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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 51, 2021 - Issue 13
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Articles

Bis(sulfanediyl)bis(6-aminopyrimidin-4-ones): Versatile precursors for novel bis(sulfanediyl)bis(tetrahydropyrimido[4,5-b]quinoline-4,6-diones) linked to aliphatic spacer via multi-component reactions

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Pages 2001-2015 | Received 04 Feb 2021, Published online: 12 May 2021
 

Abstract

A synthesis of novel bis(sulfanediyl)bis(tetrahydropyrimido[4,5-b]quinoline-4,6-diones), linked to aryl, heteroaryl, and spirocyclic-oxindole moieties at position-5, as novel hybrid molecules was reported. 2,2'-(Butane-1,4-diylbis(sulfanediyl))bis(6-aminopyrimidin-4(1H)-one) was utilized as a precursor to our target compounds via a multicomponent reaction with two equivalents of both of the appropriate aldehyde and dimedone. The target compounds were alternatively obtained by bis-(alkylation) of the appropriate 5-aryl-2-thioxohexahydropyrimido[4,5-b]quinoline-4,6-dione with 1,4-dibromobutane in moderate basic medium.

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