Campaign achieves regio- and stereocontrol in heterocycles using C–H functionalization, suggesting novel drug discovery pathways.
Saturated heterocycles are valuable fragments in drug discovery due to their polarity, three-dimensional structure and potential for versatile binding modes, yet their controlled functionalization remains challenging. Existing methods often require pre-functionalized substrates and provide limited control over substitution patterns, restricting access to diverse exit vectors. Here, we report a campaign achieving systematic control over the position and orientation of exit vectors in heterocycles through the synthesis of a structurally diverse fragment collection using aminoquinoline-directed C–H functionalization. The study prioritizes five- and six-membered N-heterocycles, as well as rings with sulfonyl and difluoromethylene units. Aminoquinoline directing groups installed at C(2), C(3), or C(4) enable β-arylation, and are subsequently removed to reveal carboxylic acids, primary amides, primary alcohols, or nitriles. The resulting 44 fragments, now part of AbbVie’s compound collection, combine structural novelty with favourable physicochemical properties. Finally, a simple script is provided for rapid analysis of fragment properties.
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Piticari et al. (2025) studied this question.
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