340812-23-9Relevant academic research and scientific papers
One-step synthesis of substituted 3,5-dicyanospiro-4-(piperidine-4′)- 1H,4H-dihydropyridine-2-thiolates and 2,6-diamino-3,5-dicyanospiro-4- [(piperidine-4′) or (2′-oxoindole-3′)]-4H-thiopyrans
Shestopalov, Anatoliy M.,Shestopalov, Alexander A.,Rodinovskaya, Lyudmila A.,Gromova, Anna V.
experimental part, p. 1100 - 1114 (2010/02/28)
A new, one-step method for the synthesis of substituted 3,5-dicyanospiro-4(piperidine-4′)-1H,4H-dihydropyridine-3-thiolates and 2,6-diamino-3,5-dicyanospiro-4-[(piperidine-4′) or (2′ -oxoindole-3′)]-4H-thiopyrans using a multicomponent reaction of N-substituted piperidine-4-ones and isatins with derivatives of cyanoacetic acid is described. The regioselectivity of this reaction can be controlled by varying the substituents at the nitrogen atom of the piperidine-4-ones. The multicomponent reaction of N-alkylpiperidine-4-ones with malononitrile and cyanothioacetamide gives spiro-4-(1′ -alkylpiperidine-4′)-1H,4H- dihydropyridine-2-thiolates, whereas a similar reaction of N-(acyl) alkoxycarbonylpiperidine-4-ones leads exclusively to spiro-4-(1′ -(acyl)alkoxycarbonylpiperidine-4′)-4H-thiopyrans. Taylor & Francis Group, LLC.
