A simple and efficient strategy for the synthesis of novel aryloxy-functionalised 4,4′-bi-1,2,4-triazoles was successfully explored by nucleophilic aromatic substitution of tetrachloro-4,4′-bi-1,2,4-triazole by various phenols using Cs2CO3 as catalyst. The syntheses were achieved in 25–94% yields.
GarciaY., GuionneauP., BravicG., ChasseauD., HowardJ. A. K., KahnO., KsenofontovV., ReimanS., and GütlichP., Eur. J. Inorg. Chem., 2000, 2000, 1531.
2.
NforE.N., EnoE. A., Foba-TendoJ. N., IniamaG. E., DukeE. O., and OffiongO. E., J. Struct. Chem., 2012, 53, 1118.
3.
MałeckiJ.G., KruszynskiR., JaworskaM., and LodowskiP., J. Coord. Chem., 2007, 60, 741.
4.
AggarwalN., KumarR., DurejaP., and KhuranaJ. M., Eur. J. Med. Chem., 2011, 46, 4089.
5.
BrushettF.R., ThorumM. S., LioutasN. S., NaughtonM. S., TornowC., Molly JhongH.-R., GewirthA. A., and KenisP. J. A., J. Am. Chem. Soc., 2010, 132, 12185.
6.
GaoH., and ShreeveJ. M., Chem. Rev., 2011, 111, 7377.
7.
ThottempudiV., and ShreeveJ. M., J. Am. Chem. Soc., 2011, 133, 19982.
8.
YinP., ParrishD. A., and ShreeveJ. M., Angew. Chem. Int. Ed., 2014, 53, 12889.
9.
StabenS.T., and BlaquiereN., Angew. Chem. Int. Ed., 2010, 49, 325.
10.
SudheendranK., SchmidtD., FreyW., ConradJ., and BeifussU., Tetrahedron, 2014, 70, 1635.
11.
MoulinA., BibianM., BlayoA.-L., El HabnouniS., MartinezJ., and FehrentzJ.-A., Chem. Rev., 2010, 110, 1809.
12.
MaesW., VerstappenB., and DehaenW., Tetrahedron, 2006, 62, 2677.
13.
CongM., XiaY., TangJ., BorgeL., QuéléverG., IovannaJ. L., RocchiP., and PengL., New J. Chem., 2015, 39, 3889.
14.
BartlettR.K., and HumphreyI. R., J. Chem. Soc. C, 1967, 1664.
15.
GovorE.V., LysenkoA. B., RusanovE. B., ChernegaA. N., KrautscheidH., and DomasevitchK. V., Z. Anorg. Allg. Chem., 2010, 636, 209.
16.
ZhangX.-C., ChenY-H., and LiuB., Inorg. Chem. Commun., 2008, 11, 446.