An one-pot multi component synthesis of novel 1,2,4-triazolo[1,5-a]pyrimidines

Journal of Chemical and Pharmaceutical Research

Volumn 4, Issue 5, 2012, Pages 2687-2691

  Pada, Ranjit ^a   Ram, Haresh ^a   Nandaniya, Rambhai ^a   Dodiya, Dipti ^a   Shah, Viresh ^a  

^a Kachchh University   (India)

Author keywords

Acetoacetamides; Pyrimidines; Triazole microwave assisted synthesis

Indexed keywords

ACETOACETAMIDES; FTIR; HIGH YIELD; MASS SPECTRAL DATA; MICROWAVE ASSISTED SYNTHESIS; MULTICOMPONENTS; ONE POT; PYRIMIDINES;

ALDEHYDES; NITROGEN COMPOUNDS;

AROMATIC COMPOUNDS;

1,2,4 TRIAZOLOPYRIMIDINE; ACETAMIDE DERIVATIVE; ACETOACETAMIDE; ALDEHYDE; N (2 CHLOROPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (3 BROMOPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (3 CHLOROPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (3 NITROPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (4 BROMOPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (4 CHLOROPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (4 FLUOROPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (4 HYDROXYPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (4 METHOXYPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; N (4 NITROPHENYL) 4,7 DIHYDRO 5 METHYL 7 [4 (PHENOXYMETHYL)PHENYL] [1,2,4,]TRIAZOLO[1,5 A]PYRIMIDINE 6 CARBOXAMIDE; PYRIMIDINE DERIVATIVE; TRIAZOLE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; MICROWAVE IRRADIATION; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 84863086390     PISSN: None     EISSN: 09757384     Source Type: Journal    
DOI: None     Document Type: Article

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