Synthesis of pyrazolo[1,5-a]-, 1,2,4-triazolo[1,5-a]- and imidazo[1,2-a]pyrimidines related to zaleplon, a new drug for the treatment of insomnia
✍ Scribed by Carlo Mustazza; Maria Rosaria Del Giudice; Anna Borioni; Franco Gatta
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2001
- Tongue
- English
- Weight
- 119 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
This paper describes the preparation of some pyrazolo[1,5‐a]‐, 1,2,4‐triazolo[1,5‐a]‐ and imidazo[1,2‐a]‐pyrimidines substituted on the pyrimidine moiety by a 4‐[(N‐acetyl‐N‐ethyl)amino]phenyl group. A new synthesis of related benzo[h]pyrazolo[1,5‐a]‐, benzo[h]pyrazolo[5,1‐b]‐ and benzo[h]1,2,4‐triazolo[1,5‐a]‐quinazolines is also reported.
📜 SIMILAR VOLUMES
## Abstract magnified image The reaction between 3‐(dimethylamino)/3,3‐bis(methylthio)‐1‐(substituted)prop‐2‐en‐1‐ones and 4‐substituted‐5‐amino‐1__H__‐pyrazoles afforded new pyrazole[1,5‐__a__]pyrimidines structurally related to Zaleplon. The chemical modifications introduced at the 3‐, 5‐, and 7
## Abstract **Dedicated to Dr. János Császár on the occasion of his 70^th^ birthday** Ring transformation of 2‐cyanoimido‐3‐methyl‐1,3‐oxazolidine (**10**) yielded 5‐amino‐3‐[__N__‐(2‐hydrox‐yethyl)‐__N__‐methyl]amino‐1__H__‐1,2,4‐triazole (**6**) that was ring closed with different β‐keto esters
## Abstract magnified image __E__‐3‐(__N,N__‐Dimethylamino)‐1‐(3‐methylthiazolo[3,2‐__a__]benzimidazol‐2‐yl)prop‐2‐en‐1‐one (**2**) was synthesized by the reaction of 1‐(3‐methylthiazolo[3,2‐__a__]benzimidazol‐2‐yl)ethanone (**1**) with dimethylformamide‐dimethylacetal. The reaction of **2** with