124041-74-3Relevant articles and documents
Microwave-assisted synthesis of N-alkylated benzotriazole derivatives: Antimicrobial studies
Nanjunda Swamy,Basappa,Sarala,Priya,Gaonkar,Shashidhara Prasad,Rangappa
, p. 999 - 1004 (2006)
Synthesis and characterization of N-alkylated benzotriazole derivatives 2(a-g) bearing pharmaceutically important bioactive substituents and their antimicrobial studies in vitro are described. The syntheses of the compounds were achieved by N-alkylation o
Iodine-induced regioselective direct alkylation of azoles via in situ formed alkyliodide
Chen, Wenlin,Yan, Rulong,Tang, Dong,Guo, Shuaibo,Meng, Xu,Chen, Baohua
supporting information; experimental part, p. 7956 - 7959 (2012/09/21)
We have developed an efficient, metal-free, convenient and relatively cheap method for iodine-induced direct alkylation of azoles via in situ formed alkyliodide. A series of heterocyclic derivatives are readily prepared under mild conditions in moderate t
Microwave-assisted benzyne-click chemistry: preparation of 1H-benzo[d][1,2,3]triazoles
Ankati, Haribabu,Biehl, Ed
supporting information; experimental part, p. 4677 - 4682 (2009/10/26)
The benzotriazoles were prepared by three-component and two-component microwave-assisted [3+2] cycloadditions of various azides to benzyne, 3-methoxybenzyne, and 4,5-difluorobenzyne. In the three-component reaction, the aryne is generated, in the presence of an azide prepared in situ, by the reaction of an o-(trimethylsilylaryl) triflate with either CsF or KF/18-Crown-6. However, in the two-component reactions, a freshly prepared azide is added to the reaction vessel prior to aryne generation. Good to excellent yields of benzotriazoles were obtained in 15-20 min when the microwave-assisted reactions were carried out at 125 °C. These reaction times are significantly faster than similar reactions carried out using conventional heating.