Skip to content
Research Article Open access CC BY 4.0

Regioselectivity in the Multicomponent Reaction of 5-aminopyrazoles, Meldrum’s Acid and Triethyl Orthoformate

Afaf M. Abdel Hameed, Ahmed Moukhtar Nour-Eldin, Michael Magdy Ibrahim, Kamal Usef Sadek

Chemical Science International Journal · pp. 1–5 · Published 29 Jun 2015

10.9734/ACSJ/2015/18903

Abstract

A regioselective multicomponent synthesis of pyrazolo[1,5-a]pyrimdines-7(4H)-ones 5 is  reported.  The  reaction  proceeded regioselectively via initial Michael addition of exocyclic amino function to the intermediately formed 5-ethoxymethylene Meldrum’s acid followed by a ring opening of Meldrum’s acid and subsequent ring closure with the ring nitrogen. The regioselectivity of the reaction was confirmed by the isolation and characterization of the Michael adduct.  

Multicomponent reactions regioselectivity pyrazolo [1 5-a] pyrimdines

Cited by 2

Recent Developments in the Synthesis of Bicyclic Condensed Pyrimidinones

Rayees Ahmad Naikoo, Rupesh Kumar, Vipan Kumar · Current Organic Chemistry · 2022

Article metrics

Real usage data collected on this platform.

0

Page views

0

PDF downloads

0

Outbound clicks

2

Citations

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

No views recorded yet.

Traffic sources

Referring site, by host.

No traffic recorded yet.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.