Affiliation:
1. Department of Chemistry, Telangana University, Dichpally, Nizamabad-503322, India
Abstract
Novel triazolothione, thiadiazole, triazole and oxadiazole-tagged trifluoromethyl group containing
naphthyridine derivatives (6a-l and 7a-d) were synthesized from 2-amino-6-(thiophen-2-yl)-4-
(trifluoromethyl)nicotinonitrile (1) on treatment with acetophenone and obtained 2-phenyl-7-(thiophen-
2-yl)-5-(trifluoromethyl)-1,8-naphthyridin-4-amine (2), compound 2 on reaction with bromoethylacetate
and after that reaction with hydrazine hydrate and obtained carbohydrazide derivatives (4), compound
4 on reaction with different substituted phenyl isothiocyanates to obtain phenyl hydrazine carbothiamide
derivatives (5). Compound 5 is independently reaction with NaOH, H2SO4 and N2H4·H2O to obtain
triazolothione, thiadiazole, triazole-substituted naphthyridine derivatives (6a-l), respectively. The
carbohydrazide compounds 4 on reaction with diverse substituted aromatic acids and obtained
oxadiazole derivatives (7a-d). All the synthesized compounds (6a-l and 7a-d) were tested for anticancer
activity against four cancer cell lines such as “HeLa-cervical cancer (CCL-2) COLO 205-colon cancer
(CCL-222) HepG2-liver cancer (HB-8065) MCF7-breast cancer (HTB-22) and one normal cell line
(HEK 293)”. Compounds 6b, 6d and 6l are known to have good anticancer activity at micro molar
concentration and found to be non-toxic on normal cell line. And all the products 6a-o and 7a-d were
tested against Gram-positive, Gram-negative bacteria and fungal strains. All the compounds, compounds
6e-h showed more activity against Bacillus subtilis (MTCC-121) at < 6.8 micromolar concentration.
Compounds (which showed more activity) further screened for minimum bactericidal concentration
against B. subtilis MTCC 121 using ciprofloxacin as standard and known to show optimistic activity.
These compounds further tested for biofilm inhibition activity against B. subtilis MTCC 121 using
erythromycin as standard which confirmed the high activity.
Publisher
Asian Journal of Chemistry