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Hexahydroquinoline synthesis
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This study reports the design, synthesis, and calcium channel modulatory activity evaluation of a series of 14 novel fused 1,4-dihydropyridine derivatives. The molecular design of the compounds was based on modifications of nifedipine, which is a calcium channel blocker. The compounds were achieved by one-pot microwave-assisted reaction of 4,4-dimethyl-1,3-cyclohexanedione, 5-chlorosalicylaldehyde/3,5-dichlorosalicylaldehyde, an appropriate alkyl acetoacetate, and ammonium acetate in ethanol according to a modified Hantzsch reaction.
11p
langthannam
29-12-2021
8
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A simple and efficient one-pot synthesis of novel thieno[3’,2’:5,6]pyrimido[1,2-a]quinoline-2-carboxylates (5a– d) and their spirooxindole derivatives (12a–d) was accomplished. Thus, the Michael addition reaction of the cyclic β-enaminone 3 with the corresponding α, β-unsaturated nitrile derivatives 4a–d in refluxing EtOH in the presence of piperidine afforded 5a–d in good yields. On the other hand, spirooxindole derivatives 12a–d were synthesized by the reaction of cyclic β-enaminone 3 with the corresponding 3-cyanomethylidene-2-oxoindoles 11a–d in refluxing EtOH.
7p
langthannam
29-12-2021
16
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