𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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


Synthesis of a new series of pyrazolo[1,
✍ Pier Giovanni Baraldi; Francesca Fruttarolo; Mojgan Aghazadeh Tabrizi; Romeo Rom 📂 Article 📅 2007 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 371 KB

## 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

On triazoles XLIV [1]. synthesis of new
✍ Gábor Berecz; József Reiter; Gyula Argay; Alajos Kálmán 📂 Article 📅 2002 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 85 KB

## 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

Synthesis of some novel pyrazolo[1,5-a]p
✍ Hatem A. Abdel-Aziz; Nehal A. Hamdy; Issa M. I. Fakhr; Ahmad M. Farag 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 407 KB

## 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