Turkish Journal of Chemistry
Abstract
The present paper describes the reduction of 1-methyl-5-nitro-benzimidazoles ({\bf 1A, 2A}) and 1,3-dimethyl-2H-5-nitro-benzimidazol-2-one ({\bf 3}) to 5-aminobenzimidazoles ({\bf 4A, 5A}) and 1,3-dimethyl-2H-5-amino-benzimidazol-2-one ({\bf 6}) respectively with hydrazine hydrate in absolute ethanol in the presence of graphite. Compounds {\bf 5A} and {\bf 6} were converted to 2-ethyl-5-(phthaloyl-L-phenylalanyl)amino-1-methylbenzimidazole ({\bf 7}) and 1,3-dimethyl-5-(phthaloyl-L-phenylalanyl)aminobenzimidazol-2-one ({\bf 8}). Characterization of the synthesized compounds was done with the help of mass spectrometry and ^1H NMR spectroscopic studies. Optical activity of the amino acid derivatives {\bf 7} and {\bf 8} was also recorded.
DOI
-
First Page
165
Last Page
176
Recommended Citation
HASAN, M, SHAHEEN, F, YUNUS, U, & MUNIR, S (2000). Preparation of Optically Active Amino Acid Derivatives of Some Methylated 5-Amino-Azaheterocycles. Turkish Journal of Chemistry 24 (2): 165-176. https://doi.org/-
