Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

Search Results (4)

Search Parameters:
Keywords = 2-methylbenzothiazole

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
15 pages, 4284 KiB  
Article
Complexes of 2-Amino-3-methylpyridine and 2-Amino-4-methylbenzothiazole with Ag(I) and Cu(II): Structure and Biological Applications
by Muhammad Hanif, Awal Noor, Mian Muhammad, Farhat Ullah, Muhammad Nawaz Tahir, Gul Shahzada Khan and Ezzat Khan
Inorganics 2023, 11(4), 152; https://doi.org/10.3390/inorganics11040152 - 1 Apr 2023
Cited by 8 | Viewed by 3294
Abstract
Coordination complexes (14) of 2-amino-4-methylbenzothiazole and 2-amino-3-methylpyridine with Cu(CH3COO)2 and AgNO3 were prepared and characterized by UV/Vis and FT-IR spectroscopy. The molecular structure for single crystals of silver complexes (2 and 4) were [...] Read more.
Coordination complexes (14) of 2-amino-4-methylbenzothiazole and 2-amino-3-methylpyridine with Cu(CH3COO)2 and AgNO3 were prepared and characterized by UV/Vis and FT-IR spectroscopy. The molecular structure for single crystals of silver complexes (2 and 4) were determined by X-ray diffraction. The coordination complex (2) is monoclinic with space group P21/c, wherein two ligands are coordinated to a metal ion, affording distorted trigonal geometry around the central Ag metal ion. The efficient nucleophilic center, i.e., the endocyclic nitrogen of the organic ligand, binds to the silver metal. Ligands are coordinated to adopt cis arrangement, predominantly due to steric reasons. The O(2) and O(3) atoms of the NO3 group further play an important role in such type of ligand arrangement by hydrogen bonding with the NH2 group of ligands. Complex (4) is orthorhombic, P212121, comprising two molecules of 2-amino-3-methylpyridine as ligand coordinated with the metal ion, affording a polymeric structure. The coordination behavior of the ligand is identical to that in complex 2, wherein ring nitrogen is coordinated to the metal center and bridged to another metal ion through an NH2 group. The resulting product is polymeric in nature with the Ag metal in the backbone and ligand as the bridge. Compounds (24) were found to be luminescent, while 1 did not show such activity. All compounds were screened for their preliminary biological activities such as antibacterial, antioxidant and enzyme inhibition. Compounds exhibited moderate activity in these tests. Full article
(This article belongs to the Special Issue 10th Anniversary of Inorganics: Coordination Chemistry)
Show Figures

Figure 1

3 pages, 334 KiB  
Short Note
3-(2-Hydroxyethyl)-2-methylbenzothiazolium Bromide
by Stela Minkovska, Nikolay Gadjev, Nikola Burdzhiev, Alexi Alexiev and Todor Deligeorgiev
Molbank 2016, 2016(4), M920; https://doi.org/10.3390/M920 - 9 Dec 2016
Viewed by 3627
Abstract
A novel method for the preparation of 3-(2-hydroxyethyl)-2-methylbenzothiazolium bromide was developed. It consists of heating of 2-methylbenzothiazole, 2-bromoethanol and ethoxyethanol for 2 h. On the next day the precipitate was filtered and air dried. Full article
(This article belongs to the Section Organic Synthesis and Biosynthesis)
Show Figures

Scheme 1

13 pages, 300 KiB  
Article
New 4-Thiazolidinones of Nicotinic Acid with 2-Amino-6-methylbenzothiazole and their Biological Activity
by Navin B. PATEL and Faiyazalam M. SHAIKH
Sci. Pharm. 2010, 78(4), 753-766; https://doi.org/10.3797/scipharm.1009-15 - 24 Oct 2010
Cited by 46 | Viewed by 2122
Abstract
The title compounds 6a–j, 2-[(6-methyl-1,3-benzothiazol-2-yl)amino]-N- [2-(substituted phenyl/furan-2-yl)-4-oxo-1,3-thiazolidin-3-yl]nicotinamides, were prepared from 2-chloropyridine-3-carboxylic acid (1) and 2-amino-6-methylbenzothiazole (2) by known methods. All the compounds have been established by IR, 1H NMR, 13C NMR and elemental analyses. [...] Read more.
The title compounds 6a–j, 2-[(6-methyl-1,3-benzothiazol-2-yl)amino]-N- [2-(substituted phenyl/furan-2-yl)-4-oxo-1,3-thiazolidin-3-yl]nicotinamides, were prepared from 2-chloropyridine-3-carboxylic acid (1) and 2-amino-6-methylbenzothiazole (2) by known methods. All the compounds have been established by IR, 1H NMR, 13C NMR and elemental analyses. The in vitro antimicrobial screening of the compounds were carried out against two Gram positive (S. aureus, S. pyogenes), two Gram negative (E. coli, P. aeruginosa) bacteria and three fungal species (C. albicans, A. niger, A. clavatus) using the broth microdilution method. Some of the compounds are comparable with standard drugs. Full article
7 pages, 192 KiB  
Article
New Conjugated Benzothiazole-N-oxides: Synthesis and Biological Activity
by Peter Gajdoš, Peter Magdolen, Pavol Zahradník and Pavlína Foltínová
Molecules 2009, 14(12), 5382-5388; https://doi.org/10.3390/molecules14125382 - 23 Dec 2009
Cited by 15 | Viewed by 9977
Abstract
Eleven new 2-styrylbenzothiazole-N-oxides have been prepared by aldol – type condensation reactions between 2-methylbenzothiazole–N-oxide and para-substituted benzaldehydes. Compounds with cyclic amino substituents showed typical push-pull molecule properties. Four compounds were tested against various bacterial strains as well as [...] Read more.
Eleven new 2-styrylbenzothiazole-N-oxides have been prepared by aldol – type condensation reactions between 2-methylbenzothiazole–N-oxide and para-substituted benzaldehydes. Compounds with cyclic amino substituents showed typical push-pull molecule properties. Four compounds were tested against various bacterial strains as well as the protozoan Euglena gracilis as model microorganisms. Unlike previously prepared analogous benzothiazolium salts, only weak activity was recorded. Full article
Show Figures

Figure 1

Back to TopTop