The present invention discloses triazine compounds of Formula II and a process to synthesize these compounds. Particularly, the invention provides one pot method to synthesize triazines nucleus, wherein the method comprises amination followed by using Leuckart reaction conditions of pyrrole/indole-2-carboxylates of Formula I to obtain corresponding triazine compounds of Formula II.
本发明揭示了Formula II的三嗪化合物以及合成这些化合物的方法。特别地,本发明提供了一种一锅法合成三嗪核的方法,其中该方法包括
氨化,然后使用Formula I的
吡咯/
吲哚-2-羧酸酯的Leuckart反应条件,以获得相应的Formula II的三嗪化合物。