Synthesis of novel 2-alkoxy(aralkoxy)-4H-[1,2,4]triazolo[1,5-a]quinazolin- 5-ones starting with dialkyl-N-cyanoimidocarbonates

Journal of Heterocyclic Chemistry

Volumn 48, Issue 3, 2011, Pages 656-662

  Al Salahi, Rashad ^a   Geffken, Detlef ^b  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

^b UNIVERSITY OF HAMBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1,2,4 TRIAZOLE DERIVATIVE; 2 ALLYLOXY 4,5 DIHYDRO[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; 2 ALLYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 ALLYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 THIONE; 2 BENZYLOXY 4,5 DIHYDRO[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; 2 BENZYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 BENZYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 THIONE; 2 BENZYLOXY 5 METHYLSULFANYL[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; 2 ETHOXY 4 PROP 2 YNYL 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 ETHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 ETHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 THIONE; 2 ISOPROPOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 METHOXY 4 PHENETHYL 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 METHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 METHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 THIONE; 2 PENTYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 PHENETHYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 2 PHENETHYLOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 THIONE; 4 (2,4 DICHLOROBENZYL) 2 ETHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE 5 ONE; 4 (4 BROMOBENZYL) 2 METHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 4 ALLYL 2 METHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 4 BENZYL 2 METHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 4 CYCLOPROPYLMETHYL 2 ETHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 4 ETHYL 2 METHOXY 4H [1,2,4]TRIAZOLO[1,5 A]QUINAZOLIN 5 ONE; 4,5 DIHYDRO 2 ETHOXY[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; 4,5 DIHYDRO 2 METHOXY[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; 4,5 DIHYDRO 2 PHENETHYLOXY[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; 5 ALLYLSULFANYL 2 METHOXY[1,2,4]TRIAZOLO[1,5 A]QUINAZOLINE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; BIOTRANSFORMATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGENOLYSIS; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE;

EID: 79957467954     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.574     Document Type: Article

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