Design and Synthesis Of 2-(2-{3-Chloro-4[1- (Arylamido/Imido-Alkyl)-1h-Benzimidazol-2-Yl] Phenyl} Ethyl) Isoindol-1, 3-Diones for Studying their Anti-Japanese Encephalitis Virus (Jev) Activity
Journal: International Journal of Science and Research (IJSR) (Vol.8, No. 9)Publication Date: 2019-09-05
Authors : Amar Singh; V.K. Pandey;
Page : 1840-1842
Keywords : Benzimidazole derivative; Enviroxime; Minimum Essential Medim;
Abstract
Phthalic anhydride on heating with -ethanolamine (cholamine) at 210�C furnished 2- (2-hydroxyethyl) -isoindol-1, 3-dione (1) which reacted with 2-chlorobenzoic acid in H2SO4 to give 2-chloro-4- [2- (1, 3-dioxo-1, 3-dihydro-isoindol-2-yl) ethyl] benzoic acid (2). Reaction of 2 with o-phenylenediamine in dry pyridine afforded 2-{2- [4- (lH-benzimidazol-2-yl) -3-chlorophenyl] ethyl} isoindol-l, 3-dione (3), which on condensation with amido/imidoalcanols resulted in 2- (2-{3-chloro-4- [1- (arylamidol/ imidoalkyl) -l Hbenzimidazol-2-yl] phenyl} ethyl) -isoindol-l, 3-diones (4). Compounds 4 were evaluated for their antiviral activity against Japanese Encephalitis Virus (JEV), a highly human pathogenic virus.
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