“…The dihydrochloride 4·2HCl was treated with a 10% solution of NaOH to give the 4-(1-adamantyl)-1,2-diaminobenzene 4 as white crystals with mp 135-137ºC, unstable in air. 1-(4-Acetamido-3-aminophenyl)adamantane (5). A solution of nitroamide 2 (2.62 g, 8 mmol) in absolute ethanol (80 ml) was hydrogenated using molecular hydrogen at 21ºC for 6 h (736 mm Hg) in the presence of Raney nickel.…”
“…We have previously reported [4,5] the synthesis and reactions of 5(6)-(1-adamantyl)benzimidazoles. The synthesized benzimidazoles were assayed for their biocide, antihelmintic, antitumor, and anti HIV activity [6,7] revealing compounds with identified activity.…”
4-(1-Adamantyl)-1,2-diaminobenzene, previously unreported in the literature, has been prepared and a novel series of 5(6)-(1-adamantyl)benzimidazole derivatives synthesized. Nitration, hydrogenation, and side chain reactions have been carried out.
“…The dihydrochloride 4·2HCl was treated with a 10% solution of NaOH to give the 4-(1-adamantyl)-1,2-diaminobenzene 4 as white crystals with mp 135-137ºC, unstable in air. 1-(4-Acetamido-3-aminophenyl)adamantane (5). A solution of nitroamide 2 (2.62 g, 8 mmol) in absolute ethanol (80 ml) was hydrogenated using molecular hydrogen at 21ºC for 6 h (736 mm Hg) in the presence of Raney nickel.…”
“…We have previously reported [4,5] the synthesis and reactions of 5(6)-(1-adamantyl)benzimidazoles. The synthesized benzimidazoles were assayed for their biocide, antihelmintic, antitumor, and anti HIV activity [6,7] revealing compounds with identified activity.…”
4-(1-Adamantyl)-1,2-diaminobenzene, previously unreported in the literature, has been prepared and a novel series of 5(6)-(1-adamantyl)benzimidazole derivatives synthesized. Nitration, hydrogenation, and side chain reactions have been carried out.
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