Department of Chemistry, University of Sheffield, Brook Hill, Sheffield S3 7HF, U.K.
Org Lett. 2023 Feb 17;25(6):987-991. doi: 10.1021/acs.orglett.3c00074. Epub 2023 Feb 3.
Piperazines are important heterocycles in drug compounds. We report the asymmetric synthesis of arylpiperazines by photocatalytic decarboxylative arylation (metallaphotoredox catalysis) then kinetic resolution using -BuLi/(+)-sparteine. This gave a range of piperazines with very high enantioselectivities. Further functionalizations gave enantioenriched 2,2-disubstituted piperazines, and either N-substituent can be removed selectively. Late-stage functionalizations of enantioenriched piperazine derivatives were demonstrated, including synthesis of a drug compound with glycogen synthase kinase (GSK)-3β inhibitor activity with potential for treating Alzheimer's disease.
哌嗪是药物化合物中重要的杂环。我们报告了通过光催化脱羧芳基化(金属光氧化还原催化)然后使用 -BuLi/(+)-辛可宁进行动力学拆分来不对称合成芳基哌嗪。这得到了一系列具有非常高对映选择性的哌嗪。进一步的官能化得到了对映体富集的 2,2-二取代哌嗪,并且可以选择性地去除任一 N-取代基。对映体富集的哌嗪衍生物的后期官能化得到了证明,包括具有糖原合酶激酶 (GSK)-3β 抑制剂活性的药物化合物的合成,该化合物可能用于治疗阿尔茨海默病。