10.22376/ijpbs.2019.10.1.p1-12 Volume 4 Issue 1 2013 (January - March) A series of N', N''-[1-(1H-benzimidazole-2-yl)-2-(4-substituted phenyl ethane-1, 2-diyl)] substituted aromatic amines (AK lessThan sub greaterThan 1 lessThan /sub greaterThan - AK lessThan sub greaterThan 6 lessThan /sub greaterThan ) and hydrazides (AKH lessThan sub greaterThan 6 lessThan /sub greaterThan – AKH lessThan sub greaterThan 11 lessThan /sub greaterThan ) were synthesized by treating 2-methyl benzimidazole with different substituted aromatic aldehydes in the presence of ethanol to produce 2-[2-(4 chlorophenyl)-vinyl]-1H-benzimidazole. It was brominated to 2-[1, 2 dibromo 2-(4-substituted phenyl) ethyl]-1H-benzimidazole, which on treatment with different substituted amines and hydrazides in absolute alcohol brings forth the newer compounds. The structures attributed to the newly synthesized compounds were elucidated using IR, NMR, MASS techniques besides elemental analysis. The compounds were evaluated for their anti-inflammatory potentials by carrageenan induced paw edema bio-assay in rats. Many of the target compounds showed good anti-inflammatory activity. A most distinctive derivative, 1-[1-H-benzimidazol-2-yl]-N, N',2-tris (4-chlorophenyl)-ethane-1,2-diamine (AK lessThan sub greaterThan 5 lessThan /sub greaterThan ) was identified in the present study, due to its remarkable anti-inflammatory potentials and was found to be equipotent with that of Indomethacin, observed after the introduction of p-chloro anilino group with 2- methyl benzimidazole moiety. The acute toxicity study of the compounds indicated that they were well tolerated. Therefore, such a compound would represent a fruitful matrix for the development of anti-inflammatory candidates. KUNNAMBATH KRISHNAKUMAR A,ANILCHANDRA RAMAKANT BHATB AND KUPPUSWAMY UMAAC Methyl amino, hydrazino benzimidazoles, anti-inflammatory potentials, 53-62