1,2,3,4-TETRAHYDROPYRIMIDO[1,2-a]BENZIMIDAZOL-2- AND -4-ONES
Abstract
We have studied the reaction of 2-aminobenzimidazole with esters of substituted cinnamic acids and arylidene derivatives of Meldrum's acid, and have established the direction of formation of the tetrahydrooxopyrimidine ring. We have conducted an X-ray diffraction study of 2-phenyl-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-4-one.
Authors: V. V. Lipson, V. D. Orlov, S. M. Desenko, S. V. Shishkina, O. V. Shishkin, and M. G. Shirobokova.
English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (9), pp 1039-1043
Keywords
2-aminobenzimidazole; arylidene derivatives of Meldrum's acid; partially hydrogenated pyrimido[1,2-a]benzimidazoles; esters of substituted cinnamic acids; X-ray diffraction study; ring condensation
Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv