Chemistry Department, Boehringer Ingelheim (Canada) Ltd., Research and Development, 2100 Cunard Street, Laval, Québec, Canada H7S 2G5.
Org Lett. 2010 May 21;12(10):2334-7. doi: 10.1021/ol100685p.
Thermal or microwave-mediated heating of 2- or 3-haloindoles with azoles (pK(a) < 8) provides a straightforward, metal-free, and environmentally friendly access to novel 2-(azol-1-yl)indoles. Furthermore, previously unknown 2,3-bis(azolyl-1-yl)indoles can be prepared from 2,3-dihaloindoles by sequential reaction with two distinct azoles. This operationally simple acid-catalyzed process delivers novel indole derivatives in fair to excellent yields and expands the chemical diversity of substitutions that can be introduced on this medicinally important scaffold.
2-或 3-卤代吲哚与唑类化合物(pK(a) < 8)的热或微波介导加热提供了一种直接的、无金属和环保的方法,可用于合成新型 2-(唑基-1-基)吲哚。此外,通过与两种不同唑类化合物的顺序反应,可以从未知的 2,3-二卤代吲哚制备以前未知的 2,3-双(唑基-1-基)吲哚。这种操作简单的酸催化过程以良好至优异的收率提供了新型吲哚衍生物,并扩展了可在该具有重要医学意义的支架上引入的取代基的化学多样性。