Superacid group in "Organic Synthesis" team - Université de Poitiers, CNRS UMR 7285 IC2MP; 4, avenue Michel Brunet F-86022 Poitiers Cedex, France.
Org Biomol Chem. 2013 Nov 21;11(43):7540-9. doi: 10.1039/c3ob41538d.
A series of tertiary (fluorinated) benzenesulfonamides was synthesized in superacid HF-SbF5. To circumvent the problem of the in situ iminium ion formation, proved by low temperature NMR experiments, a tandem superacid catalysed cross-coupling reaction was employed to synthesize the benzofuzed sultams analogues. These tertiary benzenesulfonamides were tested as inhibitors of human carbonic anhydrases (hCAs, EC 4.2.1.1). These compounds did not inhibit the widespread off target hCA II isoform and showed strong selectivity toward tumor-associated carbonic anhydrase isoform IX. A dramatic effect of the electronic and structural shape of the inhibitors on selectivity was demonstrated, confirming the non-zinc-bonding mode of inhibition of this class of sulfonamides. This work allowed identifying a highly selective hCA IX inhibitor lead in this series.
一系列的三氟苯磺酰胺在超强酸 HF-SbF5 中合成。为了避免原位亚胺离子形成的问题,通过低温 NMR 实验证明,采用串联超强酸催化的交叉偶联反应来合成苯并稠合磺酰胺类似物。这些三氟苯磺酰胺被用作人碳酸酐酶(hCA,EC 4.2.1.1)的抑制剂。这些化合物不抑制广泛存在的非靶标 hCA II 同工酶,并且对肿瘤相关的碳酸酐酶同工酶 IX 表现出很强的选择性。抑制剂的电子和结构形状对选择性的显著影响得到了证实,证实了这类磺酰胺的非锌结合抑制模式。这项工作允许在这个系列中确定一个高度选择性的 hCA IX 抑制剂先导化合物。