1992
DOI: 10.1501/commub_0000000427
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Synthesis of some pyrimidine derivatives via the reduction of schiff base type intermediates

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Cited by 2 publications
(3 citation statements)
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“…The pale brown of 2-methyl-quinazolinone was prepared according to published method [20,21] by heating of 10 mmol 2-methyl-3,1-(4H)-benzoxazin-4-one and 25 mL of formamide for 3 h in oil bath and the reaction mixture was left aside at room temperature until the precipitation occurs, the solution was filtered under vacuum and the solid product was recrystallized from suitable solvent (ethanol).…”
Section: Synthesis Of 2-methyl-quinazolinonementioning
confidence: 99%
“…The pale brown of 2-methyl-quinazolinone was prepared according to published method [20,21] by heating of 10 mmol 2-methyl-3,1-(4H)-benzoxazin-4-one and 25 mL of formamide for 3 h in oil bath and the reaction mixture was left aside at room temperature until the precipitation occurs, the solution was filtered under vacuum and the solid product was recrystallized from suitable solvent (ethanol).…”
Section: Synthesis Of 2-methyl-quinazolinonementioning
confidence: 99%
“…Nien representative compounds 2, 3,7,8,10,12,14,15, and 17 were studied with respect to these properties. Initially the acute toxicity of the compounds was assayed determining their LD 50 .…”
Section: Pharmacological Screeningmentioning
confidence: 99%
“…In previous work we prepared certain substituted pyridines, pyrimidines derivatives and their pharmacological screening [1][2][3][4][5][6][7][8]. Pyrimidines and fused pyrimidines, being an integral part of DNA and RNA in it, play an essential role in several biological processes and have considerable chemical and pharmacological importance, particularly, the pyrimidine ring can be found in nucleoside antibiotics, antibacterials, cardio-vascular as well as agro chemical and veterin products [9][10][11][12][13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%