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Relevant bibliographies by topics / 4-amino-N-(5-methyl-1; 2-oxazol-3-yl)-benzenesulfonamide

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Journal articles

Academic literature on the topic '4-amino-N-(5-methyl-1; 2-oxazol-3-yl)-benzenesulfonamide'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "4-amino-N-(5-methyl-1; 2-oxazol-3-yl)-benzenesulfonamide"

1

Valarmathy, Govindaraj, Ramanathan Subbalakshmi, Rajendran Nithya, Ragu Nandhini, Balachandaran Sabarika, and Elanchleiyan Aarthy. "Synthesis, Spectral Characterisation and Cytotoxic Evaluation of Substituted Sulfonamide Schiff Bases." Indian Journal of Science and Technology 14, no. 34 (2021): 2731–41. https://doi.org/10.17485/IJST/v14i34.888.

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Abstract <strong>Objectives:</strong> To synthesize Schiff bases i.e 4-((2-hydroxybenzylidene)-amino–N-(5-methyl-1,2-oxozol-3- yl)benzene sulphonamide (L1), 4-((2-hydroxy benzylidene)-amino-N-(thiazol-yl)benzene sulphonamide (L2), 4-((2-hydroxybenzylidene)amino-N-(pyridin-2-yl)benzene sulphonamide by theaction of 2-hydroxybenzaldehyde with sulfathiazole/ sulfamethoxazole/ sulfapyridine in ethanolic media. <strong>Methods:</strong> The Schiff bases obtained were characterized by analytical data, IR, UV, 1H- NMR, 13C-NMR, Mass spectrum and monitored for cytotoxic activity ag

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2

Tahir, M. Nawaz, Abdul Haleem Khan, Mohammad S. Iqbal, Christy Munir, and Tariq Aziz. "4-{[(E)-2,3-Dihydroxybenzylidene]amino}-N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2125. http://dx.doi.org/10.1107/s1600536812026657.

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3

Gupta, Apoorva, and Anand K. Halve. "Synthesis & Antifungal Screening of Novel Azetidin-2-ones." Open Chemistry Journal 2, no. 1 (2015): 1–6. http://dx.doi.org/10.2174/1874842201502010001.

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A new series of 4-[3-chloro-2-(4-hydroxy-3-methoxybenzyllidene)-4-oxoazetidin-1-yl]amino-N-(substituted)benzenesulfonamide, 4-{3-chloro-2-[5-methoxy-2-nitro-4-(prop-2-en-1-yloxy)benz yllidene]-4-oxoazetidin-1-yl}]amino}-N-(substituted)benzenesulfonamide and 4-{3-chloro-2-[4-hydroxy-3-methoxy-5-(prop-2-en-1-yl)benzylidene]-4-oxoazetidin-1-yl}amino}-N-(substituted) benzenesulfonamide were synthesized using appropriate synthetic route. The chemical structures of all the synthesized compounds were deduced on the basis of elemental analysis and spectroscopic data. The antifungal activity of the syn

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4

Hülya, Akgün, Kaya Betül, Mulazim Yusuf, et al. "Synthesis and Biological Activity Studies of Substituted N-(1,3-Dioxohexahydro-2H-Isoindol-2-yl) Benzenesulfonamide Derivatives." Pharmaceutical and Chemical Journal 6, no. 2 (2019): 91–102. https://doi.org/10.5281/zenodo.13936063.

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In this study, ten substituted <em>N </em>- ([1,3-dioxoindolin-2-yl] phenyl] sulfonyl) structures (compound <strong>1-10</strong>), which seven of them were original synthesized using conventional and microwave synthesis methods.  In the first method the cis-1,2-cyclohexanecarboxylic anhydride and sulfa derivatives reacted under  reflux for 2-3 hours in acetic acid. In the second method the cis-1,2-cyclohexanecarboxylic anhydride and sulfa derivatives were dissolved in DMF and radiated by microwave. Structure elucidation of the synthesized compounds were confirmed by UV, IR <sup>1</s

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5

Özbey, Süheyla, Arzu Akbaş, Gülgün Ayhan-Kilcigil, and Rahmiye Ertan. "Antibacterial 4-amino-N-(5-methylisoxazol-3-yl)-N-[(4-oxo-2-phenyl-4H-1-benzopyran-6-yl)methyl]benzenesulfonamide." Acta Crystallographica Section C Crystal Structure Communications 61, no. 9 (2005): o559—o561. http://dx.doi.org/10.1107/s0108270105023759.

