A reaction of equimolar equivalents 1-(4-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbohydrazide (1) and indoline-2,3-dione (2) in boiling ethanol for 4 h under acidic conditions gave 1-(4-methoxyphenyl)-5-methyl-N’-(2-oxoindolin-3-ylidene)-1H-1,2,3-triazole-4-carbohydrazide (3) 88% yield. The structure 3 was ascertained by NMR spectroscopy single-crystal X-ray diffraction.

The reactions of the p-tolyl radical with allene-d4 and methylacetylene-d4 as well as of the p-tolyl-d7 radical with methylacetylene-d1 and methylacetylene-d3 were carried out under single collision conditions at collision energies of 44-48 kJ mol(-1) and combined with electronic structure and statistical (RRKM) calculations. Our experimental results indicated that the reactions of p-tolyl with...

Novel derivatives of heterocyclic azo compounds have been synthesized through a free catalyst reaction. The structures the were confirmed by using different techniques such as 1H-NMR, 13C-NMR, and mass spectroscopy. prepared evaluated corrosion inhibitors for mild steel after inhibitory performance toward in 0.1 M HCl solution. derivatives, i.e. (1,1'-(((1E,1'E)-1,4-Phenylenebis(diazene-2,1-diy...

This study includes synthesis and characterization of new derivatives 3-(2-(6-oxo-1,3-thiazinan-3-yl)-R)-1,3-oxazepane-4,7-dione N-Bromo amines 1,3-oxazepane-4,7-dione derivatives. Schiff's bases reactions through one step process in inert solvents. Some employing [1- 4]; addition, synthesized by the reaction different with (Salicylaldehyde) absolute ethanol under reflux. Heterocyclic rings pre...

A one-pot three-component [2+3] cycloaddition for the synthesis of 1-alkyl 1H-naphtho[2,3-d][1,2,3]triazole-4,9-dione and 2-alkyl 2H-naphtho[2,3-d][1,2,3]triazole-4,9-dione has been developed. By taking the advantage of difference in basicity, both products can be obtained in good purity. The unique heterocyclic scaffolds of these two products could exert interesting chemical and biological pro...

(E)-5-(Methoxyimino)-1,3,4,5-tetrahydro-2H-benzo[b]azepin-2-one was prepared by a condensation reaction from 3,4-dihydro-1H-benzo[b]azepin-2,5-dione and O-methylhydroxylamine. The configuration at the C=N double bond determined X-ray crystallography.