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ChemInform Abstract: Synthesis of 5(6)-(1-Adamantyl)benzimidazoles.
β Scribed by D. S. ZURABISHVILI; M. O. LOMIDZE; SH. A. SAMSONIYA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Synthesis of 5( 6)-(1-Adamantyl)benzimidazoles.
-The synthesis of some novel 5( 6)-adamantylbenzimidazoles (III) by reaction of the o-phenylenediamine (I) with carboxylic acids or acid chlorides is presented. The benzimidazoles (III) are shown to smoothly undergo N-acylation to afford the 1-N-acyl-5-adamantylbenzimidazoles [β (V)]. N-alkylation requires more rigid reaction conditions. -(ZURABISHVILI, D. S.; LOMIDZE, M. O.;
π SIMILAR VOLUMES
Synthesis of 2-(Alkylamino)benzimidazoles. -Reaction of an alkylamine and a 1,2-phenylenediamine with thiocarbonyldiimidazole (I) forms the corresponding mixed thioureas, e.g. (IV). These undergo cyclodesulfurization to produce the title compounds. -(PERKINS,