1997
DOI: 10.1007/bf02464260
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Synthesis and psychotropic activity of 3-oxo-1,2,3,5-tetrahydropyrido[1,2-a]-benzimidazole-4-carboxylic acid arylamides

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Cited by 2 publications
(3 citation statements)
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“…The appearance of C]O stretch in the range of 1630e1600 cm À1 indicated the formation of tertiary amides (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20) by the reaction of acid chlorides with the 4-(1H-benzoimidazol-2yl)-benzenesulfonic acid. The primary amino group in compound 1 is depicted by the presence of NH asymmetric stretch at 3481.81 cm À1 .…”
Section: Chemistrymentioning
confidence: 99%
See 1 more Smart Citation
“…The appearance of C]O stretch in the range of 1630e1600 cm À1 indicated the formation of tertiary amides (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20) by the reaction of acid chlorides with the 4-(1H-benzoimidazol-2yl)-benzenesulfonic acid. The primary amino group in compound 1 is depicted by the presence of NH asymmetric stretch at 3481.81 cm À1 .…”
Section: Chemistrymentioning
confidence: 99%
“…Furthermore, the topological parameter, Balaban index (J) followed by the electronic parameter, LUMO and topological parameter, valence second order molecular connectivity index ( 2 c v ) is describing the antimicrobial activity of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20).…”
Section: Development Of Multi-target Qsar Modelmentioning
confidence: 99%
“…3 These compounds are the core of many strategic and widely used drugs that have received excellent feedback in the medical and the chemical field as efflux pumps Inhibitors A, 4 GABA-A receptors (RWJ-16979) B, 5 adrenoreceptors C, 6 RWJ-51204 D, 7 and fluorescence microscopy E. 8 Also, these compounds have biological properties such as anxiolytic agents, 5 anticonvulsive, 9 antimicrobial, 10 relaxant agents, 5 as cell proliferation inhibitors or quadruplex nucleotide stabilizers in DNA, 11 anticancer, 12 antimalarial agents, 13 and human estrogenic receptor activators (Figure 1). 14 Because the benzo [4,5]imidazo [1,2-a]pyridine scaffold show interesting biological activities, the synthesis of this group of compounds has been realised via several routes, including cycloaddition reactions, 6,9,15 condensation reactions, [16][17][18] multicomponent reactions, 10,[19][20][21][22][23] and multistep approaches. 5,[24][25][26] Also, metallic and non-metallic catalysts, [27][28][29][30] microwave irradiation, 31 and a series of transition metal catalysts have been used for the preparation of these compounds.…”
Section: Introductionmentioning
confidence: 99%