positional isomers

One-pot synthesis and structure of isomeric aryl-substituted triazolohexahydroquinazolines

Aryl-substituted triazolohexahydroquinazolines have been synthesized by means of three-component condensation of pnitro(pbromo) benzaldehydes, cyclohexanone, 1,2,4-triazol-3-amine. A scheme of the reaction mechanism is proposed, which makes it possible to explain the features of the behavior of p-nitro(bromo) benzaldehydes in condensation reactions in comparison with their ortho-substituted analogs.

Synthesis and Ways of Formation of Hydroxyphenyl Substituted Triazolohexahydroquinazolines

With three-component condensation of 1,2,4-triazol-3-amine, hydroxy-substituted aromatic aldehyde (2-hydroxybenzaldehyde, 4-hydroxybenzaldehyde, 4-hydroxy-3-methoxybenzaldehyde, 2-naphthalene-carbaldehyde), cyclohexanone, the aldehyde component has a defining impact on the shaping of triazologic hydroquinazolines with different types of rings articulation and the position of the double bond in them (C4a–C5 and C4a–C8a). When salicylic aldehyde is used, the positional isomers of the triazologic hexahydroquinazolines of angular and linear structure are formed in an equimolar ratio.

Synthesis and Ways of Formation of Hydroxyphenyl Substituted Benz[4,5]imidazole-1,2,3,4,5,6- hexahydro[1,2-a]quinazolines

To synthesize new potentially biologically active benzimidazoloquinazolines, a three-component condensation of 2-aminobenzimidazole, cyclohexanone and hydroxylatedbenzaldehydes was studied. The reaction proceeds regioselectively when the equimolar ratios of the reagents are boiled for 3 hours in N,N-dimethylformamide and is accompanied by the formation of ortho-phenyl substituted hexahydrobenz[4,5]imidazolo [1,2-a]quinazolines having an angular articulation of the rings and a different number and position of hydroxyl groups in the phenyl substituent.

Synthesis of Opto-R-Phenyl Benzimidazoloheksahydroquinazoline with Angular Articulation Rings

Condensation of 2-aminobenzimidazole, ortho-substituted benzaldehydes and cyclohexanone proceeds with the formation of 10-o-Rsubstituted phenyl benz[4,5]imidazolo-6,7,8,9,10,11-hexahydro[1,2-a] quinazolines having angular articulation rings, strukture which is set using IR, NMR, 1 H, 13C spectra.

Reaggregation Positional Isomers Tetrazologeksahidroquinazoline

9-phenyl-4,5,6,7,8,9-geksagidrotetrazolo[5,1-b]quinazoline in solution undergoes reaggregation ent via an azide to form a positional isomer corner structure that is installed involving spectral methods (1H-NMR, IR -spectra), TLC, chromato-mass spectrometry.