“…The IR spectra were recorded in KBr disc on Perkin-Elmer-720 spectrophotometer. The 1 H NMR spectra were recorded in CDCl 3 /DMSO-d 6 on Varian A-60D spectrophotometer. The chemical shifts are recorded in d ppm down field from TMS, which are used as an internal standard.…”
Section: Methodsmentioning
confidence: 99%
“…They are used as colouration of paints, varnishes, lacquers in the field of industry 3,4 . These derivatives are used as anti-oxidant 5 for rubber , linseed oil and as disperse dyes 6 . They possess wide range of pharmacological activities as hypoglycemic 7 , antimicrobial 8,9 , anticonvulsive 10 , antiinflammatory 11 , antihistaminic 12 , anti coagulant 13 , and anti-rheumatic 14 agents etc.…”
ABSTRACT4-Arylmethylene-2,4-dihydro-2-arylthioanilido-5-methyl-3H-pyrazol-3-ones(2) were prepared by the condensation of 2,4-dihydro-2-arylthioanilido-5-methyl-3H-pyrazol -3-ones (1) with aromatic aldehydes in the presence of glacial acetic acid. The synthesized compounds (2) reacted with phenyl thiourea in presence of alcoholic KOH at reflux temperature to give 1-arylthioanilido-3-methyl-4-aryl-6-phenylimino -4,7-dihydro-1, 3-thiazino [5,4-d] pyrazoles (3). The synthesised compounds (3) have been screened for their fungicidal activities against fungi A. fumigatus and C. albicans at different concentrations.
“…The IR spectra were recorded in KBr disc on Perkin-Elmer-720 spectrophotometer. The 1 H NMR spectra were recorded in CDCl 3 /DMSO-d 6 on Varian A-60D spectrophotometer. The chemical shifts are recorded in d ppm down field from TMS, which are used as an internal standard.…”
Section: Methodsmentioning
confidence: 99%
“…They are used as colouration of paints, varnishes, lacquers in the field of industry 3,4 . These derivatives are used as anti-oxidant 5 for rubber , linseed oil and as disperse dyes 6 . They possess wide range of pharmacological activities as hypoglycemic 7 , antimicrobial 8,9 , anticonvulsive 10 , antiinflammatory 11 , antihistaminic 12 , anti coagulant 13 , and anti-rheumatic 14 agents etc.…”
ABSTRACT4-Arylmethylene-2,4-dihydro-2-arylthioanilido-5-methyl-3H-pyrazol-3-ones(2) were prepared by the condensation of 2,4-dihydro-2-arylthioanilido-5-methyl-3H-pyrazol -3-ones (1) with aromatic aldehydes in the presence of glacial acetic acid. The synthesized compounds (2) reacted with phenyl thiourea in presence of alcoholic KOH at reflux temperature to give 1-arylthioanilido-3-methyl-4-aryl-6-phenylimino -4,7-dihydro-1, 3-thiazino [5,4-d] pyrazoles (3). The synthesised compounds (3) have been screened for their fungicidal activities against fungi A. fumigatus and C. albicans at different concentrations.
“…The synthesis of 3-hydrazinyl-4,5-diphenyl-1H-pyrazolo [3,4-c]pyridazine (2) [8], and azobenzene compounds (5a-i) [9], were conducted according to known procedures (Scheme 1). Spectral data for compounds 5a-i were described in the previous parts [9][10].…”
Section: Synthesismentioning
confidence: 99%
“…Also, they are used as key starting material for the synthesis of commercial aryl/ hetarylazopyrazole dyes [4]. All these properties aroused our interest in synthesis new heterocyclic compounds including the pyrazolo [3,4-c]pyridazine moiety which is a continuation of our previous work [5][6][7][8][9].…”
“…For instance, aminosubtituted pyrazole, thiazole, thiophene compounds afforded very electronegative diazo components and, consequently, provide a pronounced benzenenoid compounds [2]. We have previously reported the synthesis of novel heterocyclic systems such as 3-substituted azo-3H-pyrazolo [3,4-c]pyridazines [3], 4-[(4-arylazo-3,5-dimethylpyrazol-1-yl)carbonyl]-3,6-diphenyl pyridazine-3(2H)-one (Part 30) [4], 3-(4-arylazo-3,5-disubstituted pyrazol-1-yl)-4,5,6-triphenylpyridazines [5] and 5amino-6-[[4-arylazo-3,5-dimethylpyrazol-1-yl]-carbonyl]-3,4diphenylthieno [2,3-c]pyridazines [6] and their application to polyester fibers as disperse dyes, which gave encouraging results.…”
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