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American Journal of PharmTech Research

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Eco-Friendly Synthesis and Antimicrobial Activity of N-[7-(5-Substitutedimino-3-Amino)-1,2,4-Dithiazo-4-Yl]-N,N-Diethyl-Pentane-1,4-Diamine

Published in February 2014 Issue 1 (Vol. 4, Issue 1, 2014)

Eco-Friendly Synthesis and Antimicrobial Activity of N-[7-(5-Substitutedimino-3-Amino)-1,2,4-Dithiazo-4-Yl]-N,N-Diethyl-Pentane-1,4-Diamine - Issue cover

Abstract

Heteroacyclic and Heterocyclic containing drugs showed remarkable and noticeable drug absorption, transmission and drug effects; hence they created their own identity and importance in pharmaceutical, medicinal, agricultural and drug sciences. Benzonido and pyridino, dithiazolo, quinolino and alkylamino heterocycles showed important applications in industrial, pharmaceutical, medicinal and drug chemistry.  Considering all these facts into consideration recently in this laboratory interaction of N-(7-chloroquinoline-4-yl)-N,N-diethyl-pentane-1,4-diamine (1) was carried out with thiourea (2) in ethanol medium to isolate N-(7-thiocarbamidoquinoline-4-yl)-N,N-diethyl-pentane-1,4-diamines (3). N-(7-thiocarbamido quinoline-4-yl)-N,N-diethyl-pentane-1,4-diamines on further interactions with various isothiocynates (4) in acetone-ethanol medium produces N-[7-(1- substituted) -2,4-dithiobiureto)-4-yl]-N,N-diethyl-pentane-1,4-diamine (5) which were successfully  oxidatively cyclised into N-[7-(5-substitutedimino-3-amino)-1,2,4-dithiazo-4-yl]-N,N-diethyl-pentane-1,4-diamine (6) these reactions are hither to unknown. The justification and identification of the structure of these newly synthesized compounds had been established on the basis of chemical characterization, elemental analysis and through spectral data.

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Article Information

AJPTR41039

AJPTR-01-001041

2014-02-01

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How to Cite

Wanjari (2014). Eco-Friendly Synthesis and Antimicrobial Activity of N-[7-(5-Substitutedimino-3-Amino)-1,2,4-Dithiazo-4-Yl]-N,N-Diethyl-Pentane-1,4-Diamine. American Journal of PharmTech Research, 4(1), xx-xx. https://ajptr.com/articles/AJPTR41039

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