## Abstract A novel series of 2โalkoxy(aralkoxy)โ4__H__โ[1,2,4]triazolo[1,5โ__a__]quinazolines were synthesized employing __Nโ__cyanoimidocarbonates and 2โhydrazinobenzoic acid as building blocks. Chemical transformation of the inherent lactam moiety in the targeted 2โalkoxy(aralkoxy)[1,2,4]triazol
ChemInform Abstract: Synthesis of Novel 2-Alkoxy(aralkoxy)-4H-[1,2,4]triazolo[1,5-a]quinazolin-5-ones Starting with Dialkyl-N-cyanoimidocarbonates.
โ Scribed by Rashad Al-Salahi; Detlef Geffken
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 28 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
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Novel Synthesis of 2-Alkoxy(aralkoxy)-5-chloro[1,2,4]triazolo[1,5-a]quinazolines and Their Derivatives. -Title compounds (I) are obtained by chlorination of triazoloquinazolinones with either oxalyl chloride or phosphorus oxychloride. Replacing the chlorine atom at the 5-position with multifunctiona
## Abstract magnified image A novel series of 2,4โdisubstitutedโ1,2,4โtriazolo[1,5โ__a__]quinazolinโ5(4__H__)โones were prepared by Dimroth rearrangement of their respective isomers namely 1,4โdisubstitutedโ[1,2,4]triazolo[4,3โ__a__]โquinazolinโ5(4__H__)โones. The latter were prepared __via__ new