Previous Page  4 / 16 Next Page
Information
Show Menu
Previous Page 4 / 16 Next Page
Page Background

Notes:

Page 46

Respiratory Medicine 2016

October 17-18, 2016

Volume 6, Issue 5(Suppl)

J Pulm Respir Med

ISSN: 2161-105X JPRM, an open access journal

conferenceseries

.com

October 17-18, 2016 Chicago, USA

Respiratory and Pulmonary Medicine

2

nd

International Conference on

Varsha Kashaw et al., J Pulm Respir Med 2016, 6:5(Suppl)

http://dx.doi.org/10.4172/2161-105X.C1.017

Design, synthesis and anti-tubercular potential of some new substituted 1,2,4-triazoles derived from

isonicotinic acid hydrazides

Varsha Kashaw

1, 2

, Vaibhav Rajoriya

1

, Rakesh Kumar Jain

1

and Sushil Kumar Kashaw

2

1

SVN University, India

2

Dr Harisingh Gour University, India

O

bjective of the study was to design and synthesize some new substitutes of 1,2,4-triazoles derived from isonicotinic acid

hydrazides and screen for anti-tubercular activity. A series of new substituted 1,2,4-triazoles; isonicotinic acid hydrazide

derivative (1–28) were synthesized. Potassium dithiocarbazinate (1) was obtained from the reaction of isonicotinic acid

hydrazide with carbon disulfide in basic medium (KOH) and converted into 4-amino-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-

thiol (2) by the treatment with hydrazine hydrate. The synthesis of the other compound was performed from the reaction of

(2) with seven different benzaldehyde resulted in the formation of 4-[(substituted phenyl)-methylene]-amino-5-(pyridine-4-

yl)-4H-1,2,4-triazol-3-thiol (3). The final compound synthesized from the reaction of 3 with four different acetanilide resulted

in the formation of 4-[substituted phenyl)-methylene]-amino-3- (N-substitutedcarboxamidomethylthio)-5-(pyridine-4-yl)-

4H-1,2,4-triazoles (4). The structures of the synthesized compounds (1-28) were characterized by IR, 1H NMR, 13C NMR,

mass spectroscopy and elemental method of analysis. IR data, 1HNMR spectra, 13C NMR spectra, mass spectra and elemental

analysis indicates that 28 compounds were synthesized as proposed. In conclusion, their biological activities and study for

toxicity are required.

Biography

Varsha Kashaw has completed her PhD in 2007 from Dr Harisingh Gour University, (A Central University; ‘A’ Grade by UGC-NAAC), India. Currently, she is working

at the Department of Pharmaceutical Sciences, SVN University, India as an Associate Professor. To her credit, she is handling two research projects which are

sponsored by State and Indian Government. She has published many research papers in the journals of great repute. At present she is pursuing her MBA from

Global University.

varshakashaw@gmail.com