Overcoming the limitations of directed C–H functionalizations of heterocycles

A robust and synthetically useful method is reported that overcomes the complications associated with performing C–H functionalization reactions on heterocycles; a reactive PdX 2 (X = ArCONOMe) species is generated in situ , and is directed to the appropriate C–H bond by an N -methoxy amide group. Heterocycle poisoning bypassed in C–H activation Heterocycles containing nitrogen and suphur atoms are commonly found in drug candidates, presenting organic chemists with a problem, as these elements can poison any metal catalysts used for direct activation of C–H bonds to allow the introduction of new functional groups. This paper describes a robust and synthetically useful method that overcomes thisdifficulty. Jin-Quan Yu and colleagues use a simple N -methoxy amide as a directing group and an anionic ligand that promotes the in situ generation of the reactive palladium species PdX 2 . The N -methoxy amide group acts to localize PdX 2 to the target C–H bond. This method of bypassing heterocycle poisoning using a Pd(0) catalyst under aerobic conditions should be broadly applicable in synthesis and pharmaceutical manufacturing. In directed C–H activation reactions, any nitrogen or sulphur atoms present in heterocyclic substrates will coordinate strongly with metal catalysts. This coordination, which can lead to catalyst poisoning or C–H functionalization at an undesired position, limits the application of C–H activation reactions in heterocycle-based drug discovery 1 , 2 , 3 , 4 , 5 , in which regard they have attracted much interest from pharmaceutical companies 3 , 4 , 5 . Here we report a robust and synthetically useful method that overcomes the complications associated with performing C–H functionalization reactions on heterocycles. Our approach employs a simple N -methoxy amide group, which serves as both a directing group and an anionic ligand that promotes the in situ generation of the reactive PdX 2 (X = ArCONOMe) species from a Pd(0) source using air as the sole oxidant. In this way, the PdX 2 species is localized near the target C–H bond, avoiding interference from any nitrogen or sulphur atoms present in the heterocyclic substrates. This reaction overrides the conventional positional selectivity patterns observed with substrates containing strongly coordinating heteroatoms, including nitrogen, sulphur and phosphorus. Thus, this operationally simple aerobic reaction demonstrates that it is possible to bypass a fundamental limitation that has long plague