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
- Journal of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 136 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.574
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
A novel series of 2โalkoxy(aralkoxy)โ4__H__โ[1,2,4]triazolo[1,5โa]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]triazolo[1,5โa]quinazolines was offered access to a variety of derivatives. J. Heterocyclic Chem., (2011).
๐ SIMILAR VOLUMES
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