A new convenient synthesis of 2,4-disubstituted-1,2,4-triazolo[1,5-a] quinazolin-5(4H)-ones
✍ Scribed by Ahmad S. Shawali; Hamdi M. Hassaneen; Nabil Kh. Shurrab
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 215 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
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A novel series of 2,4‐disubstituted‐1,2,4‐triazolo[1,5‐a]quinazolin‐5(4__H__)‐ones were prepared by Dimroth rearrangement of their respective isomers namely 1,4‐disubstituted‐[1,2,4]triazolo[4,3‐a]‐quinazolin‐5(4__H__)‐ones. The latter were prepared via new synthetic strategy based on 1,5‐elecrocyclization of the respective N‐(4‐oxo‐3‐phenylquinazolin‐2‐yl)nitrilimines.
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## Abstract A novel series of 2‐alkoxy(aralkoxy)‐4__H__‐[1,2,4]triazolo[1,5‐__a__]quinazolines were synthesized employing __N‐__cyanoimidocarbonates and 2‐hydrazinobenzoic acid as building blocks. Chemical transformation of the inherent lactam moiety in the targeted 2‐alkoxy(aralkoxy)[1,2,4]triazol
## Abstract A series of 2‐[mercapto(cyano)methylene]‐1,2,3,4‐tetrahydroquinazolin‐4‐ones and 2‐amino‐4‐methylpyrazolo[1,5‐a]quinazolin‐5(4__H__)‐one were prepared from 2‐cyanomethylquinazolin‐4(3__H__)‐ones __via__ α‐bromo derivatives 4 and amide oxime 8, respectively. The new compounds have been c