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Photoinduced Alkylation of Diazines with N -(Acyloxy)phthalimides in the Presence of Triethylamine

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GEORG THIEME VERLAG KG
DOI: 10.1055/a-2182-7416

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N -(acyloxy)phthalimides; diazines; radicals; electron donor-acceptor (EDA) complexes; Minisci-type alkylation

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A photochemical protocol has been developed for the alkylation of diazines (pyrimidines, pyrazines, and pyridazines) with N-(acyloxy)phthalimides. The process is facilitated by the presence of triethylamine under irradiation with 427-390 nm light, enabling rapid cross-coupling reactions to construct a wide range of alkylated diazines.
A photochemical protocol for the alkylation of diazines (pyrimidines, pyrazines, and pyridazines) with N-(acyloxy)phthalimides has been developed. The process is facilitated by the presence of triethylamine under irradiation with 427-390 nm light; this enables rapid cross-coupling reactions to construct a wide range of alkylated diazines.

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