163071-38-3Relevant academic research and scientific papers
Reactions of 2-cyano-2-nitrosomethylbenzthiazole: One-pot synthesis of new polyfunctional pyrazine derivatives
Abd El Latif, Fawi M.,Ei Rady, Eman A.,Khalil, Mohamed A.
, p. 2497 - 2505 (2002)
2-Cyano-2-nitrosomethylbenzthiazole reacts with some active methylene and nucleophile derivatives to yield new fused and isolated polyfunctional pyrazine, -[1,2,4]triazine, -[1,4,5]benzoxadiazepin, -[1,4, 5]benzothiadiazepine, [1,4,5]benzotriazepine, -triazole and -triazolo-[3,2-c]triazine derivatives in one-pot reaction. The structures were based on IR, MS, and 1H NMR spectra and elemental data.
Synthesis of 1H-1,2,3-triazole derivatives by the cyclization of aryl azides with 2-benzothiazolylacetonone, 1,3-benzo-thiazol-2-ylacetonitrile, and (4-aryl-1,3-thiazol-2-yl)acetonitriles
Pokhodylo,Matiychuk,Obushak
experimental part, p. 483 - 488 (2010/02/28)
The cyclization of aryl azides with 2-benzothiazolylacetone, 1,3-benzothiazol-2-ylacetonitrile, and (4-aryl-1,3-thiazol-2-yl)acetonitriles in methanol in the presence of sodium methylate gives high yields of new products, 2-(5-methyl(amino)-1-aryl-1H-1,2,
THERMOLYSIS OF 4-HETEROARYL SUBSTITUTED 5-AZIDO-1H-1,2,3-TRIAZOLES : COMPETITION BETWEEN REARRANGEMENT AND DECOMPOSITION
L'abbe, Gerrit,Vercauteren, Karin,Dehaen, Wim
, p. 321 - 328 (2007/10/02)
5-Azidotriazoles bearing a thiazole or pyridine ring at the 4-position were synthesized and thermolyzed at 60 deg C.Whereas the 5-azido-4-(thiazol-2-yl)triazole 4 decomposed with extrusion of nitrogen and formation of the triazene 5 as the sole reaction p
