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Synthesis and Biological Activity of 4,5,6,7-Tetrahydro-2H-indazole Derivatives

机译:4,5,6,7-四氢-2H-吲唑衍生物的合成和生物活性

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摘要

Novel 4,5,6,7-tetrahydro-2H-indazole derivatives were obtained via the reaction of N-1,N-3,2-triaryl-6-hydroxy-6-methyl-4-oxocyclohexane-1,3-dicarboxamides with hydrazine hydrate. The reaction of 4-oxocyclo-hexane-1,3-dicarboxamides with phenylhydrazine led to the formation of hydrazones instead of indazoles. The synthesized compounds were tested for antimicrobial, analgesic and anti-inflammatory activities
机译:通过N-1,N-3,2-三芳基-6-羟基-6-甲基-4-氧己烷-1,3-二氨基甲酰胺的反应获得新的4,5,6,7-四氢-2H-吲唑衍生物 用肼水合物。 4-氧中环-1,3-二羧酸与苯肼的反应导致含有腙代替吲唑的形成。 测试合成的化合物,用于抗微生物,镇痛和抗炎活性

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