ONE POT SYNTHESIS, OF 2(1H)-QUINAZOLINONE DERIVATIVES
Abd El-Samii, Z. (1997). ONE POT SYNTHESIS, OF 2(1H)-QUINAZOLINONE DERIVATIVES. EKB Journal Management System, 6(1), 21-25. doi: 10.21608/zjps.1997.184950
Zakaria Abd El-Samii. "ONE POT SYNTHESIS, OF 2(1H)-QUINAZOLINONE DERIVATIVES". EKB Journal Management System, 6, 1, 1997, 21-25. doi: 10.21608/zjps.1997.184950
Abd El-Samii, Z. (1997). 'ONE POT SYNTHESIS, OF 2(1H)-QUINAZOLINONE DERIVATIVES', EKB Journal Management System, 6(1), pp. 21-25. doi: 10.21608/zjps.1997.184950
Abd El-Samii, Z. ONE POT SYNTHESIS, OF 2(1H)-QUINAZOLINONE DERIVATIVES. EKB Journal Management System, 1997; 6(1): 21-25. doi: 10.21608/zjps.1997.184950

ONE POT SYNTHESIS, OF 2(1H)-QUINAZOLINONE DERIVATIVES

Zagazig Journal of Pharmaceutical Sciences
Article 4, Volume 6, Issue 1, June 1997, Pages 21-25    PDF (3.74 M)
Document Type: Original Article
DOI: 10.21608/zjps.1997.184950
Author
Zakaria Abd El-Samii*
Department of Organic Pharmaceutical Chemistry, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt
Abstract
Condensation of (3-methoxyphenyl)urea or guanidine derivatives (la-e) with a variety of acyl chlorides in polyphosphoric acid leads to intramolecular cyclization with formation of the title compounds (2a-j). Attempted one pot preparation of new tricyclic pyrrolo [3,2,1-ij]-2(2H)-quinazolinone derivatives (3) using (1f) carboxamidoindoline (1f) and acyl chlorides were carried out.
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