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6

Asiri, Abdullah M., Hassan M. Faidallah, Khalid A. Alamry, Seik Weng Ng, and Edward R. T. Tiekink. "4-[5-(Furan-2-yl)-3-trifluoromethyl-1H-pyrazol-1-yl]benzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o1168—o1169. http://dx.doi.org/10.1107/s1600536812011920.

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In the title compound, C14H10F3N3O3S, there are significant twists in the molecule, as seen in the values of the dihedral angles between the pyrazole ring and each of the furan [31.1 (2)°] and benzene rings [55.58 (10)°]. The amino N atom occupies a position almost normal to the benzene ring [N—S—Car—Car(ar = aromatic) torsion angle = 83.70 (19)°]. One amino H atom forms a hydrogen bond to the tricoordinate pyrazole N atom and the other interacts with a sulfonamide O atom, forming a supramolecular chain along [010]. The chains are consolidated into a supramolecular layersviaC—H...O interaction

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7

Tailor, Sanjay M., and Urmila H. Patel. "Hirshfeld surface analysis of sulfameter (polymorph III), sulfameter dioxane monosolvate and sulfameter tetrahydrofuran monosolvate, all at 296 K." Acta Crystallographica Section C Structural Chemistry 71, no. 11 (2015): 944–53. http://dx.doi.org/10.1107/s2053229615017520.

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The ability of the antibacterial agent sulfameter (SMT) to form solvates is investigated. The X-ray crystal structures of sulfameter solvates have been determined to be conformational polymorphs. Both 1,4-dioxane and tetrahydrofuran form solvates with sulfameter in a 1:1 molar ratio. 4-Amino-N-(5-methoxypyrimidin-2-yl)benzenesulfonamide (polymorph III), C11H12N4O3S, (1), has two molecules of sulfameter in the asymmetric unit cell. 4-Amino-N-(5-methoxypyrimidin-2-yl)benzenesulfonamide 1,4-dioxane monosolvate, C11H12N4O3S·C4H8O2, (2), and 4-amino-N-(5-methoxypyrimidin-2-yl)benzenesulfonamide tet

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8

Anderson, Randy L. "Broadleaf Weed Control in Safflower (Carthamus tinctorius) with Sulfonylurea Herbicides." Weed Technology 1, no. 3 (1987): 242–46. http://dx.doi.org/10.1017/s0890037x00029614.

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Safflower (Carthamus tinctorius L. ‘Hartman’) in the rosette growth stage or early bolting stage tolerated thiameturon {3-[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl] amino] sulfonyl]-2-thiophenecarboxylic acid} at 5, 10, and 15 g ai/ha. Safflower also tolerated chlorsulfuron {2-chloro-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl] benzenesulfonamide} at 18 g/ha if safflower was taller than 15 cm at time of application. The fresh weight of above-ground biomass of common sunflower (Helianthus annuus L. #3 HELAN), treated at two plant sizes with thiameturon, was reduc

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9

Al-Khatib, Kassim, Robert Parker, and E. Patrick Fuerst. "Rose (Rosa dilecta) Response to Simulated Herbicide Drift." HortTechnology 2, no. 3 (1992): 394–98. http://dx.doi.org/10.21273/horttech.2.3.394.

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This study evaluated the response of rose to different herbicides applied as simulated drift. Chlorsulfuron {2-chloro-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]benzenesulfonamide}, thifensulfuron {3[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]amino]sulfonyl]-2-thiophenecarboxylic acid}, bromoxynil(3,5-dibromo-4-hydroxybenzonitrile), 2,4-D[(2,4-dichlorophenoxy)acetic acid], glyphosate [N-(phosphonomethyl) glycine], and a combination of 2,4-D and glyphosate were applied over the top of established rose plants at 1/3, 1/10,1/33, and 1/100 of the maximum labeled rate f

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10

Vaghasiya, Yogesh, Rathish Nair, Mayur Soni, Shipra Baluja, and Sumitra Shanda. "Synthesis, structural determination and antibacterial activity of compounds derived from vanillin and 4-aminoantipyrine." Journal of the Serbian Chemical Society 69, no. 12 (2004): 991–98. http://dx.doi.org/10.2298/jsc0412991v.

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Schiff bases derived from 4-aminoantipyrine and vanillin were evaluated for their potential as antibacterial agents against some Gram positive and Gram negative bacterial strains. The antibacterial activity was studied against P. pseudoalcaligenes ATCC 17440, P. vulgaris NCTC 8313, C. freundii ATCC 10787 E. aerogenes ATCC 13048, S. subfava NCIM 2178 and B. megaterium ATCC 9885. The determination of the antibacterial activity was done using the Agar Ditsh method. The Schiff bases produced were: (1) 4-(4-hydroxy 3-methoxybenzylideneamino) -1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one [VV1]; (

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