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M739
Received: 23 August 2011; in revised form: 24 September 2011 / Accepted: 8 October 2011 / Published: 13 October 2011
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| Download PDF Full-text (83 KB) | Abstract: 4-Amino-N -(2-hydroxy-4-pentadecylbenzylidene)benzenesulfonamide has been synthesized by reaction of 2-hydroxy-4-pentadecylbenzaldehyde with 4-aminobenzenesulfonamide in the presence of acetic acid in ethanol. The structure of this new compound was confirmed by elemental analysis, IR, 1 H-NMR, 13 C-NMR and mass spectral analysis.
M740
Received: 7 September 2011 / Accepted: 30 September 2011 / Published: 14 October 2011
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| Download PDF Full-text (175 KB) | Abstract: The title compound, N-(4-methylsulfonamido-3-phenoxyphenyl)-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboximide was synthesized in high yield by reaction of N-(4-amino-2-phenoxyphenyl)methanesulfonamide and 9,10-dihydroanthracene-9,10-endo-α,β-succinic anhydride in glacial acetic acid. The structure of the compound was fully characterized by IR, 1H and 13C NMR, mass spectral analysis and elemental analysis.
M741
Received: 16 August 2011 / Accepted: 23 September 2011 / Published: 18 October 2011
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| Download PDF Full-text (191 KB) | Abstract: The title compound, 2-(6-methoxynaphthalen-2-yl)propionic acid (1,3-dimethylbutylidene)hydrazide was synthesized in high yield by the reaction of 2-(6-methoxynaphthalen-2-yl)propionic acid hydrazide and 4-methylpentan-2-one in PEG 400. This compound was fully characterized by IR, 1 H NMR, mass spectra and elemental analysis. The in vitro antibacterial activity of this compound was evaluated against gram positive and gram negative bacteria.
M742
Received: 3 August 2011 / Accepted: 8 November 2011 / Published: 10 November 2011
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| Download PDF Full-text (174 KB) | Abstract: A simple solvent-free synthesis of 3-[1-(4-methylphenyl)-3-oxo-1,3,4,5,6,7-hexahydro-2H -isoindol-2-yl]propanoic acid 3 was achieved by fusion of cis -2-[(4-methylphenyl)carbonyl]cyclohexanecarboxylic acid 1 with 3-aminopropanoic acid 2 . The structure of this new compound was confirmed by elemental analysis, IR, EI-MS, 1 H-NMR and 13 C-NMR spectral data.
M743
Received: 16 August 2011 / Accepted: 13 October 2011 / Published: 10 November 2011
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| Download PDF Full-text (186 KB) | Abstract: Novel ethyl (1,3-diphenyl-1H -pyrazolo[4,3-e ][1,2,4]triazolo[1,5-c ]pyrimidin-5-yl)acetate (5 ), was prepared via heating of 5-amino-1,3-diphenyl-4,5-dihydro-4-imino-1H -pyrazolo[3,4-d ] pyrimidine (1 ) and diethyl malonate (2 ) under reflux. The structure of the synthesized compound was assigned on the basis of its elemental analysis, IR, 1 H-NMR and mass spectral data.
M744
Received: 23 September 2011 / Accepted: 11 November 2011 / Published: 16 November 2011
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| Download PDF Full-text (161 KB) | Abstract: 1-(8-Chloro-3-methyl-1H -pyrazolo[4,3-c ]cinnolin-1-yl)-2-(2-chlorophenyl)ethanone 2 has been synthesized through condensation of 3-acetyl-6-chloro-1H -cinnolin-4-one 1 with 2-(2-chlorophenyl)acetohydrazide in polar aprotic solvent containing catalytic amount of conc. HCl. The structure of the title compound 2 was established on the basis of IR, 1 H-NMR, 13 C-NMR and mass spectral data.
M745
Received: 3 August 2011 / Accepted: 18 November 2011 / Published: 23 November 2011
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| Download PDF Full-text (180 KB) | Abstract: A simple and novel route for the synthesis of new terphenyl derivative as well as oxidative aromatization of α,β-unsaturated cyclohexenone to the corresponding phenol derivative is developed. The present work involves the condensation of ethylacetoacetate with 4,4'-difluoro chalcone followed by the aromatization using chloramine-T in acetic acid to yield the title compound (3 ). The synthesized compound (3 ) is well characterized by IR, NMR, LCMS and elemental analysis.
M746
Received: 30 November 2011 / Accepted: 13 December 2011 / Published: 20 December 2011
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| Download PDF Full-text (120 KB) | Abstract: Novel (E )-ethyl 3-(dimethylamino)-2-(7,9-diphenyl-7H -pyrazolo[4,3-e ][1,2,4]triazolo[1,5-c ]pyrimidin-2-yl)acrylate (3A ), was prepared via condensation of ethyl (1,3-diphenyl-1H -pyrazolo[4,3-e ][1,2,4]triazolo[1,5-c ]pyrimidin-5-yl)acetate (1 ) and dimethylformamide-dimethylacetal under reflux. The structure of the synthesized compound was assigned on the basis of elemental analysis, IR, 1 H NMR and mass spectral data.
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