiro, Baran, Phil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988686/
https://www.ncbi.nlm.nih.gov/pubmed/24611732
http://dx.doi.org/10.1021/ja5007838
Descripción
Sumario:[Image: see text] A practical C–H functionalization method for the methylation of heteroarenes is presented. Inspiration from Nature’s methylating agent, S-adenosylmethionine (SAM), allowed for the design and development of zinc bis(phenylsulfonylmethanesulfinate), or PSMS. The action of PSMS on a heteroarene generates a (phenylsulfonyl)methylated intermediate that can be easily separated from unreacted starting material. This intermediate can then be desulfonylated to the methylated product or elaborated to a deuteriomethylated product, and can divergently access medicinally important motifs. This mild, operationally simple protocol that can be conducted in open air at room temperature is compatible with sensitive functional groups for the late-stage functionalization of pharmacologically relevant substrates.